Comprar Egibren (Eldepryl) Sin Receta, Egibren

compra Egibren (Eldepryl) en linea sin receta

Egibren (Eldepryl) Explicacion

Egibren es realmente un medicamento que detiene la ruptura real hacia abajo de la sustancia quimica dentro de su mente.

Egibren se utiliza para tratar la enfermedad de Parkinson.

Egibren tambien puede ser referido como selegilina.

Egibren detiene la ruptura real hacia abajo de la sustancia quimica dentro de tu mente conocido como la dopamina, por lo tanto, se detiene la enfermedad de Parkinson.

titulo general asociada con Egibren es en realidad selegilina.

Marcas asociadas con Egibren tienden a ser Egibren, Zelapar.

Egibren (Eldepryl) Dosis

Egibren viene en:

material de friccion dosis regular 5mg

Obtener Egibren por via oral.

Obtener tabletas Egibren dos veces al dia, en la hora del desayuno, asi como la hora del almuerzo.

Por lo general, no consumen la totalidad de la pildora real. Deje que se descomponen en sus dientes sin tener mordisqueo.

Por lo general no consumen o incluso consumir nada en absoluto nada menos que un minuto despues takink Egibren.

Cuando use Egibren, usted no debe consumir las comidas que estan llenos de tiramina por ejemplo secado por aire, la carne o la carne mas vieja incluso fermentado, pollo o incluso salami (que incluye cacciatore y mortadella), sardinas en escabeche. asi como cualquier tipo de ruinas o incluso guardado incorrectamente carne, pollo, mariscos, o incluso de organos del higado; cerveza ligera del grifo, cerveza ligera que no ha sido pasteurizada ya realmente; queso viejo, como el azul brillante, Boursault, paquete, brie, camembert, queso cheddar, queso emmenthal, gruyere, parmesano, pontificio, roquefort, stilton, asi como suiza; chucrut, los granos de cafe de coco, especias coco, queso de soja, sopas de miso, pulsa la cuajada, los granos de cafe fava; componentes candida (por ejemplo porque Marmite).

Las comidas mas adecuadas a lo largo de la utilizacion Egibren tienden a ser refrescante carnes, pollo, o incluso mariscos (incluyendo carnes hora del almuerzo, los caninos muy calientes, pollo la hora del desayuno, asi como preparados rellenos de jamon); cualquier tipo de verduras que no sean de ancho legumbres vainas (habas); queso parmesano preparado, mozzarella, ricotta, queso cottage (especialmente bajo o sin grasa); pizzas hechas de queso bajo en tiramina; lacteos coco, yogur sin grasa.

Si usted desea lograr mejores resultados por lo general no dejar de usar Egibren, de repente.

Egibren (Eldepryl) Careciendo asocia con dosis

Por lo general, no reciben doble dosis. En caso de que salte la dosis que necesita para llevar una vez se tiene en cuenta en lo que respecta a su deficiente. Cuando es hora de la dosis que necesita para llevar a cabo su propia rutina de dosificacion normal.

Egibren (Eldepryl)

En el caso de una sobredosis Egibren y que tambien se evita gran usted necesita comprobar hacia fuera su medico o incluso el medico de inmediato. Asociado con Egibren sobredosis: dolor de cabeza grave, alucinaciones, problemas de vision, la transpiracion, impresionante o incluso los poros y la piel sudorosa, rapida o incluso ritmo cardiaco desigual, sensacion de mareo, desmayos, convulsiones.

Egibren (Eldepryl) Espacio de almacenamiento

Tienda en temperaturas de espacio entre 10 y 30 niveles de D (59, asi como ochenta y seis niveles F) de humedad, asi como la temperatura. Fortalecer cualquier tipo de medicamento sin tocar a partir del dia de vencimiento. Mantener desde el lograr de los ninos.

Egibren (Eldepryl) Efectos negativos

Egibren ofrece los efectos negativos. El mas tipico tienden a ser:

material de friccion fatiga

un poco de material de friccion debilidad

material de friccion insomnio

nasal o material de friccion zona nasal incluso tapada

friccion material de dolor de espalda baja

material de friccion congestion

Mucho menos tipicos y graves efectos negativos en todo usando Egibren:

respuestas reaccion alergica (urticaria, inhalando y exhalando, cuestiones de alergia, asi como la erupcion) material de friccion

material de friccion dolor de cabeza inesperado y grave

material de friccion confusio

material de friccion vision borrosa

problemas con hablar o material de friccion incluso la estabilidad

nauseas o vomitos material de friccion

vomitando material de friccion

material de friccion problemas del corazon

material de friccion provocacion

hormigueo inesperado o incluso un poco de material de friccion debilidad

desagradable o incluso hacer pipi duro material de friccion

espasmos musculares acciones de masas material de friccion

Los efectos negativos indicaciones se basan en medicamentos que podrian estar utilizando pero, ademas, se basan en su condicion de bienestar y otros aspectos .

Egibren (Eldepryl) Contraindicaciones

Por lo general no reciben Egibren si usted es sensible a fin de elementos Egibren.

Por lo general no reciben Egibren en caso de que se espera, va a conseguir la lactancia materna embarazada o impar.

Tenga cuidado con la utilizacion de Egibren para aquellos que tienen enfermedad renal, enfermedades del higado, problemas de corazon, mas alto o incluso disminuir la presion arterial baja, problemas de convulsiones.

Tenga cuidado con la utilizacion de Egibren para medicamentos de venta libre que usted utiliza, tales como vitaminas, nutrientes, asi como los elementos naturales, carbamazepina (Tegretol), pastillas para bajar de peso o medicamentos incluso frias que contienen efedrina, pseudoefedrina o incluso fenilefrina. nafcilina (Unipen), fenobarbital (Luminal, Solfoton), rifampicina (Rifadin, Rifater, Rifamate, Rimactane), antidepresivos, por ejemplo, amitriptilina (Elavil), amoxapina (Ascendin), bupropion (Wellbutrin, Zyban), citalopram (Celexa), clomipramina (Anafranil), desipramina (Norpramin), doxepina (Sinequan), duloxetina (Cymbalta), escitalopram (Lexapro), fluoxetina (Prozac), fluvoxamina (Luvox), imipramina (Tofranil), nortriptilina (Pamelor), paroxetina (Paxil), protriptilina (Vivactil), sertralina (Zoloft), la venlafaxina (Effexor), o incluso trimipramina (Surmontil).

Cuando use Egibren, usted no debe consumir las comidas que estan llenos de tyraminesuch porque secado por aire, la carne mas vieja o incluso fermentados de carne, pollo o incluso salami (que incluye cacciatore y mortadella), sardinas en escabeche, asi como cualquier tipo de ruinas o incluso guardado incorrectamente carne, pollo, mariscos, o incluso de organos del higado; cerveza ligera del grifo, cerveza ligera que no ha sido pasteurizada ya realmente; queso viejo, como el azul brillante, Boursault, paquete, brie, camembert, queso cheddar, queso emmenthal, gruyere, parmesano, pontificio, roquefort, stilton, asi como suiza; chucrut, los granos de cafe de coco, especias coco, queso de soja, sopas de miso, pulsa la cuajada, los granos de cafe fava; componentes candida (por ejemplo porque Marmite).

Por lo general no reciben Egibren si usted esta usando suplementos dieteticos de venta libre o incluso tos, asi como medicamentos de frio que contienen tiramina.

Puede ser danino para evitar el uso de Egibren, de repente.

Egibren (Eldepryl) Preguntas comunes

Queen: ?Que es exactamente Egibren?

El: Egibren es realmente un medicamento que detiene la ruptura real hacia abajo de la sustancia quimica dentro de su mind. a

Queen: Exactamente lo Egibren se utiliza en relacion con?

El: Egibren se utiliza para hacer frente a illness. A de Parkinson

Queen: Entonces, ?como exactamente hace funcion Egibren?

El: Egibren detiene la ruptura real hacia abajo de la sustancia quimica dentro de tu mente conocido como la dopamina, por lo tanto, deja de illness. A de Parkinson

Queen: Exactamente ?que debo FAG situacion asociada con la dosis falta?

El: En el caso de la dosis carente de lo necesario para el fin de la pildora tan pronto como sea posible. Por lo general, no reciben doble dosis. Y cuando lo que realmente es el tiempo mas afortunado para la dosis que necesita para llevar a cabo su propia rutina normal asociada con el general Eldepyl using. A

Queen: ?Cuales son la restriccion de las comidas, mientras que la utilizacion Egibren?

El: Al usar Egibren, usted no debe consumir las comidas que estan llenos de tiramina por ejemplo secado por aire, la carne o la carne mas vieja incluso fermentado, pollo o incluso salami (que incluye cacciatore y mortadella), sardinas en escabeche, asi como cualquier tipo de ruinas o incluso guardado incorrectamente carne, pollo, mariscos, o incluso de organos del higado; cerveza ligera del grifo, cerveza ligera que no ha sido pasteurizada ya realmente; queso viejo, como el azul brillante, Boursault, paquete, brie, camembert, queso cheddar, queso emmenthal, gruyere, parmesano, pontificio, roquefort, stilton, asi como suiza; chucrut, los granos de cafe de coco, especias coco, queso de soja, sopas de miso, pulsa la cuajada, los granos de cafe fava; componentes candida (por ejemplo porque Marmite).A

Queen: ?Cuales son los sintomas de la alergia sobre Egibren?

El: sintomas sobre Egibren alergia: urticaria; problemas para inhalar y exhalar; inflamacion del encuentro, zona de los labios, lengua o incluso tonsils. A

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Finol V, Finol

FINOL v. FINOL

Enrique A. FINOL, Petitioner, v. Carmen FINOL, Respondent.

No. 4D03-4909.

Decided: March 31, 2004

H. T. Maloney of Patterson & Maloney, Ft. Lauderdale, for petitioner. Michael A. Hymowitz of the Law Offices of Braverman and Rossi, Ft. Lauderdale, for respondent.

Petitioner husband seeks certiorari review of a trial court order allowing discovery of his attorney's fee retainer agreements and billing and payment records. He contends they are protected by the attorney/client privilege and apparently assumes, without citing any authority, that billing information in and of itself is not discoverable.

If this billing information contained descriptions of services rendered which would reveal the mental impressions and opinions of counsel, that information should be redacted as privileged, Old Holdings, Ltd. v. Taplin, Howard, Shaw & Miller, P. A. 584 So.2d 1128 (Fla. 4th DCA 1991); however, the remaining information is not privileged and therefore discoverable.

This court has recently allowed discovery of defense counsel's billing records because they were relevant to plaintiff's claim for prevailing party attorney's fees. Brown Distrib. Co. of West Palm Beach v. Marcel, 866 So.2d 160 (Fla. 4th DCA 2004). In this case it is relevant to the issue of alimony, child support, equitable distribution, and attorney's fees. The petition for certiorari is therefore dismissed for lack of jurisdiction.

GUNTHER and WARNER, JJ. concur.

Tetracycline - Fda Prescribing Information, Side Effects And Uses, Tetraciclina

Tetracycline

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Tetracycline hydrochloride and other antibacterial drugs, Tetracycline hydrochloride should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

Tetracycline Description

Tetracycline is a yellow, odorless, crystalline powder. Tetracycline is stable in air but exposure to strong sunlight causes it to darken. Its potency is affected in solutions of pH below 2 and is rapidly destroyed by alkali hydroxide solutions. Tetracycline is very slightly soluble in water, freely soluble in dilute acid and in alkali hydroxide solutions, sparingly soluble in alcohol, and practically insoluble in chloroform and in ether. The chemical name for Tetracycline hydrochloride is 4 - (Dimethylamino)1,4,4a,5,5a,6,11,12a - octahydro - 3,6,10,12, - 12a - pentahydroxy - 6 - methyl - 1,11 - dioxo2 - naphthacenecar - boxamide monohydrochloride.

Each capsule, for oral administration, contains Tetracycline hydrochloride USP, 250 mg or 500 mg.

Inactive Ingredients: Lactose, magnesium stearate, and sodium lauryl sulfate.

The 250 mg capsule shell contains D&C yellow no. 10, FD&C yellow no. 6, gelatin, sodium lauryl sulfate, and titanium dioxide. It may also contain benzyl alcohol, butylparaben, D&C red no. 22, edetate calcium disodium, methylparaben, propylparaben, silicon dioxide, and sodium propionate.

The imprinting ink for the 250 mg capsule contains pharmaceutical glaze, and synthetic black iron oxide. It may also contain D&C yellow no. 10 (aluminum lake), dimethylpolysiloxane, distilled water, ethylene glycol monoethyl ether, FD&C blue no. 1 (aluminum lake), FD&C blue no. 2 (aluminum lake), FD&C red no. 40 (aluminum lake), lecithin, n-butyl alcohol, propylene alcohol, and SDA-3A alcohol.

The 500 mg capsule shell contains D&C yellow no. 10, FD&C blue no.1, FD&C red no. 40, gelatin, sodium lauryl sulfate, and titanium dioxide. It may also contain benzyl alcohol, butylparaben, edetate calcium disodium, FD&C yellow no. 6, methylparaben, propylparaben, silicon dioxide, and sodium propionate.

The imprinting ink for the 500 mg capsule contains titanium dioxide. It may also contain dimethyl polysiloxane, distilled water, ethyl alcohol, ethylene glycol monoethyl ether, pharmaceutical glaze, pharmaceutical shellac, and soya lecithin.

Its structural formula is as follows:

CLINICAL PHARMACOLOGY

Tetracyclines are readily absorbed and are bound to plasma proteins in varying degrees. They are concentrated by the liver in the bile and excreted in the urine and feces at high concentrations in a biologically active form.

Microbiology

Tetracyclines are primarily bacteriostatic and exert their antimicrobial effect by the inhibition of protein synthesis. Tetracycline is active against a wide range of gram-negative and gram-positive organisms. The drugs in the Tetracycline class have closely similar antimicrobial spectra, and cross-resistance among them is common.

While in vitro studies have demonstrated the susceptibility of most strains of the following microorganisms, clinical efficacy for infections other than those included in the INDICATIONS AND USAGE section has not been documented.

Gram-negative Bacteria

Neisseria gonorrhoeae Haemophilus ducreyi Haemophilus influenzae Yersinia pestis (formerly Pasteurella pestis) Francisella tularensis (formerly Pasteurella tularensis) Vibrio cholera (formerly Vibrio comma) Bartonella bacilliformis Brucella species

Because many strains of the following groups of gram-negative microorganisms have been shown to be resistant to Tetracyclines, culture and susceptibility testing are recommended:

Escherichia coli Klebsiella species Enterobacter aerogenes Shigella species Acinetobacter species (formerly Mima species and Herellea species) Bacteroides species

Gram-positive Bacteria

Because many strains of the following groups of gram-positive microorganisms have been shown to be resistant to Tetracycline, culture and susceptibility testing are recommended. Up to 44 percent of strains of Streptococcus pyogenes and 74 percent of Streptococcus faecalis have been found to be resistant to Tetracycline drugs. Therefore, Tetracyclines should not be used for streptococcal disease unless the organisms have been demonstrated to be susceptible.

Streptococcus pyogenes Streptococcus pneumoniae Enterococcus group (Streptococcus faecalis and Streptococcus faecium) Alpha-hemolytic Streptococci (viridans group)

Other microorganisms

Chlamydia psittaci Chlamydia trachomatis Ureaplasma urealyticum Borrelia recurrentis Treponema pallidum Treponema pertenue Clostridia species Fusobacterium fusiforme Actinomyces species Bacillus anthraxis Propionibacterium acnes Entamoeba species Balantidium coli

Susceptibility Testing

Quantitative methods are used to determine antimicrobial minimal inhibitory concentrations (MICs). These MICs provide estimates of the susceptibility of bacteria to antimicrobial compounds. The MICs should be determined using a standardized procedure. Standardized procedures are based on a dilution method (Ref1, Ref3, Ref4) (broth or agar) or equivalent with standardized inoculum concentrations and standardized concentrations of Tetracycline powder. The MIC values should be interpreted according to the following criteria:

For testing Enterobacteriaceae, Acinetobacter species, Staphylococcus spp. Enterococcus spp. and Vibrio cholerae :

A report of “Susceptible” indicates that the pathogen is likely to be inhibited if the antimicrobial compound in the blood reaches the concentrations usually achievable. A report of “Intermediate” indicates that the result should be considered equivocal, and, if the microorganism is not fully susceptible to alternative, clinically feasible drugs, the test should be repeated. This category implies possible clinical applicability in body sites where the drug is physiologically concentrated or in situations where high dosage of drug can be used. This category also provides a buffer zone which prevents small uncontrolled technical factors from causing major discrepancies in interpretation. A report of “Resistant” indicates that the pathogen is not likely to be inhibited if the antimicrobial compound in the blood reaches the concentrations usually achievable; other therapy should be selected.

Standardized susceptibility test procedures require the use of laboratory control microorganisms to control the technical aspects of the laboratory procedures. Standard Tetracycline powder should provide the following MIC values:

MIC Range (mcg/mL)

Escherichia coli ATCC 25922

Enterococcus faecalis ATCC 29212

Staphylococcus aureus ATCC 29213

Pseudomonas aeruginosa ATCC 27853

Haemophilus influenzae ATCC 49247

Streptococcus pneumoniae ATCC 49619

Neisseria gonorrhoeae ATCC 49226

Quantitative methods that require measurement of zone diameters also provide reproducible estimates of the susceptibility of bacteria to antimicrobial compounds. One such standardized procedure ( Ref2, Ref3, Ref4 ), uses paper disks impregnated with 30 mcg Tetracycline to test the susceptibility of microorganisms to Tetracycline.

Reports from the laboratory providing results of the standard single-disk susceptibility test with a 30 mcg Tetracycline disk should be interpreted according to the following criteria:

For testing Enterobacteriaceae, Acinetobacter spp. and Vibrio cholera:

Zone Diameter (mm)

These interpretative standards are applicable only to disk diffusion testing using Mueller-Hinton agar adjusted with 5% sheep blood and a 30 mcg Tetracycline disk.

As with standardized dilution techniques, diffusion methods require the use of laboratory control microorganisms that are used to control the technical aspects of the laboratory procedures. For the diffusion technique, the 30 mcg Tetracycline disk should provide the following zone diameters in these laboratory test quality control strains:

Zone Diameter Range (mm)

Escherichia coli ATCC 25922

Staphylococcus aureus ATCC 25923

Haemophilus influenzae ATCC 49247

Neisseria gonorrhoeae ATCC 49226

Streptococcus pneumoniae ATCC 49619

INDICATIONS AND USAGE

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Tetracycline hydrochloride capsules USP and other antibacterial drugs, Tetracycline hydrochloride capsules USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Tetracycline hydrochloride, USP is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the conditions listed below:

Upper respiratory tract infections caused by Streptococcus pyogenes. Streptococcus pneumoniae and Haemophilus influenzae. Note: Tetracycline should not be used for streptococcal disease unless the organism has been demonstrated to be susceptible.

Lower respiratory tract infections caused by Streptococcus pyogenes. Streptococcus pneumoniae. Mycoplasma pneumoniae (Eaton agent, and Klebsiella sp.)

Skin and soft tissue infections caused by Streptococcus pyogenes. Staphylococcus aureus . (Tetracyclines are not the drugs of choice in the treatment of any type of staphylococcal infections.)

Infections caused by rickettsia including Rocky Mountain spotted fever, typhus group infections, Q fever, rickettsialpox.

Psittacosis or ornithosis caused by Chlamydia P sittaci .

Infections caused by Chlamydia trachomatis such as uncomplicated urethral, endocervical, or rectal infections, inclusion conjunctivitis, trachoma and lymphogranuloma venereum.

Granuloma inquinale caused by Calymmatobacterium granulomatis .

Relapsing fever caused by Borrelia sp.

Bartonellosis caused by Bartonella bacilli formis .

Chancroid caused by Haemophilus ducreyi .

Tularemia caused by Francisella tularensis .

Plaque caused by Yersinia pestis .

Cholera caused by Vibrio cholerae .

Brucellosis caused by Brucella species (Tetracycline may be used in conjunction with an aminoglycoside).

Infections due to Campylobacter fetus .

As adjunctive therapy in intestinal amebiasis caused by Entamoeba histolytica .

Urinary tract infections caused by susceptible strains of Escherichia coli. Klebsiella. etc.

Other infections caused by susceptible gram-negative organisms such as E. coli. Enterobacter aerogenes, Shigella sp. Acinetobacter sp. Klebsiella sp. and Bacteroides sp.

In severe acne, adjunctive therapy with Tetracycline may be useful.

When penicillin is contraindicated, Tetracyclines are alternative drugs in the treatment of the following infections:

Syphilis and yaws caused by Treponema pallidum and pertenue. respectively,

Vincent’s infection caused by Fuso bacterium fusiforme ,

Infections caused by Neisseria gonorrhoeae ,

Anthrax caused by Bacillus anthracis ,

Infections due to Listeria monocytogenes ,

Actinomycosis caused by Actinomyces species,

Infections due to Clostridium species.

Contraindications

This drug is contraindicated in persons who have shown hypersensitivity to any of the Tetracyclines.

Warnings

THE USE OF DRUGS OF THE Tetracycline CLASS DURING TOOTH DEVELOPMENT (LAST HALF OF PREGNANCY, INFANCY AND CHILDHOOD TO THE AGE OF 8 YEARS) MAY CAUSE PERMANENT DISCOLORATION OF THE TEETH (YELLOW-GRAY-BROWN). This adverse reaction is more common during long-term use of the drugs but has been observed following repeated short-term courses. Enamel hypoplasia has also been reported. Tetracycline DRUGS, THEREFORE, SHOULD NOT BE USED IN THIS AGE GROUP UNLESS OTHER DRUGS ARE NOT LIKELY TO BE EFFECTIVE OR ARE CONTRAINDICATED.

All Tetracyclines form a stable calcium complex in any bone forming tissue. A decrease in fibula growth rate has been observed in premature infants given oral Tetracycline in doses of 25 mg/kg every six hours. This reaction was shown to be reversible when the drug was discontinued.

Results of animal studies indicate that Tetracyclines cross the placenta, are found in fetal tissues and can have toxic effects on the developing fetus (often related to retardation of skeletal development). Evidence of embryotoxicity has also been noted in animals treated early in pregnancy. If this drug is used during pregnancy or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus. Tetracycline drugs should not be used during pregnancy unless absolutely necessary.

If renal impairment exists, even usual oral or parenteral doses may lead to excessive systemic accumulation of the drug and possible liver toxicity. Under such conditions, lower than usual total doses are indicated, and, if therapy is prolonged, serum level determinations of the drug may be advisable.

Photosensitivity manifested by an exaggerated sunburn reaction has been observed in some individuals taking Tetracyclines. Patients apt to be exposed to direct sunlight or ultraviolet light should be advised that this reaction can occur with Tetracycline drugs. Treatment should be discontinued at the first evidence of skin erythema.

The antianabolic action of the Tetracyclines may cause an increase in BUN. While this is not a problem in those with normal renal function, in patients with significantly impaired renal function, higher serum levels of Tetracycline may lead to azotemia, hyperphosphatemia and acidosis.

PRECAUTIONS

General

As with other antibiotics, use of this drug may result in overgrowth of nonsusceptible organisms, including fungi. If superinfection occurs, the antibiotic should be discontinued and appropriate therapy should be instituted.

All infections due to Group A beta - hemolytic streptococci should be treated for at least ten days.

Bulging fontanels in infants and benign intracranial hypertension in adults have been reported in individuals receiving Tetracyclines. These conditions disappeared when the drug was discontinued.

Incision and drainage or other surgical procedures should be performed in conjunction with antibiotic therapy, when indicated.

Prescribing Tetracycline in the absence of proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

Information for Patients

Patients should be counseled that antibacterial drugs including Tetracycline should only be used to treat bacterial infections. They do not treat viral infections (e. g. the common cold). When Tetracycline is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by Tetracycline or other antibacterial drugs in the future.

Laboratory Tests

In venereal diseases, when coexistent syphilis is suspected, dark field examinations should be done before treatment is started and the blood serology repeated monthly for at least four months.

In long-term therapy, periodic laboratory evaluation of organ systems, including hematopoietic, renal and hepatic studies, should be performed.

Drug Interactions

Since bacteriostatic drugs may interfere with the bactericidal action of penicillin, it is advisable to avoid giving Tetracycline in conjunction with penicillin or other bactericidal antibiotics.

Because the Tetracyclines have been shown to depress plasma prothrombin activity, patients who are on anticoagulant therapy may require downward adjustment of their anticoagulant dosage.

The concurrent use of Tetracycline and methoxyflurane has been reported to result in fatal renal toxicity.

Absorption of Tetracyclines is impaired by antacids containing aluminum, calcium or magnesium and preparations containing iron, zinc, or sodium bicarbonate.

Concurrent use of Tetracycline may render oral contraceptives less effective.

Carcinogenesis, Mutagenesis, Impairment of Fertility

Long-term animal studies are currently being conducted to determine whether Tetracycline hydrochloride has carcinogenic potential.

Some related antibiotics (oxyTetracycline, minocycline) have shown evidence of oncogenic activity in rats.

In two in vitro mammalian cell assay systems (L 51784y mouse lymphoma and Chinese hamster lung cells), there was evidence of mutagenicity at Tetracycline hydrochloride concentrations of 60 and 10 mcg/mL, respectively.

Tetracycline hydrochloride had no effect on fertility when administered in the diet to male and female rats at a daily intake of 25 times the human dose.

Pregnancy

Pregnant women with renal disease may be more prone to develop Tetracycline-associated liver failure.

Labor and Delivery

The effect of Tetracyclines on labor and delivery is unknown.

Nursing Mothers

Because of the potential for serious adverse reaction in nursing infants from Tetracyclines, a decision should be made whether to discontinue the drug, taking into account the importance of the drug to the mother (see WARNINGS ).

Pediatric Use

ADVERSE REACTIONS

Gastrointestinal:

anorexia, nausea, epigastric distress, vomiting, diarrhea, glossitis, black hairy tongue, dysphagia, enterocolitis, and inflammatory lesions (with monilial overgrowth) in the anogenital region.

Rare instances of esophagitis and esophageal ulceration have been reported in patients receiving particularly the capsule and also the tablet forms of Tetracyclines. Most of the patients were reported to have taken medication immediately before going to bed (see DOSAGE AND ADMINISTRATION ).

Teeth:

permanent discoloration of teeth may be caused during tooth development. Enamel hypoplasia has also been reported (see WARNINGS ).

Skin:

maculopapular and erythematous rashes. Exfoliative dermatitis has been reported but is uncommon. Onycholysis and discoloration of the nails have been reported rarely. Photosensitivity is discussed in WARNINGS .

Renal toxicity:

rise in BUN has been reported and is apparently dose related.

Liver:

hepatotoxicity and liver failure have been observed in patients receiving large doses of Tetracycline and in Tetracycline-treated patients with renal impairment.

Hypersensitivity reactions:

urticaria, angioneurotic edema, anaphylaxis, anaphylactoid purpura, pericarditis, exacerbation of systemic lupus erythematosus, and serum sickness-like reactions, as fever, rash, and arthralgia.

Blood:

hemolytic anemia, thrombocytopenia, thrombocytopenic purpura, neutropenia and eosinophilia have been reported.

Other:

bulging fontanels in infants and intracranial pressure in adults (see PRECAUTIONS, General ).

When given over prolonged periods, Tetracyclines have been reported to produce brown-black microscopic discoloration of thyroid glands. No abnormalities of thyroid function studies are known to occur.

To report SUSPECTED ADVERSE EVENTS, contact Actavis at 1-800-272-5525 or FDA at 1-800-FDA - 1088 or h ttp://www. fda. gov/ for voluntary reporting of adverse reactions.

Overdosage

In case of overdosage, discontinue medication, treat symptomatically and institute supportive measures. Tetracycline is not dialyzable.

Tetracycline Dosage and Administration

Adults

Usual daily dose, 1 gram as 500 mg twice daily or 250 mg four times a day. Higher doses such as 500 mg four times a day may be required for severe infections or for those infections which do not respond to the smaller doses

Children above eight years of age

Usual daily dose, 10 to 20 mg/lb (25 to 50 mg/kg) body weight divided in four equal doses.

Therapy should be continued for at least 24 to 48 hours after symptoms and fever have subsided.

For treatment of brucellosis, 500 mg Tetracycline four times a day for three weeks should be accompanied by streptomycin, 1 gram intramuscularly twice daily the first week and once daily the second week.

For the treatment of syphilis in patients allergic to penicillin, the following dosage of Tetracycline is recommended: early syphilis (less than one year’s duration), 500 mg four times a day for 15 days. Syphilis of more than one year’s duration (except neurosyphilis), 500 mg four times a day for 30 days.

For treatment of gonorrhea, the recommended dose is 500 mg by mouth four times a day for seven days.

In cases of moderate to severe acne which, in the judgement of the clinician, require long-term treatment, the recommended initial dosage is 1 gram daily in divided doses. When improvement is noted, dosage should be gradually reduced to maintenance levels ranging from 125 mg to 500 mg daily. In some patients it may be possible to maintain adequate remission of lesions with alternate day or intermittent therapy. Tetracycline therapy of acne should augment the other standard measures known to be of value. Duration of long-term treatment which can safely be recommended has not been established (see WARNINGS and Carcinogenesis, Mutagenesis , Impairment of Fertilit y ).

Concomitant therapy

Absorption of Tetracyclines is impaired by antacids containing aluminum, calcium or magnesium and preparations containing iron, zinc, or sodium bicarbonate.

Food and some dairy products also interfere with absorption.

In the treatment of streptococcal infections, a therapeutic dose of Tetracycline should be administered for at least ten days.

In patients with renal impairment (see WARNINGS ) total dosage should be decreased by reduction of recommended individual doses and/or by extending time intervals between doses.

Uncomplicated urethral, endocervical or rectal infections in adults caused by Chlamydia trachomatis. 500 mg, by mouth, four times a day for at least seven days.

Administration of adequate amounts of fluid with the capsule formulation of Tetracycline is recommended to wash down the drug and reduce the risk of esophageal irritation and ulceration (see ADVERSE REACTIONS ).

How is Tetracycline Supplied

Tetracycline Hydrochloride Capsules, USP are available as: 250 mg: Orange/yellow capsules, imprinted with “ WPI ” on cap and “ 2234 ” on body.

Available in bottles of:

100 NDC 0591-2474-01 1000 NDC 0591-2474-10

500 mg: Black/yellow capsules, imprinted with “ WPI ” on cap and “ 2235 ” on body.

Available in bottles of:

100 NDC 0591-2475-01 1000 NDC 0591-2475-10

Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).

Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

ANIMAL PHARMACOLOGY AND ANIMAL TOXICOLOGY

Hyperpigmentation of the thyroid has been produced by members of the Tetracycline class in the following species: in rats by oxyTetracycline, doxycycline, minocycline, Tetracycline PO4 and methacycline; in minipigs by doxycycline, minocycline, Tetracycline PO4 and methacycline; in dogs by doxycycline and minocycline; in monkeys by minocycline. Minocycline, Tetracycline PO4, methacycline, doxycycline, Tetracycline base, oxyTetracycline HCl and Tetracycline HCl were goitrogenic in rats fed a low iodine diet. This goitrogenic effect was accomplished by high radioactive iodine uptake. Administration of minocycline also produced a large goiter with high radioiodine uptake in rats fed a relatively high iodine diet. Treatment of various animal species with this class of drugs has also resulted in the induction of thyroid hyperplasia in the following: in rats and dogs (minocycline), in chickens (chlorTetracycline) and in rats and mice (oxyTetracycline). Adrenal gland hyperplasia has been observed in goats and rats treated with oxyTetracycline.

REFERENCES

1. Clinical and Laboratory Standards Institute (CLSI). Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically; Approved Standard - Ninth Edition. CLSI document M07-A9, Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA, 2012.

2. Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Disk Diffusion Susceptibility Tests; Approved Standard – Eleventh Edition. CLSI document M02-A11, Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA, 2012.

3. Clinical and Laboratory Standards Institute (CLSI). Methods for Antimicrobial Dilution and Disk Susceptibility Testing of Infrequently Isolated or Fastidious Bacteria; Approved Guideline – Second Edition. CLSI document M45-A, Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA, 2010.

4. Clinical and Laboratory Standards Institute (CLSI). Methods for Antimicrobial Susceptibility Testing of Anaerobic Bacteria; Approved Standard - Eight Edition. CLSI document M11-A8. Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, PA 19087 USA, 2012.

5. Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing; Twenty-third Informational Supplement. CLSI document M100-S23. CLSI document M100-S23, Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087, USA, 2013.

Manufactured by: Watson Pharma Private Limited Verna, Salcette Goa 403 722 INDIA

Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA

Revised: January 2016

PRINCIPAL DISPLAY PANEL

NDC 0591- 2474 -01 Tetracycline Hydrochloride Capsules, USP 250 mg 100 Capsules Rx Only

PRINCIPAL DISPLAY PANEL

NDC 0591- 2475 -01 Tetracycline Hydrochloride Capsules, USP 500 mg 100 Capsules Rx Only

Glucoryl Mv(2), Glucoryl

Glucoryl Mv(2)

Metformin Is Used In The Treatment Of Diabetes Mellitus, Insulin Resistance, And Obesity.

Mechanism of action of Metformin :

The Exact Mechanism Of Action Of Metformin Is Not Clear But It Appears To Act By Decreasing Glucose Absorption From The Intestine, Decreasing Production Of Glucose From Proteins And Fats In Liver, And Enhancing Insulin Sensitivity In Muscle By Increasing Glucose Uptake And Utilization.

Drug Interaction of Metformin :

Taking Metformin With Other Anti-diabetic Drugs May Lead To Excessive Lowering Of Bloodsugar. If You Go For An X-ray Or Scan, Do Not Take Metformin Before And At Least 48 Hours Afterwards. Metformin With Diuretics (furosemide), Anti-asthmatic Drugs Such As Salbutamol Or Terbutaline, Or Corticosteroids (prednisone) May Affect The Glucose Control. Always Consult Your Physician For The Change Of Dose Regimen Or An Alternative Drug Of Choice That May Strictly Be Required.

Side effects of Metformin :

The Common Side Effects Are Urge To Vomit, Vomiting, Diarrhea, Abdominal Pain, Loss Of Appetite, Malabsorption Of Vitamin B12, Taste Disturbance, And Altered Liver Functions. Also, The Patient May Have The Side Effects Of Lactic Acidosis (symptoms Are Vomiting, Abdominal Pain With Muscle Cramps, Not Feeling Well With Severe Tiredness, And Difficulty In Breathing), And Skin Reactions Such As Redness Of Skin, Itching, Hives (pale Red, Raised, Itchy Bumps Of Skin).

INTERACTIONS OF METFORMIN

How Metformin will impact on Pregnancy ?

Information Not Available.

To Reduce High Post Meal Glucose Level In Diabetes Mellitus In Patients Who Have Been Using Other Diabetic Medications.

Mechanism of action of Voglibose :

Voglibose Delays The Digestion And Absorption Of Carbohydrate In The Intestine By Inhibiting Intestinal Enzyme (alpha Glucosidase) Which Results In Reduction Of Increase In Blood Glucose Level After Meal.

Drug Interaction of Voglibose :

Voglibose When Used In Combination With Sulfonylamide, Sulfonylurea, Biguanide, Insulin, Atenolol, Aspirin, Symptoms Associated With Low Blood Sugar May Occur. It Also Interacts With Drugs Like Selegiline, Warfarin, Fenofibrate, Epinephrine And Thyroxine. Always Consult Your Physician For The Change Of Dose Regimen Or An Alternative Drug Of Choice That May Strictly Be Required.

Side effects of Voglibose :

Diarrhea, Loose Stools, Abdominal Pain, Constipation, Loss Of Appetite, Urge To Vomit (nausea),vomiting, Heartburn, Increased Gas, And Intestinal Obstruction Like Symptoms Due To Increased Intestinal Gas. Hypoglycemia, Delay In Digestion And Absorption Of Disaccharides, Fulminant Hepatitis, Serious Liver Dysfunction With Increased Liver Enzymes, Jaundice, Anemia, Numbness, Edema, Blurred Vision, Hot Flushes, Malaise, Weakness, Increased Potassium Levels, Hyperkalemia, Increased Pancreatic Enzyme (serum Amylase).

INTERACTIONS OF VOGLIBOSE

How Voglibose will impact on Pregnancy ?

Information Not Available.

Panzo, Panzo

Wine

Parties

General Information

Private dining at PAZO is perfect for business, social, or just for fun, we specialize in celebrations, presentations and more. PAZO is Baltimore's premier private event location for small intimate affairs to groups of 350. We welcome you to reserve one of our lounge seating areas, private rooms, or the entire restaurant for your next event.

Whether you're looking for a warm and inviting space or something on a grander scale, the management and service staff at PAZO are prepared to assist in creating events that provide wonderful memories of your special occasion or business affair. PAZO is open for dinner service seven days a week starting at 5pm through closing. For select occasions, we are pleased to accommodate breakfast meetings, luncheons and full restaurant buy-outs.

Click here to download a PDF of our private dining room options

When emailing, please consider including the following: your phone number, date of your event, number of guests, and any other information that can help us help you better! PRIVATE ROOMS PAZO offers two private rooms for your exclusive use. With built in plasma screens, the Avellino and Villa Rosa are perfect for business presentations, meetings and private events. Both spaces are located on the spectacular mezzanine at PAZO. LOUNGE & MAIN DINING AREA Enjoy the expansive and lively atmosphere at PAZO for business networking, social gatherings or a special night out.

Weddings

PAZO provides an extraordinary backdrop for weddings and commitment ceremonies for up to 350 guests. From your rehearsal dinner to vows to your reception, the romantic setting is perfect as you indulge in sophisticated southern Italian cuisine and an award-winning wine list. This unique venue features vaulted ceilings, rich jewel-toned décor, iron chandeliers, plush seating and a 500 square foot dance floor.

PAZO is delighted to work in partnership with Charm City Cakes. Owned by acclaimed Baltimore baker, Duff Goldman, Charm City Cakes creations are beautiful, challenging, and unique.

When emailing, please consider including the following: your phone number, date of your event, number of guests, and any other information that can help us help you better!

Menus

Upcoming Events

$5 Happy Hour

Enjoy a $5 menu of small platesand pizzas, plus $5 select drinks in the bar and lounge area.

Late Night Lounge

Just because the kitchen is closed, doesn't mean the drinks have to stop. Come in and enjoy a late night drink in our bar and lounge area.

View Full Site

Motrin - Pain Relief, Farsifen

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Motrin is used for treating rheumatoid arthritis, osteoarthritis, menstrual cramps, or mild to moderate pain. Motrin is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Motrin as directed by your doctor.

Take Motrin by mouth with or without food. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Motrin with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Motrin and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose. Go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about the proper use of Motrin .

Store Motrin at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Motrin out of the reach of children and away from pets.

Active Ingredient: Ibuprofen.

Do NOT use Motrin if:

you are allergic to any ingredient in Motrin

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Motrin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal product, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver disease, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, lupus, asthma, or growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders, bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you drink alcohol, or you have a history of alcohol abuse.

Some medicines may interact with Motrin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Probenecid because it may increase the risk of Motrin 's side effects

Cyclosporine, lithium, methotrexate, or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Motrin

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Motrin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Motrin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Motrin may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Motrin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Motrin. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Motrin with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Motrin has ibuprofen in it. Before you start any new medicine, check the label to see if it has ibuprofen in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Motrin unless your doctor tells you to.

Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be done to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

Use Motrin with caution in the elderly; they may be more sensitive to its effects, including stomach bleeding and kidney problems.

Motrin should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Motrin may cause harm to the fetus. Do not take it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Motrin while you are pregnant. It is not known if Motrin is found in breast milk. Do not breastfeed while taking Motrin .

All medicines can cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; gas; headache; heartburn; nausea; stomach pain or upset.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; stiff neck; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Amiodarone Uses, Dosage - Side Effects, Amiodarona

Amiodarone

What is amiodarone?

Amiodarone affects the rhythm of your heartbeats. It is used to help keep the heart beating normally in people with life-threatening heart rhythm disorders of the ventricles (the lower chambers of the heart that allow blood to flow out of the heart).

Amiodarone is for use only in treating life-threatening heart rhythm disorders. You will receive your first few doses in a hospital setting, where your heart rhythm can be monitored using an electrocardiograph or ECG (sometimes called an EKG).

Important information

Amiodarone is for use only in treating life-threatening heart rhythm disorders.

You should not take this medicine if you are allergic to amiodarone or iodine, or if you have a serious heart condition such as "AV block" (unless you have a pacemaker), a history of slow heart beats, or if your heart cannot pump blood properly.

This medicine can cause dangerous side effects on your liver or your lungs.

Call your doctor at once if you have: chest pain, trouble breathing, upper stomach pain, dark urine, jaundice (yellowing of the skin or eyes), or if you cough up blood.

Do not use amiodarone without telling your doctor if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

To be sure this medication is not causing harmful effects, your blood may need to be tested on a regular basis. Your thyroid and liver function may also need to be tested, and you may need eye exams and chest x-rays. Do not miss any scheduled appointments.

Before taking this medicine

You should not use this medicine if you are allergic to amiodarone or iodine, or if you have:

certain serious heart conditions, especially "AV block" (unless you have a pacemaker);

a history of slow heart beats that have caused you to faint; or

if your heart cannot pump blood properly.

Amiodarone can cause dangerous side effects on your heart, liver, lungs, or thyroid.

To make sure amiodarone is safe for you, tell your doctor if you have:

asthma or another lung disorder;

a thyroid disorder;

high or low blood pressure;

an electrolyte imbalance (such as low levels of potassium or magnesium in your blood); or

if you have a pacemaker or defibrillator implanted in your chest.

Do not use amiodarone if you are pregnant. Taking amiodarone during pregnancy can harm the unborn baby or cause thyroid problems or abnormal heartbeats after the baby is born. Amiodarone may also affect the child's growth or development (speech, movement, academic skills) later in life. Use effective birth control to prevent pregnancy during treatment.

Amiodarone can pass into breast milk and may harm a nursing baby. You should not breast-feed while using this medicine.

How should I take amiodarone?

Take amiodarone exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

If you have been taking another heart rhythm medicine, you may need to gradually stop taking it when you start using amiodarone. Follow your doctor's dosing instructions very carefully.

You may take this medicine with or without food, but take it the same way each time.

It may take up to 2 weeks before your heart rhythm improves. Keep using the medicine as directed even if you feel well.

While using amiodarone, you will need frequent medical tests and chest x-rays to check your thyroid, vision, lungs, and liver function. Amiodarone can have long lasting effects on your body. You may need medical tests for several months after you stop using this medicine.

If you need surgery (including laser eye surgery), tell the surgeon ahead of time that you are using amiodarone. You may need to stop using the medicine for a short time.

Amiodarone can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using this medicine.

Store at room temperature away from moisture, heat, and light.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of amiodarone can be fatal.

Overdose symptoms may include weakness, slow heart rate, feeling light-headed, or loss of consciousness.

What should I avoid while taking amiodarone?

Grapefruit and grapefruit juice may interact with amiodarone and lead to unwanted side effects. Avoid the use of grapefruit products while taking amiodarone.

Avoid exposure to sunlight or tanning beds. Amiodarone can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

This medicine may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Amiodarone side effects

Get emergency medical help if you have signs of an allergic reaction to amiodarone: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Amiodarone takes a long time to completely clear from your body. You may continue to have side effects after you stop using it. It could take up to several months for the medicine to completely clear from your body.

Call your doctor at once if you have any of these side effects, even if they occur up to several months after you stop using amiodarone:

wheezing, cough, chest pain, coughing up blood, breathing problems that get worse;

a new or a worsening irregular heartbeat pattern (fast, slow, or pounding heartbeats);

a light-headed feeling, like you might pass out;

blurred vision, vision loss, headache or pain behind your eyes, sometimes with vomiting;

liver problems--nausea, upper stomach pain, itching, tired feeling, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

signs of overactive thyroid--weight loss, thinning hair, feeling too hot or too cold, increased sweating, irregular menstrual periods, swelling in your neck (goiter); or

signs of underactive thyroid--extreme tired feeling, dry skin, joint pain or stiffness, muscle pain or weakness, hoarse voice, feeling more sensitive to cold temperatures, weight gain.

Common amiodarone side effects may include:

dizziness, vision problems, seeing halos around lights;

loss of coordination, feeling weak or tired;

nausea, vomiting, constipation;

numbness or tingling;

abnormal liver function tests.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Amiodarone dosing information

Usual Adult Dose for Arrhythmias:

Initial dose (IV): 1000 mg over the first 24 hours of therapy, delivered by the following infusion regimen: 150 mg over the first 10 minutes (15 mg/min), followed by 360 mg over the next 6 hours (1 mg/min). Maintenance infusion: 540 mg over the remaining 18 hours (0.5 mg/min).

Initial dose (PO): Loading doses of 800 to 1600 mg/day are required for 1 to 3 weeks (occasionally longer) until initial therapeutic response occurs. When adequate arrhythmia control is achieved, or if side effects become prominent, the dose should be reduced to 600 to 800 mg/day for one month and then to the maintenance dose, usually 400 mg/day. Some patients may require up to 600 mg/day. Amiodarone may be administered as a single daily dose, or in patients with severe gastrointestinal intolerance, as a twice daily dose.

Usual Pediatric Dose for Supraventricular Tachycardia:

less than 1 month: Limited data available: oral loading dose: 10 to 20 mg/kg/day orally in 2 divided doses for 7 to 10 days; dosage should then be reduced to 5 to 10 mg/kg/day once daily and continued for 2 to 7 months; this protocol was used in 50 infants (less than 9 months of age) and neonates (as young as 1 day of life); intravenous loading dose: 5 mg/kg given over 60 minutes; Note: Bolus infusion rates should generally not exceed 0.25 mg/kg/minute unless clinically indicated; most studies used bolus infusion time of 60 minutes to avoid hypotension; may repeat initial loading dose to a maximum total initial load: 10 mg/kg; do not exceed total daily bolus of 15 mg/kg/day.

less than 1 year: Initial dose: 600 to 800 mg/1.73 m?/day orally for 4 to 14 days given in 1 to 2 divided doses/day. Maintenance dose: 200 to 400 mg/1.73 m?/day orally given once a day.

greater than 1 year: Initial dose: 10 to 15 mg/kg/day orally for 4 to 14 days given in 1 to 2 divided doses/day. Maintenance dose: 5 to 10 mg/kg/day orally given once a day.

What other drugs will affect amiodarone?

Many drugs can interact with amiodarone. Not all possible interactions are listed here. Tell your doctor about all your current medicines and any you start or stop using, especially:

an antibiotic - azithromycin, ciprofloxacin, clarithromycin, erythromycin, levofloxacin, moxifloxacin, pentamidine, rifampin, and others;

an antidepressant - amitriptyline, citalopram, desipramine, doxepin, imipramine, nortriptyline, trazodone, and others;

a blood thinner - warfarin, Coumadin, Jantoven;

a diuretic or "water pill";

"statin" cholesterol medicine - atorvastatin, lovastatin, simvastatin, Lipitor, Zocor, Vytorin, and others;

heart or blood pressure medication - digoxin, disopyramide, dofetilide, flecainide, procainamide, propranolol, quinidine, sotalol, verapamil, and many others;

hepatitis C medication - ledipasvir, simeprevir, sofosbuvir, Harvoni, Olysio, Sovaldi;

HIV or AIDS medication - indinavir, nelfinavir, rilpivirine, ritonavir, saquinavir; or

medicine to treat mental illness - chlorpromazine, fluphenazine, haloperidol, lithium, pimozide, promethazine, thioridazine, ziprasidone, and others.

This list is not complete and many other drugs can interact with amiodarone. This includes prescription and over-the-counter medicines, vitamins, and herbal products. Give a list of all your medicines to any healthcare provider who treats you.

Amiodarone takes a long time to completely clear from your body, and drug interactions are possible for up to several months after you stop using amiodarone. Talk to your doctor before taking any medication during this time. Keep track of how long it has been since your last dose of amiodarone.

More about amiodarone

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your doctor or pharmacist can provide more information about amiodarone.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use amiodarone only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 6.03. Revision Date: 2016-05-16, 10:45:21 AM.

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Mirt - What Does Mirt Stand For The Free Dictionary, Mirt

Callers will be asked for brief details so a MIRT member can call them back at an agreed time.

The role of MIRT is to offer help, support and where appropriate, refer members of the public on to more specialist services.

Call MIRT via Hambleton/Richmondshire 01609 779999; Whitby/ Scarborough/Ryedale 01723 501555 or low cost 0845 9501555.

At a minimum, officials can envision chaotic situations at intersections with multiple MIRT equipped vehicles vying for signal control.

Lawmakers are responding by prohibiting interferences with traffic signals or the use of MIRTs by anyone other than emergency personnel.

The average survival rate of a myeloma patient used to be three years upon diagnosis; thanks to research funded in part by the National Cancer Institute (NCI), the MIRT has extended the average survival rate of its patients to seven years and beyond.

The study was funded by a project program grant from the NCI, which in 2004 announced its third five-year renewal -- for nearly $18 million -- of grant support for the MIRT .

A computer-generated "digital puppet" of Mario, known as MIRT (Mario in Real-Time), also delivered a special message to the children of the hospital.

Barlogie's efforts in research innovations, MIRT is one of the leading myeloma treatment centers worldwide.

MIRT (Mario In Real Time), a "virtual reality" computer

County + USC Pediatric Pavilion; -- Patients and their families; and -- Celebrity participants Photo Opportunities: -- Kirk Cameron and Chelsea Noble -- Jenna von Oy -- "Blossom" -- Candace Cameron, Mary Kate and Ashley Olsen -- "Full House" -- MIRT (Mario In Real Time), a "virtual reality" computer graphics Mario presentation.

Current Northrop equipment is exemplified by the MIRTS (Modular IR Transmitting Set), used on some examples of the A300, B-707, B-747, DC-8, DC-10, Mirage Fl, Northrop F-5, Falcon 20, C-130 and BAe 125.

Meclizine - Side Effects, Dosage, Interactions, Meclozine

Meclizine

Meclizine is the generic name for the prescription drug called Antivert and the over-the-counter (OTC) medicines known as Dramamine and Bonine. Meclizine is used to treat motion sickness and dizziness.

The drug belongs to a class of drugs called antihistamines, which are generally used to treat allergies. However, meclizine works a little differently, reducing nausea and muscle spasms.

Meclizine was originally approved by the Food and Drug Administration (FDA) in 1957 under the brand name Antivert, manufactured by Citron Pharmaceuticals.

The 'Meclizine High' and Abuse

Because meclizine causes drowsiness, there may be potential for abuse.

Dramamine comes in two versions with different active ingredients. There is more concern about abuse of the original version of Dramamine, because it contains the antihistamine dimenhydrinate, which can cause euphoria and hallucinations at high doses.

The other Dramamine contains meclizine and is referred to as the "less drowsy" version.

Meclizine Warnings

Meclizine can create or worsen problems for some people. You should talk to your doctor before taking meclizine if:

You have an allergy to meclizine or any of its ingredients

You take other medications that dull the nervous system

You are a person of advanced age

If you live where there is extremely hot weather

Before taking meclizine, you should talk to your doctor if you have any of the following conditions:

Poor kidney function

Poor liver function

Glaucoma or increased pressure between the eyes (intraocular pressure, or IOP)

Overactive thyroid

Heart disease

A breathing condition, such as asthma

Emphysema or chronic obstructive pulmonary disease (COPD)

Blockage in your stomach or intestines

Acid reflux or stomach ulcers

Trouble urinating or an enlarged prostate

Blockage in the neck of your bladder

You should not take meclizine if you are taking any of the following:

Sodium oxybate (Xyrem), used to treat narcolepsy and some kinds of muscle problems

Potassium drugs, including potassium phosphate (K Phos), chloride (Klor Con), or citrate (Urocit-K)

Pregnancy and Meclizine

Meclizine falls under the FDA's Pregnancy Category B, which means it has not been shown to harm a fetus.

Regardless, you should tell your doctor if you are pregnant or plan to become pregnant before taking this medication.

You should also alert your physician if you are breastfeeding or plan to breastfeed. It's recommended that breastfeeding mothers not take this medication.

Meclizine Side Effects

Common Side Effects of Meclizine

If you experience any of these more common side effects and they do not get better, or they become severe, tell your doctor or seek emergency medical attention:

Mild sleepiness

Mild headache

Stomach or digestive discomfort

Dry mouth, dry nose, and dry eyes

Serious Side Effects and Reactions

Tell your doctor right away or get emergency medical help if you experience any of the following symptoms:

A swollen tongue or a feeling like your throat is closing up

A severe rash or hives

Swelling or red eyes

Trouble breathing

Signs of abnormal bleeding caused by low blood-clotting cells, such as: easy bruising, red pin-prick spots on the skin, gums bleeding when you brush your teeth

Irregular heartbeat (arrhythmia)

Seizures

Abnormal changes in mental state or behavior, personality changes, hallucinations, or delusions (psychosis)

Heat stroke

You should get medical attention if any of the following occur as well:

Excessive sleepiness

Dizziness

Poor coordination

Unusual excitement or nervousness

Blurred or double vision

Irregular or racing heartbeat

Skin that has become sensitive to the sun

Sweating

Constipation or problems urinating

Problems getting an erection

Itching and swelling in the ear (labyrinthitis)

Meclizine Interactions

It is always important to tell your doctor and pharmacist about all of your treatments, including over-the-counter (OTC) medications; vitamins, nutritional shakes, protein powders, and other supplements; herbal treatments or other alternative medicines; and any illegal or recreational drugs.

The following drugs are known to interact with meclizine:

Pain medications that are related to opium, such as: alfentanil (Alfenta), codeine (Tylenol # 3), cihydrocodeine (Synalog), hydrocodone (Vicodin, Lortab, Percocet), levorphanol (Levo Dromoran), meperidine (Demerol), reminifentanil (Ultiva), and sufentanil (Sufenta)

Dichloralphenazone

Sleeping medicines, such as: zaleplon (Sonata), zolipidem (Ambien), eszopiclone, and chloral hydrate

Muscle relaxants, such as baclofen, cyclobenzaprine (Flexeril), carisoprodol (Soma), and orphenadrine (Zanaflex)

You should talk your doctor if you are taking allergy medications or any drugs for anxiety, mood, or depression, when taking meclizine, so you will know about special drug-interaction symptoms you need to monitor. These include:

Mood or depression drugs amitriptyline (Elavil), amoxapine (Asendin), aripiprazole (Ability), loxapine (Loxitane), nortiptyline (Pamelor), and oxazepam (Serax).

Anxiety medicines estazolam (Prosom), diazepam (Valium), alprazolam (Xanax), clonazepam (Klonopin), lorazepam (Ativan), flurazepam (Dalmane, Dalmadorm), and Midazolam.

Antihistamine allergy medications: brompheniramine (Bromfed, Brom-fed DM), chlorpheniramine (often in children's cold and allergy drugs, such as Tylenol Children's Cough and Cold, and Dimetapp products for Children), and diphenhydramine (Benadryl)

Meclizine and Alcohol

Drinking alcohol while taking meclizine may worsen the side effects of the drug.

Meclizine and Grapefruit Juice

Grapefruit juice is not likely to affect how meclizine works. Both the drug and grapefruit juice are broken down by the liver, but the process for each is different.

Meclizine and Other Interactions

In general, you should be careful taking meclizine if you are already taking medications that cause drowsiness, dry mouth, difficulty using the bathroom, or appear to slow the nervous system, because adding meclizine to your medications can make all of these symptoms worse.

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El XII Congreso que tendra lugar los proximos 11 y 12 de junio en Madrid desarrollara el tema “La experiencia y el talento senior, valores imprescindibles para la Fundacion Mujer, Familia y Trabajo”. En el Congreso se abordaran temas tan importantes como el valor esencial del senior en las distintas culturas del mundo, los nuevos […]

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Drugs And Medications, Remethan

ANALGESIC, ANTIPYRETIC, ANTI-INFLAMMATORY

Composition The active ingredient of Remethan is Diclofenac Sodium.

Properties Remethan is a non-steroidal phenylacetic acid derivative which has marked analgesic, and anti-inflammatory properties. Remethan is absorbed from the gastrointestinal tract reaching peak plasma concentrations in two hours after ingestion of the enteric-coated tablets. Remethan is metabolised and excreted mainly in the urine.

Mechanism of Action inhibits prostaglandin synthesis by decreasing the activity of the enzyme, cyclo-oxygenase, which results in decreased formation of prostaglandin precursors.

Absorption. Completely absorbed.

Protein binding. 99%

Metabolism. Metabolised in the liver to inactive metabolites.

Half-life. 2 hours.

Time to peak serum concentration. Within 2 hours

Elimination. Excreted primarily in the urine.

Indications Remethan is indicated for the treatment of rheumatoid arthritis; ankylosing spondylitis, osteoarthrosis; low back pain, frozen shoulder, tendinitis, tenosynovitis, bursitis, strains, sprains and acute gout Remethan is also indicated for the control of pain and inflammation in orthopedic, dental and other minor surgery. In children, Remethan is indicated for the treatment of Juvenile chronic arthritis.

Dosage For enteric-coated tablets: The recommended adult dose of Remethan is 75-150mg daily given in two/or three divided doses.

Children should be given 1,3mg/kg per day in divided doses. For elderly patients the standard adult dose may be used.

For sustained release tablets: Remethan Retard: One tablet daily, taken whole with liquid, preferably at meal times. If necessary, the daily dosage can be increased to 150mg by supplementation with conventional Remethan tablets. For milder cases, where a lower dosage is sufficient other dosage forms of Remethan may be used.

Remethan suppositories are not suitable for use in children.

For Suppositories: The recommended adult dose is one lOOmg suppository daily, usually administered at night. In more severe cases, combined therapy with 25 or 60mg tablets is recommended. The total daily dose should not 150mg.

Side-effects Remethan is relatively free from serious side-effects. The side-effects are often transient and disappear with continuation of medication. These may include epigastric pain, nausea, diarrhoea, headache, slight dizziness, skin rashes, peripheral oedema and abnormalities of serum transaminases. Very rarely peptic ulcer and haematemesis or melaena have been reported. In such cases Remethan should be withdrawn.

Dermatological : Occasional rashes or skin eruptions. Cases of hair loss, bullous eruptions, erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell's syndrome) and photo-sensitivity reactions have been reported.

Suppository : Local reactions include itching, burning and increased frequency of bowel movement.

Precautions and Warnings Remethan should be given with caution to patients with a history of peptic ulcer, haematemesis or melaena, or bleeding diathesis or with severe hepatic or renal insufficiency.

Severe cutaneous reactions, including Steven-Johnson Syndrome and toxic epidermal necrolysis ( Lyell's syndrome ), have been reported with Diclofenac Sodium. Patients treated with Diclofenac Sodium should be closely monitored for signs of hypersensitivity reaction. Discontinue Diclofenac Sodium immediately if rash occurs.

Patients with severe hepatic, cardiac or renal insufficiency or the elderly should be kept under close surveillance. All patients who are receiving long-term treatment with non-steroidal anti-inflammatory agents should be monitored as a precautionary measure eg renal, hepatic function and blood counts.

Us of Diclofenac in patients with hepatic prophyria may trigger an attack.

Pregnancy Remethan should not be prescribed during pregnancy, unless there are compelling reasons for doing so.

Drug Interactions Remethan may cause increased blood concentrations of Digoxin and Lithium. Although studies have demonstrated a pharmacokinetic interaction between Remethan and Salicylates it has been stated that this has no clinical significance. It has also been reported that Remethan, unlike some other non-steroidal anti-inflammatory agents, does not potentiate the effects of oral anticoagulants or hypoglycaemics. The natriuretic effects of Frusemide type diuretics have been reported to be inhibited by some non-steroidal anti-inflammatory drugs.

Methotrexate excretion is inhibited by non-steroidal anti-Inflammatory drugs. Simultaneous administration of Methotrexate and non-steroidal anti-inflammatory drugs should probably be avoided. Occasional fatalities from renal failure have been reported. Severe cutaneous reactions, including Stevens-Johnson Syndrome and Mncspidermai necrolysis (Lyell's synorome) have been reported with Diclofenac Sodium. Patients treated with Diclofenac Sodium should be closely monitored for signs of hypersensitivity reactions. Discontinue I Diclofenac Sodium immediately if rash occurs.

Clinical investigations do not appear to indicate that Remethan affects the activity of anticoagulants but there have been isolated reports of an increased risk of haemorrhage with the combined use of these agents. Close monitoring is therefore recommeded. Clinical studies have shown that remethan can be given together with oral antidiabetic agents without influencing their clinical effect.

However, there have been isolated reports of hypoglycaemic and hyperglycaemic effects which have required adjustments to the dosage of hypoglycaemic agents.

Cyclosporin nephrotoxicity may be increased by the effect of non-steroidal anti-inflammatory drugs on renal prostaglandins.

Caution should be exercised if NSAIDs and Methotrexate are administered within 24 hours of each other, since NSAIDs may increase Methotrexate plasma levels, resulting in increased toxicity. Concomitant therapy with other systemic NSAIDs may increase the frequency of side-effects.

Various NSAIDs are liable to inhibit the activity of diuretics. Concomitant treatment with Potassium-sparing diuretics may be associated with increased serum Potassium levels, hence serum Potassium should be monitored.

RISK OF GI ULCERATION, BLEEDING AND PERFORATION WITH NSAID.

Serious GI toxicity such as bleeding, ulceration and perforation can occur at any time, with or without warning symptoms, in patients treated with NSAID therapy. Although minor GI problems ( eg dyspepsia ) are common, usually developing early in therapy, prescribers should remain alert for ulceration and bleeding in patients treated with NSAIDs even in the absence of previous GI tract symptoms.

Studies to date have not identified any subset of patients not at risk of developing peptic ulceration and bleeding. Patients with prior history of adverse events and other risk factors associated with peptic ulcer disease ( eg alcoholism, smoking, corticosteroid therapy ) are at increased risk. Elderly or debilitated patients seem to tolerate ulceration of bleeding less than other individuals and account for most spontaneous reports for fatal GI events.

Contraindications Remethan is contra-indicated in patients with peptic ulcer, previous sensitivity to Remethan and during pregnancy.

Overdosage Management of a non-steroidal anti-inflammatory drug-intoxication is primarily supportive and symptomatic. Fluid therapy is commonly effective in managing the hypotension that may occur following acute NSAID overdosage, except when this is due to an acute blood loss. The therapeutic measures to be taken are: absorption should be prevented as soon as possible after over dosage by means of gastric lavage and treatment with activated charcoal.

Remethan should be stored below 25?C, protected from light and moisture.

Anti Fungal Buy Mycelex-G At, Hongogen

Mycelex-G (Clotrimazole) is an antifungal medication. It prevents fungus from growing.

Clotrimazole vaginal is used to treat vaginal candida (yeast) infections.

Clotrimazole vaginal may also be used for purposes other than those listed in this medication guide.

Use Mycelex-G exactly as directed by your doctor, or follow the directions that accompany the package. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.

Wash your hands before and after using this medication.

Insert the tablet, suppository, or cream into the vagina using the applicator as directed.

Use this medication continuously for the prescribed amount of time, even during your menstrual period.

You can use a sanitary napkin to prevent the medication from staining your clothing but do not use a tampon.

If the infection does not clear up after you have finished one course of therapy, or if it appears to get worse, see your doctor. You may have another type of infection.

Avoid getting this medication in your eyes, nose, or mouth. Store clotrimazole vaginal at room temperature away from moisture and heat.

Active ingredient: Clotrimazole

Clotrimazole is an antifungal medication. It prevents fungus from growing.

Clotrimazole vaginal is used to treat vaginal candida (yeast) infections.

It also may be used for purposes other than those listed in this medication guide.

Safety information

Do not use clotrimazole vaginal if you have ever had an allergic reaction to it.

If this is the first time that you have ever had symptoms of a vaginal yeast infection, consult your doctor before using this medication.

Do not use clotrimazole vaginal if you have a fever, abdominal pain, foul-smelling discharge, diabetes, HIV, or AIDS. Consult your doctor. Do not use this medication without first talking to your doctor if you are pregnant. Do not use clotrimazole vaginal without first talking to your doctor if you are breast-feeding a baby. Do not use this medication if you are younger than 12 years of age.

Important safety information

Use this medication for the full amount of time prescribed by your doctor or recommended in the package even if you begin to feel better. Your symptoms may improve before the infection is completely healed.

Avoid wearing tight-fitting, synthetic clothing (e. g. panty hose) that does not allow air circulation. Wear loose-fitting clothing made of cotton and other natural fibers until the infection is healed. Avoid getting this medication in your eyes, nose, or mouth.

Side effects

Stop using clotrimazole vaginal and seek emergency medical attention if you experience an allergic reaction (shortness of breath; closing of your throat; swelling of your lips, face, or tongue; or hives).

Other, less serious side effects may be more likely to occur. These include burning, itching, irritation of the skin, and an increased need to urinate.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Avoid using other vaginal creams or douches at the same time as clotrimazole unless your doctor approves.

Drugs other than those listed here may also interact with clotrimazole vaginal. Talk to your doctor and pharmacist before taking any prescription or over the counter medicines.

Packaging

Your order will be packed safely and secure and dispatched within 24 hours. This is how your parcel will look like, the images are photographs of real shipments. It has the size of a normal protected envelope and it does not disclose its contents.

Special offers

Euphyllin Retard - (Tablets), Euphyllin

PROPRIETARY NAME (and dosage form):

EUPHYLLIN RETARD ® (Tablets)

COMPOSITION One Euphyllin Retard ® filmcoated tablet contains: 250 mg anhydrous theophylline

PHARMACOLOGICAL CLASSIFICATION A.10.2 Bronchodilator.

PHARMACOLOGICAL ACTION Euphyllin Retard ® is a delayed release formulation of anhydrous theophylline and has a bronchodilator action.

INDICATIONS Reversible airways obstruction in chronic obstructive bronchitis, emphysema and bronchial asthma.

CONTRA-INDICATIONS Hypersensitivity to theophylline or other xanthine derivates. Acute myocardial infarction. Safety in pregnancy has not been established.

DOSAGE AND DIRECTIONS FOR USE Euphyllin Retard ® tablets are scored and can be halved for individual dosage titration. Breaking the tablet does not affect the retard-mechanism because the tablet contains a large number of micro-pellets each of which is individually retard-coated. Unless prescribed otherwise by the physician, Euphyllin Retard ® is dosed as follows: Adults . Generally, one tablet taken twice a day (every 10-12 hours) after meals, preferably with some water. Depending upon the effect achieved and in severe cases one tablet can be administered 3 times a day (at intervals of 8 hours, or half tablets can be added to the dosage. As a general guideline the average daily dosage can be given as 10-14 mg/kg body mass/day. Therapeutic serum levels of theophylline are considered to be between 10 and 20 ug/mL; higher levels may produce toxic effects. There is wide interpatient variation in the dosage needed to achieve and maintain therapeutic serum levels. Because of these wide variations and the relatively narrow range between therapeutic and toxic serum levels, dosage must be individualized, and serum level monitoring is recommended particularly when prolonged use is planned. Dosage should be calculated on the basis of lean (ideal) body weight since theophylline does not distribute into fatty tissue. Giving theophylline with food may prevent stomach irritation, although absorption may be slower, it is still complete.

Measurement of serum theophylline concentrations: The pharmacokinetics of theophylline in an individual patient can only be determined by means of a blood level profile because of the individual biotransformation variation. For the purposes of these measurements, serum should be obtained at the time of peak drug absorption. An average peak concentration of Euphyllin Retard ® is attained approximately 2 to 5 hours after ingestion of the tablet.

DOSAGE ADJUSTMENT IS BASED ON SERUM THEOPHYLLINE MEASUREMENTS AND WHEN THESE INSTRUCTIONS HAVE NOT BEEN FOLLOWED, THERE MAY BE A RISK OF TOXICITY TO THE PATIENT.

Adolescents: older than 14 years (body mass of approxiately 45 kg or more) may be given half a tablet twice daily.

Babies, infants and children: up to the age of 14 years should not be given Euphyllin Retard ® .

Any additional treatment should only be taken in accordance with the instructions of a physician.

SIDE-EFFECTS AND SPECIAL PRECAUTIONS Side-effects relate to a great extent, to plasma concentrations and are seen frequently with theophylline concentrations exceeding 20 mg/L. The most common side-effects include insomnia, headache, nausea, vomiting, diarrhoea, diuresis, tremor, malaise, excitation, anorexia, dizziness, gastralgia, tachycardia and palpitations, reduced exercising ability, excessive sweating, metallic taste in the mouth, gastro-intestinal bleeding, visual disorders, confusion and anxiety. If side-effects appear, plasma levels of theophylline should be monitored. Euphyllin Retard ® should be administered with caution and the dosage must be reduced in the elderly and in patients with cardiac failure and impaired hepatic function. Use with caution in the following conditions: hyperfunction of the thyroid (hyperthyroidism), epilepsy, recent myocardial infarction and tachycardia. Care should be taken in patients with a history of peptic ulceration.

Interactions Concurrent use of cimetidine, antibiotics of the macrolid type (e. g. erythromycin), lincomycin, allopurinol, furosemide and oral contraceptives may enhance the effect of Euphyllin Retard ®. While barbiturates, phenytoin, carbamazepine and sulphinpyrazone may weaken it. Theophylline weakens the effect of lithium carbonate. Additional medication with beta-sympathomimetics, other theophylline-containing preparations and ephedrine may produce untoward effects or potentiate existing ones.

KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT Severe overdosage or idiosyncracy may lead to maniacal behaviour, repeated vomiting with extreme thirst, delirium, hypotension, hyperthermia and convulsions. Treatment is symptomatic. Gastric lavage may be used. Fluid and electrolyte balance should be maintained with intravenous fluids and sedatives and oxygen given if necessary.

IDENTIFICATION Light blue, convex, oblong, scored, filmcoated tablets.

PRESENTATION Packs of 60 and 500 tablets.

STORAGE INSTRUCTIONS Store in a dry place below 25°C. Protect from light. KEEP OUT OF REACH OF CHILDREN.

REGISTRATION NUMBER K/10.2/311.

NAME AND BUSINESS ADDRESS OF THE APPLICANT Byk Madaus (Pty) Ltd. Reg. No. 82/11215/07 2nd Road (cnr. 16th Road) Randjespark, Midrand 1685

DATE OF PUBLICATION OF THIS PACKAGE INSERT 26 October 1993.

ER PI 06/97/01 BUSI-FORMS (011) 706-0421 SAEPI HOME PAGE TRADE NAME INDEX GENERIC NAME INDEX FEEDBACK Information presented by Malahyde Information Systems © Copyright 1996,1997,1998

Seaze, Seaze

seize

Verb Edit

( transitive ) To deliberately take hold of; to grab or capture .

( transitive ) To take advantage of (an opportunity or circumstance ).

( transitive ) To take possession of (by force, law etc.). to seize smuggled goods to seize a ship after libeling

( transitive ) To have a sudden and powerful effect upon.

2010 . Antonio Saggio, A Secret van Gogh: His Motif and Motives . ISBN 9781447507932. 11. This sensation of an object becoming alive is a characteristic that, I believe, seizes all viewers of a van Gogh. The Bible goes beyond being a simple still-life object to become a living thing, an expression of strength, an existence that emanates from itself, beyond the painting surface to participate in our very lives.

a panic seized the crowd a fever seized him

( transitive. nautical ) To bind. lash or make fast. with several turns of small rope, cord, or small line. to seize two fish-hooks back to back to seize or stop one rope on to another

( transitive. obsolete ) To fasten. fix .

( intransitive ) To lay hold in seizure. by hands or claws (+ on or upon ). to seize on the neck of a horse The text which had seized upon his heart with such comfort and strength abode upon him for more than a year. ( Southey . Bunyan, p. 21)

( intransitive ) To have a seizure.

2012 . Daniel M. Avery, Tales of a Country Obstetrician Nearing what she thought was a climax, he started seizing and fell off her. Later, realizing he was dead, she became alarmed and dragged the body to his vehicle to make it look like he had died in his truck.

( intransitive ) To bind or lock in position immovably ; see also seize up . Rust caused the engine to seize . never to run again.

( Britain. intransitive ) To submit for consideration to a deliberative body.

Derived terms Edit

Terms derived from seize

Related terms Edit

Translations Edit

take possession of (by force, law etc)

to have a sudden and powerful effect upon

to have a seizure

References Edit

^ C. T. Onions, ed. Oxford Dictionary of English Etymology, s. v. "seize" (Oxford: Clarendon Press, 1996), 807.

seize in The Century Dictionary . The Century Co. New York, 1911

“seize ” in OED Online . Oxford University Press, 1989.

French cardinal numbers

Omesec News - Updates, Omesec

Omesec News

Posted 6 Jun 2016 by Drugs. com

-- If you've eaten too much or indulged in a food that's greasy, fatty or spicy, you may have an uncomfortable feeling known as indigestion. Here are common symptoms, courtesy of the Cleveland Clinic: A burning sensation in the stomach or upper abdomen. An acidic taste in the mouth. Pain in the abdomen. Occasional diarrhea. Bloatedness or gassiness. Vomiting or nausea. Growling stomach. Read more

Posted 10 May 2016 by Drugs. com

TUESDAY, May 10, 2016 – A popular over-the-counter heartburn medication accelerated aging of blood vessel cells in lab tests, raising red flags about its long-term effect on heart health, researchers say. Faster aging of blood vessel cells exposed to the antacid Nexium (esomeprazole) might potentially hinder the tasks these cells perform to prevent heart attack and stroke, the new study suggests. These lab results could explain why other studies have shown increased risk of heart disease in people who use proton pump inhibitors (PPIs) – the class of heartburn medication that includes Nexium, said study senior author Dr. John Cooke. "Our finding that the lining of blood vessels is impaired by proton pump inhibitors is a unifying mechanism for the reports that PPI users are at increased risk for heart attack, stroke and renal failure," said Cooke, chair of cardiovascular sciences at the. Read more

Posted 27 Apr 2016 by Drugs. com

WEDNESDAY, April 27, 2016 – Despite reported risks, nearly one in four infants in neonatal intensive care units (NICUs) are given stomach acid-suppressing drugs, researchers report. However, they noted that the use of these medications has started to decline some in recent years. A number of studies have linked the use of stomach acid-suppressing drugs in hospitalized high-risk infants with infections, necrotizing enterocolitis (a serious disease where intestinal tissue begins to die off) and increased risk of death, the researchers said. These drugs include histamine-2 receptor antagonists such as ranitidine (Zantac), and proton pump inhibitors such as esomeprazole (Nexium). Researchers at Nationwide Children's Hospital in Columbus, Ohio, analyzed data from 43 children's hospitals across the United States from 2006 to 2013. They found that nearly 24 percent of roughly 122,000 newborns. Read more

Posted 15 Apr 2016 by Drugs. com

THURSDAY, April 14, 2016 – People who use certain drugs for chronic heartburn may be at increased risk of developing kidney disease, a new study suggests. The research is the latest to highlight potential risks from drugs called proton pump inhibitors (PPIs). PPIs include prescription and over-the-counter drugs, such as Prilosec, Prevacid and Nexium. But prolonged use of PPIs has been linked to certain nutrient deficiencies and bone-density loss. According to the U. S. Food and Drug Administration, bone fractures are considered a safety concern when people use PPIs for a year or more. More recently, research has hinted at additional hazards. Last year, for example, a study tied the medications to a slight increase in heart attack risk. However, neither that study nor this new one prove that PPIs are directly to blame for these problems. "I cannot say for certain that this is. Read more

Posted 15 Feb 2016 by Drugs. com

MONDAY, Feb. 15, 2016 – A popular class of heartburn medications might raise a senior's risk of dementia, a new study suggests. Called proton pump inhibitors (PPIs), this group of drugs includes Prilosec, Nexium and Prevacid. They work by lowering the amount of acid produced by the stomach. But German researchers found that people 75 or older who regularly take the medications had a 44 percent increased risk of dementia, compared with seniors not using the drugs. The study only found an association, however, and not a cause-and-effect link. "To evaluate cause-and-effect relationships between long-term PPI use and possible effects on cognition in the elderly, randomized, prospective clinical trials are needed," said corresponding author Britta Haenisch, from the German Center for Neurodegenerative Diseases in Bonn. In the meantime, "Clinicians should follow guidelines for PPI. Read more

Posted 13 Feb 2016 by Drugs. com

FRIDAY, Feb. 12, 2016 – Patients with the leading form of lung cancer may be able to look to Coca-Cola Classic to solve a common medicinal challenge, new research suggests. As the Dutch scientists explain it, the effectiveness of the powerful lung cancer drug Tarceva (erlotinib) depends on the pH level of the stomach. But many people on Tarceva must also take a proton pump inhibitor heartburn medication – such as Nexium or Prilosec – which raises stomach pH to more alkaline levels. That higher pH can lower the absorption rate for Tarceva, cutting its effectiveness in fighting non-small-cell lung cancer, research suggests. One prior study involving healthy volunteers found the use of Prilosec lowered blood concentrations of Tarceva by 61 percent. What to do? In the new study, researchers led by Dr. Roelof van Leeuwen, of Erasmus MC Cancer Institute in Rotterdam, the Netherlands. Read more

Posted 11 Jan 2016 by Drugs. com

MONDAY, Jan. 11, 2016 – A type of heartburn medication called proton pump inhibitors may be linked to long-term kidney damage, a new study suggests. Prilosec, Nexium and Prevacid belong to this class of drugs, which treat heartburn and acid reflux by lowering the amount of acid produced by the stomach. People who use proton pump inhibitors (PPIs) have a 20 percent to 50 percent higher risk of chronic kidney disease compared with nonusers, said lead author Dr. Morgan Grams, an assistant professor of epidemiology at Johns Hopkins University in Baltimore. The study was published Jan. 11 in JAMA Internal Medicine. The study doesn't establish a direct cause-and-effect relationship between the drugs and chronic kidney disease. However, Grams said, "We found there was an increasing risk associated with an increasing dose. That suggests that perhaps this observed effect is real." Proton pump. Read more

Posted 27 Oct 2015 by Drugs. com

TUESDAY, Oct. 27, 2015 – A common type of heartburn medication called proton pump inhibitors (PPIs) seem to be linked with increased risk of chronic kidney disease, two new studies suggest. Prilosec, Nexium and Prevacid belong to this class of drugs, which treat heartburn and acid reflux by lowering the amount of acid produced by the stomach. While the current studies have shown an association between these drugs and the development of chronic kidney disease, they did not prove a cause-and-effect relationship. Still, the lead author of one of the studies believes, "It is very reasonable to assume that PPIs themselves can cause chronic kidney disease," said Dr. Pradeep Arora, a nephrologist and associate professor at the SUNY Buffalo School of Medicine and Biomedical Science in Buffalo, N. Y. "Patients should only use PPIs for [U. S. Food and Drug Administration]-approved indications, and. Read more

Posted 10 Jun 2015 by Drugs. com

WEDNESDAY, June 10, 2015 – People who use certain heartburn drugs for a long period of time may have a slightly heightened risk of suffering a heart attack, a new study suggests. Using medical records from nearly 300,000 U. S. adults with acid reflux disease (commonly called heartburn), researchers found that the risk of heart attack was slightly elevated among those using proton pump inhibitors. Proton pump inhibitors are a group of acid-suppressing drugs that include brand-names such as Prevacid, Prilosec and Nexium. In 2009, they were the third most commonly used type of drug in the United States, the researchers said. The study, funded by the U. S. National Institutes of Health, does not prove the drugs cause heart attack. And experts were divided over what to make of the connection. Another class of heartburn drug – so-called H2-blockers – was not linked to any increase in heart. Read more

Posted 2 Dec 2014 by Drugs. com

TUESDAY, Dec. 2, 2014 – Using antacids to control acid reflux may improve head and neck cancer patients' chances of survival, a new study suggests. The researchers examined the effects that two types of antacids – proton pump inhibitors and histamine 2 blockers – had on head and neck cancer patients. More than two-thirds of the nearly 600 patients in the study took one or both types of the antacids after their cancer diagnosis. Acid reflux – commonly known as heartburn – is a common side effect of chemotherapy or radiation treatment, according to the researchers. Proton pump inhibitors include drugs such as Prilosec, Nexium and Prevacid, while histamine 2 blockers include drugs such as Tagamet, Zantac and Pepcid. Compared to patients who didn't take antacids, those who took proton pump inhibitors had a 45 percent lower risk of death, according to the researchers. They also found. Read more

Posted 25 Nov 2014 by Drugs. com

TUESDAY, Nov. 25, 2014 – Heartburn drugs such as Prilosec and Nexium may disrupt the makeup of bacteria in the digestive system, potentially boosting the risk of infections and other problems, a small new study suggests. The research doesn't confirm that these changes make it more likely users will become ill, and study authors aren't recommending that anyone stop taking the so-called proton pump inhibitors. However, these antacids "should be used at the lowest dose that provides adequate relief of symptoms, and attempts to discontinue their use should be considered periodically," said study co-author Dr. John DiBaise, professor of medicine at the Mayo Clinic in Scottsdale, Ariz. According to Harvard Medical School, billions of dollars are spent annually on antacid drugs in an attempt to combat heartburn, ulcers and gastroesophageal reflux disease, also known as GERD. Old standbys such. Read more

Posted 11 Jun 2014 by Drugs. com

WEDNESDAY, June 11, 2014 – Many people with heartburn aren't taking their acid-reducing medicine at the right time, which makes the drugs less effective and wastes money, according to new research. Only about one-third of those buying these medications – such as Nexium, Prevacid and Prilosec – over-the-counter used them properly compared to just under half of those who were prescribed the drugs by their primary care doctor. Those who were given a prescription by a gastroenterologist were most likely to use the drugs as they're supposed to be used, with seven out of 10 taking the drugs properly, according to the study. These drugs are activated once in the body, said the study's senior author, Dr. M. Michael Wolfe, a gastroenterologist and chair of the department of medicine at MetroHealth System. "In order to activate the medicine, you must eat. For that reason, you take it before. Read more

Posted 10 Dec 2013 by Drugs. com

TUESDAY, Dec. 10, 2013 – People who take certain acid-reflux medications might have an increased risk of vitamin B-12 deficiency, according to new research. Taking proton pump inhibitors (PPIs) to ease the symptoms of excess stomach acid for more than two years was linked to a 65 percent increase in the risk of vitamin B-12 deficiency. Commonly used PPI brands include Prilosec, Nexium and Prevacid. Researchers also found that using acid-suppressing drugs called histamine-2 receptor antagonists – also known as H2 blockers – for two years was associated with a 25 percent increase in the risk of B-12 deficiency. Common brands include Tagamet, Pepcid and Zantac. "This study raises the question of whether or not people who are on long-term acid suppression need to be tested for vitamin B-12 deficiency," said study author Dr. Douglas Corley, a research scientist and gastroenterologist at. Read more

Posted 23 May 2013 by Drugs. com

THURSDAY, May 23 – People who suffer from frequent heartburn may be at increased risk for cancers of the throat and vocal cords even if they don't smoke or drink alcohol, a new study says. Interestingly, common over-the-counter antacids seemed to protect against these cancers while prescription medications such as Prilosec, Nexium and Prevacid didn't, the researchers said. "There has been a controversy about whether heartburn contributes to cancers of the larynx or pharynx," said lead researcher Scott Langevin, a postdoctoral research fellow at Brown University in Providence, R. I. "And we found out that it does elevate the risk of these cancers. There is about a 78 percent increase in the risk for cancer in people who experience heavy heartburn," he said. "This is important in figuring out who to monitor more closely." The other finding, which Langevin called "surprising," was the. Read more

Posted 5 Apr 2013 by Drugs. com

-- A proton pump inhibitor, a drug commonly taken for heartburn, may cause side effects. The American Academy of Family Physicians lists these factors to consider before using a proton pump inhibitor (PPI): If you're a postmenopausal woman, talk with your doctor because a PPI could increase your risk for bone fractures. If you've been treated for a C. difficile infection, check with your doctor because PPIs may increase the risk of the infection returning. If you have problems with your immune system or are elderly, check with your doctor because PPIs may increase the risk of pneumonia. Read more

Razo Surname, Family Crest & Coats Of Arms, Razo

From the historical and enchanting region of France emerged a multitude of noble families, including the distinguished Razo family. Originally, the French people were known only by a single name. The process by which hereditary surnames were adopted in France is extremely interesting. Surnames evolved during the Middle Ages when people began to assume an extra name to avoid confusion and to further identify themselves. Often they adopted names that were derived from nicknames. Nickname surnames were derived from an eke-name, or added name. They usually reflected the physical characteristics or attributes of the first person that used the name. The name Razo is a nickname type of surname for a person of regal bearing or a person who played a king in a local festival. Looking back further, we find the name Razo was derived from the Old French word "roy," meaning "king."

Razo Early Origins

PDF Coat of Arms + Extended History

The surname Razo was first found in Burgundy (French: Bourgogne), an administrative and historical region of east-central France, where the family has held a family seat since ancient times.

Other References

D'Hozier Charles. Armorial G?n?ral de France . Paris: Dillon, 1875. Print.

Rolland, and H. V. Rolland. Illustrations to the Armorial general by J. B. Rietstap 6 volumes in 3 . Baltimore: Heraldic Book Company, 1976. Print.

Vaillancourt, Emile. La Conquete du Canada par les Normands. Biographie de la premiere generation Normande du Canada . Montreal: G. Ducharme, 1930. Print.

De Ville, Winston. Gulf Coast Colonials, A Compendium of French Families in Early Eighteenth Century Louisiana . Baltimore, MD: Clearfield, 1999. Print.

Rietstap, Johannes Baptist. Armorial G?n?ral . Baltimore: Genealogical Publishing Co. Print.

de la Porte, A. Tresor Heraldique . Paris: F. Casterman, 1864. Print.

Annuaire G?n?ral H?raldique Universel . Paris: Institut H?raldique, 1901. Print.

Gu?rard, Albert L?on. France: a Modern History . Ann Arbor: University of Michigan Press, 1959. Print.

Hanks, Patricia and Flavia Hodges. A Dictionary of Surnames . Oxford: Oxford University Press, 1988. Print. (ISBN 0-19-211592-8).

Doyle, William. The Oxford History of the French Revolution . Oxford: Oxford University Press, 1990. Print. (ISBN 0192852213).

.

The Razo Family Crest was acquired from the Houseofnames. com archives. The Razo Family Crest was drawn according to heraldic standards based on published blazons. We generally include the oldest published family crest once associated with each surname.

This page was last modified on 18 May 2014 at 22:33.

Sign Up

From the historical and enchanting region of France emerged a multitude of noble families, including the distinguished Razo family. Originally, the French people were known only by a single name. The process by which hereditary surnames were adopted in France is extremely interesting. Surnames evolved during the Middle Ages when people began to assume an extra name to avoid confusion and to further identify themselves. Often they adopted names that were derived from nicknames. Nickname surnames were derived from an eke-name, or added name. They usually reflected the physical characteristics or attributes of the first person that used the name. The name Razo is a nickname type of surname for a person of regal bearing or a person who played a king in a local festival. Looking back further, we find the name Razo was derived from the Old French word "roy," meaning "king."

Razo Early Origins

PDF Coat of Arms + Extended History

The surname Razo was first found in Burgundy (French: Bourgogne), an administrative and historical region of east-central France, where the family has held a family seat since ancient times.

Other References

de la Porte, A. Tresor Heraldique . Paris: F. Casterman, 1864. Print.

D'Hozier Charles. Armorial G?n?ral de France . Paris: Dillon, 1875. Print.

Rolland, and H. V. Rolland. Illustrations to the Armorial general by J. B. Rietstap 6 volumes in 3 . Baltimore: Heraldic Book Company, 1976. Print.

Doyle, William. The Oxford History of the French Revolution . Oxford: Oxford University Press, 1990. Print. (ISBN 0192852213).

Annuaire G?n?ral H?raldique Universel . Paris: Institut H?raldique, 1901. Print.

Rietstap, Johannes Baptist. Armorial G?n?ral . Baltimore: Genealogical Publishing Co. Print.

Hanks, Patricia and Flavia Hodges. A Dictionary of Surnames . Oxford: Oxford University Press, 1988. Print. (ISBN 0-19-211592-8).

Vaillancourt, Emile. La Conquete du Canada par les Normands. Biographie de la premiere generation Normande du Canada . Montreal: G. Ducharme, 1930. Print.

Gu?rard, Albert L?on. France: a Modern History . Ann Arbor: University of Michigan Press, 1959. Print.

De Ville, Winston. Gulf Coast Colonials, A Compendium of French Families in Early Eighteenth Century Louisiana . Baltimore, MD: Clearfield, 1999. Print.

.

The Razo Family Crest was acquired from the Houseofnames. com archives. The Razo Family Crest was drawn according to heraldic standards based on published blazons. We generally include the oldest published family crest once associated with each surname.

This page was last modified on 18 May 2014 at 22:33.

Sign Up

Trump Is Evoking Memories Of Hitler And This Is His Big Lie -Commentary, Levoking

Sam Altman: Trump is evoking memories of Hitler and this is his 'big lie'

Mon, 20 Jun '16 | 5:03 PM ET CNBC. com

Lucas Jackson | Reuters

Republican U. S. presidential candidate Donald Trump is surrounded by family members as he speaks during a campaign victory party at Trump Tower in New York on May 3, 2016, after rival candidate Senator Ted Cruz dropped out of the race for the Republican presidential nomination following the results of the Indiana state primary.

This commentary originally appeared on Sam Altman's blog .

I'm going to say something very unpopular in my world: Trump is right about some big things.

He's right that many Americans are getting screwed by the system. He's right that the economy is not growing nearly fast enough. He's right that we're drowning in political correctness, and that broken campaign finance laws have bred a class of ineffective career politicians. He may even be right that free trade is not the best policy. Trump supporters are not dumb.

But Trump is wrong about the more important part: how to fix these problems. Many of his proposals, such as they are, are so wrong they're difficult to even respond to.

Even more dangerous, though, is the way he's wrong. He is not merely irresponsible. He is irresponsible in the way dictators are.

Trump's casual racism, misogyny and conspiracy theories are without precedent among major presidential nominees. He has said that a judge of Mexican descent couldn't treat him fairly because of his heritage, and that we should ban Muslims from entering the country.

When his supporters beat up a homeless Hispanic man and cited Trump, he called them "very passionate." He has accused Obama of somehow being responsible for the recent shooting in Orlando.

To anyone familiar with the history of Germany in the 1930s, it's chilling to watch Trump in action. Though I know intellectually it's easy in hard economic times to rile people up with a hatred of outsiders, it's still surprising to watch this happen right in front of us.

It's hard to tell, as it often is with demagogues, how much is calculation and how much is genuine belief. But it's a real and terrifying possibility that Trump actually believes much of what he says. In any case, when he says it, it signals to other people that it's OK to believe.

Demagogic hate-mongers lead down terrible paths. It would be particularly embarrassing for us to fall for this — we are a nation of immigrants, and we know that immigrants built this country (and Trump, of course, is the grandson of immigrants and married to an immigrant).

Hitler taught us about the big lie — the lie so big, and so often repeated, that people end up believing it.

Trump's big lie is hiding in plain sight. His big lie is that he's going to make America great by keeping us safe from outsiders.

But he has no serious plan for how to restore economic growth, which is what we actually need. Without it, we'll be in a zero-sum game and face continued infighting. And without it, we'll lose our position as the most powerful country in the world.

He distracts us with hate of outsiders in the hopes that we don't notice he has no plan for the inside. He has failed to put forward a serious plan for major investments in research and technology that we so desperately need. Instead, he tries to distract us with fear of Them.

At least Trump is willing to talk about the fact that the U. S. is not on an acceptable growth trajectory. The big truth in Trump's slogan is "again" — we do need a fundamental change to get back to where we were. Clinton's dangerously bad big lie is that there's no big problem here at all.

Trump is right about the problem, but horribly wrong about the solution.

I take some risk by writing this (even though I've supported some Republicans in the past), and I'll feel bad if I end up hurting Y Combinator by doing so. I understand why other people in the technology industry aren't saying much. In an ordinary election, it's reasonable for people in the business world to remain publicly neutral. But this is not an ordinary election.

This would be a good time for us all — even Republicans, especially Republican politicians who previously endorsed Trump — to start speaking up.

Commentary by Sam Altman, the president of start-up incubator Y Combinator. He was also co-founder and CEO of Loopt, which was funded by Y Combinator and acquired by Green Dot in 2012. He was CTO at Green Dot and is currently on their board of directors. Follow him on Twitter @sama .

Lithioderm () - No Prescription Needed, Lithioderm

Lithium (Lithioderm)

Lithium carbonate is indicated for the treatment of manic episodes of manic-depressive illness. Maintenance therapy prevents or diminishes the intensity of subsequent episodes in those manic-depressive patients with a history of mania. Lithium is an element of the alkali-metal group. Preclinical studies have shown that lithium alters sodium transport in nerve and muscle cells and effects a shift toward intraneuronal metabolism of catecholamines.

Use Lithium Carbonate as directed by your doctor.

Take Lithium Carbonate by mouth after meals or with food or milk to decrease stomach upset.

Drinking extra fluids while you are taking Lithium Carbonate is recommended. Check with your doctor for instructions.

Do not change your diet, including the amount of salt in your diet, unless instructed by your doctor.

If you miss a dose of Lithium Carbonate, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Lithium Carbonate.

Store Lithium Carbonate at 77 degrees F (25 degrees C) in a tightly closed container. Store away from heat, light, and moisture. Keep Lithium Carbonate out of the reach of children and away from pets.

Do NOT use Lithium Carbonate if:

you are allergic to any ingredient in Lithium Carbonate

you have moderate to severe kidney, heart, or blood vessel problems

you have low blood sodium levels

you are severely dehydrated, ill, or weakened

you are taking an angiotensin-converting enzyme (ACE) inhibitor (eg, enalapril) or a diuretic (eg, furosemide, hydrochlorothiazide).

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Lithium Carbonate. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have diarrhea, vomiting, excessive sweating, dehydration, fever, infection, or illness, or you are in a weakened state

if you have kidney, heart, blood vessel, or thyroid problems

if you have brain or nerve problems (eg, organic brain syndrome)

if you are on a low-salt diet.

Some medicines may interact with Lithium Carbonate. Tell your health care provider if you are taking any other medicines, especially any of the following:

Acetazolamide, urea, urinary alkalinizers (eg, sodium bicarbonate), or xanthines (eg, theophylline) because they may decrease Lithium Carbonate's effectiveness

ACE inhibitors (eg, enalapril), angiotensin II receptor antagonists (eg, losartan), calcium channel blockers (eg, verapamil), carbamazepine, diuretics (eg, furosemide, hydrochlorothiazide), hydantoins (eg, phenytoin), methyldopa, metronidazole, nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, indomethacin, celecoxib), or selective serotonin reuptake inhibitor (SSRI) antidepressants (eg, fluoxetine) because the risk of toxicity of Lithium Carbonate may be increased

Butyrophenones (eg, haloperidol) or other medicines for mental or mood problems because the risk of serious side effects, such as confusion, involuntary muscle movements, fever, and brain damage, may be increased

Iodide preparations (eg, potassium iodide) because the risk of low thyroid levels may be increased

Nondepolarizing neuromuscular blockers (eg, vecuronium) or succinylcholine because the risk of their side effects may be increased by Lithium Carbonate.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Lithium Carbonate may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Lithium Carbonate may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Lithium Carbonate with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Do NOT take more than the recommended dose without checking with your doctor.

It may take 1 to 3 weeks for Lithium Carbonate to work. Do not stop using Lithium Carbonate without checking with your doctor.

Tell your doctor or dentist that you take Lithium Carbonate before you receive any medical or dental care, emergency care, or surgery.

Fever, infection, vomiting, diarrhea, or excessive sweating may affect the levels of Lithium Carbonate in your blood. If you experience any of these conditions, contact your doctor. Talk to your doctor about how to replace the salt lost through sweating during exercise.

Do not change the amount of salt in your diet unless instructed by your doctor. Check with your doctor before restricting your salt intake. Tell your doctor if you are on a low-salt diet.

Lab tests, including blood lithium levels and kidney function tests, may be performed while you use Lithium Carbonate. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Lithium Carbonate with caution in the elderly; they may be more sensitive to its effects.

Lithium Carbonate should not be used in children younger 12 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Lithium Carbonate may cause harm to the fetus. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Lithium Carbonate while you are pregnant. Lithium Carbonate is found in breast milk. Do not breastfeed while taking Lithium Carbonate.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Mild hand tremor; mild thirst; temporary, mild nausea and general discomfort at the beginning of treatment.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision; confusion; diarrhea; drowsiness; excessive weight gain; fainting; giddiness; inability to control the bladder or bowels; increased thirst; increased or decreased urination; involuntary twitching or muscle movements; loss of consciousness; loss of coordination; muscle weakness; persistent headache; persistent or severe nausea; ringing in the ears; seizures; slow or irregular heartbeat; slurred speech; swelling of the ankles or wrists; unsteadiness; vision changes; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

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Brevinor (Ethinyloestradiol And Norethisterone) Drug, Brevinor

Brevinor

NOTICE: This Consumer Medicine Information (CMI) is intended for persons living in Australia. This page contains answers to some common questions about Brevinor. It does not contain all the information that is known about Brevinor. It does not take the place of talking to your doctor or pharmacist. All medicines have risks and benefits. Your doctor has weighed the risk of you using this medicine against the benefits he/she expects it will have for you. If you have any concerns about using this medicine, ask your doctor or pharmacist. Bookmark or print this page, you may need to read it again.

What Brevinor is used for

Brevinor is a birth control pill commonly known as a "Combined Oral Contraceptive". It contains both an oestrogen (ethinyloestradiol) and progestogen (norethisterone) hormone.

Oral contraceptives belonging to this group produce their birth control (or contraceptive) effect by preventing ovulation (the release of an egg from the ovary) during each menstrual cycle. Combined Oral Contraceptives also cause changes to the mucus of the cervix and the lining of the womb which contribute to the contraceptive action.

Ask your doctor if you have any questions about why Brevinor has been prescribed for you.

Your doctor may have prescribed Brevinor for another reason.

Brevinor is only available on a prescription from your doctor.

This medicine is not expected to affect your ability to drive a car or operate machinery.

Before you start to take Brevinor

When you must not take it

Do not take Brevinor if you have an allergy to:

any medicine containing ethinyloestradiol or norethisterone

any of the ingredients listed at the end of this leaflet

any other similar medicines (such as other oral contraceptives).

Some of the symptoms of an allergic reaction may include:

shortness of breath

wheezing or difficulty breathing

swelling of the face, lips, tongue or other parts of the body

rash, itching or hives on the skin.

Do not take it if:

you have had a stroke or heart attack

you have or have had inflammation, infection or clotting in any blood vessel(s), including a clot in the lung

you have or have had liver disease (including tumours of any type), a history of jaundice or cholestatic jaundice of pregnancy, or severe generalised itch in the body during pregnancy, Dubin-Johnson Syndrome or Rotor Syndrome

you have abnormal vaginal bleeding, the cause of which is unknown

you are pregnant or suspect that you may be pregnant

you have cancer or suspected cancer of the breast or sex organs (e. g. cervix, vagina, ovaries, endometrium, womb) and known or suspected oestrogen-dependent tumours

you have a family history of breast nodules, fibrocystic disease or have had an abnormal mammograph

you have sickle cell anaemia

you have lipid metabolism disorders such as congenital hyperlipidaemia

you have diabetes with blood vessel damage

you have a history of herpes of pregnancy

you have otosclerosis (an ear disorder) which worsened in past pregnancies.

If you are not certain whether these may apply to you, or you are worried by anything in this list, tell your doctor.

Tell your doctor about any existing medical condition as this may be affected by taking the birth control pill.

Do not take Brevinor if the packaging is torn or shows signs of tampering.

If it is expired or is damaged, return it to your pharmacist for disposal.

If you are not sure whether you should start taking this medicine, talk to your doctor.

Before you start to take it

Tell your doctor if you are allergic to any foods, dyes, preservatives or any other medicines.

You must tell your doctor if:

you are a heavy smoker (15 or more cigarettes per day), especially if you are aged over 35 years.

Oral contraceptives increase your risk of having a stroke or heart attack. Smoking, while taking oral contraceptives, further increases this risk.

Tell your doctor if you have any other health problems, especially:

liver, kidney or heart disease

Omeprazole Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Omeprazolum

omeprazole

GENERIC NAME(S): OMEPRAZOLE

Uses

Omeprazole is used to treat certain stomach and esophagus problems (such as acid reflux. ulcers). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn. difficulty swallowing, and persistent cough. This medication helps heal acid damage to the stomach and esophagus, helps prevent ulcers, and may help prevent cancer of the esophagus. Omeprazole belongs to a class of drugs known as proton pump inhibitors (PPIs).

If you are self-treating with this medication, over-the-counter omeprazole products are used to treat frequent heartburn (occurring 2 or more days a week). Since it may take 1 to 4 days to have full effect, these products do not relieve heartburn right away.

For over-the-counter products, carefully read the package instructions to make sure the product is right for you. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar brand names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.

How to use omeprazole

Read the Patient Information Leaflet if available from your pharmacist before you start taking omeprazole and each time you get a refill.

Take this medication by mouth as directed by your doctor, usually once daily, before a meal. If you are self-treating, follow all directions on the product package. Dosage and length of treatment are based on your medical condition and response to treatment. In children, the dosage is also based on weight. Do not increase your dose or take this drug more often than directed. If you have any questions, ask your doctor or pharmacist.

Do not crush, break, or chew the tablets. Swallow this medication whole with a glass of water.

If needed, antacids may be taken along with this medication. If you are also taking sucralfate, take omeprazole at least 30 minutes before sucralfate.

Use this medication regularly to get the most benefit from it. To help you remember, take it at the same time each day. Continue to take this medication for the prescribed length of treatment even if you are feeling better. If you are self-treating with the over-the-counter product, do not take it for more than 14 days unless directed by your doctor.

Tell your doctor if your condition persists or worsens. If you are self-treating, tell your doctor if your heartburn persists after 14 days or if you need to use this medication more than once every 4 months. If you think you may have a serious medical problem, get medical help right away.

Side Effects

See also Precautions section.

Headache or abdominal pain may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

If your doctor has directed you to use this product, remember that he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

Tell your doctor right away if you have any serious side effects, including: symptoms of a low magnesium blood level (such as unusually fast/slow/irregular heartbeat. persistent muscle spasms. seizures ).

This medication may rarely cause a severe intestinal condition (Clostridium difficile - associated diarrhea ) due to a type of bacteria. Do not use anti-diarrhea products or narcotic pain medications if you have any of the following symptoms because these products may make them worse. Tell your doctor right away if you develop: persistent diarrhea, abdominal or stomach pain/cramping, fever, blood /mucus in your stool.

Rarely, proton pump inhibitors (such as omeprazole) have caused vitamin B-12 deficiency. The risk is increased if they are taken every day for a long time (3 years or longer). Tell your doctor right away if you develop symptoms of vitamin B-12 deficiency (such as unusual weakness. sore tongue. or numbness/tingling of the hands/feet).

A very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction. including: rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing. kidney problems (such as change in the amount of urine).

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before taking omeprazole, tell your doctor or pharmacist if you are allergic to it; or to similar drugs (such as esomeprazole. lansoprazole. pantoprazole ); or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: liver disease.

Some symptoms may actually be signs of a more serious condition. Get medical help right away if you have: heartburn with lightheadedness/sweating /dizziness, chest/jaw/arm/shoulder pain (especially with shortness of breath, unusual sweating ), unexplained weight loss .

In addition, before you self-treat with this medication, get medical help right away if you have any of these signs of a serious condition: trouble/pain swallowing food, bloody vomit, vomit that looks like coffee grounds, bloody/black stools, heartburn for over 3 months, frequent chest pain. frequent wheezing (especially with heartburn), nausea /vomiting. stomach pain.

Proton pump inhibitors (such as omeprazole) may increase your risk for bone fractures. especially with longer use, higher doses, and in older adults. Talk with your doctor or pharmacist about ways to prevent bone loss /fracture, such as by taking calcium (such as calcium citrate ) and vitamin D supplements .

Children may be more sensitive to the side effects of this drug, especially fever, cough, and infections of the nose/throat/airways.

Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).

During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.

This medication passes into breast milk. The effects on a nursing infant are unknown. Consult your doctor before breast-feeding.

Interactions

See also How to Use section.

Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval.

Some products that may interact with this drug include: cilostazol, clopidogrel, methotrexate (especially high-dose treatment), rifampin, St John's wort.

Some products need stomach acid so that the body can absorb them properly. Omeprazole decreases stomach acid, so it may change how well these products work. Some affected products include atazanavir, erlotinib, nelfinavir, pazopanib, rilpivirine, certain azole antifungals (itraconazole, ketoconazole, posaconazole), among others.

Omeprazole is very similar to esomeprazole. Do not use any medications containing esomeprazole while using omeprazole.

This medication may interfere with certain laboratory tests, possibly causing false test results. Make sure laboratory personnel and all your doctors know you use this drug.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center. Symptoms of overdose may include: confusion, unusual sweating, blurred vision, unusually fast heartbeat.

Notes

If your doctor has prescribed this medication for you, do not share it with others.

If your doctor instructs you to use this medication regularly for a long time, laboratory and medical tests (such as a magnesium blood test, vitamin B-12 levels) may be performed periodically to monitor your progress or check for side effects. Keep all regular medical and laboratory appointments.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature away from light and moisture. Do not store in the bathroom. Keep all medications away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

Images

Klonamicin Compuesto Suspension Oftalmica Esteril - Productos De Linea Farmacias - Laboratorios Klon

KLONAMICIN COMPUESTO Suspension Oftalmica Esteril - Tobramicina - Dexametasona

Excipientes autorizados: Cloruro de benzalconio, Polisorbato 20, EDTA, Metilhidroxietilcelulosa, Cloruro de sodio, Fosfato de sodio, Agua destilada

DESCRIPCION : KLONAMICIN COMPUESTO (Tobramicina y Dexametasona) Suspensión Oftálmica y Ungüento oftálmico son una combinación estéril de esteroide y antibiótico para uso oftálmico tópico.

FARMACOLOGIA CLINICA : Los corticoides suprimen la respuesta inflamatoria frente a una variedad de agentes, y probablemente retardan o alargan la cicatrización. Debido a que los corticoides pueden inhibir los mecanismos de defensa corporales contra la infección se recomienda el uso concomitante de una droga antimicrobiana cuando esta inhibición es considerada clínicamente significativa. La dexametasona es un corticoide potente. El componente antibiótico de la combinación (tobramicina), se incluye para actuar acción contra organismos susceptibles. Estudios in vitro han demostrado que el antibiótico tobramicina, componente anti-infeccioso de este producto, es activo contra cepas susceptibles de los siguientes micro-organismos: Estafilococos incluyendo S. aureus y S. epidermidis (coagulasa-positivos y coagulasa-negativos), y cepas resistentes a la penicilina. Estreptococos, incluyendo algunos del grupo A beta-hemolítico, y algunas especies no hemolíticas y algunas cepas de Strepococcus pneumoniae, Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Enterobacer aerogenes, Proteus mirabilis, Morganella morganii, la mayoria de las cepas de Proteus vulgarís, Haemophilus influenzae y H. aegyptius, Moraxella Iacunata y Acinetobacter calcoaceticus, y algunas especies de Neisseria. Estudios de sensibilidad bacteriana demuestran que en algunos casos, micro-organismos resistentes a la gentamicina pueden permanecer susceptibles a la tobramicina. No se ha detectado aún una significativa población bacteriana resistente a la tobramicina; sin embargo la resistencia bacteriana puede desarrollarse luego de su utilización prolongada. No existen datos disponibles sobre la extensión de absorción sistémica a partir de Klonamicin Compuesto Suspensión ó Ungüento oftálmico; sin embargo se conoce que la absorción sistémica puede ocurrir con drogas aplicadas topicamente a nivel ocular. Si se administra la máxima dosis de Klonamicin compuesto suspensión Oftálmica, durante las primeras 48 horas (dos gotas en cada ojo cada dos horas) y ocurre una absorción sistémica completa, lo cual es altamente improbable, la dosificación diaria de dexametasona sería 2.4 mg. El reemplazo fisiológico usual es 0.75 mg diariamente. Si KLONAMICIN COMPUESTO suspensión Oftálmica se administra luego de las primeras 48 horas con una frecuencia de dos gotas en cada ojo cada 4 horas, la dosis administrada de dexametasona es 1.2 mg diarios. La dosis de aplicación de KLONAMICIN COMPUESTO Ungüento Oftálmico en ambos ojos 4 veces al día proporciona una dosificación de dexametasona diaria de 0.4 mg.

INDICACIONES Y USO : KLONAMICIN COMPUESTO Suspensión y Ungüento Oftálmico están indicados en condiciones oculares inflamatorias que responden a los esteroides y en las cuales además existe riesgo de una infección ocular bacteriana superficial, o la existencia de la misma. Se encuentran también indicados en la uveítis anterior crónica y heridas corneales debidas a quemaduras químicas, térmicas, o radioactivas, o presencia de cuerpos extraños.

CONTRAINDICACIONES : Queratitis epitelial por herpes simple (queratitis dendrítica), vaccinia, varicela, y muchas otras enfermedades virales de la córnea y conjuntiva. Infección ocular micobacteriana. Infección fúngica de las estructuras oculares. Hipersensibilidad a algún componente de la medicación. El uso de esta combinación se encuentra siempre contraindicado luego de la remoción no complicada de un cuerpo extraño.

ADVERTENCIA . PARA USO TOPICO SOLAMENTE - NO INYECTAR. Puede presentarse hipersensibilidad frente a los aminoglucósidos aplicados tópicamente en algunos pacientes. Si una reacción de hipersensibilidad ocurre, se debe discontinuar el uso. El uso prolongado de esteroides puede provocar glaucoma, con daño del nervio óptico, defectos en la agudeza visual y campo visual, y formación de catarata subcapsular posterior. La presión intraocular debe ser registrada rutinariamente, aun si esto resulta dificultoso en niños y en pacientes poco cooperadores. El uso prolongado puede suprimir la respuesta de defensa del paciente e incrementar así el riesgo de infecciones oculares secundarias. En aquellas enfermedades que causan un adelgazamiento de la córnea o esclera, se han reportado perforaciones con el uso de esteroides tópicos. En las infecciones purulentas agudas del globo ocular, los esteroides pueden enmascarar la infección y así favorecerlas.

PRECAUCIONES : Generales: la posibilidad de infecciones fúngicas en la córnea debe ser considerada siempre luego de la dosificación prolongada de esteroides. Como cualquier otra preparación antibiótica, el uso prolongado puede resultar en el desarrollo de organismos no susceptibles incluyendo hongos. De ocurrir una superinfección se debe recurrir a la terapia apropiada. Cuando se requieren prescripciones múltiples, o cuando el juicio clínico lo dicta, el paciente debe ser examinado con la ayuda de magnificación con una lámpara de biomicroscopía, y de ser apropiado, tinción con fluoresceina. Información para los pacientes: Para evitar contaminar el contenido, no tocar ninguna superficie con la punta del gotero. Carcinogénesis, mutagénesis, alteración de la fertilidad: No existen estudios para evaluar el potencial carcinogénico o mutagénico. No se ha detectado alteración de la fertilidad en estudios con tobramicina subcutánea en ratas a dosis de 50 a 100 mg/Kg/día. Uso durante el embarazo: Los corticosteroides han resultado teratogénicos en estudios en animales. La administración ocular de dexametasona 0.1% resultó en una incidencia de anomalías fetales de 15.6% y 32.3% en dos grupos de conejas preñadas. Se han observado retardos del crecimiento fetal y aumento del indice de mortalidad en ratas con terapia crónica con dexametasona. Estudios de reproducción han sido llevados a cabo en ratas y conejos con tobramicina a dois de hasta 100mg/kg/día en forma parenteral y los mismos no han revelado evidencia alguna de alteración de la fertilidad o daño al feto. No existen estudios bien controlados y adecuados en mujeres embarazadas. KLONAMICIN COMPUESTO Suspensión y Ungüento Oftálmico pueden ser utilizados durante el embarazo sólo si el beneficio justifica el riesgo potencial al feto. Madres durante la lactancia: Se desconoce si esta droga es excretada en la leche materna. Debido a que muchas drogas son excretadas en la leche materna, debe considerarse discontinuar la lactancia temporalmente para utilizar KLONAMICIN COMPUESTO Suspensión y Ungüento Oftálmicos. Uso Pediátrico: La Seguridad y efectividad en niños no han sido establecidas. REACCIONES ADVERSAS: han ocurrido reacciones adversas con la combinación de esteroides y anti-infecciosos que pueden ser atribuídas al componente esteroideo, al componente anti-infeccioso o a la combinación de ambos. Las cifras de incidencia exacta se desconocen. Las reacciones adversas más frecuentes frente a la administración ocular tópica de tobramicina (KLONAMICIN COMPUESTO) son toxicidad e hipersensibilidad ocular localizadas, incluyendo prurito, edema palpebral y eritema conjuntival. Estas reacciones ocurren en menos del 4% de los pacientes. Reacciones similares pueden ocurrir con el uso tópico de otros antibióticos aminoglucósidos. No se han reportado otras reacciones adversas: sin embargo, si la tobramicina ocular tópica es administrada concomitantemente con aminoglucósidos sistémicos, debe actuarse con precaución para mantener una concentración sérica total adecuada del antibiótico. Las reacciones debidas al componente esteroideo son: elevación de la presión intraocular (PIO) con posible desarrollo de glaucoma, e infrecuentemente daño en el nervio óptico, formación de cataratas subcapsulares posterior y retardo de la cicatrización. Infección secundaria: El desarrollo de infección secundaria ha occurrido luego del uso de combinaciones conteniendo esteroides y antimicrobianos. Las infecciones fúngicas de la córnea son particularmente proclives a desarrollarse concomitantemente con la aplicación prolongada de esteroides. La posibilidad de invasión fúngica debe considerarse frente a cualquier úlcera corneal persistente sobre la cual se hayan aplicados esteroides. También ocurre infección ocular bacteriana secundaria después de la suspensión de la respuesta inflamatoria del paciente.

DOSIS Y ADMINISTRACION : Suspensión: AGITAR BIEN ANTES DE USAR. Una ó dos gotas instiladas en el saco conjuntival cada cuatro a seis horas. Durante 24 a 48 horas iniciales. La dosificación puede incrementarse a una o dos gotas cada dos (2) horas. La frecuencia debe ser disminuida gradualmente a medida que se obtiene una mejoría de los signos clínicos. Actuar con precaución para no discontinuar la terapia en forma prematura. Ungüento: Aplicar 1-1,5 cm de Ungüento en el saco conjuntival hasta tres o cuatro veces al día. Luego de la aplicación del Ungüento, dirigir la mirada hacia abajo antes de cerrar los párpados. KLONAMICIN COMPUESTO Ungüento Oftálmico puede ser utilizado antes del sueño nocturno concomitantemente con KLONAMICIN COMPUESTO Suspensión Oftálmica utilizada durante el día. No deben prescribirse inicialmente más de 20 ml u 8 g, y la prescripción no debe ser renovada sin evaluación adecuada según se explica más arriba bajo el subtítulo PRECAUCIONES.

CONSERVACION : Suspensión: Conservar entre 8 y 27ºC y en posición vertical. Se recomienda descartar un mes después de abierto el envase. Ungüento: Conservar entre 8 y 27ºC. Mantener el envase herméticamente cerrado.

PRESENTACIONES . Envases conteniendo 1 y 100 frascos goteros por 5 ml de suspensión oftálmica estéril, siendo este último de uso hospitalario exclusivo. Envases conteniendo 1 y 100 pomos por 3,5 g de ungüento oftálmico estéril, siendo este último de uso hospitalario exclusivo.

SOBREDOSIFICACIÓN . Consultar con el hospital Posadas a los telefonos: (011) 4654-6648/4658-7777 o al Hospital de Pediatría R. Gutierrez al (011) 4962-6666/2247. «ESTE MEDICAMENTO DEBE SER UTILIZADO EXCLUSIVAMENTE BAJO PRESCRIPCIÓN Y VIGILANCIA MÉDICA Y NO PUEDE REPETIRSE SIN NUEVA RECETA».

MANTENER FUERA DEL ALCANCE DE LOS NIÑOS

Paracetamol Tablets 500mg - Patient Information Leaflet (Pil), Mexalen

The Patient Information Leaflet (PIL) is the leaflet included in the pack with a medicine. It is written for patients and gives information about taking or using a medicine.

This PIL is in PDF format and so you must have a PDF reader installed on your device to read it.

Text only version for the visually impaired Below is a text only representation of the Patient Information leaflet. The original may contain images or tables and can be viewed in PDF format using the link above. This PIL may be available from the RNIB in large print, Braille or audio CD. For further information please call the RNIB Medicine Leaflet line on 0800 198 5000. The product code(s) for this leaflet is/are: PL 00142/5554R.

Paracetamol Tablets 500mg

PATIENT INFORMATION LEAFLET

Paracetamol 500mg tablets

Read all of this leaflet carefully before you start taking this medicine.

Keep this leaflet. You may need to read it again.

If you have any further questions, ask your doctor or pharmacist.

This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.

1 What Paracetamol tablets are and what they are used for 2 Before you take 3 How to take 4 Possible side effects 5 How to store 6 Further information

1 What Paracetamol tablets are and what they are used for

Paracetamol tablets belong to a group of medicines called analgesics. They are used for the relief of mild to moderate pain and feverish conditions such as headache, toothache, colds, influenza, joint pain and period pains.

2 Before you take

Do not take Paracetamol tablets and tell your doctor if you:

are allergic (hypersensitive) to paracetamol or any of the ingredients in the tablet (see section 6).

Check with your doctor or pharmacist before taking Paracetamol tablets if you have:

suffered from alcoholism

severe kidney or liver disease.

Other important warnings:

taking painkillers for headaches too often or for too long can make them worse.

Taking other medicines

Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Especially:

medicines to prevent blood clotting such as warfarin

metoclopramide or domperidone (to prevent sickness)

colestyramine (to treat high cholesterol levels). Should not be taken at least one hour before and after taking paracetamol

imatinib (used to treat leukaemia and some stomach tumours).

Pregnancy and breastfeeding

Ask your doctor or pharmacist for advice before taking any medicines.

Always take Paracetamol tablets exactly as your doctor has told you. If you are not sure, check with your doctor or pharmacist.

Swallow the tablets with water. Take this medicine for as long as your doctor tells you to.

Adults including elderly and children over 12 years . 1or 2 tablets every 4 to 6 hours as required, to a maximum of 8 tablets in a day.

Children 6-12 years . half to 1 tablet every 4-6 hours as required, to a maximum of 4 tablets in a day.

Children under 6 years . Not recommended.

If you take more than you should

Seek immediate medical advice in the event of an overdose, even if you feel well, because of the risk of delayed, serious liver damage.

If you (or someone else) swallow a lot of tablets at the same time, or you think a child may have swallowed any contact your nearest hospital casualty department or tell your doctor immediately. Symptoms of an overdose include feeling or being sick, loss of appetite, stomach pain or liver damage.

If you forget to take the tablets

Do not take a double dose to make up for a forgotten dose. If you forget to take a dose take it as soon as you remember it and then take the next dose at the right time.

4 Possible side effects

Like all medicines, Paracetamol tablets can cause side effects, although not everybody gets them.

Tell your doctor if you notice any of the following side effects or notice any other effects not listed:

Allergic reactions - skin rash

Blood - changes in numbers and types of blood cells. If you have an increase in number of nose bleeds or notice that you bruise more easily or have more infections talk to your doctor. Very rare cases of serious skin reactions have been reported

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www. mhra. gov. uk/yellowcard

By reporting side effects you can help provide more information on the safety of this medicine.

Keep out of the reach and sight of children.

Store below 25°C in a dry place, protected from light.

Do not use Paracetamol tablets after the expiry date stated on the label/carton/ bottle. The expiry date refers to the last day of that month.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

6 Further information

What Paracetamol tablets contain

The active substance (the ingredient that makes the tablets work) is 500mg of paracetamol.

The other ingredients are pregelatinised maize starch, maize starch, stearic acid.

What Paracetamol tablets look like and contents of the pack

Paracetamol are white, uncoated tablets.

Pack sizes are 30, 32 or 100 tablets.

Not all pack sizes will be marketed

Marketing Authorisation Holder and Manufacturer

This leaflet was last revised in July 2014

If you would like a leaflet with larger text, please contact 01271 385257.

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Kopen Afugin (Lamisil) Zonder Recept, Afugin

Afugin (Lamisil) Kopen Online Zonder Recept

Afugin (Lamisil) Toelichting

Afugin is echt een ideale medicijn binnen battle richting gist bacteriele infecties van de teen nagel en nagel.

Afugin werkt door het voorkomen van de uitbreiding in verband met schimmel. Het is echt antifungale.

Afugin kan ook worden aangeduid als Terbinafine, Tebina, Terbisil, Zabel.

General titel geassocieerd met Afugin is eigenlijk Terbinafine.

Merk geassocieerd met Afugin is eigenlijk Afugin.

Afugin (Lamisil) Dosis

Afugin wordt geleverd in:

250mg normale dosis frictiemateriaal

Krijg Afugin pillen via de mond, samen met het drinken van water, zonder of met maaltijden. Krijg Afugin gelijktijdig dagelijks.

De therapie kan produceren direct na zes of twaalf enkele weken.

Naakte deze medicatie van kinderen en doe dit niet een aantal andere personen in verband met gebruik te maken.

Meestal niet te malen of zelfs kauwen dit.

Wilt u beste resultaten te bereiken meestal niet stoppen met het gebruik Afugin ineens.

Afugin (Lamisil) ontbreekt in verband met de dosering

Meestal krijgt niet de dubbele dosering. In het geval u de dosering die u nodig hebt om het te dragen als je eenmaal in het achterhoofd te houden met betrekking tot uw ontbreekt overslaan. Wanneer het tijd is voor de dosering die u nodig hebt om te dragen op je eigen normale dosering routine.

Afugin (Lamisil) Overdose

In het geval u Afugin overdosis en je ook voorkomen dat geweldig je nodig hebt om direct te controleren uw arts of zelfs arts.

Afugin (Lamisil) Opslagruimte

Shop in de ruimte temperaturen onder vijfentwintig niveaus D (77 niveaus F) tegen vocht, verlichting en temperatuur. Versterken elke vorm van ongerepte medicatie na het verstrijken dag. Handhaven van het bereiken van kinderen.

Afugin (Lamisil) Negatieve effecten

Afugin biedt de negatieve effecten. De meest typische neiging om:

buik ongemak frictiemateriaal

pruritus frictiemateriaal

diarree frictiemateriaal

vermoeidheid wrijving materiaal

binnen smaak of zelfs gebrek aan smaak frictiemateriaal

Veel minder typische en ernstige nadelige gevolgen voor het hele gebruik Afugin:

allergische reactie reacties (urticaria, en uitademen problemen, allergie, evenals eruptie) frictiemateriaal

vermoeidheid die niet verdwijnt frictiemateriaal

een verminderd hongergevoel frictiemateriaal

ernstige vermoeidheid frictiemateriaal

overgeven, donkere plas frictiemateriaal

licht barkrukken frictiemateriaal

pijnlijke amandelen frictiemateriaal

aanwijzingen van contaminatie frictiemateriaal

ongemak in de juiste bovenste gedeelte van de stomachhigh temperaturen frictiemateriaal

Negatieve effecten indicaties worden afhankelijk van medicijnen die u zou kunnen worden met behulp van, maar bovendien rekenen op uw welzijn conditie en andere aspecten

Afugin (Lamisil) Contra-indicaties

Meestal hoeft Afugin niet te gebruiken in het geval dat u gevoelig om Afugin elementen zijn.

Normaal gesproken niet te gebruiken Afugin wanneer u verwacht en hebben nurseling.

Wees voorzichtig met het gebruik van Afugin voor antidepressiva zoals amitriptyline (Elavil), amoxapine (Asendin), clomipramine (Anafranil), desipramine (Norpramin), doxepine (Adapin, Sinequan), imipramine (Tofranil), nortriptyline (Aventyl. Pamelor), protriptyline (Vivactil), alsmede trimipramine (Surmontil); beta-blokkers zoals atenolol (Tenormin), labetalol (Normodyne), metoprolol (Lopressor, Toprol XL), nadolol (Corgard), alsook propranolol (Inderal); cimetidine (Tagamet); geneesmiddelen die het immuunsysteem regelen bijvoorbeeld azathioprine (Imuran), ciclosporine (Neoral, Sandimmune), methotrexaat (Rheumatrex), sirolimus (Rapamune), evenals tacrolimus (Prograft); rifampicine (Rifadin, Rimactane); evenals selegiline (Eldepryl), anticoagulantia (bloedverdunners) zoals warfarine (Coumadin).

Wees voorzichtig, samen met Afugin in het geval u worden getroffen door en hebben een korte geschiedenis geassocieerd met nier - of zelfs ziekten in de lever, de mens immunodeficiency pathogeen (HIV), of zelfs verkregen immunodeficientie symptomen (AIDS), renale of zelfs ziekten in de lever.

Het kan schadelijk zijn voor het gebruik van Afugin ineens voorkomen.

Afugin (Lamisil) Veelgestelde vragen

Queen: Very best essentieel Afugin info?

De: Afugin is echt een uitstekend medicijn dat wordt verbruikt bij het verhelpen van gist bacteriele infecties van de teen nagel en nagel. Meestal Afugin niet krijgen in geval van een allergische reactie op dit medicijn of de onderdelen. Speel de rol van voorzichtige gebruik te maken van Afugin voor antidepressiva zoals amitriptyline (Elavil), amoxapine (Asendin), clomipramine (Anafranil), desipramine (Norpramin), doxepine (Adapin, Sinequan), imipramine (Tofranil), nortriptyline (Aventyl, Pamelor), protriptyline (Vivactil), alsmede trimipramine (Surmontil); beta-blokkers zoals atenolol (Tenormin), labetalol (Normodyne), metoprolol (Lopressor, Toprol XL), nadolol (Corgard), alsook propranolol (Inderal); cimetidine (Tagamet); geneesmiddelen die het immuunsysteem regelen bijvoorbeeld azathioprine (Imuran), ciclosporine (Neoral, Sandimmune), methotrexaat (Rheumatrex), sirolimus (Rapamune), evenals tacrolimus (Prograft); rifampicine (Rifadin, Rimactane); evenals selegiline (Eldepryl), anticoagulantia (bloedverdunners) zoals warfarine (Coumadin). Afugin mag niet worden gebruikt als u verwacht op een andere manier je van plan bent om een ??kind te bezitten, anders wordt je echt een medische moeder. Het kan schadelijk zijn voor het gebruik van Afugin in het geval u worden getroffen door en hebben een korte geschiedenis geassocieerd met nier - of zelfs ziekten in de lever, de mens immunodeficiency pathogeen (HIV), of zelfs verkregen immunodeficientie symptomen (AIDS), nier - of zelfs ziekten in de liver. A

Queen: Wat zijn precies Afugin negatieve effecten?

De: Afugin biedt de typische negatieve effecten bijvoorbeeld: buik ongemak, jeuk, diarree, vermoeidheid, binnen smaak of zelfs gebrek aan smaak. Maar in de situatie in verband met zijn afgewezen in verband met Afugin componenten die u in staat om meer ernstige negatieve effecten tegenkomen zijn: vermoeidheid, die niet zal verdwijnen, minder honger, ernstige vermoeidheid, overgeven, donkere plas, licht barkrukken, pijnlijke amandelen, aanwijzingen van besmetting, ongemak binnen de juiste bovenste deel van de buik, in verband met allergische reactie (moeilijkheden samen met in-en uitademen, ontsteking, porien en huid allergie of zelfs netelroos), warm. A

Queen: Wat zijn precies het algemeen en als merken verbonden Afugin?

De: Brand in verband met Afugin is eigenlijk Afugin. Algemene titel in verband met Afugin is eigenlijk Terbinafine. A

Kopen Afugin (Lamisil) online, kopen Afugin (Lamisil) online zonder voorschrift, kopen Afugin (Lamisil) zonder recept, kopen Afugin (Lamisil) goedkoop, kopen Afugin (Lamisil) zonder voorschrift, kopen Afugin (Lamisil) uit Canada, kopen Afugin (Lamisil) Canada, inkopen Afugin (Lamisil) online, inkopen Afugin (Lamisil) online no prescription, bestelling Afugin (Lamisil) zonder recept, Afugin (Lamisil) orale pil

Permoxin

Permoxin is indicated for: Dogs: Tick control (including Paralysis Ticks), Flea Control; Management of Flea Allergic Dermatitis; Horses: Fly Nuisance (stable fly, buffalo fly, sandfly); Management of Queensland Itch.

Use as a Spray or Rinse

Safe for use on pregnant and lactating animals

Active constituents: 4.0% Permethrin 25:75(cis:trans) A highly effective insecticide and tickicide with insect repellent activity.

Highly Effective Tickicide and Insecticide. In laboratory trials, a single application of PERMOXIN prevents tick attachment for over two weeks and resulted in greater than 98% flea control for 20 days.

Flea and Insect Repellent. When applied daily to flea allergic dogs, PERMOXIN repels fleas and gives relief to the pruritic dog. In fact, the high safety margin means that Permoxin can be applied as often as needed, to maintain the repellent action.

Binds to the Hair Coat. PERMOXIN utilises advanced technology which allows it to bind to clean hair and skin for long acting effectiveness. Peak activity is maintained by regular weekly top up rinses to produce saturation of the hair coat.

Resists Inactivation by Light. This ensures a longer duration of action than the natural pyrethrins which decompose rapidly on exposure to air and light

DIRECTIONS FOR USE Dilute to 1:40 (as directed by label) in water, or methylated spirits if a rapid drying spray is required. Spray or rinse as directed.

NOT TO BE USED ON CATS

Available in 250ml and 1L

Alsidol, Alsidol

Alsidol

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Ultracet (Tramadol Hydrochloride And Acetaminophen Tablets) Drug Information Warnings And Precaution

WARNINGS

Hepatotoxicity

ULTRACET® containstramadol HCl and acetaminophen. Acetaminophen has been associated with cases of acute liver failure, at times resulting in liver trans plant and death. Most of the cases of liver injury are associated with the use of acetaminophen at doses that exceed 4,000 milligrams per day, and often involve more than one acetaminophen-containing product. The excessive intake of acetaminophen may be intentional to cause self-harm or unintentional as patients attempt to obtain more pain relief or unknowingly take other acetaminophen-containing products (see BOXED WARNING ).

The risk of acute liver failure is higher in individuals with underlying liver disease and in individuals who ingest alcohol while taking acetaminophen.

Instruct patients to look for acetaminophen or APAP on package labels and not to us e more than one product that contains acetaminophen. Instruct patients to seek medical attention immediately upon ingestion of more than 4,000 milligrams of acetaminophen per day, even if they feel well.

Serious Skin Reactions

Rarely, acetaminophen may cause serious skin reactions such as acute generalized exanthematous pustulosis (AGEP), Stevens-Johnson Syndrome (SJS ), and toxic epidermal necrolysis (TEN), which can be fatal. Patients should be informed about the signs of serious skin reactions, and use of the drug should be discontinued at the first appearance of skin rash or any other sign of hypersensitivity.

Seizure Risk

Seizures have been reported in patients receiving tramadol within the recommended dosage range. Spontaneous post-marketing reports indicate that seizure risk is increased with doses of tramadol above the recommended range. Concomitant use of tramadol increases the seizure risk in patients taking:

Selective serotonin reuptake inhibitors (SSRI antidepressants or anorectics),

Tricyclic antidepressants (TCAs ), and other tricyclic compounds (e. g. cyclobenzaprine, promethazine, etc.), or

Other opioids.

Administration of tramadol may enhance the seizure risk in patients taking:

MAO inhibitors (see also WARNINGS, Use with MAO Inhibitors and Serotonin Re-uptake Inhibitors ),

Neuroleptics, or

Other drugs that reduce the seizure threshold.

Risk of convulsions may also increase in patients with epilepsy, those with a history of seizures, or in patients with a recognized risk for seizure (such as head trauma, metabolic disorders, alcohol and drug withdrawal, or CNS infections). In tramadol overdose, naloxone administration may increase the risk of seizure.

Suicide Risk

Do not prescribe ULTRACET® for patients who are suicidal or addiction-prone.

Prescribe ULTRACET with caution for patients taking tranquilizers or antidepressant drugs and patients who us e alcohol in excess and who suffer from emotional disturbance or depression.

The judicious prescribing of tramadol is essential to the safe use of this drug. With patients who are depressed or suicidal, consideration should be given to the use of non-narcotic analgesics.

Tramadol-related deaths have occurred in patients with previous histories of emotional disturbances or suicidal ideation or attempts as well as histories of misuse of tranquilizers, alcohol, and other CNSactive drugs (see WARNINGS . Risk of Overdosage ).

Serotonin Syndrome Risk

The development of a potentially life-threatening s erotonin s yndrome may occur with the use of tramadol products, including ULTRACET®, particularly with concomitant use of serotonergic drugs such as SSRIs, SNRIs, TCAs, MAOIs, and triptans, with drugs which impair metabolism of serotonin (including MAOIs), and with drugs which impair metabolism of tramadol (CYP2D6 and CYP3A4 inhibitors). This may occur within the recommended dose (see CLINICAL PHARMACOLOGY. Pharmacokinetics).

Serotonin syndrome may include mental-status changes (e. g. agitation, hallucinations, coma), autonomic instability (e. g. tachycardia, labile blood pressure, hyperthermia), neuromuscular aberrations (e. g. hyperreflexia, incoordination), and/or gas trointestinal symptoms (e. g. nausea, vomiting, diarrhea).

Hypersensitivity/Anaphylaxis

Serious and rarely fatal anaphylactic reactions have been reported in patients receiving therapy with tramadol. When these events do occur it is often following the first dose. Other reported allergic reactions include pruritus. hives, bronchospasm, angioedema. toxic epidermal necrolysis, and Stevens - Johnson syndrome. Patients with a history of anaphylactoid reactions to codeine and other opioids may be at increased risk and therefore should not receive ULTRACET® (see CONTRAINDICATIONS ).

There have been post-marketing reports of hypersensitivity and anaphylaxis associated with the use of acetaminophen. Clinical signs included swelling of the face, mouth, and throat, respiratory distress, urticaria. rash, pruritus, and vomiting. There were infrequent reports of life-threatening anaphylaxis requiring emergency medical attention. Instruct patients to discontinue ULTRACET immediately and seek medical care if they experience these symptoms. Do not prescribe ULTRACET for patients with acetaminophen allergy .

Respiratory Depression

Administer ULTRACET® cautiously in patients at risk for respiratory depression. In these patients, alternative non-opioid analgesics should be considered. When large doses of tramadol are administered with anesthetic medications or alcohol, respiratory depression may result. Respiratory depression should be treated as an overdose. If naloxone is to be administered, use cautiously because it may precipitate seizures (see WARNINGS . Seizure Risk and OVERDOSAGE ).

Interaction With Central Nervous System (CNS) Depressants

ULTRACET should be used with caution and in reduced dosages when administered to patients receiving CNS depressants such as alcohol, opioids, anesthetic agents, narcotics, phenothiazines, tranquilizers, or sedative hypnotics. Tramadol increases the risk of CNS and respiratory depression in these patients.

Interactions With Alcohol And Drugs Of Abuse

Tramadol may be expected to have additive effects when used in conjunction with alcohol, other opioids, or illicit drugs that cause central nervous system depression.

Increased Intracranial Pressure Or Head Trauma

ULTRACET® should be used with caution in patients with increased intracranial pressure or head injury. The respiratory depressant effects of opioids include carbon dioxide retention and secondary elevation of cerebrospinal fluid pressure and may be markedly exaggerated in these patients. Additionally, pupillary changes (miosis ) from tramadol may obscure the existence, extent, or course of intracranial pathology. Clinicians should also maintain a high index of suspicion for adverse drug reactions when evaluating altered mental status in these patients if they are receiving ULTRACET® (see WARNINGS . Respiratory Depression ).

Use In Ambulatory Patients

Tramadol may impair the mental and or physical abilities required for the performance of potentially hazardous tasks such as driving a car or operating machinery. The patient using this drug should be cautioned accordingly.

Use With MAO Inhibitors and Serotonin Re-uptake Inhibitors

Use ULTRACET® with great caution in patients taking monoamine oxidase inhibitors. Animal studies have shown increased deaths with combined administration of MAO inhibitors and tramadol. Concomitant use of tramadol with MAO inhibitors or SSRIs increases the risk of adverse events, including seizure and serotonin syndrome.

Use With Alcohol

ULTRACET® should not be used concomitantly with alcohol consumption. The use of ULTRACET® in patients with liver disease is not recommended.

Use With Other Acetaminophen-containing Products

Due to the potential for acetaminophen hepatotoxicity at doses higher than the recommended dose, ULTRACET® should not be used concomitantly with other acetaminophen-containing products.

Misuse, Abuse And Divers ion

Tramadol has mu-opioid agonist activity. ULTRACET®, a tramadol-containing product, can be sought by drug abusers and people with addiction disorders and may be subject to criminal diversion. The possibility of illegal or illicit use should be considered when prescribing or dispensing ULTRACET® in situations where the physician or pharmacist is concerned about an increased risk of misuse, abuse, or diversion. Misuse or abuse poses a significant risk to the abuser that could result in overdose and death (see Drug Abuse And Dependence and OVERDOSAGE ).

Concerns about abuse, addiction, and diversion should not prevent the proper management of pain. The development of addiction to opioid analgesics in properly managed patients with pain has been reported to be rare. However, data are not available to establish the true incidence of addiction in chronic pain patients.

Risk Of Overdosage

Patients taking tramadol should be warned not to exceed the dose recommended by their physician. Tramadol products in excessive doses, either alone or in combination with other CNS depressants, including alcohol, are a cause of drug-related deaths. Patients should be cautioned about the concomitant use of tramadol products and alcohol because of potentially serious CNS additive effects of these agents. Because of its added depressant effects, tramadol should be prescribed with caution for those patients whose medical condition requires the concomitant administration of sedatives, tranquilizers, muscle relaxants, tricyclic antidepressants. or other CNS depressant drugs. Patients should be advised of the additive depressant effects of these combinations.

Serious potential consequences of overdosage with tramadol are central nervous system depression, respiratory depression, and death. Some deaths have occurred as a consequence of the accidental ingestion of excessive quantities of tramadol alone or in combination with other drugs. In treating an overdose, primary attention should be given to maintaining adequate ventilation along with general supportive treatment (see OVERDOSAGE ).

A serious potential consequence of overdosage with acetaminophen is hepatic (centrilobular) necrosis. leading to hepatic failure and death. Emergency help should be sought immediately and treatment initiated immediately if overdose is suspected, even if symptoms are not apparent.

Withdrawal

Withdrawal symptoms may occur if ULTRACET® is discontinued abruptly (see also Drug Abuse And Dependence ). Reported symptoms have included anxiety, sweating, insomnia, rigors, pain, nausea, tremors, diarrhea, upper respiratory symptoms, piloerection. and rarely hallucinations. Other symptoms that have been reported less frequently with ULTRACET® discontinuation include: panic attacks, severe anxiety, and paresthesias. Clinical experience suggests that withdrawal symptoms may be avoided by tapering ULTRACET® at the time of discontinuation.

PRECAUTIONS

General

The recommended dose of ULTRACET® should not be exceeded.

Do not co-administer ULTRACET® with other tramadol or acetaminophen-containing products (see WARNINGS . Use With Other Acetaminophen-containing Products and Risk of Overdosage ).

Pediatric Use

The safety and effectiveness of ULTRACET® has not been studied in the pediatric population.

Geriatric Use

In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function; of concomitant disease; and multiple drug therapy.

Acute Abdominal Conditions

The administration of ULTRACET® may complicate the clinical assessment of patients with acute abdominal conditions.

Use In Renal Disease

ULTRACET® has not been studied in patients with impaired renal function. Experience with tramadol suggests that impaired renal function results in a decreased rate and extent of excretion of tramadol and its active metabolite, M1. In patients with creatinine clearances of less than 30 mL/min, it is recommended that the dosing interval of ULTRACET be increased, not to exceed 2 tablets every 12 hours.

Use In Hepatic Disease

ULTRACET® has not been studied in patients with impaired hepatic function. The use of ULTRACET® in patients with hepatic impairment is not recommended (see WARNINGS . Use With Alcohol ).

Carcinogenesis, Mutagenesis, Impairment Of Fertility

There are no animal or laboratory studies on the combination product (tramadol and acetaminophen) to evaluate carcinogenesis, mutagenesis. or impairment of fertility.

A slight but statistically significant increase in two common murine tumors, pulmonary and hepatic, was observed in a mouse carcinogenicity study, particularly in aged mice. Mice were dosed orally up to 30 mg/kg (90 mg/m² or 0.5 times the maximum daily human tramadol dosage of 185 mg/m²) for approximately two years, although the study was not done with the Maximum Tolerated Dose. This finding is not believed to suggest risk in humans. No such finding occurred in a rat carcinogenicity study (dosing orally up to 30 mg/kg, 180 mg/m², or 1 time the maximum daily human tramadol dosage).

Tramadol was not mutagenic in the following assays: Ames Salmonella microsomal activation test, CHO/HPRT mammalian cell assay, mouse lymphoma assay (in the absence of metabolic activation), dominant lethal mutation tests in mice, chromosome aberration test in Chinese hamsters, and bone marrow micronucleus tests in mice and Chinese hamsters. Weakly mutagenic results occurred in the presence of metabolic activation in the mouse lymphoma assay and micronucleus test in rats. Overall, the weight of evidence from these tests indicates that tramadol does not pose a genotoxic risk to humans.

No effects on fertility were observed for tramadol at oral dose levels up to 50 mg/kg (350 mg/m²) in male rats and 75 mg/kg (450 mg/m²) in female rats. These dosages are 1.6 and 2.4 times the maximum daily human tramadol dosage of 185 mg/m².

Pregnancy

Teratogenic Effects

Pregnancy Category C

No drug-related teratogenic effects were observed in the progeny of rats treated orally with tramadol and acetaminophen. The tramadol/acetaminophen combination product was shown to be embryotoxic and fetotoxic in rats at a maternally toxic dose, 50/434 mg/kg tramadol/acetaminophen (300/2604 mg/m² or 1.6 times the maximum daily human tramadol/acetaminophen dosage of 185/1591 mg/m²), but was not teratogenic at this dose level. Embryo and fetal toxicity consisted of decreased fetal weights and increased supernumerary ribs.

Non-teratogenic Effects

Tramadol alone was evaluated in peri - and post-natal studies in rats. Progeny of dams receiving oral (gavage) dose levels of 50 mg/kg (300 mg/m² or 1.6 times the maximum daily human tramadol dosage) or greater had decreased weights, and pup survival was decreased early in lactation at 80 mg/kg (480 mg/m² or 2.6 times the maximum daily human tramadol dosage).

There are no adequate and well-controlled studies in pregnant women. ULTRACET® should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Neonatal seizures, neonatal withdrawal syndrome, fetal death and stillbirth have been reported with tramadol hydrochloride during post-marketing.

Labor And Delivery

ULTRACET® should not be used in pregnant women prior to or during labor unless the potential benefits outweigh the risks. Safe use in pregnancy has not been established. Chronic use during pregnancy may lead to physical dependence and post-partum withdrawal symptoms in the newborn (see Drug Abuse And Dependence ). Tramadol has been shown to cross the placenta. The mean ratio of serum tramadol in the umbilical veins compared to maternal veins was 0.83 for 40 women given tramadol during labor.

The effect of ULTRACET®, if any, on the later growth, development, and functional maturation of the child is unknown.

Nursing Mothers

ULTRACET® is not recommended for obstetrical preoperative medication or for post-delivery analgesia in nursing mothers because its safety in infants and newborns has not been studied.

Following a single IV 100 mg dose of tramadol, the cumulative excretion in breast milk within 16 hours post-dose was 100 μg of tramadol (0.1% of the maternal dose) and 27 μg of M1.

This monograph has been modified to include the generic and brand name in many instances.

Last reviewed on RxList: 9/13/2016

Rapidus - Local, Professional, Same-Day Delivery On The App Store, Rapidus

Rapidus - Local, Professional, Same-day Delivery

Description

Rapidus delivers 24/7, professional, same-day delivery service.

It is your own affordable package delivery courier, on-demand, and anywhere you need it with touch of a button.

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iPhone Screenshots

Digoxin - Heart Disease, Halfdigoxin

Digoxin is used for treating heart failure and slowing the heart rate in patients with chronic atrial fibrillation, a type of abnormal heart rhythm. Digoxin is a digitalis glycoside. It works by increasing the force of contraction of the heart and slowing heart rate.

Use Digoxin as directed by your doctor.

Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Take Digoxin with a full glass of water.

Try to take the medication at the same time every day.

To be sure Digoxin is not causing harmful effects, your blood may need to be tested on a regular basis. Your kidney function may also need to be tested. Do not miss any scheduled appointments.

Keep taking Digoxin as directed, even if you feel well.

Do not stop taking Digoxin without first talking to your doctor. Stopping suddenly may make your condition worse.

If you miss a dose of Digoxin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Digoxin.

Store Digoxin at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Digoxin out of the reach of children and away from pets.

Do NOT use Digoxin if:

you are allergic to any ingredient in Digoxin or other digitalis medicines

you have beriberi heart disease

you have certain types of heart rhythm problems, such as ventricular fibrillation.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Digoxin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have severe heart failure, inflammation of the heart, coronary artery disease, heart attack, heart block, extra heart beats (PVCs), certain abnormal heart rhythms, or fainting due to a heart problem

if you have severe kidney, liver, or lung problems, or a thyroid problem

if you have low blood levels of calcium, magnesium, or potassium, or high blood levels of potassium or calcium.

Some medicines may interact with Digoxin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Amiodarone, amphotericin B, anticholinergics (eg, propantheline), beta-blockers (eg, propranolol), bupivacaine, calcium, certain stimulants (eg, albuterol, amphetamine, pseudoephedrine), cyclosporine, diltiazem, diphenoxylate, diuretics (eg, hydrochlorothiazide, furosemide), indomethacin, itraconazole, macrolides (eg, erythromycin), propafenone, quinidine, quinine, spironolactone, succinylcholine, tetracyclines (eg, doxycycline), thioamines (eg, methimazole), or verapamil because they may increase the risk of Digoxin's side effects, especially on the heart

Acarbose, certain anticancer medicines, cholestyramine, colestipol, kaolin-pectin, metoclopramide, penicillamine, rifampin, sulfasalazine, or thyroid hormones (eg, levothyroxine) because they may decrease Digoxin's effectiveness

Oral aminoglycosides (eg, neomycin) because the action and side effects of Digoxin may be increased or decreased

Spironolactone because it may interfere with certain lab tests for digoxin blood levels and give false readings.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Digoxin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Digoxin may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Digoxin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Tell your doctor or dentist that you take Digoxin before you receive any medical or dental care, emergency care, or surgery.

Lab tests, including electrocardiogram (ECG), electrolytes, and blood digoxin levels, may be performed while you use Digoxin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Digoxin with caution in the elderly; they may be more sensitive to its effects.

Use Digoxin with extreme caution in infants who are premature or immature; they may be more sensitive to its effects.

Poisoning may occur in children who accidently swallow Digoxin or receive too much medicine. In case of an overdose, call a doctor or poison control center right away.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Digoxin while you are pregnant. Digoxin is found in breast milk. If you are or will be breast-feeding while you use Digoxin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision, yellow vision, or other vision changes; confusion; fast, slow, or irregular heartbeat; hallucinations; mood or mental changes (eg, depression); severe or persistent nausea, vomiting, or stomach pain; unusual bruising or bleeding; unusual tiredness or weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Digoxin is used for treating heart failure and slowing the heart rate in patients with chronic atrial fibrillation, a type of abnormal heart rhythm. Digoxin is a digitalis glycoside. It works by increasing the force of contraction of the heart and slowing heart rate.

Use Digoxin as directed by your doctor.

Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Take Digoxin with a full glass of water.

Try to take the medication at the same time every day.

To be sure Digoxin is not causing harmful effects, your blood may need to be tested on a regular basis. Your kidney function may also need to be tested. Do not miss any scheduled appointments.

Keep taking Digoxin as directed, even if you feel well.

Do not stop taking Digoxin without first talking to your doctor. Stopping suddenly may make your condition worse.

If you miss a dose of Digoxin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Digoxin.

Store Digoxin at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Digoxin out of the reach of children and away from pets.

Do NOT use Digoxin if:

you are allergic to any ingredient in Digoxin or other digitalis medicines

you have beriberi heart disease

you have certain types of heart rhythm problems, such as ventricular fibrillation.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Digoxin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have severe heart failure, inflammation of the heart, coronary artery disease, heart attack, heart block, extra heart beats (PVCs), certain abnormal heart rhythms, or fainting due to a heart problem

if you have severe kidney, liver, or lung problems, or a thyroid problem

if you have low blood levels of calcium, magnesium, or potassium, or high blood levels of potassium or calcium.

Some medicines may interact with Digoxin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Amiodarone, amphotericin B, anticholinergics (eg, propantheline), beta-blockers (eg, propranolol), bupivacaine, calcium, certain stimulants (eg, albuterol, amphetamine, pseudoephedrine), cyclosporine, diltiazem, diphenoxylate, diuretics (eg, hydrochlorothiazide, furosemide), indomethacin, itraconazole, macrolides (eg, erythromycin), propafenone, quinidine, quinine, spironolactone, succinylcholine, tetracyclines (eg, doxycycline), thioamines (eg, methimazole), or verapamil because they may increase the risk of Digoxin's side effects, especially on the heart

Acarbose, certain anticancer medicines, cholestyramine, colestipol, kaolin-pectin, metoclopramide, penicillamine, rifampin, sulfasalazine, or thyroid hormones (eg, levothyroxine) because they may decrease Digoxin's effectiveness

Oral aminoglycosides (eg, neomycin) because the action and side effects of Digoxin may be increased or decreased

Spironolactone because it may interfere with certain lab tests for digoxin blood levels and give false readings.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Digoxin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Digoxin may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Digoxin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Tell your doctor or dentist that you take Digoxin before you receive any medical or dental care, emergency care, or surgery.

Lab tests, including electrocardiogram (ECG), electrolytes, and blood digoxin levels, may be performed while you use Digoxin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Digoxin with caution in the elderly; they may be more sensitive to its effects.

Use Digoxin with extreme caution in infants who are premature or immature; they may be more sensitive to its effects.

Poisoning may occur in children who accidently swallow Digoxin or receive too much medicine. In case of an overdose, call a doctor or poison control center right away.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Digoxin while you are pregnant. Digoxin is found in breast milk. If you are or will be breast-feeding while you use Digoxin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision, yellow vision, or other vision changes; confusion; fast, slow, or irregular heartbeat; hallucinations; mood or mental changes (eg, depression); severe or persistent nausea, vomiting, or stomach pain; unusual bruising or bleeding; unusual tiredness or weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Digoxin is used for treating heart failure and slowing the heart rate in patients with chronic atrial fibrillation, a type of abnormal heart rhythm. Digoxin is a digitalis glycoside. It works by increasing the force of contraction of the heart and slowing heart rate.

Use Digoxin as directed by your doctor.

Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.

Take Digoxin with a full glass of water.

Try to take the medication at the same time every day.

To be sure Digoxin is not causing harmful effects, your blood may need to be tested on a regular basis. Your kidney function may also need to be tested. Do not miss any scheduled appointments.

Keep taking Digoxin as directed, even if you feel well.

Do not stop taking Digoxin without first talking to your doctor. Stopping suddenly may make your condition worse.

If you miss a dose of Digoxin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Digoxin.

Store Digoxin at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Digoxin out of the reach of children and away from pets.

Do NOT use Digoxin if:

you are allergic to any ingredient in Digoxin or other digitalis medicines

you have beriberi heart disease

you have certain types of heart rhythm problems, such as ventricular fibrillation.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Digoxin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have severe heart failure, inflammation of the heart, coronary artery disease, heart attack, heart block, extra heart beats (PVCs), certain abnormal heart rhythms, or fainting due to a heart problem

if you have severe kidney, liver, or lung problems, or a thyroid problem

if you have low blood levels of calcium, magnesium, or potassium, or high blood levels of potassium or calcium.

Some medicines may interact with Digoxin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Amiodarone, amphotericin B, anticholinergics (eg, propantheline), beta-blockers (eg, propranolol), bupivacaine, calcium, certain stimulants (eg, albuterol, amphetamine, pseudoephedrine), cyclosporine, diltiazem, diphenoxylate, diuretics (eg, hydrochlorothiazide, furosemide), indomethacin, itraconazole, macrolides (eg, erythromycin), propafenone, quinidine, quinine, spironolactone, succinylcholine, tetracyclines (eg, doxycycline), thioamines (eg, methimazole), or verapamil because they may increase the risk of Digoxin's side effects, especially on the heart

Acarbose, certain anticancer medicines, cholestyramine, colestipol, kaolin-pectin, metoclopramide, penicillamine, rifampin, sulfasalazine, or thyroid hormones (eg, levothyroxine) because they may decrease Digoxin's effectiveness

Oral aminoglycosides (eg, neomycin) because the action and side effects of Digoxin may be increased or decreased

Spironolactone because it may interfere with certain lab tests for digoxin blood levels and give false readings.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Digoxin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Digoxin may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Digoxin with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Tell your doctor or dentist that you take Digoxin before you receive any medical or dental care, emergency care, or surgery.

Lab tests, including electrocardiogram (ECG), electrolytes, and blood digoxin levels, may be performed while you use Digoxin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Digoxin with caution in the elderly; they may be more sensitive to its effects.

Use Digoxin with extreme caution in infants who are premature or immature; they may be more sensitive to its effects.

Poisoning may occur in children who accidently swallow Digoxin or receive too much medicine. In case of an overdose, call a doctor or poison control center right away.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Digoxin while you are pregnant. Digoxin is found in breast milk. If you are or will be breast-feeding while you use Digoxin, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision, yellow vision, or other vision changes; confusion; fast, slow, or irregular heartbeat; hallucinations; mood or mental changes (eg, depression); severe or persistent nausea, vomiting, or stomach pain; unusual bruising or bleeding; unusual tiredness or weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Cefuroxime - Side Effects, Dosage, Interactions, Famicef

Cefuroxime

Cefuroxime is a prescription drug available under the brand names Ceftin and Zinacef.

It's an antibiotic used to treat certain infections caused by bacteria, such as sinus infections, throat infections, Lyme disease. and gonorrhea.

Cefuroxime was originally approved by the Food and Drug Administration (FDA) under the brand name Ceftin, manufactured by GlaxoSmithKline, in 1987.

Cefuroxime Warnings

You should not take cefuroxime if you:

Are allergic to cefuroxime or any of the other ingredients contained in the drug

Are taking Theracrys (BCG live intravesical)

Talk to your doctor before taking cefuroxime if you:

Are allergic to penicillin

Are allergic to other antibiotics such as ceflacor, cefdinir, Keflex (cephalexin), or antibiotics in the cephalosporin class

Have kidney or liver problems

Have seizures

Have poor eating habits or suffer from malnutrition

Have recently had an either infection or inflammation of your intestines while or after taking antibiotics

Cefuroxime may reduce the effects of your birth control (pills, patches, or injections).

You may need to use a back-up form of birth control while taking cefuroxime.

Pregnancy and Cefuroxime

Cefuroxime falls under the FDA's Pregnancy Category B, which means that it's generally safe for your unborn baby.

Regardless, you should tell your doctor if you are pregnant or plan to become pregnant before taking this medication.

Cefuroxime is found in breast milk. Tell your doctor if you are breastfeeding or plan to breastfeed before you take this medication.

Cefuroxime (Ceftin) Side Effects

Common side effects of cefuroxime include:

Nausea, vomiting, and diarrhea

Kidney problems

Diaper rash

Yeast infection

An allergic reaction

Serious side effects of cefuroxime include but are not limited to:

Life-threatening allergic reaction called anaphylaxis in which you may have trouble breathing, your throat closes up, and your skin breaks out into hives

Swelling of the face, including eyes, lips, mouth, tongue, and throat

Severe and possibly life-threatening skin-reactions like Steven-Johnsons syndrome or toxic epidermal necrolysis (TENs)

Blood disorders like low platelet count or low levels of all blood cells

Low levels of white blood cells

Seizures

A severe form of diarrhea noted by loose, watery stool and a foul smell that is much worse than normal

Cefuroxime (Ceftin) Interactions

It's always important to share with your doctor and pharmacist all of the medications you are taking.

This includes prescription and over-the-counter (OTC) medications, supplements like vitamins and other dietary supplements (nutritional shakes, protein powders, etc.), herbals, and any illegal or recreational drugs.

You should not take cefuroxime if you are taking Theracrys (BCG live intravesical).

Some other medications that have serious interactions with Cefuroxime include:

Acid-reflux medications like Tagamet (cimetidine), Dexilant (deslansoprazole), and Aciphex (rabeprazole)

Other acid-reflux medications like Pepcid (famotidine), Zantac (ranitidine), and Axid (nizatidine)

Vivotif (live typhoid vaccine)

Aluminum hydroxide, calcium carbonate, magnesium hydroxide, sodium bicarbonate

Cellcept (mycophenolate mofetil) and Myfortic (mycophenolic acid)

Cefuroxime and Alcohol

You should avoid or limit alcohol consumption while taking cefuroxime.

Cefuroxime and Grapefruit Juice

You should avoid eating grapefruit and drinking grapefruit juice while taking cefuroxime.

Grapefruit juice slows down how quickly the body is able to break down cefuroxime, which could cause levels in the blood to rise dangerously high.

Cefuroxime (Ceftin) Dosage

Cefuroxime comes in 250 mg and 500 mg tablets.

Doses typically range from 250 mg twice a day to 500 mg twice a day to be taken for 5 to 10 days for most infections.

Lyme disease symptoms may be treated for up to 20 days.

For gonorrhea, your doctor may prescribe a one-time dose of 1000 mg.

It is very important to take cefuroxime exactly as your doctor prescribes and to finish taking all of the medication -- even if you start to feel better or your symptoms disappear.

Otherwise, the infection might return and become much more difficult to treat.

Cefuroxime Overdose

If you suspect an overdose of cefuroxime you should contact a poison control center or emergency room immediately.

You can get in touch with a poison control center at (800) 222-1222.

Missed Dose of Cefuroxime

If you miss a dose of Cefuroxime, try to take it as soon as you remember.

If it's almost time for the next dose, skip the missed dose and take your next dose at the regular time.

Do not take two doses of the medication at the same time.

Doxycycline User Reviews For Acne At, Doxicap

User Reviews for Doxycycline

Reviews for Doxycycline to treat Acne

"I've been on doxy for sometime now Atleast 3 months+, I had a horrible experience with the drug at the start, I saw no improvements for about a month then my skin just increasingly got worse, it was extremely painful and it was mostly all down the sides of my face from ear to lips. It played a lot with my mental state because I wasn't sure if it was the breakout before it got better or my skin was just going crazy and this was just my life now. It took over a month for the breakouts to calm down and now I've been left with scarring that looks terrible. I've got quite pale skin so it is very noticeable. So at this point even though my skin has had slight improvements I don't think this was the right path for me."

Al_Pal123 September 8, 2016

1 users found this comment helpful. Did you? Yes No

"So 4 years ago, having suffered through my teenage years and the start of my 20s with acne (usual places like face, chest and back) and after several doctors giving me cream my face, chest and back (not the easiest to apply cream on your back) i eventually go and see a GP who also specialises in skin. He explained as by now if acne was going to go away, it would have done (by 22/23yo) so puts me on doxycycline. Worked wonders, still suffered spots occasionally but my back when it flairs up is like i have lots of little volcanoes on my back and they are extemely itchy and so the occasional spot wasnt bothering me. 4 years on and 26, spots are back with a vengence but back to skin doc and back on doxy for 3 months. Eat before taking!!"

Kaazz September 6, 2016

0 users found this comment helpful. Did you? Yes No

"This helped my acne to a good amount, while I was on it. I took this religiously for 6 months. I did not see any improvements until around the third month, and up until this point I just kept asking why I'm the only one my age with acne, and why it won't go away. For the last three months of my prescription though, my acne was kept at bay. I still had 2-3 pimples on my face at all times, but it was better than the usual amount. I had scarring left over, but I think the biggest disappointment of this regimen was in is the fact that my acne came back with vengeance about a month after I stopped taking it. After 3 months of trying every drugstore/high end option, I'm going to go back to the dermatologist and try something new."

AlexaTaylor September 5, 2016

2 users found this comment helpful. Did you? Yes No

"Do not get the monohydrate. It will make your acne ten times worse and it will not get better for weeks you are much better getting the other kind."

Heheh September 3, 2016

0 users found this comment helpful. Did you? Yes No

"I have had severe acne ever since I was about 14; when my period started. I have tried proactiv, every topical treatment and over the counter wash almost I know. I also have changed my diet and went on the candida cleanse as well as tried minocycline. But nothing, absolutely nothing has helped as it should have until I went on doxycycline and I am 18 now! It is the best thing I have ever tried! Within a week, I noticed a huge improvement and it is week three now and all my cystic acne is gone and I am almost acne free expect a few hormonal pimples that I am about to go on birth control for. I am so thankful and I thank God everyday for letting me find it. Thank you, Lord!"

FutureGaMeteorologistGirl17 (taken for less than 1 month) August 31, 2016

9 users found this comment helpful. Did you? Yes No

"I've been on doxycycline (100 mg daily for three months) twice, a year apart. The first time cleared my skin up beautifully. I had horrible cystic acne with new pimples popping up every day before I went to my dermatologist. I started clearing up within the first month. A year later, I started to break out again so I went back on it and my skin is back to being clear. I definitely recommend taking it with food, though. I got really bad heartburn for a week because I took this pill without eating."

MissxMegan August 28, 2016

5 users found this comment helpful. Did you? Yes No

"Used for stubborn chin and jawline acne. I'm a 23 y/o woman and 110lbs. I have been on a lower dose, 100mg once a day. I avoid dairy/calcium around the time I take this medication. My acne started to clear significantly at two months, by three months it was completely gone. I stopped taking antibiotics after three months and two months later my acne came back. Now I'm back on the same dose again. Hopefully with time I will see long term improvement."

Anonymous (taken for 1 to 6 months) August 28, 2016

4 users found this comment helpful. Did you? Yes No

"I have been struggling with severe acne for the past two years. seems like nothing I did could help me so I tried to use ucerin which is a very rich body lotion on my face this caused me to get cystic acne which was horrible I stopped using the ucerin and that went away. I have to put benzol peroxide on my face 24 seven usually and I use xout and moisturizer every day twice a day. This was horrible I was depressed I hated my life and my face looked horrible overall. My doctor prescribed me doxycycline and as soon as I started using that I saw results today is the 14th day and my face is already almost perfectly clear. This drug is amazing and I 100% recommend it cause plain and simple it works. No initial breakout from this."

Tatethegreat August 27, 2016

7 users found this comment helpful. Did you? Yes No

"I'm an African American female 20 yr old female & I've had acne since high school. Recently. this summer. I was prescribed the doxycycline 150mg to take once a day. Originally. the summer before I was prescribed another formula of doxycycline. to take twice daily. I took two pills at once by accident and about 45 minutes later. I threw up. Even though. I didn't take the correct dose. I could still tell this pill was not going to sit well in my stomach. The formula (150mg) I am taking now is much better. It was a struggle hanging in there for the first month because my body had to get used to it. But I did. I advice to eat with food or on a full stomach. Hang in there. I'm waiting on my second refill. Definetly see results ."

AnonymousGirl1108 August 22, 2016

5 users found this comment helpful. Did you? Yes No

"I have got severe acne all over my face apart from forehead this is my third week and I have seen no improvement it has made it worse to be honest my derm prescribed me 100 mg once daily for three months also my acne has become extremely painfull"

Nz4lyf (taken for less than 1 month) August 22, 2016

3 users found this comment helpful. Did you? Yes No

"I'm currently taking this for a bad skin infection and it's clearing my pimples as well. I read some comments of people saying they're taking this for months and months with "no side effects". You may not see visible side effects but taking this even twice can make it resilient for something serious like staph or MRSA. Trust me, I have MRSA and I'm on my 3rd antibiotic and it's resilient to the antibiotics. These infections can kill you. acne is awful, I had it as a teen but there are natural ways to cure it without antibiotics."

Be careful (taken for less than 1 month) August 20, 2016

0 users found this comment helpful. Did you? Yes No

"I developed cystic acne, I'm guessing as a result of hormones, stress, and genetics. My doctor and I changed what we were using during the second visit, since we were doing some trial and error (figuring out what works). Since my skin is not sensitive, we went from a combination of doxycycline, tretinoin, and clyndimicine (idk how to spell it) to a combination of tretinoin of higher strength, erythromycin/BP gel, and minocycline. My skin has cleared up in a matter of 2 months with the occasional pimples and some acne scarring. I had to switch from doxy to mono because after my first round of doxy, my insurence would not cover any form of it for some reason, I which is why I gave it a 5."

Sabrina L (taken for 1 to 6 months) August 15, 2016

2 users found this comment helpful. Did you? Yes No

"I'm an eighteen year old female and I started taking these 100mg doxycycline monohydrate pills only four days ago because they worked great for my brothers. I've been taking them with tons of water and food. They seem to work so far but I've been waking up with terrible migraine-like headaches and confusion. I'm usually an early riser and a morning person but these make me feel really nauseated. I don't recommend them for anyone who gets migraines like I do."

18 years old (taken for less than 1 month) August 15, 2016

3 users found this comment helpful. Did you? Yes No

"I've had horrible cystic acne for about 2 years now. It left horrible scarring that still remains but after my first 3 months it went away completely. Not even the occasional pimple, I just believe it makes me gain weight and lose harder. Besides that, works really well with no side effects."

beachgothic (taken for 1 to 2 years) August 6, 2016

6 users found this comment helpful. Did you? Yes No

"Hi! I'm Krissy. About a month ago I had a terrible breakout with cystic acne all over my cheeks & chin. It got so bad that it hurt to go to sleep at night. About a week ago I went & seen the doctor & he prescribed me doxycycline 100 mg to take once a day & he also prescribed me benzaclin which is benzoyl peroxide & I've been on all this for about a week & I've noticed good improvement. Its drying up all my acne. There not completely gone but before this month is over they will be. It just takes time & patience."

• Krissy • August 6, 2016

8 users found this comment helpful. Did you? Yes No

"I'm 15 years old and have had horrible acne on my face, body, and chest since 6th grade. It's been tearing down my self esteem to the point of not wanting to go outside, I even stopped swimming one summer. So about 2 weeks ago, I went to my dermatologist and he prescribed me 150mg of Acticlate (doxycycline) and I've been taking it every night along with using SulfaCleanse and Atralin. So far, I've seen no improvement in my acne whatsoever. My chest acne has gotten worse, and my face and back have stayed the same. I see my dermatologist next week and if no improvement is seen before then, I'm hoping there's another option."

Fauna S. August 3, 2016

6 users found this comment helpful. Did you? Yes No

"Over the summer before I enter college, I had severe acnes all over my face, it came to the point where I don't want to go outside because my acnes ate all my self confidence. My derma gave me different creams but none of them works. So at last, my derma made me try doxycycline and after a week my face had cleared up. I took it for 3 months, even if I ate lots of chocolates, and even if I have slept late, there will be no appearance of pimples while I'm taking the pill. But after the 3 months, I stopped and my pimples are starting to appear again but not as worse as before. So I am taking it again. I would definitely recommend it but you have to continuously use it or else your pimple will come back. But maybe It will not be the same for yo"

Anonymous August 1, 2016

11 users found this comment helpful. Did you? Yes No

"I have acne all over my face for four years. I'M turning 20.I have oily and too much bumps on my chin and I really hate it! It minimize my confidence. I almost tried everything otc for my condition. I tried cetaphil but it doesnt work. Now, my derma suggested me to take doxy 100mg twice a day. I also have a soap named Bactazil and I use benzoyl peroxide 5%. so far so good. Its my 6th day. Yes, redness is still there. But my pimples become less. There are no pus on my chin and cheek. I'm looking forward for the next step which is accutane. anw, Hello there from philippines!."

Celerypeps July 30, 2016

5 users found this comment helpful. Did you? Yes No

Monodox (doxycycline): "My daughter had had horrible acne for years. Nothing has worked, tried everything except birth control pills. She had her wisdom teeth pulled and was prescribed this and within 3 days her face was clear. Totally amazing! Shocked to find such a simple solution that has not given her any side effects."

Mam8 July 23, 2016

6 users found this comment helpful. Did you? Yes No

"I've been using it for 3 weeks, whilst also using cetaphil, moisturising, exercising, drinking a lot of water. It hasn't helped that much at all, it seemed to work, but all the acne is still winning. After 4 weeks I'm ditching it if I see no significant improvements"

Jimmy R G July 22, 2016

0 users found this comment helpful. Did you? Yes No

"I took Doxycycline for severe cystic acne for six months. My skin cleared up beautifully, however once I stopped taking it, within a week, my skin broke out 10x worse than it was before I started taking Doxycycline. I ended up not only with the usual painful cystic acne, but also on top of that developed acne rosacea. So my face was lumpy, painful, and terribly red."

LouH83 (taken for 6 months to 1 year) July 19, 2016

6 users found this comment helpful. Did you? Yes No

"I'm 15 and had pretty bad acne for about three years. My dermatologist percribed 150mg doxycycline haplate to take once in the AM, also paired with 0.1% adapalene gel 2 or 3 times a week and cetaphil gentle face clenser every night This has tremendously helped my acne. Also i use PanOxyl face wash (recommend by dermatologist) and a moisturizer every morning, You can buy it at Walmart or Walgreens. As for the doxycycline I haven't had any side effects other than little stomach aches but that's it. (I've only been using this routine for 14 days So I don't know about what will happen but as for now it's pretty great :)"

* READ (taken for less than 1 month) July 18, 2016

4 users found this comment helpful. Did you? Yes No

"I am 18 years old, and had severe acne on my cheeks and chin area since I was about 14. Acne was the hardest thing I have ever went through and was ruining my confidence. I went to the dermatologist and got prescribed .1% tretinoin cream and doxycycline 100mg twice a day. I was on doxy for 4 months and my acne stayed EXACTLY the same. I always read the review on this site for this product, and promised myself I would write one. I did not work for me, but that doesn't mean it won't work for you. I have been off doxy for about four weeks now and I have ZERO pimples. I do have a lot of redness and LOTS of acne scars, but use mederma and have had one laser treatment for scars and am planning on having 2 more. Stay positive. it gets better!!"

sav1234 July 16, 2016

8 users found this comment helpful. Did you? Yes No

"I'm 16 years old, my skin was really clear in the beginning of my freshman year, but my acne started at the end of freshman year. Obviously occasional breakouts but i started to pick at my face and it just got progressively worse. My acne isn't cystic or all over my face, my breakouts occur in certain areas such as my forehead/hairline. A few blackheads in my T zone and on my lower checks. The pimples i suffer most with are whiteheads and blackheads. I always popped whiteheads and blackheads and they have left scars on my face, I tried Retin-A and other medications but im now using Doxy and ive seen few results but I honestly hope to see greater results at the end of summer 2016 just in time for when i go back to school for my junior year."

Anonymous July 12, 2016

9 users found this comment helpful. Did you? Yes No

"I'm a 36 year old female who is managing face, chest and back acne with doxy and differin gel .3%. I take 200 mgs of doxy in the AM and at night I apply differin to my face, chest and back. I have been on this routine since 6/30/16. Since that time no new acne has sprouted and existing acne has significantly improved. Doxy and differin is an interim solution as my derm believes acne outbreak is hormonal. As interim solution, I recommend doxy and differin."

Yosprala Yosprala (aspirin and omeprazole) is a platelet aggregation inhibitor and proton pump inhibitor.

Cuvitru Cuvitru (immune globulin subcutaneous (human)) is indicated as replacement therapy in the treatment.

Erelzi Erelzi (etanercept-szzs) is a tumor necrosis factor (TNF) blocker biosimilar to Enbrel indicated.

Troxyca ER Troxyca ER (oxycodone hydrochloride and naltrexone hydrochloride) is an extended-release.

Doxycycline 100 mg

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Dipyridamole - Blood Pressure, Asasantine Lp

Dipyridamole is used for evaluating coronary artery disease in patients who cannot exercise adequately before thallium imaging (cardiac blood flow scan). Dipyridamole is a coronary vasodilator. It works by increasing blood flow to the heart, which mimics an exercise test. It is followed by the thallium test.

Use Dipyridamole as directed by your doctor.

Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Take Dipyridamole with a full glass (8 ounces) of water.

Dipyridamole is often taken together with other medications to prevent blood clots. To best treat your condition, use all of your medications as directed by your doctor.

To be sure this medication is not causing harmful effects, your doctor may need to check your progress on a regular basis. Do not miss any scheduled visits to your doctor.

If you miss a dose of Dipyridamole, take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Ask your health care provider any questions you may have about how to use Dipyridamole.

Store Dipyridamole at room temperature, between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not freeze. Keep Dipyridamole out of the reach of children and away from pets.

Do NOT use Dipyridamole if:

you are allergic to any ingredient in Dipyridamole.

Some medical conditions may interact with Dipyridamole. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have asthma; chest pain (angina); heart disease; heart block; or abnormal, rapid, slow, or irregular heartbeat

if you have severe muscle weakness.

Some medicines may interact with Dipyridamole. Tell your health care provider if you are taking any other medicines, especially any of the following:

Theophyllines (eg, aminophylline) because they may decrease Dipyridamole's effectiveness

Adenosine because the risk of its side effects, including low blood pressure and irregular heartbeat, may be increased by Dipyridamole

Anticholinesterases (eg, pyridostigmine) because their effectiveness may be decreased by Dipyridamole.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dipyridamole may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Dipyridamole may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Dipyridamole with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Avoid food or drink that has caffeine (eg, coffee, tea, cocoa, cola, chocolate) before you use Dipyridamole.

Dipyridamole should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Dipyridamole while you are pregnant. Dipyridamole is found in breast milk. Do not breastfeed while taking Dipyridamole.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Dizziness; fatigue; flushing; headache; nausea.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; confusion; fast, irregular, or slow heartbeat; one-sided weakness; seizures; slurred speech.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Dipyridamole is used for evaluating coronary artery disease in patients who cannot exercise adequately before thallium imaging (cardiac blood flow scan). Dipyridamole is a coronary vasodilator. It works by increasing blood flow to the heart, which mimics an exercise test. It is followed by the thallium test.

Use Dipyridamole as directed by your doctor.

Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Follow the directions on your prescription label.

Take Dipyridamole with a full glass (8 ounces) of water.

Dipyridamole is often taken together with other medications to prevent blood clots. To best treat your condition, use all of your medications as directed by your doctor.

To be sure this medication is not causing harmful effects, your doctor may need to check your progress on a regular basis. Do not miss any scheduled visits to your doctor.

If you miss a dose of Dipyridamole, take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.

Ask your health care provider any questions you may have about how to use Dipyridamole.

Store Dipyridamole at room temperature, between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not freeze. Keep Dipyridamole out of the reach of children and away from pets.

Do NOT use Dipyridamole if:

you are allergic to any ingredient in Dipyridamole.

Some medical conditions may interact with Dipyridamole. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have asthma; chest pain (angina); heart disease; heart block; or abnormal, rapid, slow, or irregular heartbeat

if you have severe muscle weakness.

Some medicines may interact with Dipyridamole. Tell your health care provider if you are taking any other medicines, especially any of the following:

Theophyllines (eg, aminophylline) because they may decrease Dipyridamole's effectiveness

Adenosine because the risk of its side effects, including low blood pressure and irregular heartbeat, may be increased by Dipyridamole

Anticholinesterases (eg, pyridostigmine) because their effectiveness may be decreased by Dipyridamole.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Dipyridamole may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Dipyridamole may cause dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Dipyridamole with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Avoid food or drink that has caffeine (eg, coffee, tea, cocoa, cola, chocolate) before you use Dipyridamole.

Dipyridamole should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Dipyridamole while you are pregnant. Dipyridamole is found in breast milk. Do not breastfeed while taking Dipyridamole.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Dizziness; fatigue; flushing; headache; nausea.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; confusion; fast, irregular, or slow heartbeat; one-sided weakness; seizures; slurred speech.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

Lokev, Si Photographers, Lokev

29 Lokev, SI Photographers

List your business here for free - Learn More

What Is a Home Photographer?

A home photographer is trained to make your home look its best. If you are a design professional — an architect, an interior designer or a contractor, for example — consider hiring a photographer to capture your work to enhance your portfolio, and to attract and engage new clients. They understand what buyers and renters are looking for, and they have the equipment and editing skills to fulfill those expectations.

Professional home photographers vary quite widely in the services that they offer. Some photographers include home staging in their rate, some include editing and some want to come prior to the shoot date to set up shots. Others will not offer these services unless asked or will charge an additional rate. Make sure you ask the photographer beforehand what is included in the cost. If he or she does not offer everything you need, you might want to consider reaching out to other professionals to get the best finished product. Here are some related professionals and vendors to complement the work of photographers: Home Stagers. Interior Designers & Decorators. Architects & Building Designers. Real Estate Agents.

Before you call any potential photographers, make sure they have good references. Friends who've sold or rented homes before are great resources, as are local real estate agents. Look through each photographer's online portfolio to make sure what you're looking for is being offered. Once you've done that, it's a good idea to walk around your home and write down exactly how many and what types of shots you'll need. Include any specifications you might have, such as angles, things to consider about your home’s Lokev, SI site, the time of day you think will be best and aspects of your home you want to highlight.

Questions to ask a home photographer:

Is photo editing included in your rate?

How long will it take for you to provide the photos?

Do you do home staging?

What happens if I don't like the first round of photos?

Do you offer consultations prior to the shoot?

Find a home photographer on Houzz. Narrow your search in the Professionals section of the website to Lokev, SI photographers. You can also look through Lokev, SI photos by style to find a room you like, then contact the professional who photographed it.

Professional Categories in Lokev

Professional Metro Areas

Diltahexal Cd Extended Release Capsules, Diltahexal

Diltahexal CD capsules

Consumer Medicine Information

What is in this leaflet

This leaflet answers some common questions about Diltahexal CD capsules. It does not contain all the available information.

It does not take the place of talking to your doctor or pharmacist.

All medicines have risks and benefits. Your doctor has weighed the risks of you taking these medicines against the benefits they expect it will have for you.

Keep this leaflet with the medicine. You may need to read it again.

What this medicine is used for

You have been prescribed Diltahexal CD capsules. This medicine contains an active ingredient called diltiazem hydrochloride. Diltahexal CD is designed to release the active ingredient slowly so that it works over 24 hours and can be taken once a day (CD stands for “controlled delivery”).

This medicine belongs to a group of medicines called calcium channel blockers or calcium antagonists. They work by opening up blood vessels, which lowers blood pressure and lets more blood and oxygen reach the heart. They do not change the amount of calcium in your blood or bones.

Diltahexal CD capsules are used to prevent angina or to treat hypertension (high blood pressure).

Angina is a pain or uncomfortable sensation in the chest, often spreading to the arms or neck and sometimes to the shoulders and back. The pain of angina is due to a shortage of oxygen to the heart.

High blood pressure can have many different causes including kidney disease, hardening of the arteries and some hormone imbalances. However, the vast majority of people with high blood pressure have no identifiable cause for it. If left untreated, high blood pressure can lead to serious health problems such as a stroke or heart attack.

Your doctor may have prescribed this medicine for another reason. Ask your doctor if you have any questions about why this medicine has been prescribed for you.

There is no evidence that this medicine is addictive.

This medicine is available only with a doctor’s prescription.

Before you take this medicine

When you must not take them:

Do not take this medicine:

If you have an allergy to: Diltiazem hydrochloride or any of the ingredients listed at the end of this leaflet

Symptoms of an allergic reaction to these medicines may include:

asthma, wheezing or shortness of breath

swelling of the face, lips or tongue, which may cause difficulty in swallowing or breathing

hives, itching or skin rash

fainting

If you are pregnant, or intend to become pregnant. This medicine may affect your developing baby if they are taken during pregnancy.

If you are breastfeeding or intend to breastfeed. The active ingredient of this medicine passes into breast milk and may affect your baby.

If the packaging is torn or shows signs of tampering or if capsules do not look quite right.

If the expiry date (EXP) printed on the pack has passed. If you take this medicine after the expiry date has passed, it may not work as well.

If you are not sure whether you should start taking this medicine, contact your doctor.

Do not give this medicine to a child. The safety and effectiveness of this medicine has not been established in children.

Before you start to take it

Tell your doctor:

If you have any allergies to:

any other medicines

any other substances, such as foods, preservatives or dyes

If you are pregnant or intend to become pregnant. Diltahexal CD capsules should not be used during pregnancy.

If you are breastfeeding or plan to breastfeed. Your doctor will discuss this situation with you. A decision will have to be made whether to discontinue breastfeeding or discontinue therapy taking into consideration the importance of the medicine.

if you have or have had any medical conditions, especially the following:

Abnormal heart beat rhythm

Hypotension (low blood pressure)

Heart attack or other heart-related complications

Impaired renal (kidney) or hepatic (liver) function

Diabetes

Taking other medicines

Tell your doctor if you are taking any other medicines, including any that you buy without a prescription from your pharmacy, supermarket or health food shop.

Some medicines may interfere with Diltahexal CD capsules. These include:

Dantrolene (a muscle relaxant)

Some other medicines for your heart or high blood pressure (eg. beta blockers, digoxin, amiodarone, nitrates)

Cyclosporin which you may have been given after an operation or because of rheumatoid arthritis

Rifampicin (an antibiotic)

Cimetidine or ranitidine (for ulcers or reflux)

Diazepam (for depression, alcohol withdrawal or anxiety)

Carbamazepine (for bipolar disorder or epilepsy)

Lithium (for bipolar disorder)

Theophylline (for asthma and other breathing problems)

Certain drugs used to treat prostate problems

Inhaled anaesthetic agents such as halothane, isoflurane, enflurane (for surgery)

Drugs used to lower your blood cholesterol (including simvastatin, lovastatin)

Benzodiazepines or medicines used as sedatives or to treat anxiety such as midazolam, triazolam

Corticosteroids such as methylprednisolone, prednisone, cortisone

Antiarrhythmics or medicines used to treat irregular heart beats

Diltahexal CD capsules may themselves be affected, or they may affect how well these medicines work. You may need to take different amounts of your medicine, or you may need to take different medicines. Your doctor will advise you.

Your doctor and pharmacist may have more information on medicines to be careful with or to avoid while taking Diltahexal CD capsules.

How to take this medicine

How much to take

Diltahexal CD capsules can be taken once a day, preferably at the same time every day. Your doctor will tell you how often and how much Diltahexal CD to take. Follow all directions given to you by your doctor and pharmacist carefully. Write them down if necessary.

If you do not understand the instructions on the packaging of these medicines, ask your doctor or pharmacist for help.

How to take it

Swallow the capsules with a glass of water. Do not chew them.

When to take it

Take this medicine at the same time every day.

How long to take it

If you are not sure how long to take your medicine, talk to your doctor.

If you forget to take it

If you are taking this medicine for angina, do not suddenly stop taking it since this can cause severe angina for a day or two.

If you forget to take a dose and it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to. Otherwise, take it as soon as you remember, and then go back to taking your capsules as you would normally.

Do not take a double dose to make up for the dose that you missed.

If you have trouble remembering to take your medicine, ask your pharmacist for some hints.

If you take too much (overdose)

If you think that you or anyone else may have taken too much of this medicine, immediately telephone your doctor or Poisons Information Centre (Australia telephone 13 11 26, New Zealand telephone 0800 764766), or go to the Accident and Emergency Department at your nearest hospital.

If you take too much of this medicine, you may:

feel continuously light headed or dizzy

notice your heart beating very slowly

feel pain, which could be severe, in your left arm and chest.

If any of these occur, you should get medical attention immediately.

While you are using this medicine

Things you must do

Take this medicine exactly as your doctor has prescribed. If you do not follow your doctor's instructions, you may not get relief from your attacks of angina, or your blood pressure may not be as well controlled as it could be.

If you are taking this medicine for angina, tell your doctor if you continue to have angina attacks or if they become more frequent.

Tell all your doctors, dentists and pharmacists that you are taking this medicine.

Tell your doctor or pharmacist that you are taking Diltahexal CD capsules if you are about to be started on any new medicine.

Things you must not do

Do not use this medicine to treat any other complaints unless your doctor says to.

Do not give this medicine to anyone else, even if they have the same condition as you.

As mentioned previously, if you are taking this medicine for angina, do not suddenly stop taking your medicine since this can cause severe angina for a day or two.

Things to be careful of

Be careful driving or operating machinery until you know how this medicine affects you. This medicine may cause dizziness and fainting in some patients, especially when you first start to use them. Make sure you know how you react to these medicines before you drive a car, operate machinery, or do anything else that could be dangerous if this happens to you.

Be careful not to overdo physical activities when you first start using this medicine. You may feel better when you start taking this medicine, but you will need time to improve your physical fitness.

Get up slowly when getting out of bed or standing up if you feel lightheaded, dizzy or faint. If this is a problem and it gets worse or continues, talk to your doctor.

Side effects

Tell your doctor or pharmacist as soon as possible if you do not feel well while you are using this medicine. This medicine helps most people with angina, and Diltahexal CD will help control most people’s blood pressure, but it may have unwanted effects in a few people.

All medicines can have side effects. Sometimes they are serious, but most of the time they are not. You may need medical treatment if you get some of the side effects.

Ask your doctor or pharmacist any questions you may have.

Tell your doctor if you notice any of the following and they worry you:

swelling or flushing (feeling hot suddenly)

headache

nausea, vomiting, constipation, diarrhoea, indigestion, gastric pain

dizziness

confusion, hallucinations, abnormal dreams, mental depression or mood changes

trouble sleeping

nervousness, tremor

ringing or other persistent noise in the ears

loss of memory

dry mouth

loss of appetite

weight increase

increased sensitivity to the sun

unusual movements or uncontrollable movements

rash or an itchy, burning or prickly sensation

small round, raised itchy areas on the skin

weakness or tiredness

These side effects are usually mild.

Tell your doctor immediately if you notice any of the following:

you feel continuously lightheaded or dizzy

you notice your heart beating irregularly, slowly or very quickly

you feel pain, which may be severe, in your left arm and chest

you have blisters and bleeding in the lips, eyes, mouth, nose or genitals

you have skin reactions such as red, painful or itchy spots, blisters or peeling of the skin.

These are serious side effects. You may need urgent medical attention. Serious side effects are rare.

Other side effects not listed above may also occur in some patients. Tell your doctor if you notice anything else that is making you feel unwell.

Ask your doctor or pharmacist if you do not understand anything in this section.

Do not be alarmed by this list of possible side effects. You may not experience any of them.

After taking these medicines

Storage

Keep this medicine in its container until it is time to take it. If you take the medicine out of its container it may not keep well.

Keep this medicine in a cool, dry place where it stays below 25°C. Do not store it, or any other medicine, in a bathroom or near a sink. Do not leave them in the car or on a windowsill. Heat and dampness can destroy some medicines.

Keep this medicine where young children cannot reach it. A locked cupboard at least one-and-a half metres above the ground is a good place to store medicines.

Disposal

If your doctor tells you to stop taking your Diltahexal CD medication, or it has passed its expiry date, ask your pharmacist what to do with any capsules that are left over.

Product description

What your medicine looks like

Diltahexal CD are available in bottles of 30 capsules.

All doses (180 mg, 240 mg and 360 mg) are two component capsules:

The 180 mg capsules are blue and light turquoise

The 240 mg capsules are blue/blue

The 360 mg capsules are white and light blue

Ingredients

Diltahexal CD 180 and 240 mg capsules contain:

Diltiazem hydrochloride 180 mg or 240 mg, fumaric acid, purified talc, nonpareil seeds (sucrose), colloidal silica, white beeswax, ethylcellulose, castor oil, stearic acid, methacrylic acid copolymers, tributyl acetylcitrate, simethicone, gelatin, Brilliant Blue FCF CI 42090 and titanium dioxide.

Diltahexal CD 360mg capsules contain:

Diltiazem hydrochloride 360mg, non-pareil seed (sucrose), povidone, sodium lauryl sulfate, diethyl pthalate, purified talc, methacrylic acid copolymers, tributyl acetylcitrate, simethicone, titanium dioxide, Brilliant Blue FCFand gelatin.

Supplier

Diltahexal CD capsules are supplied by: Sandoz Pty Ltd 100 Harris Street Pyrmont NSW 2009 Australia

Australian Registration Numbers: 180 mg: AUST R 131298 240 mg: AUST R 131300 360mg: AUST R 131304

Date of Preparation: August 2009.

Published by MIMS January 2010

Consumers should be aware that the information provided by the Consumer Medicines Information (CMI) search (CMI Search) is for information purposes only and consumers should continue to obtain professional advice from a qualified healthcare professional regarding any condition for which they have searched for CMI. CMIs are provided by MIMS Australia. CMI is supplied by the relevant pharmaceutical company for each consumer medical product. All copyright and responsibility for CMI is that of the relevant pharmaceutical company. MIMS Australia uses its best endeavours to ensure that at the time of publishing, as indicated on the publishing date for each resource (e. g. Published by MIMS/myDr January 2007), the CMI provided was complete to the best of MIMS Australia's knowledge. The CMI and the CMI Search are not intended to be used by consumers to diagnose, treat, cure or prevent any disease or for any therapeutic purpose. Cirrus Media Pty Limited, its servants and agents shall not be responsible for the continued currency of the CMI, or for any errors, omissions or inaccuracies in the CMI and/or the CMI Search whether arising from negligence or otherwise or from any other consequence arising there from.

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Vaclo, Vaclo

Clopidogrel is an inhibitor of platelet aggregation. A variety of drugs that inhibit platelet function have been shown to decrease morbid events in people with established atherosclerotic cardiovascular disease as evidenced by stroke or transient ischemic attacks, myocardial infarction, or need for bypass or angioplasty. This indicates that platelets participate in the initiation and/or evolution of these events and that inhibiting them can reduce the event rate.

Clopidogrel is a prodrug. The active metabolite, a thiol derivative, is formed by oxidation of clopidogrel to 2-oxo-clopidogrel and subsequent hydrolysis.

Clopidogrel selectively inhibits the binding of adenosine diphosphate (ADP) to its platelet receptor and the subsequent ADP-mediated activation of the glycoprotein GPIIb/IIIa complex, thereby inhibiting platelet aggregation. Biotransformation of clopidogrel is necessary to produce inhibition of platelet aggregation, but an active metabolite responsible for the activity of the drug has not been isolated. Clopidogrel also inhibits platelet aggregation induced by agonists other than ADP by blocking the amplification of platelet activation by released ADP. Clopidogrel does not inhibit phosphodiesterase activity.

Clopidogrel acts by irreversibly modifying the platelet ADP receptor. Consequently, platelets exposed to clopidogrel are affected for the remainder of their lifespan.

Dose dependent inhibition of platelet aggregation can be seen 2 hours after single oral doses of Clopidogrel . Repeated doses of 75 mg Clopidogrel per day inhibit ADP-induced platelet aggregation on the first day, and inhibition reaches steady state between Day 3 and Day 7. At steady state, the average inhibition level observed with a dose of 75 mg Clopidogrel per day was between 40% and 60%. Platelet aggregation and bleeding time gradually return to baseline values after treatment is discontinued, generally in about 5 days.

Administration of clopidogrel with meals did not significantly modify the bioavailability of clopidogrel as assessed by the pharmacokinetics of the main circulating metabolite.

Clopidogrel is rapidly absorbed after oral administration of repeated doses 75 mg clopidogrel (base), with peak plasma levels ( @ 3 mg/L) of the main circulating metabolite occurring approximately 1 hour after dosing. The pharmacokinetics of the main circulating metabolite are linear (plasma concentration increased in proportion to dose) in the dose range of 50 to 150 mg of clopidogrel . Absorption is at least 50% based on urinary excretion of clopidogrel - related metabolites.

Clopidogrel and the main circulating metabolite bind reversibly in vitro to human plasma protein (98% and 94%, respectively). The binding is nonsaturable in vitro up to a concentration of 100 µg/mL.

In vitro and in vivo, clopidogrel undergoes rapid hydrolysis into its carboxylic acid derivative. In plasma and urine, the glucuronide of the carboxylic acid derivative is also observed.

Clopidogrel is indicated for the reduction of atherosclerotic events (myocardial infarction, stroke and vascular death) in patients with atherosclerotic documented by recent stroke, recent myocardial infarction, or established peripheral arterial disease.

The use of Clopidogrel is contraindicated in the following conditions:

Hypersensitivity to the drug substance or any component of the product

Active pathological bleeding such as peptic ulcer or intracranial hemorrhage

. DOSAGE and ADMINISTRATION.

The recommended dose of Clopidogrel is 75 mg once daily with or without food. No dosage adjustment is necessary for elderly patients or patients with renal disease

Autonomic nervous system disorders: Syncope, palpitation. Body as a whole-general disorders: Arthenia, hernia. Rarely reported (<1%): Allergic reaction, necrosis ischemic.

Cardiovascular disorders: Cardiac failure, edema generalized rarely reported (<1%).

Central and pheripheral nervous system disorders: Cramps legs, hypoaesthesia, neuralgia, paraesthesia, vertigo.

Gastrointestinal system disorders: Constipation, vomiting. Rarely reported (<1%): gastric ulcer perforated, gastritis hemorrhagic, upper GI ulcer hemorrhagic.

Heart rate and rhythm disorders: Fibrillation atrial.

Liver and biliary system disorders: Hepatic enzymes increased. Rarely reported (<1%): Billirubinemia, hepatitis infectious, liver fatty.

Metabolic and nutritional disorders: Gout, hyperuricemia, non-protein nitrogen (NPN) increased.

Musculo-skeletal system disorders: Arthritis, arthrosis.

Platelet, bleeding and clotting disorders: GI hemorrhage, hematoma, platelets decrease. Rarely reported (<1%): Hemarthrosis, hematuria, hemoptysis, hemorrhage of operative wound, ocular hemorrhage, pulmonary hemorrhage, purpura allergic, thrombocytopenia.

Psychiatric disorders: Anxiety, insomnia.

Red blood cell disorders: anemia. Rarely reported (<1%): Anemia aplastic, anemia hypochromic.

Respiratory system disorders: Pneumonia, sinusitis. Rarely reported (<1%): Hemothorax.

Skin and appendage disorders: eczema, skin ulceration. Rarely reported (<1%): Bullous eruption, rash erythematous, rash maculopapular, urticaria.

Urinary system disorders: cystitis.

Vision disorders: Cataract, conjunctivitis.

Other potentially serious adverse events which may be of clinical interest but were rarely reported (<1%):

Reproductive disorders, female: Menorrhagia

White cell and reticuloendothelial system disorders: Agranulocytosis, granulocytopenia, leukemia, leukopenia, neutrophils decreased.

. WARNINGS and PRECAUTIONS.

In patients with acute myocardial infarction, clopidogrel therapy should not be initiated within the first few days following myocardial infarction.

As with other anti-platelet agents, clopidogrel should be used with caution in patients who may be at risk of increased bleeding from trauma, surgery or other pathological conditions and in patients receiving treatment with ASA, NSAID, heparin, glycoprotein Iib/IIIa inhibitors or thrombolytics. Patients should be followed carefully for any signs of bleeding including occult bleeding, especially during the first weeks of treatment and/or after invasive cardiac procedures of surgery. If a patient is to undergo elective surgery and an antiplatelet effect is not desired, clopidogrel should be discontinued 7 days prior to surgery.

Clopidogrel prolongs bleeding time and should be used with caution in patients who have lesions with a propensity to bleed (particulary gastrointestinal and intraocular). Patients should be told that it may take longer than usual to stop bleeding when they take clopidogrel (alone or in combination with ASA), and that they should report any unusual bleeding (site or duration) to their physician. Patients should inform physicians and dentists that they are taking clopidogrel before any surgery is scheduled and before any new drug is taken.

Therapeutic experience with clopidogrel is limited in patients with renal impairment. Therefore clopidogrel should be used with caution in these patients.

Experience is limited in patients with moderate hepatic disease who may have bleeding diatheses. Clopidogrel should therefore be used with caution in this population.

Due to the risk of bleeding and haematological undesirable effects, blood cell count determination and/or other appropriate testing should be promptly considered whenever clinical symptoms suggestive of bleeding arise during the course of treatment.

. PREGNANCY and LACTAION.

Pregnancy: Reproduction studies performed in rats and in rabbits revealed no evidence of impaired fertility or harm to the foetus due to clopidogrel . There are, however, no adequate and well-controlled studies in pregnant women. In view of the lack of date, clopidogrel is not recommended during pregnancy.

Lactation: Studies in rats shown that clopidogrel and/or its metabolites are excreted in the milk. It is not known whether this medical product is excreted in human milk.

Safety and effectiveness in the patient under 18 years old have not been established.

The concomitant administration of clopidogrel with warfarin is not recommended since it may increase the intensity of bleedings.

Drugs that might induce gastrointestinal lesions (such as Non-Steroidal Anti-Inflammatory Drugs) should be used with caution in patients taking clopidogrel .

In a clinical study conducted in healthy subjects, clopidogrel did not necessitate modification of the heparin dose or alter the effect of heparin on coagulation. Co-administration of heparin had no effect on the inhibition of platelet aggregation induced by clopidogrel . However, the safety pf this combination has not been established and concomitant use should be undertaken with caution.

The safety of concomitant administration of clopidogrel . rt-PA and heparin was assessed in patients with recent myocardial infarction. The incidence of clinically significant bleeding was similar to that observed when rt-PA and heparin was assessed in patients with recent myocarial infarction. The incidence of administration of clopidogrel with other thrombolytic agents has not been establised and should be undertaken with caution.

The pharmacokinetics of digoxin or theophylline were not modified by the co-administration of clopidogrel .

Antacids did not modify the extent of clopidogrel absorption.

Glycoprotein IIb/IIIa inhibitors: clopidogrel should be used with caution in patients who may be at risk of increased bleeding from trauma, surgery or other pathological conditions that receive concomitant glycoprotein IIb/IIIa inhibitors.

Acetylsalicylic (ASA): ASA did not modify the clopidogrel mediated inhibition of ADP-induced platelet agregation, but clopidogrel potentiated the effect of ASA on collagen-induced platelet aggregation

Thrombolytics: The safety of the concomitant administration of clopidogrel . rt-PA and heparin was assessed in patients with recent myocardial infarction. The incidence of clinically significant bleeding was similar to that observed when rt-PA and heparin are co-administered with ASA. The safety of the concomitant administration of clopidogrel with other thrombolytic agents has not been formally established and should undertaken with caution.

. PRESENTATION and REGISTRATION NUMBER.

VACLO film-coated tablet, Box, 5 strips @ 6 film-coated tablets; No. Reg. DKL0834607717A1

ON MEDICAL PRESCRIPTION ONLY

STORE AT TEMPERATURE BELOW 30?C

PROTECT FROM LIGHT

Manufactered by PT DEXA MEDICA JL. LETJEN BAMBANG UTOYO 138 PALEMBANG – INDONESIA for PT FERRON PAR PHARMACEUTICALS CIKARANG - INDONESIA

Clopidogrel is an inhibitor of platelet aggregation. A variety of drugs that inhibit platelet function have been shown to decrease morbid events in people with established atherosclerotic cardiovascular disease as evidenced by stroke or transient ischemic attacks, myocardial infarction, or need for bypass or angioplasty. This indicates that platelets participate in the initiation and/or evolution of these events and that inhibiting them can reduce the event rate.

Clopidogrel is a prodrug. The active metabolite, a thiol derivative, is formed by oxidation of clopidogrel to 2-oxo-clopidogrel and subsequent hydrolysis.

Clopidogrel selectively inhibits the binding of adenosine diphosphate (ADP) to its platelet receptor and the subsequent ADP-mediated activation of the glycoprotein GPIIb/IIIa complex, thereby inhibiting platelet aggregation. Biotransformation of clopidogrel is necessary to produce inhibition of platelet aggregation, but an active metabolite responsible for the activity of the drug has not been isolated. Clopidogrel also inhibits platelet aggregation induced by agonists other than ADP by blocking the amplification of platelet activation by released ADP. Clopidogrel does not inhibit phosphodiesterase activity.

Clopidogrel acts by irreversibly modifying the platelet ADP receptor. Consequently, platelets exposed to clopidogrel are affected for the remainder of their lifespan.

Dose dependent inhibition of platelet aggregation can be seen 2 hours after single oral doses of Clopidogrel . Repeated doses of 75 mg Clopidogrel per day inhibit ADP-induced platelet aggregation on the first day, and inhibition reaches steady state between Day 3 and Day 7. At steady state, the average inhibition level observed with a dose of 75 mg Clopidogrel per day was between 40% and 60%. Platelet aggregation and bleeding time gradually return to baseline values after treatment is discontinued, generally in about 5 days.

Administration of clopidogrel with meals did not significantly modify the bioavailability of clopidogrel as assessed by the pharmacokinetics of the main circulating metabolite.

Clopidogrel is rapidly absorbed after oral administration of repeated doses 75 mg clopidogrel (base), with peak plasma levels ( @ 3 mg/L) of the main circulating metabolite occurring approximately 1 hour after dosing. The pharmacokinetics of the main circulating metabolite are linear (plasma concentration increased in proportion to dose) in the dose range of 50 to 150 mg of clopidogrel . Absorption is at least 50% based on urinary excretion of clopidogrel - related metabolites.

Clopidogrel and the main circulating metabolite bind reversibly in vitro to human plasma protein (98% and 94%, respectively). The binding is nonsaturable in vitro up to a concentration of 100 µg/mL.

In vitro and in vivo, clopidogrel undergoes rapid hydrolysis into its carboxylic acid derivative. In plasma and urine, the glucuronide of the carboxylic acid derivative is also observed.

Clopidogrel is indicated for the reduction of atherosclerotic events (myocardial infarction, stroke and vascular death) in patients with atherosclerotic documented by recent stroke, recent myocardial infarction, or established peripheral arterial disease.

The use of Clopidogrel is contraindicated in the following conditions:

Hypersensitivity to the drug substance or any component of the product

Active pathological bleeding such as peptic ulcer or intracranial hemorrhage

. DOSAGE and ADMINISTRATION.

The recommended dose of Clopidogrel is 75 mg once daily with or without food. No dosage adjustment is necessary for elderly patients or patients with renal disease

Autonomic nervous system disorders: Syncope, palpitation. Body as a whole-general disorders: Arthenia, hernia. Rarely reported (<1%): Allergic reaction, necrosis ischemic.

Cardiovascular disorders: Cardiac failure, edema generalized rarely reported (<1%).

Central and pheripheral nervous system disorders: Cramps legs, hypoaesthesia, neuralgia, paraesthesia, vertigo.

Gastrointestinal system disorders: Constipation, vomiting. Rarely reported (<1%): gastric ulcer perforated, gastritis hemorrhagic, upper GI ulcer hemorrhagic.

Heart rate and rhythm disorders: Fibrillation atrial.

Liver and biliary system disorders: Hepatic enzymes increased. Rarely reported (<1%): Billirubinemia, hepatitis infectious, liver fatty.

Metabolic and nutritional disorders: Gout, hyperuricemia, non-protein nitrogen (NPN) increased.

Musculo-skeletal system disorders: Arthritis, arthrosis.

Platelet, bleeding and clotting disorders: GI hemorrhage, hematoma, platelets decrease. Rarely reported (<1%): Hemarthrosis, hematuria, hemoptysis, hemorrhage of operative wound, ocular hemorrhage, pulmonary hemorrhage, purpura allergic, thrombocytopenia.

Psychiatric disorders: Anxiety, insomnia.

Red blood cell disorders: anemia. Rarely reported (<1%): Anemia aplastic, anemia hypochromic.

Respiratory system disorders: Pneumonia, sinusitis. Rarely reported (<1%): Hemothorax.

Skin and appendage disorders: eczema, skin ulceration. Rarely reported (<1%): Bullous eruption, rash erythematous, rash maculopapular, urticaria.

Urinary system disorders: cystitis.

Vision disorders: Cataract, conjunctivitis.

Other potentially serious adverse events which may be of clinical interest but were rarely reported (<1%):

Reproductive disorders, female: Menorrhagia

White cell and reticuloendothelial system disorders: Agranulocytosis, granulocytopenia, leukemia, leukopenia, neutrophils decreased.

. WARNINGS and PRECAUTIONS.

In patients with acute myocardial infarction, clopidogrel therapy should not be initiated within the first few days following myocardial infarction.

As with other anti-platelet agents, clopidogrel should be used with caution in patients who may be at risk of increased bleeding from trauma, surgery or other pathological conditions and in patients receiving treatment with ASA, NSAID, heparin, glycoprotein Iib/IIIa inhibitors or thrombolytics. Patients should be followed carefully for any signs of bleeding including occult bleeding, especially during the first weeks of treatment and/or after invasive cardiac procedures of surgery. If a patient is to undergo elective surgery and an antiplatelet effect is not desired, clopidogrel should be discontinued 7 days prior to surgery.

Clopidogrel prolongs bleeding time and should be used with caution in patients who have lesions with a propensity to bleed (particulary gastrointestinal and intraocular). Patients should be told that it may take longer than usual to stop bleeding when they take clopidogrel (alone or in combination with ASA), and that they should report any unusual bleeding (site or duration) to their physician. Patients should inform physicians and dentists that they are taking clopidogrel before any surgery is scheduled and before any new drug is taken.

Therapeutic experience with clopidogrel is limited in patients with renal impairment. Therefore clopidogrel should be used with caution in these patients.

Experience is limited in patients with moderate hepatic disease who may have bleeding diatheses. Clopidogrel should therefore be used with caution in this population.

Due to the risk of bleeding and haematological undesirable effects, blood cell count determination and/or other appropriate testing should be promptly considered whenever clinical symptoms suggestive of bleeding arise during the course of treatment.

. PREGNANCY and LACTAION.

Pregnancy: Reproduction studies performed in rats and in rabbits revealed no evidence of impaired fertility or harm to the foetus due to clopidogrel . There are, however, no adequate and well-controlled studies in pregnant women. In view of the lack of date, clopidogrel is not recommended during pregnancy.

Lactation: Studies in rats shown that clopidogrel and/or its metabolites are excreted in the milk. It is not known whether this medical product is excreted in human milk.

Safety and effectiveness in the patient under 18 years old have not been established.

The concomitant administration of clopidogrel with warfarin is not recommended since it may increase the intensity of bleedings.

Drugs that might induce gastrointestinal lesions (such as Non-Steroidal Anti-Inflammatory Drugs) should be used with caution in patients taking clopidogrel .

In a clinical study conducted in healthy subjects, clopidogrel did not necessitate modification of the heparin dose or alter the effect of heparin on coagulation. Co-administration of heparin had no effect on the inhibition of platelet aggregation induced by clopidogrel . However, the safety pf this combination has not been established and concomitant use should be undertaken with caution.

The safety of concomitant administration of clopidogrel . rt-PA and heparin was assessed in patients with recent myocardial infarction. The incidence of clinically significant bleeding was similar to that observed when rt-PA and heparin was assessed in patients with recent myocarial infarction. The incidence of administration of clopidogrel with other thrombolytic agents has not been establised and should be undertaken with caution.

The pharmacokinetics of digoxin or theophylline were not modified by the co-administration of clopidogrel .

Antacids did not modify the extent of clopidogrel absorption.

Glycoprotein IIb/IIIa inhibitors: clopidogrel should be used with caution in patients who may be at risk of increased bleeding from trauma, surgery or other pathological conditions that receive concomitant glycoprotein IIb/IIIa inhibitors.

Acetylsalicylic (ASA): ASA did not modify the clopidogrel mediated inhibition of ADP-induced platelet agregation, but clopidogrel potentiated the effect of ASA on collagen-induced platelet aggregation

Thrombolytics: The safety of the concomitant administration of clopidogrel . rt-PA and heparin was assessed in patients with recent myocardial infarction. The incidence of clinically significant bleeding was similar to that observed when rt-PA and heparin are co-administered with ASA. The safety of the concomitant administration of clopidogrel with other thrombolytic agents has not been formally established and should undertaken with caution.

. PRESENTATION and REGISTRATION NUMBER.

VACLO film-coated tablet, Box, 5 strips @ 6 film-coated tablets; No. Reg. DKL0834607717A1

ON MEDICAL PRESCRIPTION ONLY

STORE AT TEMPERATURE BELOW 30?C

PROTECT FROM LIGHT

Manufactered by PT DEXA MEDICA JL. LETJEN BAMBANG UTOYO 138 PALEMBANG – INDONESIA for PT FERRON PAR PHARMACEUTICALS CIKARANG - INDONESIA

Amoxicillin Uses, Side Effects - Dosage Guide, Moxicillin

Amoxicillin

What is amoxicillin?

Amoxicillin is a penicillin antibiotic that fights bacteria.

Amoxicillin is used to treat many different types of infection caused by bacteria, such as tonsillitis, bronchitis, pneumonia, gonorrhea, and infections of the ear, nose, throat, skin, or urinary tract.

Amoxicillin is also sometimes used together with another antibiotic called clarithromycin (Biaxin) to treat stomach ulcers caused by Helicobacter pylori infection. This combination is sometimes used with a stomach acid reducer called lansoprazole (Prevacid).

There are many brands and forms of amoxicillin available and not all brands are listed on this leaflet.

Important information

Do not use this medication if you are allergic to amoxicillin or to any other penicillin antibiotic, such as ampicillin (Omnipen, Principen), dicloxacillin (Dycill, Dynapen), oxacillin (Bactocill), penicillin (Beepen-VK, Ledercillin VK, Pen-V, Pen-Vee K, Pfizerpen, V-Cillin K, Veetids), and others.

Before using amoxicillin, tell your doctor if you are allergic to cephalosporins such as Omnicef, Cefzil, Ceftin, Keflex, and others. Also tell your doctor if you have asthma, liver or kidney disease, a bleeding or blood clotting disorder, mononucleosis (also called "mono"), or any type of allergy.

Amoxicillin can make birth control pills less effective. Ask your doctor about using a non-hormone method of birth control (such as a condom, diaphragm, spermicide) to prevent pregnancy while taking this medicine. Take this medication for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Amoxicillin will not treat a viral infection such as the common cold or flu. Do not share this medication with another person, even if they have the same symptoms you have.

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop taking amoxicillin and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Before taking this medicine

You should not use amoxicillin if you are allergic to any penicillin antibiotic, such as ampicillin, dicloxacillin, oxacillin, penicillin, or ticarcillin.

To make sure amoxicillin is safe for you, tell your doctor if you have:

liver or kidney disease;

mononucleosis (also called "mono");

a history of diarrhea caused by taking antibiotics; or

food or drug allergies (especially to a cephalosporin antibiotic such as Omnicef, Cefzil, Ceftin, Keflex, and others).

If you are being treated for gonorrhea, your doctor may also have you tested for syphilis, another sexually transmitted disease.

Amoxicillin is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment.

Amoxicillin can make birth control pills less effective. Ask your doctor about using non hormonal birth control (condom, diaphragm with spermicide) to prevent pregnancy while taking this medicine.

Amoxicillin can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

The amoxicillin chewable tablet may contain phenylalanine. Talk to your doctor before using the chewable tablets if you have phenylketonuria (PKU).

How should I take amoxicillin?

Take amoxicillin exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Take this medicine at the same time each day.

The Moxatag brand of amoxicillin should be taken with food, or within 1 hour after eating a meal.

Some forms of amoxicillin may be taken with or without food. Check your medicine label to see if you should take your medicine with food or not.

You may need to shake the liquid medicine well just before you measure a dose. Follow the directions on your medicine label.

Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one. You may place the liquid directly on the tongue, or you may mix it with water, milk, baby formula, fruit juice, or ginger ale. Drink all of the mixture right away. Do not save any for later use.

The chewable tablet should be chewed before you swallow it.

Do not crush, chew, or break an extended-release tablet . Swallow it whole.

While using amoxicillin, you may need frequent blood tests. Your kidney and liver function may also need to be checked.

If you are taking amoxicillin with clarithromycin and/or lansoprazole to treat stomach ulcer, use all of your medications as directed. Read the medication guide or patient instructions provided with each medication. Do not change your doses or medication schedule without your doctor's advice.

Use this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Amoxicillin will not treat a viral infection such as the flu or a common cold.

Do not share this medicine with another person, even if they have the same symptoms you have.

This medicine can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using amoxicillin.

Store at room temperature away from moisture, heat, and light.

You may store liquid amoxicillin in a refrigerator but do not allow it to freeze. Throw away any liquid medicine that is not used within 14 days after it was mixed at the pharmacy.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include confusion, behavior changes, a severe skin rash, urinating less than usual, or seizure (black-out or convulsions).

What should I avoid while taking amoxicillin?

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, stop using amoxicillin and call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Amoxicillin side effects

Get emergency medical help if you have any of these signs of an allergic reaction to amoxicillin: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have:

diarrhea that is watery or bloody;

fever, swollen gums, painful mouth sores, pain when swallowing, skin sores, cold or flu symptoms, cough, trouble breathing;

swollen glands, rash or itching, joint pain, or general ill feeling;

pale or yellowed skin, yellowing of the eyes, dark colored urine, fever, confusion or weakness;

severe tingling, numbness, pain, muscle weakness;

easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin; or

severe skin reaction--fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Common amoxicillin side effects may include:

stomach pain, nausea, vomiting, diarrhea;

vaginal itching or discharge;

swollen, black, or "hairy" tongue.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect amoxicillin?

Other drugs may interact with amoxicillin, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

More about amoxicillin

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about amoxicillin.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 9.05. Revision Date: 2016-07-22, 8:38:25 AM.

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Kop Bicrolid (Biaxin) Utan Recept, Bicrolid

Kopa Bicrolid (Biaxin) Natet Utan Recept

Bicrolid (Biaxin) Forklaring

Bicrolid anvands for att hantera olika typer av transmissioner som paverkar huden och andas. Bicrolid kan ocksa anvandas tillsammans med nagra andra lakemedel for att hantera magen sar som beror pa den Helicobacter pylori.

Bicrolid Dee bakterier i kroppen.

Bicrolid kan ocksa kallas Clarithromycin, Maclar, Klaricid, Klacid, Clarimac, Claribid.

Allmant Titel forknippas med Bicrolid ar faktiskt Klaritromycin.

Varumarke associerade med Bicrolid tenderar att vara Bicrolid, Bicrolid XL, Bicrolid XL-Pak.

Bicrolid (Biaxin) Dose

Bicrolid kommer in:

250mg lagre dos friktionsmaterial

500mg Regular Dos friktionsmaterial

Bicrolid kommer i piller samt tandvard fordrojning, paus.

Get Bicrolid genom munnen.

Get Bicrolid tillsammans med komplett koppen i samband med dricksvatten.

Get Bicrolid utan eller med maltider.

Vanligtvis inte slipa, tugga upp, eller ens knacka sjalva Bicrolid piller. Konsumera p-piller hela.

Darra sjalva Bicrolid dental fordrojning, pausa en stund innan berakning av dosen. Berakna den verkliga Bicrolid dental fordrojning, pausa med en markbar berakning plats eller ens medicinering mugg.

Get Bicrolid vad galler med avseende pa sju for att fjorton dagar.

Den faktiska dosen och aven typ av lakemedel ar beroende av tillstandet och dess rekommenderade terapi.

Vanligtvis inte sluta anvanda Bicrolid helt plotsligt.

Bicrolid (Biaxin) I brist forknippas med doserings

Vanligtvis far inte dubbel dos. Om du hoppar over dosen du behover for att bara den nar du kom ihag nar det galler din saknas. Nar det ar dags for dosering du behover bara pa din egen normal dosering rutin.

Bicrolid (Biaxin) Overdosering

Om du overdoserar Bicrolid och du undviker ocksa stor att du behover kolla din lakare eller ens lakare omedelbart. Forknippas med Bicrolid overdosering: illamaende eller krakningar, kasta upp, diarre, magont.

Bicrolid (Biaxin) Lagringsutrymme

Shop i rymden temperaturer mellan tjugo liksom tjugofem nivaer D (68 liksom Seventy Seven nivaer F) fran fukt och temperatur. Behall text ordentligt stangd. Skyddsatgarder genom belysning. Starka nagon form av orord medicinering efter utgangen dagen. Behall fran uppna barnen.

Bicrolid (Biaxin) Negativa effekter

Bicrolid erbjuder de negativa effekterna. Den mest typiska tenderar att vara:

mattlig magen obehag friktionsmaterial

illamaende eller krakningar friktionsmaterial

kastar upp friktionsmaterial

diarre friktionsmaterial

irriterad mage friktionsmaterial

ovanligt eller ens obekvam smak pa tanderna friktionsmaterial

missfargning friktionsmaterial

trotthet friktionsmaterial

huvudvark friktionsmaterial

angest friktionsmaterial

missforstand friktionsmaterial

porer och hudallergi friktionsmaterial

genital klada eller ens slappa friktionsmaterial

Mycket mindre typiska och allvarliga negativa effekter i hela anvander Bicrolid:

allergiska reaktion reaktioner (urtikaria, andas in och utandning fragor, allergi, samt utbrott) friktionsmaterial

ojamlika hjartslag; friktionsmaterial

hjartproblem friktionsmaterial

brist i samband med andning friktionsmaterial

vattning eller ens vekling avforing friktionsmaterial

magen obehag friktion material

lagre temperatur friktionsmaterial

brist pa hunger friktionsmaterial

gulsot friktionsmaterial

temperaturfriktionsmaterial

varkande tonsiller friktionsmaterial

huvudvark med en allvarlig brannande friktionsmaterial

rodfargade porer och hudallergi friktionsmaterial

problem med att lyssna pa friktionsmaterial

Negativa effekter indikationer beroende av medicin du kanske anvander men dessutom lita pa ditt valbefinnande villkor och ytterligare aspekter

Bicrolid (Biaxin) Kontraindikationer

Vanligtvis gor inte utnyttjar Bicrolid om du ar kanslig for att Bicrolid element eller klaritromycin eller motsvarande mediciner till exempel azitromycin (Zithromax), diritromycin (Dynabac), erytromycin (E. Electronic. H. E-mycin, Ery-Tab, Erythrocin), troleandomycin (Tao).

Bli forsiktig om du vantar annars du tanker ha ett barn, annars ar du verkligen en medicinsk mamma.

Vanligtvis inte utnyttjar Bicrolid for astemizol (Hismanal), cisaprid (Propulsid), mjoldryga medicinering till exempel ergotamin (Ergomar, Ergostat, Cafergot, Ercaf, Wigraine), eller till och med dihydroergotamin (D. De skulle. Electronic. fyrtiofem, Migranal nasspray), pimozid (Orap), terfenadin (Seldane).

Spela rollen av forsiktiga tillsammans med Bicrolid nyttjande vid att fa sjukdomar i levern, njur sjukdom, myasthenia gravis, porfyri, individ eller ens slaktforskning forknippas med "langt QT-syndrom".

Spela rollen av forsiktiga tillsammans med Bicrolid utnyttjande bor du anvanda nagon form av lakare ordinerats eller receptfria lakemedel, naturlig beredning, eller ens komplettera.

Forhindra alkoholhaltiga drycker.

Det kan vara skadligt att forhindra Bicrolid anvander helt plotsligt.

Bicrolid (Biaxin) Vanliga fragor

Queen: Vad exakt ar Bicrolid?

Bicrolid ar verkligen ett lakemedel i samband med makrolid antibiotika laget. Bicrolid Dee bakterier i din body. A

Queen: Exakt vad det galler verkligen Bicrolid utnyttjad?

Bicrolid anvands for att hantera olika typer av transmissioner som paverkar huden och andas. Bicrolid kan ocksa anvandas tillsammans med nagra andra lakemedel for att hantera magen sar som beror pa den Helicobacter pylori. A

Queen: Mycket basta allmanna titeln i samband med Bicrolid?

General avdelning ar faktiskt Clarithromycin. A

Queen: Vilka andra marken an Bicrolid?

Varumarken tenderar att vara Bicrolid, Bicrolid XL, Bicrolid XL-Pak. A

Queen: Om vilka typer ar faktiskt Bicrolid tillganglig?

Bicrolid kommer i piller samt tandvard forseningar pause. A

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Buy Carpiaton - Spironolactone - Online Without Prescriptions, Carpiaton

Aldactone (Carpiaton)

Aldactone is used for treating swelling and fluid retention in patients with congestive heart failure, liver cirrhosis, or kidney problems (nephrotic syndrome). It is also used for treatment of high blood pressure. It may also be used to treat or prevent low blood potassium. It may also be used to treat excess secretion of the hormone aldosterone by the adrenal gland. Aldactone is a potassium-sparing diuretic. It works by blocking the hormone aldosterone, causing the kidney to eliminate excess water, save potassium, and lower blood pressure.

Use Aldactone as directed by your doctor.

Take Aldactone by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

Aldactone may increase the amount of urine or cause you to urinate more often when you first start taking it. To keep this from disturbing your sleep, try to take your dose before 6 pm.

If you miss a dose of Aldactone, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. If more than one dose is missed, restart the medication and advise your doctor or pharmacist at your next appointment.

Ask your health care provider any questions you may have about how to use Aldactone.

Store Aldactone at room temperature, between 59 and 77 degrees F (15 and 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Aldactone out of the reach of children and away from pets.

Active Ingredient: Spironolactone.

Do NOT use Aldactone if:

you are allergic to any ingredient in Aldactone

you are unable to urinate, have severe kidney problems, or have high blood potassium levels

you are taking a potassium supplement, another potassium-sparing diuretic (eg, amiloride, triamterene), or another aldosterone-blocker (eg, eplerenone).

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Aldactone. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have high acidity in your body fluids; low blood sodium levels; high blood potassium levels; kidney, liver, or heart disease; diabetes; or high urea or nitrogen in your blood

if you have menstrual disease.

Some medicines may interact with Aldactone. Tell your health care provider if you are taking any other medicines, especially any of the following:

Adrenocorticotropic hormone (corticotropin) (ACTH) or corticosteroids (eg, prednisone) or because low blood electrolyte levels may occur

Barbiturates (eg, phenobarbital) or narcotics (eg, morphine) because dizziness upon standing may occur

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril), angiotensin II receptor antagonists (eg, valsartan), cyclosporine, macrolide immunosuppressives (eg, tacrolimus), other aldosterone-blockers (eg, eplerenone), other potassium sparing diuretics (eg, amiloride, triamterene), or potassium supplements because high blood potassium levels may occur (eg, listlessness, confusion, abnormal skin sensations of the arms and legs, heaviness of limbs, slowed heart rate, irregular heart rhythm, potentially life-threatening slow or irregular heartbeat)

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, indomethacin) because they may decrease Aldactone's effectiveness and increase the risk of kidney problems and high blood potassium

Digoxin, digitoxin, lithium, nondepolarizing muscle relaxants (eg, tubocurarine), or quinidine because the risk of their side effects and toxicity may be increased by Aldactone

Pressor amines (eg, norepinephrine) because their effectiveness may be decreased by Aldactone.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Aldactone may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Aldactone may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Aldactone with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

Aldactone can raise your body's potassium levels. This is more likely to occur in people with kidney problems or diabetes, in the elderly, or if the patient is severely ill. Potassium levels must be closely monitored in people with any of these problems or illnesses. If not treated, high potassium levels can be fatal.

Check with your doctor before you use a salt substitute or a product that has potassium in it.

Lab tests, including kidney function, blood pressure, blood potassium, and chemistries, may be performed while you use Aldactone. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Aldactone with caution in the elderly; they may be more sensitive to its effects.

Aldactone should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Aldactone while you are pregnant. Aldactone is found in breast milk. Do not breast-feed while taking Aldactone.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Diarrhea; drowsiness; headache; nausea; stomach cramping; vomiting.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry, or bloody stools; change in the amount of urine produced; confusion; dark urine; decreased sexual ability; enlarged breasts in men; irregular or missed menstrual periods; pale stools; severe or persistent stomach pain; symptoms of abnormal fluid or electrolyte levels (eg, fast, slow, or irregular heartbeat; increased thirst; muscle weakness; severe or persistent dry mouth, nausea, or vomiting; severe or persistent dizziness or drowsiness; unusual fatigue or sluggishness; tingling sensation); yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

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Rulid (Roxithromycine ) The Antibiotic Besigned For Bacterial And Soft Tissue Infections - Antiaging

Rulid Antibiotics fight a host of bacterial infections

Rulid target a wide range of bacterial infections and are commonly used to treat respiratory tract conditions such as acute bronchitis, tonsillitis and pneumonia. Rulid also combats bacterial infections in the body’s genitals, gastrointestinal tract and soft tissues.

What is Rulid?

Rulid acts as a bacteria fighting antibiotic. In common with other antibiotics, Rulid targets bacterial infections rather than viruses, so is not recommended for viral infections.

Rulid belongs to a group of antibiotics known as macrolides. It shares characteristics with other macrolide drugs including erythromycin, azithromycin and clarithromycin. Macrolide antibiotics such as Rulid fight bacterial infections by blocking the proteins at the heart of bacteria growth. They also act to kill bacteria directly (becoming what is termed as ‘bactericidal’) if the bacteria presence is high enough.

One of the reasons why macrolides are so effective in the treatment of bacterial infections is due to their propensity to form in the body’s white blood cells (leukocytes). White blood cells are an integral part of our immune system, ensuring that the macrolides are in a prime position to fight any bacterial infections.

What are bacteria?

Bacteria are omnipresent in the world. They are microscopic cells present in air, water, food, plants, people and animals that are vital to life, but can also cause infection and disease. Bacteria cells are classified as prokaryotic – a primitive, single cell structure without a nucleus or membrane. This sets them apart from human eukaryotic cells, which are more complex, multi-cellular structures.

The effectiveness of Rulid is directly linked to the differing characteristics of human eukaryotic cells and bacteria cells.

Eukaryotic and bacteria cells both contain a key protein-creating component known as ribosome. As a macrolide drug, Rulid act to kill bacteria by inhibiting the production of these ribosomes. But human eukaryotic cells are not affected by macrolide antibiotics, leaving their ribosomes intact.

What conditions does Rulid treat?

Rulid is used to target a variety of bacterial infections – including those affecting the respiratory tract, genitals, gastrointestinal tract and the body’s soft tissues. Specific conditions where Rulid treatment can help ranges from sore throats and difficulties with swallowing, through acute bronchitis, tonsillitis, sinusitis and pneumonia, to certain sexually transmitted diseases, gum infections like gingivitis, and skin infections such as impetigo – skin sores caused by bacteria.

As is the nature of antibiotics, they are only effective against particular strains of bacteria. This is true for macrolide antibiotics such as Rulid. which target the following bacteria strains:

Chlamydia trachomatis: affecting the eyes and urogenital areas of both men and women;

Listeria monocytogenes: a virulent strain of bacteria carried in food;

Helicobacter: bacteria leading to inflammation of the stomach lining and associated with ulcers and the development of stomach cancer;

Ureaplasma urealyticum: bacteria that are a normal part of the genital flora of both sexes, but also associated with conditions such as infertility, still and premature birth, and non-specific urethritis (NSU);

Gardnerella vaginalis: bacteria that causes infection of the female genital tract;

Haemophilus Ducreyi: a bacteria strain responsible for chancroid – a sexually transmitted disease characterised by genital sores;

Streptococcus agalactiae: bacteria that can cause serious and even fatal infections in newborn babies;

Streptococcus pneumoniae: a cause of bacterial meningitis and infections such as enocarditis, cellulitis, peritonitis, and acute sinusitis;

Neisseria meningitides: bacteria that can cause meningococcal meningitis and meningococcal septicaemia;

Mycoplasma pneumoniae bacteria leading to the condition of the same name;

Bordetella pertussis: bacteria that can cause whooping cough;

Moraxella Catarrhalis: bacteria responsible for infections associated with the respiratory tract;

Legionella pneumophila: bacteria that can lead to Legionnaire’s disease.

Taking Rulid

A typical Rulid dosage is one 150mg tablet taken twice a day. Rulid is well tolerated with few side effects. Although rare, side effects may stem from the gastrointestinal area – such as diarrhoea, abdominal pain and vomiting. Less common side effects include headaches, rashes and changes in the senses of smell and taste.

Rulid is a safe and effective antibiotic that targets a slightly wider range of bacteria than penicillin. Rulid is an important ally in the fight against the bacteria that have proven difficult to treat in past.

Label

Equip your body to fight off bacterial infections with Rulid

Rulid is part of a group of antibiotics called macrolides. These special types of bacterial fighter work by blocking the proteins that harmful bacteria use to grow and multiply.

Rulid is so powerful that if the bacteria are in enough proliferation, it actually kills the bacteria directly – meaning it’s ‘bactericidal’. Using the body’s defence system of white blood cells, the antibiotics in rulid form in these natural defences. They’re then in the perfect position to be employed in bolstering the immune system.

To treat bacteria infection of the respiratory tract, a Rulid dosage – also known as Rulid – Roxithromycin – is usually prescribed. As well as Rulid – Roxithromycin being used for acute bronchitis, tonsillitis and pneumonia, it’s also used to treat infections of the gastrointestinal tract and the body’s soft tissues.

Antibiotics should only be used when prescribed by your doctor, so it’s important to check to see whether you require them for a certain condition. Side effects are seldom experienced with Rulid and it’s proven itself to be handy weapon to fight off serious infections.

Chemical: Roxithromycin(e)

Polioxyethylene–polioxypropylene co-polymer, polyvinyl pyrrolidone, hydroxypropyl cellulose, precipitate silica, corn starch, magnesium stearate, talc, propylene glycol, anhydrous glucose, methylhydroxypropyl cellulose, titanium dioxide.

Adverse Effects and Precautions :

Gastro-intestinal disturbances are the most frequent adverse effect, but are less frequent than with erythromycin. A case of cholestatic hepatitis has been reported. Rashes, headache, dizziness, weakness and changes in blood cell counts have also occurred. Acute pancreatitis, with duodenal inflammation, pain, pancreatic enlargement and raised serum-amylase developed within 24 hours of substitution of roxithromycin for erythromycin ethyl succinate in a patient being treated for respiratory tract infection. Symptoms resolved rapidly once roxithromycin was withdrawn. Souweine B, et al. Acute pancreatitis associated with roxithromycin therapy. DICP Ann Pharmacother 1991- 25: 1137.

Antimicrobial Action and Resistance :

It is reported to be as active or slightly less active than erythromycin. MICs for the most sensitive strains range from about 0.03 to 1 mcg per ml but organisms with MICs up to about 2 mcg per ml are generally considered sensitive.

Following oral administration roxithromycin is well absorbed, with peak concentrations of about 6 to 8 mcg per ml occurring around 2 hours after a single dose of 150 mg. Absorption is reduced when taken after, but not before, a meal. It is widely distributed in tissues and body fluids. It is reported to be about 96% bound to plasma protein (mainly alpha (1)-acid glycoprotein) at trough concentrations, but binding is saturable, and only about 86% is bound at usual peak concentrations. Small amounts of roxithromycin are metabolized in the liver, and the majority of a dose is excreted in the faeces as unchanged drug and metabolites - about 7 to 12% is excreted in urine, and up to 15% via the lungs. The elimination half-life is reported to range between about 8 and 13 hours, but may be more prolonged in children. References. 1. Puri SK, Lassman HB. Roxithromycin: a pharmacokinetic review of a macrolide. J Antimicrob Chemother 1987- 20 (suppl B): 89-100. 2. Periti P, et al. clinical pharmacokinetic properties of the macrolide antibiotics: effects of age and various pathophysiological states (part II). Clin Pharmacokinet 1989- 16: 261-82.

Uses and Administration :

Roxithromycin is a macrolide antibiotic with actions and uses similar to those of erythromycin. It is given by mouth in a dose of 150 mg twice daily before meals, in the treatment of susceptible infections. 1. Phillips I, et al. (eds). Roxithromycin: a new macrolide. J Antimicrob Chemother 1987- 20 (suppl B): 1-187. 2. Young RA, et al. Roxithromycin: a review of its antibacterial activity, pharmacokinetic properties and clinical efficacy. Drugs 1989- 37: 8-41. Correction. ibid.,3. Bahal N, Nahata MC. The new macrolide antibiotics: azithromycin, clarithromycin, dirithromycin, and roxithromycin. Ann Pharmacother 1992- 26: 46-55.

Roxithromycin has been reported to be of benefit in patients with late-stage symptoms (neuroborreliosis, (1) arthritis (2)) of Lyme disease, given in combination with co-trimoxazole, although the contribution of the latter is uncertain. (3) 1. Gasser R, Dusleag J. Oral treatment of late borreliosis with roxithromycin plus co-trimoxazole. Lancet 1990- 336: 1189-90. 2. Pedersen LM, Friis-Moller A. Late treatment of chronic Lyme arthritis. Lancet 1991- 337: 241. 3. Bowman CA. Oral treatment of late borreliosis with roxithromycin plus co-trimoxazole. Lancet 1990- 336: 1514.

KEEP OUT OF THE REACH OF CHILDREN

The above information is the translation of the manufacturer's insert. It is provided under the supplying company's terms and conditions and should not replace the advice of your personal physician.

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