Eye Problems Using Eyedrops And Eye Ointment, Virucid

Eye Problems: Using Eyedrops and Eye Ointment

Introduction

Many eye problems are treated with eyedrops or eye ointments, and sometimes with both.

Even though drops and ointments are widely used, many people don't know the best way to put them in. But with a little preparation, you can comfortably and easily put drops or ointment in your eyes or someone else's.

Eyedrops and eye ointments can deliver medicine directly to your eyes, keep your eyes moist, and help with redness, itching, and watering.

It is important to be sure the dropper or tube is clean. Do not let it touch the eye, eyelid, lashes, or any surface. This will keep it free from bacteria.

Do not use more drops or ointment than directed.

If you have questions about this information, take it with you when you visit your doctor.

How to use eyedrops or eye ointment

Safety tips

Take these safety precautions when you use eyedrops or eye ointments:

Wash your hands well before and after you insert the drops or ointment. If you have disposable medical gloves, wear them when you put eyedrops or eye ointments into someone else's eyes. Even if you wore gloves, wash your hands afterward.

Be sure the dropper or tube is clean and does not touch the eye, eyelid, lashes, or any surface. This is to keep it free from bacteria. Eyedrops or ointments that get bacteria in them can easily spread the bacteria to the eye and cause an infection.

If the dropper is separate from the bottle and touches the eye, do not put the dropper back in the bottle. Buy a new dropper at a drugstore.

Do not use anyone else's drops or ointment.

If you have an eye infection, do not wear contact lenses while you are using eyedrops or eye ointments unless your doctor has told you it is okay.

Use them exactly as directed. Make sure you understand the directions, and do not use the drops or ointment longer or in larger amounts than your doctor tells you to. This can hurt your eyes.

If your doctor prescribed one type of eyedrop or eye ointment to treat one problem, do not use the same medicine to treat a different problem.

Using eyedrops

For older children and adults: While tilting your head back, pull the lower eyelid down with one or two fingers to create a small pouch. Gently squeeze the dropper to put 1 to 2 eyedrops (or the number of drops your doctor told you) in the pouch. Close the eye for 30 to 60 seconds to let the drops absorb.

For younger children: Have the child lie down with the eyes closed. Place an eyedrop in the inner corner of the closed eye. When the eye opens, the drop will run in.

If you are putting more than 1 drop in your eye, wait at least 5 minutes between eyedrops. This helps prevent flushing away or diluting the first drop.

If you are using both eyedrops and eye ointment, put the eyedrop in at least 10 minutes before the ointment.

Using eye ointment

The method for inserting eye ointment is slightly different than for inserting eyedrops. When using eye ointments, follow these tips:

For older children and adults: Pull the lower eyelid down with one or two fingers to create a pouch. Put a thin line of ointment in the pouch. Close the eye for 30 to 60 seconds to let the ointment absorb.

For younger children, have the child lie down with eyes closed. Pull the lower eyelid out to create a pouch. Put a thin line of ointment in the pouch. With the child's eyes closed, ask the child to move his or her eyeball from side to side to move the ointment around the eye.

Eye ointment can cause some temporary blurring of vision.

Using a mirror may make it easier to see what you are doing.

Credits

By Healthwise Staff Primary Medical Reviewer Kathleen Romito, MD - Family Medicine Martin J. Gabica, MD - Family Medicine Specialist Medical Reviewer Christopher J. Rudnisky, MD, MPH, FRCSC - Ophthalmology

Current as of September 9, 2014

WebMD Medical Reference from Healthwise

This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information. © 1995-2015 Healthwise, Incorporated. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.

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Virless Cream Acyclovir - Profil Gravatar, Virless

Copyright 2012 Iddeerz Acyclovir. All Rights Reserved.

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Sabal Stada® Uno 320 Mg Weichkapseln, Stada Uno

STADA

STADA

Beschwerden beim Wasserlassen bei einer gutartigen Vergro?erung der Prostata

Haufiges Wasserlassen, auch nachts, verzogerter Harnstrahl, Nachtraufeln. Bei Mannern ab 60 Jahren treten diese Probleme verstarkt auf. Ursache ist oft eine gutartige Vergro?erung der Prostata, die durch altersabhangige hormonelle Veranderungen im Korper entsteht.

Diese langsame Vergro?erung kann das Wassserlassen beeintrachtigen und die vollstandige Entleerung der Harnblase verhindern.

Mit naturlichen Wirkstoffen der Sageplamenfruchte hat sich Sabal STADA uno 320 mg als gut vertragliche Langzeittherapie erwiesen.

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Wirkstoff: Sagepalmenfruchte-Dickextrakt. Zur Anwendung bei Mannern gegen Beschwerden beim Wasserlassen bei einer gutartigen Vergro?erung der Prostata (Miktionsbeschwerden bei benigner Prostatahyperplasie, Stadium I bis II nach Alken bzw. II bis III nach Vahlensieck). Hinweis: Eine Behandlung mit Sabal STADA® uno sollte nur nach gesicherter Diagnose unter arztlicher Uberwachung erfolgen. Dieses Medikament bessert nur die Beschwerden bei einer vergro?erten Prostata, ohne die Vergro?erung zu beheben. Bitte suchen Sie daher in regelma?igen Abstanden Ihren Arzt auf. Insbesondere bei Blut im Urin, Harnwegsinfekt, Verschlimmerung der Beschwerden oder akuter Harnverhaltung ist umgehend eine Rucksprache mit dem Arzt erforderlich.

Zu Risiken und Nebenwirkungen lesen Sie bitte die Packungsbeilage und fragen Sie Ihren Arzt oder Apotheker.

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Oxitriptan - Information; Why It Is Recommended, Cincofarm

Oxitriptan

Source

Oxitriptan is supplied in 50mg or 10mg tablets under the trade names Cincofarm, Levotonine, Levothym, Oxyfan, Serotonyl™, Serovit, Telesol, Trimag, Tript-OG, Tript-OH, Triptene and Triptum™.

Function; Why it is Recommended

Oxitriptan is converted into the brain hormone serotonin in the body. Serotonin is a key factor in mood regulation, eating disorders, and anxiety. Serotonin is also the precursor to the pineal gland 's production of melatonin .

Oxitriptan's anti-aging benefits may include the prevention and treatment of depression. maintenance of serotonin levels as the body ages, prevention and treatment of compulsive disorders like overeating, improved daytime alertness and treatment of insomnia.

Side-Effects

Side-effects include nausea and mild gastric discomfort.

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Aliyot - Definition Of Aliyot By The Free Dictionary, Aliot

aliyah

The expressway passes through Barakahu, Murree, Phulgran, Upper Topa, Lower Topa, Bhurban, Aliyot and Phagwari before ending just outside Kohala.

Women read the Torah, are honored with aliyot during the Torah reading and even give the Sabbath "speech," tasks that for my entire life I considered exclusively male.

Torah Reading--a Torah scroll should be taken out of the ark in the morning and three aliyot should be read.

We have created policies ranging from very strict standards of Shabbat and kashrut observance, to a set of policies on assigning aliyot on Shabbat morning, to a prohibition on fake tattoos (a prohibition which my laypeople insisted on over my objections).

The book's focus on the circumstances of the evacuation also precludes it from delving into the Ethiopians' subsequent experience of absorption in Israel--no doubt a book in itself--which would modify, without undermining, the triumphal celebration of ingathering told here, and would make comparison with Israel's other aliyot possible.

That's why you have these big aliyot from Ethiopia and Russia.

In the trading city of Livorno, those who had travelled back to Spain on business were not allowed to receive the honor of aliyot to the Torah.

Gordon, then of Minneapolis, Goldman appears to have shortened the Torah reading to seven aliyot of only three verses, and also abbreviated the Haftarah (Prophetic Reading).

Many of its innovations--bat mitzvah, Sephardic Hebrew, aliyot for women--would eventually become standard in Conservative synagogues.

The most obvious breakthroughs of the past 40 years in the synagogue sphere have been women's ordination, the proliferation of the bat mitzvah, women being counted in the minyan and having aliyot. and the advent of non-sexist liturgy and God-language.

At the seasonal holiday times of the three aliyot b'regel, foot ascents, referring to the religious imperative to ascend to and pray at the Temple in Jerusalem during the Pesach, Shavuot, and Succot holidays, the population of Jerusalem must have swelled immensely, and more water was needed than the local Jerusalem springs could supply.

Throughout, a variety of elegant solutions are used to deal with the special issues related to vocalization, trope, chapter notations, verse notations, parshah divisions, and aliyot .

Pedea 5 Mg, Pedea

Pedea 5 mg/ml solution for injection

Treatment of a haemodynamically significant patent ductus arteriosus in preterm newborn infants less than 34 weeks of gestational age.

4.2 Posology and method of administration

Treatment with Pedea should only be carried out in a neonatal intensive care unit under the supervision of an experienced neonatologist.

A course of therapy is defined as three intravenous injections of Pedea given at 24-hour intervals. The first injection should be given after the first 6 hours of life.

The ibuprofen dose is adjusted to the body weight as follows:

- 1 st injection: 10 mg/kg,

- 2 nd and 3 rd injections: 5 mg/kg.

If anuria or manifest oliguria occurs after the first or second dose, the next dose should be withheld until urine output returns to normal levels.

If the ductus arteriosus does not close 48 hours after the last injection or if it re-opens, a second course of 3 doses, as above, may be given.

If the condition is unchanged after the second course of therapy, surgery of the patent ductus arteriosus may then be necessary.

Method of administration

For intravenous use only.

Pedea should be administered as a short infusion over 15 minutes, preferably undiluted. If necessary, the injection volume may be adjusted with either sodium chloride 9 mg/ml (0.9%) solution for injection or glucose 50 mg/ml (5%) solution for injection. Any unused portion of the solution should be discarded.

The total volume of solution injected should take into account the total daily fluid volume administered.

- Hypersensitivity to the active substance or to any of the excipients;

- Active bleeding, especially intracranial or gastrointestinal haemorrhage;

- Thrombocytopenia or coagulation defects;

- Significant impairment of renal function;

- Congenital heart disease in which patency of the ductus arteriosus is necessary for satisfactory pulmonary or systemic blood flow (e. g. pulmonary atresia, severe tetralogy of Fallot, severe coarctation of the aorta);

- Known or suspected necrotising enterocolitis;

4.4 Special warnings and precautions for use

Before administration of Pedea an adequate echocardiographic examination should be performed in order to detect a haemodynamically significant patent ductus arteriosus and to exclude pulmonary hypertension and ductal-dependent congenital heart disease.

Since prophylactic use in the first 3 days of life (starting within 6 hours of birth) in preterm newborn infants less than 28 weeks of gestational age was associated with increased pulmonary and renal adverse events, Pedea should not be used prophylactically at any gestational age (see sections 4.8 and 5.1). In particular, severe hypoxemia with pulmonary hypertension was reported in 3 infants within one hour of the first infusion and was reversed within 30 min after start of inhaled nitric oxide therapy.

If hypoxaemia occurs during or following Pedea infusion, close attention should be paid to pulmonary pressure.

Since ibuprofen was shown in vitro to displace bilirubin from its binding site to albumin, the risk of bilirubin encephalopathy in premature newborn infants may be increased (see section 5.2). Therefore, ibuprofen should not be used in infants with marked elevated bilirubin concentration.

As a non-steroidal anti-inflammatory drug (NSAID), ibuprofen may mask the usual signs and symptoms of infection. Pedea must therefore be used cautiously in the presence of an infection (see also section 4.3).

Pedea should be administered carefully to avoid extravasation and potential resultant irritation to tissues.

As ibuprofen may inhibit platelet aggregation, premature neonates should be monitored for signs of bleeding.

As ibuprofen may decrease the clearance of aminoglycosides, strict surveillance of their serum levels is recommended during co-administration with ibuprofen.

Careful monitoring of both renal and gastrointestinal function is recommended.

In preterm newborn infants less than 27 weeks of gestational age, the closure rate of the ductus arteriosus (33 to 50%) was shown to be low at the recommended dose regimen (see section 5.1).

This medicinal product contains less than 1 mmol sodium (15 mg) per 2 ml, i. e. essentially 'sodium-free'.

4.5 Interaction with other medicinal products and other forms of interaction

The concomitant use of Pedea with the following medicinal products is not recommended:

- diuretics: ibuprofen may reduce the effect of diuretics; diuretics can increase the risk of nephrotoxicity of NSAIDs in dehydrated patients.

- anticoagulants: ibuprofen may increase the effect of anticoagulants and enhance the risk of bleeding.

- corticosteroids: ibuprofen may increase the risk of gastrointestinal bleeding.

- nitric oxide: since both medicinal products inhibit platelet function, their combination may in theory increase the risk of bleeding.

- other NSAIDs: the concomitant use of more than one NSAID should be avoided because of the increased risk of adverse reactions.

- aminoglycosides: since ibuprofen may decrease the clearance of aminoglycosides, their co-administration may increase the risk of nephrotoxicity and ototoxicity (see section 4.4).

4.6 Pregnancy and lactation

In a clinical curative trial involving 175 preterm newborn infants less than 35 weeks of gestational age, the incidence of bronchopulmonary dysplasia at 36 weeks post-conceptional age was 13/81 (16%) for indomethacin versus 23/94 (24%) for ibuprofen.

In a clinical trial where Pedea was administered prophylactically during the first 6 hours of life, severe hypoxemia with pulmonary hypertension was reported in 3 newborn infants less than 28 weeks of gestational age. This occurred within one hour of the first infusion and was reversed within 30 minutes after the inhalation of nitric oxide. There have also been post-marketing reports of pulmonary hypertension where Pedea was administered to premature neonates in the therapeutic setting.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via

Yellow Card Scheme

Tel: +353 1 6764971

Fax: +353 1 6762517

No case of overdose has been reported with intravenous ibuprofen in preterm newborn infants.

However, overdose has been described in infants and children administered oral ibuprofen: CNS depression, seizures, gastrointestinal disturbances, bradycardia, hypotension, apnoea, abnormal renal function, haematuria have been observed.

Massive overdose (up to more than 1000 mg/kg) has been reported to induce coma, metabolic acidosis, and transient renal failure. All patients recovered with conventional treatment. Only one recorded death has been published: after an overdose of 469 mg/kg, a 16-month old child developed an apnoeic episode with seizures and a fatal aspiration pneumonia.

The management of ibuprofen overdose is primarily supportive.

5. Pharmacological properties

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: other cardiac preparations, ATC code: C01 EB16

Ibuprofen is a NSAID that possesses anti-inflammatory, analgesic and antipyretic activity. Ibuprofen is a racemic mixture of S(+) and R(-) enantiomers. In vivo and in vitro studies indicate that the S(+) isomer is responsible for the clinical activity. Ibuprofen is a non selective inhibitor of cyclo-oxygenase, leading to reduced synthesis of prostaglandins.

Since prostaglandins are involved in the persistence of the ductus arteriosus after birth, this effect is believed to be the main mechanism of action of ibuprofen in this indication.

In a dose-response study of Pedea in 40 preterm newborn infants, the ductus arteriosus closure rate associated to the 10-5-5 mg/kg dose regimen was 75% (6/8) in neonates of 27-29 weeks' gestation and 33% (2/6) in neonates of 24-26 weeks' gestation.

Prophylactic use of Pedea in the first 3 days of life (starting within 6 hours of birth) in preterm newborn infants less than 28 weeks of gestational age was associated with increased incidence of renal failure and pulmonary adverse events including hypoxia, pulmonary hypertension, pulmonary haemorrhage, as compared to curative use. Conversely, a lower incidence of neonatal grade III-IV intraventricular haemorrhage and of surgical ligation was associated with prophylactic use of Pedea.

5.2 Pharmacokinetic properties

Although a great variability is observed in the premature population, peak plasma concentrations are measured around 35-40 mg/l after the initial loading dose of 10 mg/kg as well as after the last maintenance dose, whatever gestational and postnatal age. Residual concentrations are around 10-15 mg/l 24 hours after the last dose of 5 mg/kg.

Plasma concentrations of the S-enantiomer are much higher than those of the R-enantiomer, which reflects a rapid chiral inversion of the R - to the S-form in a proportion similar to adults (about 60%).

The apparent volume of distribution is on average 200 ml/kg (62 to 350 according to various studies). The central volume of distribution may depend on the status of the ductus and decrease as the ductus closes.

In vitro studies suggest that, similarly to other NSAIDs, ibuprofen is highly bound to plasma albumin, although this seems to be significantly lower (95 %) compared with adult plasma (99 %). Ibuprofen competes with bilirubin for albumin binding in newborn infant serum and, as a consequence, the free fraction of bilirubin may be increased at high ibuprofen concentrations.

Elimination rate is markedly lower than in older children and adults, with an elimination half-life estimated at approximately 30 hours (16–43). The clearance of both enantiomers increases with gestational age, at least in the range of 24 to 28 weeks.

In preterm newborns ibuprofen significantly reduced plasma concentrations of prostaglandins and their metabolites, particularly PGE2 and 6-keto-PGF-1-alpha. Low levels were sustained up to 72 hours in neonates who received 3 doses of ibuprofen, whereas subsequent re-increases were observed at 72 hours after only 1 dose of ibuprofen.

5.3 Preclinical safety data

There are no preclinical data considered relevant to clinical safety beyond data included in other sections of this Summary of Product Characteristics. With the exception of an acute toxicity study, no further studies have been carried out in juvenile animals with Pedea.

6. Pharmaceutical particulars

6.1 List of excipients

Orphan Europe (UK) Limited

Degranol - Tablets, Degranol

PROPRIETARY NAME (and dosage form):

DEGRANOL ® TABLETS

COMPOSITION: Each tablet contains 200 mg carbamazepine .

PHARMACOLOGICAL CLASSIFICATION: A.2.5 Anticonvulsants, including anti-epileptics.

PHARMACOLOGICAL ACTION: Degranol possesses both anticonvulsant and psychotropic properties.

INDICATIONS: Epilepsy with motor and psychic manifestations: - psychomotor and temporal-lobe epilepsy - grand mal - mixed forms - focal seizures Carbamazepine is also used in the treatment of trigeminal neuralgia.

CONTRA-INDICATIONS: Hypersensitivity to carbamazepine. Carbamazepine is contra-indicated for expectant or nursing mothers or patients with liver disease. Not to be used in patients with heartblock. It should not be given to patients taking a mono-amine oxidase inhibitor or within 2 weeks of stopping such treatment. Not to be used in patients with porphyria.

WARNING: In rats treated with carbamazepine for two years, the incidence of tumours of the liver was found to be increased. There is, however, no evidence to indicate that this observation has any significance relative to the therapeutic use of the drug.

DOSAGE AND DIRECTIONS FOR USE: Trigeminal Neuralgia An initial dose of 200 mg twice daily gradually increasing until a suitable response is obtained. The usual dosage required is one tablet three or four times daily. In elderly or hypersensitive patients an initial dose of half a tablet daily is recommended.

Initially 100 mg to 200 mg once or twice a day, followed by a slow increase until usually at a level of 400 mg twice or three times a day, the best response is obtained. In some instances 1600 mg in 3 to 4 divided doses may be necessary.

Administered in several fractional doses –usually 10 to 20 mg/kg per day.

Age up to 1 year: 100 mg to 200 mg (½ to 1 tablet ) per day. 1 to 5 years: 200 mg to 400 mg (1 to 2 tablets) per day. 5 to 10 years: 400 mg to 600 mg (2 to 3 tablets) per day. 10 to 15 years: 600 mg to 1 000 mg (3 to 5 tablets) per day.

SIDE-EFFECTS AND SPECIAL PRECAUTIONS: Medical supervision during treatment is essential. The level of serum folic acid should be observed during anticonvulsant therapy since Degranol may enhance the metabolism of folic acid. Abnormalities of liver function and jaundice have been associated with long-term treatment. Blood counts and liver function tests should be performed before commencing treatment. Blood counts should then be repeated at weekly intervals during the first month of treatment and subsequently at monthly intervals; liver function tests should also be undertaken periodically, if allergic skin reactions occur, if the leucocyte and/or platelet count diminish, if tests reveal a deterioration in liver function, or if any serious adverse symptoms develop, Degranol should be withdrawn. Reaction-time may be increased by Degranol. The patient's safety as a road-user or operator of machines may be impaired in consequence. Unwanted effects - i. e. loss of appetite, dryness of the mouth, retching, diarrhoea or constipation, headache, drowsiness, dizziness, somnolence, ataxia, disorders of visual accommodation, diplopia, or, in elderly patients, states of confusion and agitation - may occur, particularly at the start of treatment. These effects may require temporary reduction in the dosage. Hyponatraemia due to the antidiuretic effect of Degranol and possibly accompanied by vomiting, headache, and mental confusion has been observed. Allergic skin reactions, as well as occurrences of exfoliative dermatitis, paraesthesia, systemic lupus erythematosus, Steven's-Johnson syndrome, photosensitivity, altered skin pigmentation, leucopenia, thrombocytopenia, agranulocytosis, aplastic anaemia, thrombo-embolism, left ventricular failure, disturbances of cardiac impulse conduction, hepatocellular and cholestatic hepatitis, acute oliguria with hypertension and proteinuria have been reported. A wide variety of other central nervous system, gastro-intestinal, cardiovascular and dermatological effects have also been reported. In patients with cardiovascular diseases, or with hepatic or renal disorders, glaucoma and in elderly subjects, Degranol should be administered with caution. Tolerance may develop to some of the untoward effects of carbamazepine and they can be minimized by gradual increase in dosage and adjustment of maintenance dosage. If treatment with Degranol is withdrawn abruptly, the change-over to another anti-epileptic should be effected under cover of diazepam or a barbiturate. INTERACTIONS: Degranol may reduce the patient's alcohol tolerance, it is therefore advisable to abstain from alcohol during treatment. Induction of hepatic enzymes in response to Degranol may have the effect of diminishing the activity of certain drugs that are metabolized in the liver. This should be borne in mind when administering Degranol concomitantly with other anti-epileptic agents, e. g. phenytoin and the tetracycline, doxycycline. Similarly, in patients receiving oral anticoagulant medication, the dosage of the anticoagulant should be readapted to clinical requirements whenever treatment with Degranol is initiated or withdrawn. Degranol may adversely affect the reliability of oral contraceptives. Pregnancy and Lactation: Safety of Degranol in pregnancy has not been demonstrated conclusively. If pregnancy occurs in a woman receiving Degranol or if the problem of initiating treatment with Degranol rises during pregnancy, the drug's potential benefits must be carefully weighed against its possible hazards, particularly in the first three months of pregnancy. The active substance of Degranol passes into the breast milk.

KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT: Agitation, tremor, abnormal reflexes, convulsions, impairment of consciousness, hypertension or hypotension, nausea, vomiting, renal insufficiency, deep sleep, coma, EEG and ECG changes. No specific antidote. The stomach should be emptied by aspiration and lavage. Ensure clear airway and maintain respiration. Treatment is mainly supportive and symptomatic. Measures to monitor and safeguard vital functions. Administration of diazepam where necessary.

CONDITIONS OF REGISTRATION: May be advertised to the professions only.

IDENTIFICATION: Flat, white bisected tablets with bevelled edges, engraved with a mortar and pestle on one side.

PRESENTATION : Packs of 100 and 500 tablets.

STORAGE INSTRUCTIONS: Store below 25°C away from moisture. KEEP OUT OF REACH OF CHILDREN.

REGISTRATION NUMBER: G/2.5/220

NAME AND BUSINESS ADDRESS OF APPLICANT: Pharmacare Limited 7 Fairclough Road PORT ELIZABETH 6001

DATE OF PUBLICATION OF THIS PACKAGE INSERT: 19./3/1985.

Information for the Patient: If the treatment is to prove successful, it is essential that the doctors instructions be carried out exactly. It is advisable to refrain from alcohol during treatment with Degranol. In addition, caution should be exercised when driving a vehicle. If a skin rash, fever, sore throat, or any other symptoms develop, the doctor should be informed without delay. You should also consult your doctor at once should you become pregnant.

G941 A&S PRINTERS

Updated on this site: October 2000 Current: March 2005 Source: Hospital Pharmacy SAEPI HOME PAGE TRADE NAME INDEX GENERIC NAME INDEX FEEDBACK Information presented by Malahyde Information Systems © Copyright 1996-2005

Nifecard, Nifecard

Nifecard

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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Soclor, Soclor

Soclor

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.

Was this page helpful?

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We accept Paypal and Visa, Mastercard, Discover and American Express. When you go to check out, you will have your choice to pay with Paypal Secure Server or go through our secure server check out.

If you prefer to pay with a check or money order, you can use Paypal to send an echeck for your order, or send your check or money order to Stuff4Beauty, PO Box 532, Shelbyville Il 62565

Once we get your order and payment, we will ship your order to you with all possible speed. If you pay with your credit card, we usually charge your card within 48 hours of the order being placed. All cancelled orders, if cancelled by you after the order was processed, will be charged a 50% restocking fee.

Orders received between Monday and Friday are usually processed within 1-4 business days. Orders received on Friday, Saturday and Sunday are usually processed by Monday or by close of business day Tuesday. Your order may be shipped in more than one package. Only one discount per customer per day please.

Most all products advertised on this site are in stock. Often you will receive your order within 4 - 7 business days of ordering, but not always. A few examples that could cause a delay (extra time) in order filling is if you order a product in high demand, gallons or large numbers or liters of product. In these special order cases please allow 1-21 days for your order to be shipped from our location - and then, please allow 4 additional days for the package to arrive after it has been shipped

If you can be patient, we can assure you that our prices will continue to be the lowest prices you will find on the internet. If you find a product that we carry at a lower price, contact us for a possible price match before you place your order!

If a product is backordered, or if there is a problem with a product that has been discontinued, we will email you within 3 weeks of your order being placed. This does not generally happen, but on occassion certain products are discontinued. Our discontinued products advertised on this site are shipped separate and treated as a separate order from regular (non-discontinued) products.

As a privately owned and operated business, we understand the need for both security and privacy.

All information gathered during your shopping experience with Stuff4Beauty. com is held in the strictest confidence. Your name, address, e-mail, and all other personal information will never be distributed or sold.

All online transactions at Stuff4Beauty. com are handled with industry-standard SSL encryption. When you enter your credit card number into the order form, it is transmitted across the Internet in an encrypted (scrambled) form, then decoded when it gets to us.

Stuff4Beauty accepts returns in accordance with the return policy guidelines outlined below.

It is our desire for you to be completely satisfied with your purchase. We trust that you choose your products carefully. All of the products for sale on our website are name brand.

We assume that if you place an order with us you have done your research and carefully selected the products you ordered. We are always here to help you select products that are right for you if you are unsure.

Before purchasing, carefully review the product description to be sure that you are interested in purchasing the product. Purchase the smaller or sample size if available if you are not sure how you will react to a product.

If we sent you a product you did not order by our mistake, contact us we will resolve the problem. If you receive a product that was damaged in transit, please contact us within 24 hours of the order arriving to you.

We provide no cash refunds or charge card credits for unauthorized items returned to us. All merchandise being returned must be authorized before you return it, and must be arranged within 5 business days of receiving your order. Merchandise being returned must be unopened, unused and in the original packaging. If your order was eligible for free shipping, all original shipping and handling costs are not refundable and will be deducted from the refund. Returned products will be assessed a 50% restocking fee.

We reserve the right to substitute a listed product for one of a different size. We will always make these substitutions on the side of the customers best interest.

We cannot accept any returns for items which are not factory sealed due to State, Federal and Local Health Laws and Concerns.

If you cancel an order that has been already processed and/or shipped, we do not refund shipping and there is a 50% restocking fee on your order. Unauthorized returns become the property of Stuff4Beauty and will be disposed of. Products on our website are priced per each unless otherwise stated. If you are unsure what a product price is, please contact us before you pay. Returns of shipped merchandise are not accepted for price reasons alone. View your cart total, product price/quantity/size before you pay. We recommend price comparison shopping before you order. Discontinued products (orders placed from our discontinued specialty product section), hair color, perfume and cosmetics cannot be returned.

Stuff4Beauty cannot be held responsible for freezing products left outside if you live in a cold climate during the winter months. Please take precaution if this applies to you. In the extreme cold winter months, please consider having your order shipped to your place of employment or where someone would be home to accept the package. Products that freeze will usually work fine once thawed, but the consistency could possibly change in some products if they have been frozen.

Packages delivered with incorrect address information

If the package has incorrect or incomplete address information, you will be charged full postage for transit both ways. Examples of incomplete addresses include missing apartment or suite numbers, or missing floor numbers. Please double-check addresses during checkout. Incorrect address fees are not charged if we catch the address error ourselves, first.

By placing an order, you entered into agreement with our policies. Only one discount per customer per day please.

There are 4 ways to contact Stuff4Beauty. Com. These four ways are by phone, snail mail, website form or email!

**By Phone: Toll Free to the USA - 1-866-458-4441 (Based in Illinois)

**Store Phone Hours:

Monday's: Noon to 5pm Central Time Tues. through Thursday: 11am to 5pm Central Time Friday's: CLOSED Weekends (Sat. and Sun): CLOSED

** Our phone hours are subject to change without notice. We do close on certain occasions for holidays, inventory updates and meetings.

Our phone and fax number is toll free to the USA 1-866-458-4441 all others, please email.

Contact By Snail Mail:

Stuff4Beauty PO Box 532 Shelbyville Il 62565

Contact By Email: customerservice at stuff4beauty. com

Check your spam box - we answer most all emails!

Stuff4Beauty. com is your premier online store where you can purchase brand name, discounted salon products, skin care products and tanning lotions. All of our customers are handled with the utmost care to ensure that your shopping experience is a quick and pleasant one. We have several locations across the USA, our main location is in Illinois. Our policies are outlined on this page.

All products ordered through our website are genuine salon products that come from reputable suppliers. We are not a bulk distributor nor are we a mass-marketer. We provide this personal shopping service to our clients as a convenience - and for their own personal consumption. We guarantee that the products sold from our Website are authentic salon-professional products. We do not condone or support diversion. We do not wholesale products for resale.

Stuff4Beauty. com is not affiliated with the product lines. The website and images and descriptions of all products displayed belong to their respected owners - along with all copyrights and trademarks.

Because of the constantly evolving nature of the beauty industry, new products being added and other products being discontinued. Products are resized and repackaged and there are seasonal changes as well. Catalogs just do not work well for us.

Ampicillin - Side Effects, Dosage, Interactions, Ampicilin„

Ampicillin

Ampicillin is the generic name of a drug that's prescribed to treat bacterial infections.

It was once sold under several brand names, such as Omnipen, Amcill, and Principen.

Though these brand names are no longer on the market, your health care provider can prescribe generic ampicillin to treat infections such as pneumonia, bronchitis, urinary tract infections. meningitis, and typhoid fever.

Dentists often prescribe ampicillin before a dental procedure for people who are at risk of endocarditis, an infection in the lining of the heart.

Ampicillin, a penicillin-like drug, is an antibiotic that belongs to a class of drugs known as aminopenicillins. It kills bacteria by preventing them from making the protein needed to build their cell walls.

Ampicillin was approved by the Food and Drug Administration (FDA) under the brand name Ominpen in 1965 and was originally manufactured by Wyeth Ayerst.

Ampicillin Warnings

You should not take ampicillin if:

You're allergic to ampicillin, any penicillin antibiotic, or any other ingredient in the medication

You have infectious mononucleosis

Talk to your doctor before taking ampicillin if you have:

Allergies to many things

Asthma or ever had asthma

Acute Lymphoid Leukemia (ALL), a type of cancer of the white blood cells

HIV/AIDS

Seizures

Kidney problems

Inflammation or an infection of the intestines caused by taking antibiotics recently

Pregnancy and Ampicillin

Ampicillin is an FDA Pregnancy Category B drug, meaning animal studies indicate there is no risk to a fetus, but there are no human studies showing it's safe for an unborn baby.

Tell your doctor if you are pregnant or plan to become pregnant before taking this medication.

Ampicillin is safe for mothers to take while breastfeeding. Still, tell your doctor know if you are breastfeeding or plan to breastfeed while taking it.

Bula Do Medicamento Zolben, Zolben

Posologia e Administracao - ZOLBEN adultos e criancas acima de 2 anos: dose unica de 1 comprimido de 400 mg, ou o conteudo de 1 frasco da suspensao oral (10 ml). Em caso de parasitose por Strongyloides stercoralis ou Taenia spp. essa dose deve ser repetida por 3 dias consecutivos.

Reacoes adversas - ZOLBEN sao raros, porem podem ocorrer desconforto gastrintestinal, cefaleia1, nauseas2 e vomitos3, diarreia4, obstipacao, secura na boca e prurido5 cutaneo. - Superdosagem: a intoxicacao e pouco provavel, pois a absorcao do albendazol e pequena. Promover lavagem gastrica6 e observacao do paciente.

Contra-Indicacoes - ZOLBEN nao devera ser usado durante a gravidez7 e em criancas com idade inferior a 2 anos.

Indicacoes - ZOLBEN tratamento das parasitoses intestinais simples ou mistas. Zolben e eficaz contra Ascaris lumbricoides, Enterobius vermicularis, Trichuris trichiura, Ancylostoma duodenale, Necator americanus, Strongyloides stercoralis e Taenia spp.

Apresentacao - ZOLBEN caixa com 1 comprimido de 400 mg; frasco com 10 ml de suspensao oral de 4%.

Oferta In English, Oferta

1 (ofrecimiento) offer

2 (Com) (gen) offer; (para contrato, concurso) tender; (en subasta) bid; (Economía) supply; (ganga) special offer

estar de o en oferta to be on offer; la ley de la oferta y la demanda the law of supply and demand; la oferta es superior a la demanda supply exceeds demand

oferta cerrada sealed bid

oferta condicional conditional offer

oferta excedentaria excess supply

oferta monetaria money supply

oferta promocional promotional offer

El Parque se abrió ayer solo para los invitados y los poseedores de pases que los hayan adquirido durante la [oferta promocional] que concluyó el pasado día 28 de mayo.

oferta pública de adquisición (de acciones) takeover bid

oferta pública de venta (de acciones) share offer

ofertas de trabajo (en periódico) situations vacant (column); job openings; (EEUU)

3 (regalo) gift; present

Imperacin (Oxytetracycline) Uk - No Prescription, Lowest Price, Imperacin

Imperacin (Oxytetracycline)

Prices shown are for comparative purposes, converted from $USD at current rates.

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HealthTip: Could Oral Contraceptives Help Ease Rheumatoid Arthritis? 8/28/2015 12:00:00 AM Read article

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Purchasing discount Imperacin (Oxytetracycline) online is secure and private. Pharmacy employees are trained to understand the importance of customer privacy and security. Pharmacies maintains physical, electronic and procedural safeguards to protect your personal information.

Imperacin - HealthCare News

Clot-Buster Doesn't Raise Bleeding Risk in Warfarin Patients: Study

THURSDAY, May 10 (HealthDay News) -- Tissue plasminogen activator (tPA), a drug used to combat clots in stroke patients, does not increase the risk of dangerous bleeding in patients also taking the blood thinner warfarin, new research found.

The study included information on more than 23,000 ischemic stroke patients treated with tPA at more than 1,200 U. S. hospitals. Ischemic stroke, the most common type of brain attack, is caused by a blocked blood vessel to the brain. The clot-busting drug tPA is sold under the brand name Activase and the generic name alteplase.

Thank you for visiting our Imperacin information page. Click Buy Imperacin Online to order.

Ampicare

Manufacturing

Practice Hypiene

Our Team

Products

Imprin

Since 1991 McBenson have offered a wide range of animal health products from pharmaceuticals to pet toys. We have built an enviable reputation providing innovativeand good value products into the veterinary market. We pride our - selves on listening to our customers, sourcingand adapting our products to fulfil their requirements.

Our aim is to renew and strengthen our product range through out the Uk and through distribution partners into other key european territories. Westrive to achieve the best levels of customer service through our highly trained customerservice team and veterinary representatives, creating a high level of customer satisfaction.

The following are trademarks of McBenson Ltd or associated companies:Amoxycare

Ampicare Identichip Animalcare Isocare Animalcare Limited Totalcare Oxycare Oxycare  Pentoject Animalcare Ltd Phenoleptil

Animalcare Pet Fresh Phenycare Anivac Prednicare Aqupharm Streptacare Aquspray Treatplast Atrocare Trimacare

Benazacare (Community) Vetaclean Buprecare Vetasept Cephacare Xylacare Deocare Enrocare Florgane Frusecare

What we do

We pride ourselves on listening to our customers, sourcing and adapting our products to fulfil their requirements. Our aim is to renew and strengthen our product range throughout the UK and through distribution partners into other key european territories. Learn more

About Us

Since 1991 McBenson have offered a wide range of animal health products from pharmaceuticals to pet toys. We have built an enviable reputation providing innovative and good value products into the veterinary market. Learn more

New & Event

We at McBenson cordially invite you to look around our website, with a click of your mouse you can now link your day-to-day practice with the latest developments from McBenson. Learn more

Manufacturing Practice Hygiene Our Team Products Imprint Copyright@McBenson Veterinary. All right reserved. McBenson is powered by cosmos@1991-2015

Ramipril - An Ace Inhibitor - Tritace, Ranopril

Ramipril - an ACE inhibitor (Tritace)

Ramipril is used to treat a number of different conditions.

The first dose may make you feel dizzy, so it is best taken at night.

Some painkillers and indigestion remedies interfere with ramipril, so ask your pharmacist for advice before you buy any medicines.

Some people taking ramipril develop a troublesome cough. If this happens to you, let your doctor know.

About ramipril

Type of medicine

An angiotensin-converting enzyme (ACE) inhibitor

High blood pressure; heart failure; and to help prevent heart, kidney or blood vessel problems in people who are at risk of these

Tritace®; Triapin® (ramipril with felodipine)

Tablets, capsules, and oral liquid medicine

Ramipril is in a class of medicines called angiotensin-converting enzyme inhibitors, or ACE inhibitors. It is prescribed for a number of different reasons. You may have been prescribed it to reduce hypertension. or to treat heart failure. or to protect your heart and blood vessels from further damage (following a heart attack. for example). Your doctor will tell you why it has been prescribed for you.

ACE inhibitors like ramipril prevent your body from creating a hormone known as angiotensin II. They do this by blocking (inhibiting) a chemical called angiotensin-converting enzyme. This widens your blood vessels and helps to reduce the amount of water put back into your blood by your kidneys.

These actions help to decrease blood pressure in people who have hypertension, which is a condition where the blood pressure is higher than normal. People with high blood pressure often do not feel unwell but, if left untreated, high blood pressure can harm the heart and damage blood vessels, leading to a heart attack or stroke.

Heart failure is a condition where your heart does not work as well as it should. Because of this, there may be too much circulating fluid in your blood vessels. Ramipril helps to reduce this. It appears to have a protective effect on the heart and slows the progression of the heart failure. Its protective action also helps to reduce the risk of heart, kidney or blood vessel problems in people who are at risk of these.

Related discussions

Side effect of ramipril - difficulty taking deep breaths

Before taking ramipril

Some medicines are not suitable for people with certain conditions, and sometimes a medicine may only be used if extra care is taken. For these reasons, before you start taking ramipril it is important that your doctor or pharmacist knows:

If you are pregnant, trying for a baby or breast-feeding.

If you have any problems with your kidneys or liver.

If you are dehydrated - for example, if you have had diarrhoea or sickness very recently.

If you have been told you have atherosclerosis (a build-up of fatty deposits on the walls of your arteries).

If you have peripheral vascular disease (a particular type of poor circulation).

If you have collagen vascular disease, such as systemic lupus erythematosus (SLE) or scleroderma .

If you have been told you have cardiomyopathy (heart muscle disease), or aortic stenosis (narrowing of the main blood vessel from your heart).

If you have ever had angio-oedema (where your face, tongue or throat swells).

If you are having desensitisation treatment to protect against bee and wasp stings.

If you have dialysis treatment, or treatment to remove cholesterol from your blood by a machine (LDL apheresis).

If you are taking any other medicines. This includes any medicines you are taking which are available to buy without a prescription, such as herbal and complementary medicines.

If you have ever had an allergic or unusual reaction to any other ACE inhibitor (such as lisinopril, captopril and perindopril), or to any other medicine.

How to take ramipril

Before you start this treatment, read the manufacturer's printed information leaflet from inside the pack. The leaflet will give you more information about ramipril and a full list of side-effects which you may experience from taking it.

Take ramipril exactly as your doctor tells you to. It is usually taken once a day, although some people may be asked to take two doses daily (such as if you have recently had a heart attack).

Your doctor may advise you to take your very first dose at bedtime. This is because you may feel dizzy when you first start taking ramipril.

With the exception of the first dose, you can generally take ramipril at a time of day that suits you. You should, however, try to take each of your doses at the same time of day, each day.

Swallow the tablets/capsules with a drink of water. You can take ramipril before or after food.

There are several strengths of ramipril tablets and capsules. It is usual to start with a low strength and then for the strength to be increased as necessary after a few weeks. This allows your doctor to make sure that you have the dose that helps your condition, but helps avoid unwanted side-effects. You may be prescribed a special titration pack which contains different strengths of tablet and allows for your dose to be increased gradually over a five-week period. Each time you collect a new supply of ramipril, check to make sure it contains the strength of tablet/capsule that you are expecting.

If you have been prescribed the combination brand Triapin®, you must swallow the tablet whole - do not crush or chew these tablets, as it will damage the way they work.

If you forget to take a dose at your usual time, take it as soon as you remember. However, if you do not remember until the following day, skip the forgotten dose. Do not take two doses together to make up for a missed dose.

Getting the most from your treatment

Try to keep your regular appointments with your doctor. This is so your progress can be monitored. Your doctor will want you to have some blood tests from time to time to check that your kidneys are working well.

It is very important that you follow any dietary and lifestyle advice that you have been given by your doctor. This may include advice about eating a healthy diet, not smoking, and taking regular exercise.

If you buy any medicines, check with a pharmacist that they are suitable to take with ramipril. This is because some medicines (such as anti-inflammatory painkillers and indigestion remedies) may interfere with your treatment.

It is likely that your doctor will advise that you do not use salt substitutes while you are taking ramipril. These products have a high content of potassium which could be harmful for you.

If you drink alcohol, ask your doctor for advice about taking ramipril and alcohol. Alcohol may make you feel light-headed or dizzy, and may not be recommended for you.

If you have diabetes you may need to check your blood glucose more frequently, as ramipril may lower the levels of sugar in your blood. Your doctor will advise you about this.

If you are having an operation or dental treatment, tell the person carrying out the treatment that you are taking ramipril. This is because if you need an anaesthetic, it may cause your blood pressure to drop.

Treatment with ramipril is often long-term unless you experience an adverse effect. Continue to take it unless you are advised otherwise.

Can ramipril cause problems?

Along with their useful effects, most medicines can cause unwanted side-effects although not everyone experiences them. These usually improve as your body adjusts to the new medicine, but speak with your doctor or pharmacist if any of the following side-effects continue or become troublesome.

Common ramipril side-effects - these affect less than 1 in 10 people who take this medicine

What can I do if I experience this?

Clomid Profile, Colmifen

Clomid (Clomiphene Citrate)

To understand how Clomid can aid this process, let’s look at how natural testosterone production is regulated.

Testosterone production is regulated by a feedback loop which senses not only testosterone or other androgen levels, but also estrogen levels. This feedback loop includes the hypothalamus, the pituitary, and the testes (often referred to as the HPTA, or hypothalamic-pituitary-testicular axis.)

When the hypothalamus senses low estrogen levels and does not sense high androgen levels, it’s stimulated to signal the pituitary by producing more LHRH, which stands for LH releasing hormone. On receiving this signal, the pituitary produces more LH (luteinizing hormone) which in turn signals the testes to produce more testosterone.

During an anabolic steroid cycle, high androgen levels shut this process down entirely. If this is for only a relatively short period such as 8 weeks, this is not a real issue. Over a longer period of time, testicular atrophy might occur, however. That can be avoided with HCG usage. Something that cannot be avoided, however, is that the hypothalamus and pituitary respond not only according to the hormone levels which they sense at a given moment, but are affected in their response by their recent exposure. When that exposure has been an extended period of anabolic steroid use, responsiveness typically is poor even after anabolic steroid use has ceased.

Clomid, as does Nolvadex, works by occupying the binding sites of estrogen receptors of cells, without activating the receptors. This reduces the extent to which estradiol can activate these receptors. In the case of the hypothalamus, this leads to the hypothalamus “concluding” that estrogen levels are low. If androgen levels are not elevated, as indeed they should not be after an anabolic steroid cycle, the hypothalamus is then stimulated to produce LHRH. This will act to increase LH and restart natural testosterone production.

Clomid ordinarily is dosed at 50 mg/day. However, it’s important to note that clomiphene has a long half life. Where this has relevance is that when a daily dose is taken, the body will have not only that dose in it, but also an accumulated amount of about five days’ worth of previous doses as well. That’s fine: it results in correct blood levels. Where there can be a problem is when first starting use. If simply taking 50 mg/day from the beginning, there is no such buildup and levels will be low.

To account for this, 300 mg is taken on the first day, as three doses of 100 mg, or optionally six doses of 50 mg. This immediately gets levels to where they should be. Ongoing 50 mg/day dosing will maintain this level.

After day 1, doses of more than 50 mg are not needed and are not recommended. They will not improve results, but may increase adverse side effects.

Adverse side effects of Clomid can include increased emotionalism or vision disturbance. If vision disturbance is experienced, Clomid should be discontinued immediately.

Clomid rarely leads to libido issues, which can be a problem with Nolvadex. For this reason some prefer it to Nolvadex. Others, who do not have that issue with Nolvadex, may prefer that drug. Both are effective for restoring natural testosterone production. I have a slightly better opinion of Clomid for effectiveness, but where a person dislikes Clomid for emotional effects, or prefers Nolvadex for any reason, Nolvadex is a perfectly acceptable substitute.

Clomid differs from Nolvadex in that while SERMs are always anti-estrogenic in some tissues, they are estrogenic in others. Fortunately, both Clomid and Nolvadex are anti-estrogenic in the hypothalamus, making them useful for post-cycle therapy (PCT), and anti-estrogenic in breast tissue, making them useful as anti-gyno agents. Clomid however is estrogenic in the pituitary, which in some instances may even enhance its value for PCT. It’s likely estrogenic to at least some other neurons in the brain as well, causing increased emotionality. With regard to body fat and muscle, or any observable physical property, Clomid and Nolvadex have no other adverse estrogenic effects, but instead are useful anti-estrogens .

PCT with Clomid should begin as soon as androgen levels have dropped to normal, and continue until confident that natural testosterone production has been fully restored.

Clomid, properly, is a brand name: typically clomiphene citrate products are used, but popularly called Clomid. Clomiphene citrate is widely available both as a pharmaceutical and even more widely as a research chemical, often in liquid form for oral use.

Clomid can and usually should be used as the only SERM in PCT. In most instances, there is no point to combining with another SERM. Where a second SERM such as Nolvadex is combined with Clomid, each should be used at half dose rather than full dose. Using full dose of each does not provide enhanced efficacy and only increases risk of side effects.

Clomiphene citrate is the chemical name of active ingredient in Clomid. Clomid is a registered trademark of Merrell Dow Pharmaceuticals in the United States and/or other countries.

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Gastral - Definition Of Gastral By The Free Dictionary, Gastrial

gastral

References in periodicals archive ?

Gastral lock for doors Painting and Undercoating Prime and finish painting shall be in strict accordance with the manufacturer s recommendations and standards The final painting should be white Armoring: 360 degree C bulletproof material Conform to CEN Euro Norms or American NIJ Vehicle shielding to be made up of ballistic steel/according to level B6 Composite material to all doors withstand B6 level All windows are to be glass( curved and bullet proof resistant) All windows at least 40 mm thick All windows to have polycarbonate film Front: Battery to be armored with steel Firewall to be armored with steel Engine sides to be armored with steel Front window frame to be armored with steel All windows fixed except driver - not to be able to be opened more than 100 mm

Gastral tergites T2-T7 with 2, 2, 2, 4, 6 and 4 setae.

Gastral antral biopsy in the differentiation of pediatric colitides.

Pribalovy Letak Melovis 15 Mg, Melovis

Pribalovy letak MELOVIS 15 MG

Humanni lecivy pripravek

MELOVIS 15 mg

Tablety Meloxicamum Prectete si pozorne tento pribalovy letak, protoze obsahuje pro vas dulezite udaje.

Ponechte si pribalovy letak pro pripad, ze si jej budete potrebovat precist znovu.

Mate-li jakekoli dalsi otazky, zeptejte se sveho lekare, lekarnika nebo zdravotni sestry.

Tento pripravek byl predepsan vyhradne Vam. Nedavejte jej zadne dalsi osobe. Mohl by ji ublizit, a to i tehdy, ma-li stejne znamky onemocneni jako Vy.

Pokud se u Vas vyskytne kterykoli z nezadoucich ucinku, sdelte to svemu lekari, lekarnikovi nebo zdravotni sestre.

Stejne postupujte v pripade jakychkoli nezadoucich ucinku, ktere nejsou uvedeny v teto pribalove informaci.

Co naleznete v tomto pribalovem letaku:

Co je MELOVIS a k cemu se pouziva

Cemu musite venovat pozornost, nez zacnete pripravek MELOVIS uzivat

Jak se pripravek MELOVIS uziva

Mozne nezadouci ucinky

Jak pripravek MELOVIS uchovavat

Obsah baleni a dalsi informace

1. Co je MELOVIS a k cemu se pouziva

MELOVIS obsahuje lecivou latku meloxikam. Meloxikam patri do skupiny leku nazyvanych nesteroidni protizanetlive leky (NSAID), ktere se pouzivaji ke zmenseni zanetu a bolesti kloubu a svalu.

ke kratkodobe lecbe pri vzplanuti osteoartrozy

k dlouhodobe lecbe

revmatoidni artritidy

ankylozujici spondylitidy (zname take jako Bechterevova choroba)

2. Cemu musite venovat pozornost, nez zacnete pripravek MELOVIS uzivat

behem poslednich tri mesicu tehotenstvi

jestlize je Vam mene nez 16 let

jestlize jste alergicky(a) na meloxikam nebo na kteroukoli dalsi slozku tohoto pripravku

jestlize jste alergicky(a) na kyselinu acetylsalicylovou nebo jine nesteroidni protizanetlive leky (NSAID)

jestlize jste meli po uziti kyseliny acetylsalicylove nebo jinych NSAID nektery z nasledujicich priznaku:

sipani, pocit tisne na hrudniku, dusnost (astma)

nosni nepruchodnost v dusledku vyvysenin nosni sliznice (nosni polypy)

kozni vyrazky/koprivka (urtikarie) o nahly otok kuze nebo sliznice, napr. otok okolo oci, otok obliceje, rtu, ust nebo hrdla, ktery muze zpusobit dychaci obtize (angioneurotic­ky edem)

jestlize jste mel(a) v souvislosti s predchozi lecbou nesteroidnimi protizanetlivymi leky (NSAID)

krvaceni do zaludku nebo strev

proderaveni (perforace) v zaludku nebo strevech

jestlize mate vredy nebo krvaceni do zaludku nebo strev

jestlize mate vred zaludku nebo dvanactniku nebo krvaceni zazivaciho traktu v soucasnosti nebo v minulosti (vredy nebo krvaceni, ktere se vyskytly nejmene dvakrat)

jestlize mate tezkou poruchu funkce jater

jestlize mate nedialyzovane tezke selhani ledvin

jestlize jste v nedavne dobe mel(a) krvaceni do mozku (cerebrovaskularni krvaceni)

jestlize mate jakoukoliv poruchu srazlivosti krve

jestlize mate zavazne srdecni selhani

Zeptejte se, prosim, sveho lekare, pokud si nejste jisti, jestli se Vas vyse uvedene informaceme tykaji.

Upozorneni a opatreni Pred uzitim pripravku MELOVIS se poradte se svym lekarem, lekarnikem nebo zdravotni sestrou. Leky jako je MELOVIS mohou pusobit mirne zvyseni rizika srdecniho zachvatu (infarktu myokardu) nebo mrtvice (apoplexie). Riziko je vice pravdepodobne, pokud jsou pouzivany vysoke davky a je dlouha doba lecby. Neprekracujte doporucenou davku. Neuzivejte MELOVIS dele, nez je Vam predepsan (viz bod 3 “Jak se pripravek Melovis uziva”). Pokud mate srdecni obtize, prodelali jste v minulosti cevni mozkovou prihodu nebo se domnivate, ze mate rizikove faktory pro rozvoj techto onemocneni (napr. vysoky krevni tlak, cukrovku, vysoky cholesterol nebo kourite), meli byste se o vhodnosti lecby poradit s lekarem nebo lekarnikem. Napr. pokud:

mate vysoky krevni tlak (hypertenze)

mate vysokou hladinu cukru v krvi (cukrovka – diabetes mellitus)

mate vysokou hladinu cholesterolu v krvi (hypercholeste­rolemie)

kourite

Pokud se u Vas objevi zavazne alergicke reakce, meli byste prestat uzivat MELOVIS pri prvnim vyskytu kozni vyrazky, lezi mekkych tkani (sliznicni leze) nebo jakychkoli jinych priznaku alergie a kontaktovat lekare. Okamzite ukoncete lecbu pripravkem MELOVIS, jakmile zaznamenate krvaceni (zpusobujici nacernalou – dehtovou barvu stolice) nebo vredy v travicim traktu (zpusobujici bolesti bricha). MELOVIS neni vhodny, pokud potrebujete ihned zmirnit akutni bolest. MELOVIS muze zakryt priznaky infekce (napr. horecku). Pokud si myslite, ze muzete mit infekci, meli byste navstivit lekare. Vzhledem k tomu, ze muze byt nutne upravit Vasi lecbu, poradte se se svym lekarem, nez zacnete uzivat pripravek MELOVIS v techto pripadech:

zanet jicnu (ezofagitida) v anamneze, zanet zaludku (gastritida) nebo jine onemocneni traviciho traktu, napr. ulcerativni kolitida, Crohnova nemoc

vysoky krevni tlak (hypertenze)

vyssi vek

onemocneni srdce, jater nebo ledvin

vysoka hladina cukru v krvi (cukrovka – diabetes mellitus)

snizeny objem krve (hypovolemie), ktery muze nastat v dusledku velke ztraty krve nebo tezkych popalenin, operace nebo nizkeho prijmu tekutin vysoka hladina drasliku v krvi drive diagnostikovana lekarem

bronchialni astma nebo jeho predchozi historie

Je treba, aby lekar sledoval zlepsovani Vaseho stavu v prubehu lecby. V souvislosti s uzivanim meloxikamu byly hlaseny potencialne zivot ohrozujici kozni vyrazky (Stevens Johnsonuv syndrom, toxicka epidermalni nekrolyza), projevujici se zpocatku jako nacervenale tercovite skvrny nebo kruhove skvrny casto s centralnimi puchyri lokalizovane na trupu. Dalsi priznaky, po kterych je treba patrat, zahrnuji vredy v ustech, hrdle, nosu, na pohlavnich organech a zanet spojivek (cervene a otekle oci). Tyto potencialne zivot ohrozujici kozni vyrazky jsou casto doprovazeny chripkovymi priznaky (priznaky podobne chripce). Vyrazka se muze vyvinout v rozsahle puchyre nebo olupovani kuze. Nejvyssi riziko vyskytu zavaznych koznich reakci je v prvnich tydnech lecby. Pokud se u Vas v souvislosti s uzivanim meloxikamu objevi Stevens Johnsonuv syndrom nebo toxicka epidermalni nekrolyza, nesmite nikdy meloxikam opet uzivat. Pokud se u Vas objevi vyrazka nebo vyse uvedene kozni priznaky, prestante uzivat meloxikam, vyhledejte okamzite lekare a reknete mu, ze uzivate tento lek.

Deti a dospivajici MELOVIS by nemel byt podavan detem a dospivajicim mladsim 16 let.

Dalsi lecive pripravky a MELOVIS MELOVIS muze ovlivnit pusobeni jinych leku nebo jeho ucinek muze byt ovlivnen jinymi leky.

Informujte sveho lekar nebo lekarnika o vsech lecich, ktere uzivate, ktere jste v nedavne dobe uzival(a) nebo ktere mozna budete uzivat. Zejmena, prosim, nformujte sveho lekare nebo lekarnika, pokud uzivate, v minulosti jste uzivala nebo pouzivate nektere z nasledujicich le­civ:

jina nesteroidni protizanetliva leciva (NSAID)

leky, ktere zabranuji srazeni krve

leky, ktere rozpousteji krevni srazeniny (trombolytika)

leky k lecbe srdecnich onemocneni

leky k lecbe ledvinovych onemocneni

kortikosteroidy (napr. leky proti zanetum nebo k lecbe alergii)

cyklosporin nebo takrolimus – pouziva se po transplantaci organu, k lecbe tezkych koznich onemocneni, revmatoidni artritidy nebo nefrotickeho syndromu

jakakoliv diuretika (“odvodnovaci tablety”)

Pokud uzivate diuretika, muze lekar sledovat funkci ledvin.

pripravky k lecbe vysokeho krevniho tlaku (napr. beta-blokatory)

lithium (k lecbe poruch nalady)

inhibitory zpetneho vychytavani serotoninu (SSRIs) (pripravky k lecbe deprese)

methotrexat (k lecbe nadoru nebo zavaznych onemocneni kuze a revmatoidni artritidy)

cholestyramin (ke snizeni hladiny cholesterolu v krvi)

jste zena, ktera pouziva nitrodelozni antikoncepcni telisko (IUD)

V pripade jakychkoli pochybnosti nebo nejasnosti pozadejte o vysvetleni sveho lekare nebolekarnika.

MELOVIS s jidlem a pitim Tablety se polykaji cele behem jidla a zapijeji se vodou nebo jinou tekutinou.

Tehotenstvi, kojeni a fertilita Pokud jste tehotna nebo kojite, domnivate se, ze muzete byt tehotna, nebo planujete otehotnet, poradte se se svym lekarem nebo lekarnikem drive, nez zacnete tento pripravek uzivat.

Tehotenstvi Pokud behem pouzivani pripravku MELOVIS zjistite, ze jste tehotna, informujte sveho lekare. Behem prvnich 6 mesicu tehotenstvi smite uzivat pripravek MELOVIS pouze s vyslovnym souhlasem Vaseho lekare. Behem poslednich tri mesicu tehotenstvi neuzivejte pripravek MELOVIS, protoze muze zpusobit vazne poskozeni Vaseho ditete, zejmena poskodit srdce, plice a ledviny, a to jiz po jednom podani.

Kojeni Uzivani tohoto pripravku se behem kojeni nedoporucuje.

Fertilita MELOVIS muze zpusobit obtize s otehotnenim. Pokud planujete otehotnet nebo mate problemy s otehotnenim, informujte o tom lekare.

Rizeni dopravnich prostredku a obsluha stroju V souvislosti s uzivanim tohoto pripravku se mohou vyskytnout poruchy zraku, ospalost, zavrate (toceni hlavy) nebo jine poruchy centralni nervove soustavy. Jestlize zpozorujete takove ucinky, neridte dopravni prostredky ani neobsluhujte stoje.

MELOVIS obsahuje laktozu Pokud Vam lekar rekl, ze nesnasite urcite druhy cukru, informujte ho drive, nez zacnete tento pripravek uzivat.

3. Jak se pripravek MELOVIS uziva

Vzdy uzivejte tento pripravek presne podle pokynu sveho lekare nebo lekarnika. Pokud si nejste jisty(a), poradte se se svym lekarem nebo lekarnikem. Doporucena davka pripravku je: vzplanuti osteoartritidy: 7,5 mg jednou denne. Davka muze byt zvysena na 15 mg jednou denne. Revmatoidni artritida: 15 mg jednou denne. Davka muze byt snizena na 7,5 mg jednou denne. Ankylozujici spondylitida: 15 mg jednou denne. Davka muze byt snizena na 7,5 mg jednou denne. Tablety se polykaji cele behem jidla a zapijeji se vodou nebo jinou tekutinou. Neprekracujte doporucenou maximalni davku 15 mg denne. Pokud se Vas tyka nektery z udaju uvedenych v bode „Upozorneni a opatreni“, lekar muze snizit Vasi davku na 7,5 mg (jedna tableta) jednou denne.

Pouziti u deti a dospivajicich MELOVIS by nemel byt podavan detem a dospivajicim do 16 let. Pokud mate pocit, ze ucinek pripravku MELOVIS je prilis silny nebo prilis slaby nebo pokud po nekolika dnech uzivani nepocitujete zadne zlepseni sveho stavu, poradte se se svym lekarem nebo lekarnikem.

Jestlize jste uzil(a) vice pripravku MELOVIS, nez jste mel(a) Jestlize jste uzil(a) prilis mnoho tablet nebo mate podezreni na predavkovani, ihned kontaktujte lekare nebo jdete do nejblizsi nemocnice.

Priznaky po akutnim predavkovani NSAID jsou obvykle:

nedostatek energie (letargie)

ospalost

zaludecni nevolnost a zvraceni

bolesti v oblasti zaludku (epigastricka bolest)

Tyto priznaky se obecne zlepsi po vysazeni pripravku MELOVIS. Muzete trpet krvacenim do zaludku nebo strev (gastrointestinalni krvaceni).

Tezke predavkovani muze vest k zavaznym nezadoucim ucinkum (viz bod 4).

vysoky krevni tlak (hypertenze)

akutni selhani ledvin

spatna funkce jater

snizene dychani nebo zastava dechu (respiracni deprese)

ztrata vedomi (koma)

krece (konvulze)

selhani krevniho obehu (kardiovaskularni kolaps)

zastava srdce

nahle alergicke (hypersenzitivni) reakce, vcetne:

mdlob

dusnosti

koznich reakci

Jestlize jste zapomnel(a) uzit pripravek MELOVIS Nezdvojnasobujte nasledujici davku, abyste nahradil(a) vynechanou davku. Pouze uzijte nasledujici davku v obvyklou dobu. Mate-li jakekoli dalsi otazky tykajici se uzivani tohoto pripravku, zeptejte se sveho lekare, lekarnika nebo zdravotni sestry.

4. Mozne nezadouci ucinky

Podobne jako vsechny leky muze mit i tento pripravek nezadouci ucinky, ktere se ale nemusi vyskytnout u kazdeho. Prestante uzivat MELOVIS a ihned se poradte s lekarem nebo navstivte nejblizsi nemocnici, jestlize zaznamenate: jakekoli alergicke reakce (reakce precitlivelosti), ktere se mohou objevit ve forme:

koznich reakci jako je svedeni (pruritus), puchyrky nebo odlupovani kuze, ktere muze byt zavazne (Stevens Johnsonuv syndrom a toxicka epidermalni nekrolyza), poskozeni mekkych tkani (poskozeni sliznic) nebo erythema multiforme. Erythema multiforme je zavazna alergicka kozni reakce, ktera se projevuje skvrnami, cervenymi nebo fialovymi podlitinami nebo puchyrky. Muze take zasahnout usta, oci a jine vlhke povrchy tela.

otok kuze nebo sliznice, napr. otok okolo oci, otok obliceje a rtu, ust nebo hrdla, ktery muze zpusobit dychaci obtize, otekle kotniky nebo nohy (edem dolnich koncetin)

dychaci obtize nebo zachvat astmatu

zanet jater (hepatitida). Ten muze zpusobit priznaky jako:

zezloutnuti kuze nebo ocniho belma (zloutenka)

bolest v oblasti bricha

nechutenstvi (ztrata chuti k jidlu)

Jakekoliv nezadouci ucinky tykajici se zazivaciho traktu, zvlaste:

krvaceni (zpusobujici nacernalou – dehtovou barvu stolice)

vredy v zazivacim traktu (zpusobujici bolesti bricha)

Krvaceni v zazivacim traktu (gastrointestinalni krvaceni), tvorba vredu, nebo proderaveni (perforace) v oblasti traviciho ustroji muze byt nekdy zavazne a muze vest k umrti, zejmena u starsich osob.

Jestlize jste drive trpel(a) vyse uvedenymi priznaky, ktere se tykaji traviciho ustroji, v souvislosti s dlouhodobym uzivanim nesteroidnich protizanetlivych leku, vyhledejte neodkladne lekarskou pomoc, zejmena pokud jste vyssiho veku. Vas lekar bude sledovat prubeh lecby. Pokud se u Vas vyskytly poruchy zraku, neridte ani neobsluhujte stroje. Obecne nezadouci ucinky nesteroidnich protizanetlivych leku (NSAID) Pouziti nekterych nesteroidnich protizanetlivych leku muze byt spojeno s mirnym zvysenim rizika arterialnich trombotickych prihod (vyskyt krevnich srazenin v tepnach), napr. infarkt myokardu nebo cevnich mozkovych prihod(apoplexie), zejmena pri uzivani vyssich davek a pri dlouhodobem uzivani. V souvislosti s lecbou nesteroidnimi protizanetlivymi leky byly hlaseny pripady zadrzovani tekutin (otoky), vysokeho krevniho tlaku (hypertzenze) a srdecniho selhani.

Nejcasteji pozorovane nezadouci ucinky se tykaly traviciho ustroji (gastrointestinalni prihody):

zaludecni vredy a vredy v horni casti tenkeho streva (pepticke/gas­troduodenalni vre­dy)

proderaveni strevni steny (perforace) nebo krvaceni v travicim ustroji (nekdy muze vest k umrti, zejmena u starsich pacientu)

V souvislosti s lecbou nesteroidnimi protizanetlivymi leky byly hlaseny nasledujici nezadouci ucinky:

nevolnost (nausea) a zvraceni

prujem

plynatost

zacpa

zazivaci potize (dyspepsie)

bolesti bricha

nacernala (dehtova) stolice z duvodu krvaceni v travicim ustroji (melena)

krev pri zvraceni (hematemesis)

zanet v souvislosti s tvorbou vridku v ustech (ulcerativni stomatitida)

zhorseni zanetu tlusteho streva (exacerbace zanetu tracniku)

zhorseni zanetu v travicim ustroji (exacerbace Crohnovy nemoci)

Mene casto byl pozorovan zanet zaludku (gastritida). Nezadouci ucinky meloxikamu Velmi caste: vyskytuji se u vice nez 1 pacienta z 10

zazivaci potize (dyspepsie)

nevolnost (nausea) a zvraceni

bolesti bricha

zacpa

plynatost

prujem

Caste: vyskytuji se u 1 az 10 pacientu ze 100

Mene caste: vyskytuji se u 1 az 10 pacientu z 1000

zavrat (pocit na omdleni)

pocit zavrati nebo pocit toceni hlavy (vertigo)

ospalost (somnolence)

anemie (chudokrevnost – nizsi mnozstvi krevniho barviva hemoglobinu)

zvyseny krevni tlak (hypertenze)

navaly (prechodne zcervenani obliceje a krku)

zadrzovani vody a sodiku v tele

zvysena hladina drasliku v krvi (hyperkalemie). To muze vest k nasledujicim priznakum:

zmeny srdecni cinnosti (arytmie)

palpitace (pocit buseni srdce)

svalova slabost

rihani

zanet zaludku (gastritida)

krvaceni v zazivacim ustroji

zanet v ustech (stomatitida)

nahle alergicke reakce (reakce precitlivelosti)

svedeni (pruritus)

vyrazka na kuzi

otoky zpusobene zadrzovanim tekutin v tele (edem), vcetne oteklych kotniku/nohou (edem dolnich koncetin)

nahle otoky kuze a sliznic, jako jsou otoky kolem oci, otoky v obliceji, rtu, ust a v krku, ktere mohou zpusobit dychaci obtize (angioneurotic­ky edem)

prechodne abnormality jaternich laboratornich testu (napr. zvysene jaterni enzymy transaminazy nebo zvyseni bilirubinu (zlucove barvivo). Tyto abnormality zjisti Vas lekar pri laboratornim vysetreni krve.

abnormality laboratornich testu zjistujicich funkce ledvin (napr. zvyseni kreatininu nebo urey)

Vzacne: vyskytuji se u 1 az 10 pacientu ze 10000

poruchy nalady

nocni mury

abnormalni krevni obraz vcetne

abnormalniho diferencialniho krevniho obrazu

snizeneho poctu bilych krvinek (leukocytopenie)

snizeneho poctu krevnich desticek (trombocytopenie)

Tyto nezadouci ucinky mohou vest ke zvysenemu riziku infekce a priznakum jako jsou modriny nebo krvaceni z nosu.

pocit zvoneni v usich (tinitus)

pocit buseni srdce (palpitace)

zaludecni vredy nebo vredy v horni casti tenkeho streva (pepticke/gas­troduodenalni vre­dy)

zanet jicnu (ezofagitida)

zanet tlusteho streva (kolitida)

zachvaty astmatu (pozorovane u pacientu, kteri jsou alergicti na kyselinu acetylsalicylovou nebo jine nesteroidni protizanetlive le­ky)

koprivka (urticaria)

poruchy zraku vcetne

rozmazaneho videni

zanetu spojivek (cervene a otekle oci)

byly hlaseny pripady potencialne zivot ohrozujici kozni vyrazky (Stevens Johnsonuv syndrom, toxicka epidermalni nekrolyza) (viz bod 2).

Velmi vzacne: vyskytuji se u mene nez 1 pacienta z 10000

puchyrky na kuzi (bulozni reakce) a erythema multiforme. Erythema multiforme je zavazna alergicka reakce kuze, ktera se projevuje skvrnami, cervenymi nebo fialovymi podlitinami nebo puchyrky. Muze take zasahnout usta, oci a jine vlhke povrchy tela.

zanet jater (hepatitida). Ten muze zpusobit priznaky jako:

zezloutnuti kuze nebo ocniho belma (zloutenka)

bolest v oblasti bricha

nechutenstvi (ztrate chuti k jidlu)

akutni selhani ledvin zejmena u pacientu s rizikovymi faktory jako je onemocneni srdce, cukrovka nebo onemocneni ledvin.

proderaveni (perforace) strevni steny

Neni znamo: cetnost neni mozne zjistit z dostupnych udaju

zmatenost

desorientace

dychaci obtize a kozni reakce (anafylakticke/a­nafylaktoidni reakce)

vyrazky zpusobene slunecnim svetlem (fotosenzitivni reakce)

byly hlaseny pripady srdecniho selhani v souvislosti s podanim nesteroidnich protizanetlivych le­ku

kompletni ztrata urciteho druhu bilych krvinek (agranulocytoza) zvlaste u pacientu, kteri uzivaji spolu s pripravkem MELOVIS leky s nezadoucimi myelotoxickymi ucinky (leky, ktere poskozuji kostni dren). To muze zpusobit:

nahlou horecku

boleni v krku

infekce

Nezadouci ucinky zpusobene nesteroidnimi protizanetlivymi leky (NSAID), ktere nebyly hlaseny po podani pripravku MELOVIS. Zmeny ledvin vedouci k akutnimu selhani ledvin:

velmi vzacne pripady zanetu ledvin (intersticialni nefritida)

nekroza (odumreni) nekterych bunek ledvin (akutni tubularni nebo papilarni nekroza)

bilkoviny v moci (nefroticky syndrom s proteinurii)

Pokud se u Vas vyskytne kterykoli z nezadoucich ucinku, sdelte to svemu lekari, lekarnikovi nebo zdravotni sestre. Stejne postupujte v pripade jakychkoli nezadoucich ucinku, ktere nejsou uvedeny v teto pribalove informaci.

5. Jak pripravek MELOVIS uchovavat

Uchovavejte tento pripravek mimo dohled a dosah deti. Nepouzivejte tento pripravek po uplynuti doby pouzitelnosti, vyznacene na obalu. Nevyhazujte zadne lecive pripravky do odpadnich vod nebo domaciho odpadu. Zeptejte se sveho lekarnika, jak mate nalozit s pripravky, ktere jiz nepouzivate. Tato opatreni pomahaji chranit zivotni prostredi.

6. Obsah baleni a dalsi informace

Co pripravek MELOVIS obsahuje Lecivou latkou je meloxicamum 15 mg v 1 tablete. Pomocnymi latkami jsou: dihydrat citronanu sodneho, monohydrat laktosy, mikrokrystalicka celulosa, krospovidon, koloidni bezvody oxid kremicity, magnesium-stearat.

Jak pripravek MELOVIS vypada a co obsahuje toto baleni Melovis 15 mg: svetle zlute, kulate, bikonvexni tablety se zkosenymi hranami, na jedne strane s pulici ryhou, nad pulici ryhou vyrazeno „B“ a pod pulici ryhou vyrazeno „19“, na druhe strane hladke. Tabletu lze delit na dve stejne davky

Velikost baleni PVC/PVDC/Al blistr: 1, 2, 7, 10, 14, 15, 20, 28, 30, 50, 60, 100, 140, 280, 300, 500 nebo 1000 tablet. Na trhu nemusi byt vsechny velikosti baleni.

Drzitel rozhodnuti o registraci Actavis Group PTC ehf. Reykjavikurvegur 76–78 220 Hafnarfjordur Island

Vyrobce Niche Generics Ltd.,Unit 5, 151 Baldozle Industrial Estate Dublin 13, Irsko Extractum Pharma Ltd. 1044 Budapest, Megyeri ut 64, Madarsko Tento lecivy pripravek je v clenskych zemich EU schvalen pod temito nazvy: Ceska republika: Melovis 15 mg Dansko: Celomix 7,5 mg, 15 mg tablets Madarsko: Meloxan 7,5 mg, 15 mg tablets Polsko: Celomix 7,5 mg, 15 mg tablets Slovenska republika: Celomix 7,5 mg, 15 mg tablets Slovinsko: Celomix 7,5 mg, 15 mg tablets

Datum posledni revize textu: 17.1.2013

Vice informaci o lecivem pripravku naleznete zde .

Upozorneni: Vyse uvedene udaje maji pouze informacni charakter. Kompletni a aktualni informace o lecivych pripravcich naleznete na webovych strankach Statniho ustavu pro kontrolu leciv www. sukl. cz .

O spravnem davkovani nebo nezadoucich ucincich se poradte se svym lekarem nebo lekarnikem.

Norvasc - Blood Pressure, Actapin

Common use This medication belongs to the group of calcium channel blockers. Norvasc selectively blocks channels of L-type (one of six types of channels in tissues) located in a vascular wall, myocard and in particular in cells of conducting and contractile systems of myocardium. By blocking Ca+ ions transfer through membrane Norvasc decreases tone of vessels, arterial pressure. The medication is used to treat hypertension, ischemic heart disease, angina.

Dosage and direction Do not take this drug if it was not administered to you. Follow all directions of your doctor. It is possible to take Norvasc with or without food. As it is metabolized in liver it should be administered cautiously in patients with liver failure.

Precautions Avoid drinking alcohol. Before taking Norvasc, inform your doctor if you have congestive heart failure or liver disease.

Contraindications Individual hypersensitivity, arterial hypotension, cardiogenic shock, pregnancy, breastfeeding. Cautiousness is important when Norvasc is administered in patients with chronic heart failure diabetes, lipid metabolism disorders, liver failure and to persons younger 18 y. o.

Possible side effect The most common side effects are edema of lower extremities and headache. Contact your doctor for medical attention if your feel them and also swelling in your hands, ankles, or feet, chest pain, slow, fast, or pounding heartbeats, easy bruising or bleeding, unusual weakness, numbness, burning, pain, or tingly feeling, jaundice.

Drug interaction Medications which contain Á2+ may decrease Norvasc effect. Non-steroid anti-inflammatory medications and estrogens may decrease effectiveness of Norvasc. Diuretics may increase Norvasc activity. Concomitant taking with medications containing lithium might aggravate their toxicity.

If you forgot to take a dose take it as soon as you remember unless it is almost time for the next intake. If so, do not take the missed dose and resume your regular schedule. Do not compensate the missed dose by taking an extra one.

Overdose If you experience tingly feeling, severe dizziness, and fainting, seek for immediate medical help.

Storage Keep at room temperature, 15-30 C (59-86 F), in a light-resistant container away from moisture.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Common use This medication belongs to the group of calcium channel blockers. Norvasc selectively blocks channels of L-type (one of six types of channels in tissues) located in a vascular wall, myocard and in particular in cells of conducting and contractile systems of myocardium. By blocking Ca+ ions transfer through membrane Norvasc decreases tone of vessels, arterial pressure. The medication is used to treat hypertension, ischemic heart disease, angina.

Dosage and direction Do not take this drug if it was not administered to you. Follow all directions of your doctor. It is possible to take Norvasc with or without food. As it is metabolized in liver it should be administered cautiously in patients with liver failure.

Precautions Avoid drinking alcohol. Before taking Norvasc, inform your doctor if you have congestive heart failure or liver disease.

Contraindications Individual hypersensitivity, arterial hypotension, cardiogenic shock, pregnancy, breastfeeding. Cautiousness is important when Norvasc is administered in patients with chronic heart failure diabetes, lipid metabolism disorders, liver failure and to persons younger 18 y. o.

Possible side effect The most common side effects are edema of lower extremities and headache. Contact your doctor for medical attention if your feel them and also swelling in your hands, ankles, or feet, chest pain, slow, fast, or pounding heartbeats, easy bruising or bleeding, unusual weakness, numbness, burning, pain, or tingly feeling, jaundice.

Drug interaction Medications which contain Á2+ may decrease Norvasc effect. Non-steroid anti-inflammatory medications and estrogens may decrease effectiveness of Norvasc. Diuretics may increase Norvasc activity. Concomitant taking with medications containing lithium might aggravate their toxicity.

If you forgot to take a dose take it as soon as you remember unless it is almost time for the next intake. If so, do not take the missed dose and resume your regular schedule. Do not compensate the missed dose by taking an extra one.

Overdose If you experience tingly feeling, severe dizziness, and fainting, seek for immediate medical help.

Storage Keep at room temperature, 15-30 C (59-86 F), in a light-resistant container away from moisture.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Repaglinide Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Repaglinid

repaglinide

Uses

Repaglinide is used alone or with other medications to control high blood sugar along with a proper diet and exercise program. It is used in people with type 2 diabetes. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. It works by stimulating the body to produce more insulin. Insulin is a natural substance that allows the body to properly use sugar from the diet.

How to use repaglinide

Read the Patient Information leaflet if one is available from your pharmacist before you start using repaglinide and each time you get a refill. If you have any questions, consult your doctor or pharmacist.

Take this medication by mouth 15 minutes before each meal, usually 2-4 times daily depending on the number of meals or as directed by your doctor. Take this drug no earlier than 30 minutes before the meal. You may also take it just before the meal if necessary. Do not take a dose of medication if you are skipping that meal or if your blood sugar is low.

The dosage is based on your medical condition and response to treatment.

If you are changing from a different anti-diabetes drug (such as chlorpropamide ) to repaglinide, follow your doctor's directions carefully for stopping the old drug and starting this medication.

Use this medication regularly as directed by your doctor in order to get the most benefit from it. Carefully follow the medication treatment plan, meal plan, and exercise program your doctor has recommended.

Check your blood sugar regularly as directed by your doctor. Keep track of the results, and share them with your doctor. This is very important in order to determine the correct dose. Tell your doctor if your blood sugar measurements are too high or too low. Your treatment plan may need to be changed.

Side Effects

Weight gain, diarrhea. and joint pain may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because 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.

Repaglinide can cause low blood sugar (hypoglycemia) especially if you are taking other medicines for diabetes. Consuming large quantities of alcohol, not getting enough calories from food, or doing unusually heavy exercise may also lead to low blood sugar. Symptoms may include chills, cold sweat, dizziness. drowsiness, shaking, fast heartbeat, weakness. headache. fainting. tingling of the hands or feet, or hunger. It is a good habit to carry glucose tablets or gel to treat low blood sugar. If you don't have these reliable forms of glucose, raise your blood sugar quickly by eating a quick source of sugar such as table sugar, honey, candy, or drinking a glass of fruit juice or non-diet soda. Check with your doctor or pharmacist to find out what you should do if you miss a meal.

Symptoms of high blood sugar (hyperglycemia ) include thirst, increased urination, confusion, drowsiness, flushing, rapid breathing, and fruity breath odor. If these symptoms occur, tell your doctor right away. Your doctor may need to adjust your diabetes medication(s).

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction. rash. itching /swelling (especially of the face/tongue /throat), severe dizziness, trouble breathing .

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 repaglinide, tell your doctor or pharmacist if you are allergic to it; 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: kidney disease. liver disease.

You may experience blurred vision. dizziness, or drowsiness due to extremely low or high blood sugar levels. Do not drive, use machinery, or do any activity that requires alertness or clear vision until you are sure you can perform such activities safely.

Limit alcohol while taking this medication because it can increase the risk of developing low blood sugar.

During times of stress, such as fever, infection, injury, or surgery, it may be more difficult to control your blood sugar. Consult your doctor because increased stress may require a change in your treatment plan, medications, or blood sugar testing.

During pregnancy this medication should be used only when clearly needed. Pregnancy may cause or worsen diabetes. Discuss a plan with your doctor for managing your blood sugar while pregnant. Your doctor may change your diabetes treatment during your pregnancy. Discuss the risks and benefits of different treatments (such as diet, exercise, and medications including insulin ).

It is not known whether this drug passes into breast milk and the effect on a nursing infant is unknown. Therefore, breast - feeding while using this drug is not recommended. Consult your doctor before breast-feeding.

Interactions

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.

A product that may interact with this drug is: NPH insulin.

Other medications can affect the removal of repaglinide from your body, which may affect how repaglinide works. Examples include clopidogrel, cyclosporine, gemfibrozil, trimethoprim, azole antifungals (such as itraconazole), macrolide antibiotics (such as erythromycin), rifamycins (such as rifabutin), St. John's wort, among others.

Many drugs can affect your blood sugar levels, making it more difficult to control your blood sugar. Examples include corticosteroids (such as prednisone), psychiatric medicines (such as olanzapine), fluoroquinolone antibiotics (such as ciprofloxacin), among others. Ask your doctor or pharmacist how often to check your blood sugar. Tell your doctor about the results and of any symptoms of high or low blood sugar. (See also Side Effects section.) Your doctor may need to adjust your diabetes medication, exercise program, or diet.

Beta-blocker medications (such as metoprolol, propranolol, glaucoma eye drops such as timolol) may prevent the fast/pounding heartbeat you would usually feel when your blood sugar level falls too low (hypoglycemia). Other symptoms of low blood sugar such as dizziness, hunger, or sweating are unaffected by these drugs.

Check the labels on all your medicines (such as cough-and-cold products) carefully. Some products may contain sugar or alcohol and may affect your blood sugar levels. Ask your doctor or pharmacist about using these products safely.

Other medications can affect the results of urine tests for sugar or ketones. Consult your doctor or pharmacist for more information.

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: very fast heartbeat, vision changes, unexplained heavy sweating, agitation, fainting, seizures.

Notes

Do not share this medication with others.

Attend a diabetes education program to learn more about diabetes and the important aspects of its treatment, including medications, diet, exercise, and getting regular eye/foot/medical exams. Learn the symptoms of high and low blood sugar and how to treat low blood sugar.

Check your blood sugar levels regularly as directed. Keep all medical appointments. Laboratory and/or medical tests (such as kidney function tests, fasting blood glucose, hemoglobin A1c) should be performed periodically to check for side effects and monitor your response to treatment.

Missed Dose

If you miss a dose, skip that dose and resume your regular dosage schedule with your next meal. Do not double the dose to catch up.

Storage

Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture. Do not store in the bathroom. Keep all medicines 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 for more details about how to safely discard your product.

MEDICAL ALERT: Your condition can cause complications in a medical emergency. For information about enrolling in MedicAlert, call 1-888-633-4298 (US) or 1-800-668-1507 (Canada).

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

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Lotriderm, Lotriderm

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Lotriderm

Lotriderm is an anti fungal / potent steroid combination containing the steroid betamethasone diproprionate plus clotrimazole for the treatment of severe inflammatory skin disorders such as scalp psoriasis which is unresponsive to less potent corticosteroids.

It belongs to the group of medicines for application to the skin called topical corticosteroids which should not be confused with anabolic steroid tablets or injections which can be misused by some athletes. Topical corticosteroids have been shown to reduce the itching, redness and inflammation of certain skin problems

It is used for the short-term topical treatment of tinea infections due to Trichophyton rubrum; T. mentagrophytes; Epidermophyton floccusum and Microsporum canis; candidiasis due to Candida albicans.

Topical Corticosteroids suppress the inflammatory reaction during use; they are not curative and on discontinuation a rebound exacerbation of the condition may occur. They are generally used to relieve symptoms and suppress signs of the disorder when other measures such as emollients are ineffective.

Topical corticosteroids are often prescribed as first-line treatment because they are so easy to use. Once-daily application is usually sufficient effect

Clotrimazole is a broad-spectrum antifungal agent with activity against Trichomones, Staphylococci and Bacteroides.

Suitable for adults and children over 12 years of age. Available on Prescription only.

For adults and children over the age of 12 years a layer of cream should be gently massaged into the affected and surrounding skin areas twice a day, in the morning and evening. Usually the cream should be used for either two weeks or four weeks, depending on the type of infection you have. Your doctor will tell you how long to use the cream for. Your skin infection should start to improve and the redness and itchiness will ease, within the first few days of treatment. If your skin infection does not appear to get any better, you should see your doctor. You should always follow these instructions when using Lotriderm:

Keep the cream away from your eyes.

Do not apply the cream to children (over 12 years of age), on any part of their body, for more than 5 days.

Do not put the cream under a dressing, such as a plaster or bandage, as this makes it easier for the active drugs to pass through the skin and possibly cause some undesirable effects.

Do not apply the cream to the face (for any more than 5 days), in places where the skin folds (e. g. the back of the knee) or on large areas of damaged skin.

You should not use a large amount of cream on large areas of the body for a long time (for example every day for many weeks or months).

What are the side effects?

Adverse reactions reported for Lotriderm include: burning and stinging, maculopapular rash, oedema and secondary infection. Reported reactions to clotrimazole include erythema, stinging, blistering, peeling, oedema, pruritis, urticaria and general irritation of the skin. Reactions to betamethasone dipropionate include: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hyperpigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae and miliaria. If you are worried by these or any other effects, you should tell your doctor or pharmacist.

Lotriderm is available on prescription and is manufactured in the UK by PLIVA Pharma Ltd.

Lotriderm

What is Lotriderm?

Lotriderm is an anti-inflammatory cream with antifungal components. It contains two active ingredients:

betamethasone, a powerful topical corticosteroid, and

clotrimazole, an antifungal medicine.

Lotriderm cream relieves skin problems such as itching, redness and swelling. Lotriderm is a prescription-only medicine.

What is Lotriderm used for?

Lotriderm cream is used to treat fungal skin infections such as:

Athlete’s foot (fungal infection of the feet);

Ringworm (ring-shaped or oval patches);

Tinea cruris (fungal infection of the groin);

Candida infections (itchy rash, usually found in skin folds, in the groin, on the genitals and in the area around the anal orifice).

Betamethasone reduces swelling, redness and itching rapidly. Clotrimazole kills the fungi and yeasts and treats the infection.

How to use Lotriderm

Apply Lotriderm cream to the affected area(s) of skin and massage in gently. Do not get the treated areas wet within half an hour of application because the medicine will rinse off. Do not apply the cream to the eyelids or the skin around the eyes. Wash your hands immediately after applying the cream. Continuous, long-term use of topical steroid medication should be avoided. For this reason, Lotriderm cream is usually prescribed as a two to four-week course. If your symptoms have not improved in one or two weeks, you should talk to your doctor.

Dosage

Unless otherwise advised by a doctor, the usual dose in adults and children is:

a thin layer applied to the affected area(s) of skin twice a day.

Do not cover the area being treated with airtight dressings such as bandages or other dressings, unless the doctor advises otherwise. This medicine should only be used on advice of a doctor in young children. The duration of treatment should be determined by a doctor. Read the package leaflet before use.

Side effects

Lotriderm may cause side effects, although not everybody gets them. Side effects that are known to be associated with this medicine include:

Skin irritation due to hypersensitivity;

Thinning of the treated skin;

Red patches and scaling around the mouth;

Striae (stripe-like skin marks);

A decrease in the production of natural hormones by the adrenal glands (only if used long term).

Consult a doctor if the side effects are severe. For more information, see the package leaflet.

When not to use Lotriderm

Lotriderm cream is not suitable for everyone and should not be used if:

You are allergic to betamethasone, clotrimazole or any other ingredient in this medicine;

Your skin problem is caused by viruses, bacteria or parasites;

Your baby has a nappy rash, your skin is broken or ulcerated, or you have acne or rosacea;

You have a skin disorder called ichthyosis vulgaris or the blood vessels in your skin are fragile.

It is important to tell your doctor what topical skin medications you are already using before you start treatment with Lotriderm cream to make sure the combination is safe.

Pregnancy/driving ability/alcohol

Lotriderm cream should not be used by pregnant or breastfeeding women without consulting a doctor first.

Lotriderm cream does not interact with alcohol or affect your ability to drive safely.

Ibuprofen Uses, Dosage - Side Effects, Ibuprofeno

Ibuprofen

Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID). It works by reducing hormones that cause inflammation and pain in the body.

Ibuprofen is used to reduce fever and treat pain or inflammation caused by many conditions such as headache, toothache, back pain, arthritis. menstrual cramps. or minor injury.

Ibuprofen is used in adults and children who are at least 6 months old.

Important information

Ibuprofen can increase your risk of fatal heart attack or stroke, especially if you use it long term or take high doses, or if you have heart disease. Do not use this medicine just before or after heart bypass surgery (coronary artery bypass graft, or CABG).

Ibuprofen may also cause stomach or intestinal bleeding, which can be fatal. These conditions can occur without warning while you are using ibuprofen, especially in older adults.

Do not take more than your recommended dose. An ibuprofen overdose can damage your stomach or intestines. Use only the smallest amount of medication needed to get relief from your pain, swelling, or fever.

Before taking this medicine

Ibuprofen can increase your risk of fatal heart attack or stroke, especially if you use it long term or take high doses, or if you have heart disease. Even people without heart disease or risk factors could have a stroke or heart attack while taking this medicine.

Do not use this medicine just before or after heart bypass surgery (coronary artery bypass graft, or CABG).

Ibuprofen may also cause stomach or intestinal bleeding, which can be fatal. These conditions can occur without warning while you are using ibuprofen, especially in older adults.

You should not use ibuprofen if you are allergic to it, or if you have ever had an asthma attack or severe allergic reaction after taking aspirin or an NSAID.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have:

heart disease, high blood pressure, high cholesterol, diabetes, or if you smoke;

a history of heart attack, stroke, or blood clot;

a history of stomach ulcers or bleeding;

liver or kidney disease;

fluid retention; or

a connective tissue disease such as Marfan syndrome, Sjogren's syndrome, or lupus.

Taking ibuprofen during the last 3 months of pregnancy may harm the unborn baby. Do not use this medicine without a doctor's advice if you are pregnant.

It is not known whether ibuprofen passes into breast milk or if it could harm a nursing baby. Do not use this medicine without a doctor's advice if you are breast-feeding a baby.

Do not give ibuprofen to a child younger than 2 years old without the advice of a doctor.

How should I take ibuprofen?

Use ibuprofen exactly as directed on the label, or as prescribed by your doctor. Do not use in larger amounts or for longer than recommended. Use the lowest dose that is effective in treating your condition.

Do not take more than your recommended dose. An ibuprofen overdose can damage your stomach or intestines. The maximum amount of ibuprofen for adults is 800 milligrams per dose or 3200 mg per day (4 maximum doses). Use only the smallest amount needed to get relief from your pain, swelling, or fever.

A child's dose of ibuprofen is based on the age and weight of the child. Carefully follow the dosing instructions provided with your child's medicine for the age and weight of your child. Ask a doctor or pharmacist if you have questions.

Take ibuprofen with food or milk to lessen stomach upset.

Shake the oral suspension ( liquid ) well just before you measure a dose. 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.

The ibuprofen chewable tablet must be chewed before you swallow it.

If you use this medicine long-term, you may need frequent medical tests.

Store at room temperature away from moisture and heat. Do not allow the liquid medicine to freeze.

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?

Since ibuprofen is used when needed, you may not be on a dosing schedule. If you are on a schedule, use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use 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 nausea, vomiting, stomach pain, drowsiness, black or bloody stools, coughing up blood, shallow breathing, fainting, or coma.

What should I avoid while taking ibuprofen?

Avoid drinking alcohol. It may increase your risk of stomach bleeding.

Avoid taking aspirin while you are taking ibuprofen.

Avoid taking ibuprofen if you are taking aspirin to prevent stroke or heart attack. Ibuprofen can make aspirin less effective in protecting your heart and blood vessels. If you must use both medications, take the ibuprofen at least 8 hours before or 30 minutes after you take the aspirin (non-enteric coated form).

Ask a doctor or pharmacist before using any cold, allergy, or pain medicine. Many medicines available over the counter contain aspirin or other medicines similar to ibuprofen. Taking certain products together can cause you to get too much of this type of medication. Check the label to see if a medicine contains aspirin, ibuprofen, ketoprofen, or naproxen.

Ibuprofen side effects

Get emergency medical help if you have signs of an allergic reaction to ibuprofen: sneezing, runny or stuffy nose; wheezing or trouble breathing; hives; swelling of your face, lips, tongue, or throat.

Get emergency medical help if you have signs of a heart attack or stroke: chest pain spreading to your jaw or shoulder, sudden numbness or weakness on one side of the body, slurred speech, feeling short of breath.

Stop using ibuprofen and call your doctor at once if you have:

changes in your vision;

shortness of breath (even with mild exertion);

swelling or rapid weight gain;

the first sign of any skin rash, no matter how mild;

signs of stomach bleeding - bloody or tarry stools, coughing up blood or vomit that looks like coffee grounds;

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

kidney problems - little or no urinating, painful or difficult urination, swelling in your feet or ankles, feeling tired or short of breath;

low red blood cells (anemia) - pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating; 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 ibuprofen side effects may include:

upset stomach, mild heartburn, nausea, vomiting;

bloating, gas, diarrhea, constipation;

dizziness, headache, nervousness;

mild itching or rash; or

ringing in your ears.

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.

Ibuprofen dosing information

Usual Adult Dose for Dysmenorrhea:

200 to 400 mg orally every 4 to 6 hours as needed.

Usual Adult Dose for Osteoarthritis:

Initial dose: 400 to 800 mg orally every 6 to 8 hours. Maintenance dose: May be increased to a maximum daily dose of 3200 mg based on patient response and tolerance.

Usual Adult Dose for Rheumatoid Arthritis:

Initial dose: 400 to 800 mg orally every 6 to 8 hours. Maintenance dose: May be increased to a maximum daily dose of 3200 mg based on patient response and tolerance.

Usual Adult Dose for Headache:

Study (n=34) - Prevention of Electroconvulsive therapy (ECT)-induced headache: 600 mg orally 90 minutes prior to the initial ECT session

Usual Adult Dose for Pain:

Oral: Mild to moderate pain: 200 to 400 mg orally every 4 to 6 hours as needed. Doses greater than 400 mg have not been proven to provide greater efficacy.

IV: (Patients should be well hydrated before IV ibuprofen administration): Pain: 400 to 800 mg intravenously over 30 minutes every 6 hours as needed.

Usual Adult Dose for Fever:

Oral: 200 to 400 mg orally every 4 to 6 hours as needed.

IV: (Patients should be well hydrated before IV ibuprofen administration): Fever: Initial: 400 mg intravenously over 30 minutes Maintenance: 400 mg every 4 to 6 hours or 100 to 200 mg every 4 hours as needed.

Usual Pediatric Dose for Fever:

Greater than 6 months to 12 years: 5 mg/kg/dose for temperature less than 102.5 degrees F (39.2 degrees C) orally every 6 to 8 hours as needed. 10 mg/kg/dose for temperature greater than or equal to 102.5 degrees F (39.2 degrees C) orally every 6 to 8 hours as needed.

The recommended maximum daily dose is 40 mg/kg.

OTC pediatric labeling (analgesic, antipyretic): 6 months to 11 years: 7.5 mg/kg/dose every 6 to 8 hours; Maximum daily dose: 30 mg/kg

Usual Pediatric Dose for Pain:

Infants and Children: 4 to 10 mg/kg orally every 6 to 8 hours as needed. The recommended maximum daily dose is 40 mg/kg.

OTC pediatric labeling (analgesic, antipyretic): 6 months to 11 years: 7.5 mg/kg/dose every 6 to 8 hours; Maximum daily dose: 30 mg/kg

Usual Pediatric Dose for Rheumatoid Arthritis:

6 months to 12 years: Usual: 30 to 40 mg/kg/day in 3 to 4 divided doses; start at lower end of dosing range and titrate; patients with milder disease may be treated with 20 mg/kg/day; doses greater than 40 mg/kg/day may increase risk of serious adverse effects; doses greater than 50 mg/kg/day have not been studied and are not recommended. Maximum dose: 2.4 g/day

Usual Pediatric Dose for Cystic Fibrosis:

Oral: Chronic (greater than 4 years) twice daily dosing adjusted to maintain serum concentration of 50 to 100 mcg/mL has been associated with slowing of disease progression in pediatric patients with mild lung disease.

Usual Pediatric Dose for Patent Ductus Arteriosus:

Ibuprofen lysine: Gestational age 32 weeks or less, birth weight: 500 to 1500 g: Initial dose: 10 mg/kg, followed by two doses of 5 mg/kg after 24 and 48 hours Note: Use birth weight to calculate all doses. Hold second or third doses if urinary output is less than 0.6 mL/kg/hour; may give when laboratory studies indicate renal function is back to normal. A second course of treatment, alternative pharmacologic therapy, or surgery may be needed if the ductus arteriosus fails to close or reopens following the initial course of therapy.

What other drugs will affect ibuprofen?

Ask your doctor before using ibuprofen if you take an antidepressant such as citalopram, escitalopram, fluoxetine (Prozac), fluvoxamine, paroxetine, sertraline (Zoloft), trazodone, or vilazodone. Taking any of these medicines with an NSAID may cause you to bruise or bleed easily.

Ask a doctor or pharmacist if it is safe for you to use ibuprofen if you are also using any of the following drugs:

a blood thinner (warfarin, Coumadin, Jantoven);

heart or blood pressure medication, including a diuretic or "water pill"; or

steroid medicine (such as prednisone).

This list is not complete. Other drugs may interact with ibuprofen, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.

Cezin Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Cezin

Cezin

Warnings

If your brand of multivitamin contains iron, it is important to keep this product out of reach of children. Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children younger than 6 years. If overdose does occur, seek immediate medical attention or call a poison control center.

Uses

This medication is a multivitamin product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins are important building blocks of the body and help keep you in good health.

How to use Cezin

Take this medication by mouth. usually once daily or as directed. Follow all directions on the product package, or take as directed by your doctor. Do not take more than the recommended dosage. If you are uncertain about any of the information, consult your doctor or pharmacist.

Take this medication regularly in order to get the most benefit from it. To help you remember, take it at the same time each day.

Side Effects

Constipation. diarrhea. or upset stomach may occur. These effects are usually temporary and may disappear as your body adjusts to this medication. If any of these effects persist or worsen, contact your doctor or pharmacist promptly.

If your doctor has prescribed this drug, 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.

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction. rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing .

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 this product, tell your doctor or pharmacist if you are allergic to any of its ingredients; or to soy/peanut found in some brands; 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 taking this medication, tell your doctor or pharmacist your medical history, especially of: use/abuse of alcohol, liver problems, stomach /intestinal problems (e. g. ulcer, colitis ).

If your brand of multivitamin also contains folic acid. be sure to tell your doctor or pharmacist if you have vitamin B12 deficiency (pernicious anemia) before taking it. Folic acid may affect certain laboratory tests for vitamin B12 deficiency without treating this anemia. Untreated vitamin B12 deficiency may result in serious nerve problems (e. g. peripheral neuropathy ). Consult your doctor or pharmacist for details.

Tell your doctor if you are pregnant before using this medication.

This medication passes into breast milk. Consult your doctor before breast - feeding.

Interactions

Your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with them first.

Before taking this medication, tell your doctor or pharmacist of all prescription and nonprescription/herbal drugs you may use, especially: other vitamin/nutritional supplements .

If your brand of multivitamin also contains iron, avoid taking this product at the same time as antacids, bisphosphonates (for example, alendronate ), levodopa, thyroid medications (for example, levothyroxine ), or some antibiotics (for example, tetracyclines, quinolones such as ciprofloxacin ). Ask your doctor or pharmacist about how long you should wait between doses and for help finding a dosing schedule that will work with all your medications.

If your brand of multivitamin also contains folic acid, be sure to tell your doctor or pharmacist if you take certain anti-seizure drugs (e. g. hydantoins such as phenytoin).

This document does not contain all possible interactions. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

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: stomach pain. nausea, vomiting. diarrhea.

Notes

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

Keep all regular medical and laboratory appointments.

Some brands may also contain ingredients such as docusate. Ask your doctor or pharmacist if you have questions about the ingredients in your brand.

This product is not a substitute for a proper diet. Remember that it is best to get your vitamins from healthy foods. Maintain a well-balanced diet and follow any dietary guidelines as directed by your doctor.

Missed Dose

If you are taking this product on a prescribed schedule and 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 between 59-86 degrees F (15-30 degrees C) away from light and moisture. Do not store in the bathroom. Keep all medicines 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 for more details about how to safely discard your product.

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

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Selected from data included with permission and copyrighted by First Databank, Inc. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, expect as may be authorized by the applicable terms of use.

CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.

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Doxiciclina Medlineplus Medicinas, Vibradox

Doxiciclina

La doxiciclina se usa para tratar las infecciones producidas por bacterias, incluyendo neumonia y otras infecciones en las vias respiratorias; enfermedad de Lyme; acne; infecciones de la piel, los genitales y del sistema urinario; y carbunco (despues de una exposicion por inhalacion). Tambien se usa para prevenir la malaria. La doxiciclina pertenece a una clase de medicamentos llamados antibioticos de tetraciclina. Funciona al prevenir el crecimiento y la propagacion de las bacterias. Los antibioticos no tienen ningun efecto en los resfrios, la gripe u otras infecciones viricas.

?Como se debe usar este medicamento?

La doxiciclina viene envasada en forma de capsulas regulares y recubiertas, tabletas, jarabe y solucion oral (liquido), todos para tomar por via oral. La doxiciclina por lo general se toma una vez o dos veces al dia. Beba un vaso lleno de agua con cada dosis de la capsula o tableta. Si usted comienza a tener malestar estomacal cuando toma doxiciclina, puede tomarla con alimentos o leche. Sin embargo, tomar doxiciclina con leche o alimentos puede disminuir la cantidad de medicamento absorbido por su estomago. Converse con su doctor o farmaceutico sobre la mejor manera de tomar doxiciclina si comienza a sentir malestar estomacal. Siga cuidadosamente las instrucciones en la etiqueta del medicamento y preguntele a su doctor o farmaceutico cualquier cosa que no entienda. Use el medicamento exactamente como se indica. No use mas ni menos que la dosis indicada ni tampoco mas seguido que lo prescrito por su doctor.

Agite bien el jarabe o la solucion liquida antes de cada uso para mezclar el medicamento en forma uniforme.

Si usted esta tomando doxiciclina para prevenir la malaria, comience a tomarla 1 o 2 dias antes de viajar a un lugar donde la malaria este presente. Continue tomando doxiciclina por 4 semanas despues de salir del lugar donde habia malaria. Usted no deberia tomar doxiciclina para prevenir la malaria por mas de 4 meses.

Siga tomando doxiciclina aunque se sienta bien. Tome el medicamento hasta que se termine, a menos que su doctor le indique de otro modo.

?Que otro uso se le da a este medicamento?

La doxiciclina puede ser tambien usada para tratar la malaria. Converse con su doctor sobre los posibles riesgos de usar este medicamento para su condicion.

Este medicamento tambien puede ser prescrito para otros usos; pidale mas informacion a su doctor o farmaceutico.

?Cuales son las precauciones especiales que debo seguir?

Antes de comenzar a tomar doxiciclina:

digale a su doctor y a su farmaceutico si usted es alergico a la doxiciclina, minociclina, tetraciclina, sulfitos (solo en el caso del jarabe de doxiciclina) o a otros medicamentos.

digale a su doctor y a su farmaceutico que medicamentos con y sin prescripcion esta tomando, especialmente antiacidos, anticoagulantes (adelgazantes de la sangre) como warfarina (Cumadina), carbamazepina (Tegretol), penicilina, fenobarbital, fenitoina (Dilantin) y vitaminas. La doxiciclina reduce la eficacia de algunos anticonceptivos orales; use otro metodo para prevenir el embarazo mientras toma este medicamento.

los antiacidos, los suplementos de calcio, los productos derivados del hierro y los laxantes que contienen magnesio interfieren con el efecto de la doxiciclina, haciendola menos eficaz. Tome doxiciclina 1 hora antes o 2 horas despues tomar antiacidos (incluyendo el bicarbonato de sodio), los suplementos de calcio y los laxantes que contienen magnesio. Tome doxiciclina 2 horas antes o 3 horas despues de tomar productos derivados del hierro y las vitaminas que contienen hierro.

digale a su doctor si tiene o alguna vez ha tenido diabetes o enfermedades al rinon o al higado.

digale a su doctor si esta embarazada, tiene planes de quedar embarazada o si esta amamantando. Si queda embarazada mientras toma este medicamento, llame a su doctor de inmediato. La doxiciclina puede danar el feto.

si va a ser sometido a cualquier cirugia, incluyendo la dental, digale al doctor o dentista que usted esta tomando doxiciclina.

evite la exposicion innecesaria o prolongada a la luz solar y use ropa que cubra su piel, gafas de sol y filtro solar. Este medicamento hace que su piel se vuelva mucho mas sensible a la luz solar

usted debe saber que cuando recibe doxiciclina para prevenir la malaria, tambien debe tomar medidas de proteccion tales como usar un repelente de insectos eficaz, mallas contra los mosquitos, ropa que cubra todo el cuerpo y estar en areas con mosquiteros, especialmente al final de la tarde y hasta que amanezca. Tomar doxiciclina no da una proteccion total contra la malaria.

Cuando se usa doxiciclina durante el embarazo, o en bebes o ninos de hasta 8 anos de edad, puede hacer que los dientes se manchen permanentemente. La doxiciclina no debe usarse en ninos menores de 8 anos salvo en los casos de carbunco por inhalacion o si su doctor decide que es necesario.

?Que dieta especial debo seguir mientras tomo este medicamento?

A menos que su doctor le indique de otro modo, continue con su regimen normal de alimentacion.

?Que tengo que hacer si me olvido de tomar una dosis?

Tome la dosis olvidada tan pronto como lo recuerde, sin embargo, si es hora para la siguiente, saltese aquella que no tomo y siga con la dosificacion regular. No tome una dosis doble para compensar la que olvido.

?Cuales son los efectos secundarios que podria provocar este medicamento?

La doxiciclina puede provocar efectos secundarios. Digale a su doctor si cualquiera de estos sintomas se vuelve grave o no desaparece:

diarrea

picazon en el recto o la vagina

dolor en la boca

Algunos efectos secundarios pueden provocar graves consecuencias para la salud. Si usted experimenta alguno de los siguientes sintomas, llame a su doctor de inmediato:

dolor de cabeza grave

vision borrosa

sarpullido (erupciones en la piel)

urticaria

dificultad para respirar o tragar

enrojecimiento de la piel (quemadura de sol)

coloracion amarillenta de la piel o los ojos

picazon

orina de color oscuro

heces de color palido

perdida del apetito

malestar estomacal

vomitos

dolor de estomago

cansancio extremo o debilidad

confusion

disminucion de la necesidad de orinar

?Como debo almacenar o desechar este medicamento?

Mantenga este medicamento en su envase, bien cerrado y fuera del alcance de los ninos. Almacenelo a temperatura ambiente y lejos del calor excesivo y la humedad (no en el bano). Deseche cualquier medicamento que este vencido o que ya no se utilice. Converse con su farmaceutico acerca del desecho adecuado de los medicamentos.

?Que debo hacer en caso de una sobredosis?

En caso de una sobredosis, llame a la oficina local de control de envenenamiento al 1-800-222-1222. Si la victima esta inconsciente, o no respira, llame inmediatamente al 911.

?Que otra informacion de importancia deberia saber?

Cumpla con todas las citas con su doctor y el laboratorio. Su doctor podria ordenar algunos examenes de laboratorio para determinar la respuesta de su cuerpo a la doxiciclina.

Antes de realizarse cualquier prueba de laboratorio, digale a su doctor y al personal del laboratorio que usted esta tomando doxiciclina.

Si usted tiene diabetes, la doxiciclina puede alterar los resultados en algunas de las pruebas para determinar el nivel de azucar en la orina. Consulte con su doctor antes de cambiar su regimen alimenticio o la dosificacion del medicamento para la diabetes.

No deje que otras personas tomen su medicamento. Probablemente su prescripcion no podra ser renovada por el farmaceutico sin autorizacion medica. Si todavia tiene sintomas de la infeccion despues de que ha terminado de tomar el medicamento, llame a su doctor.

Es importante que Ud. mantenga una lista escrita de todas las medicinas que Ud. esta tomando, incluyendo las que recibio con receta medica y las que Ud. compro sin receta, incluyendo vitaminas y suplementos de dieta. Ud. debe tener la lista cada vez que visita su medico o cuando es admitido a un hospital. Tambien es una informacion importante en casos de emergencia.

Marcas comerciales

Doryx

Doxy 100

Monodox

Vibramycin Calcium Syrup

Vibramycin Hyclate

Vibramycin Monohydrate

Vibra-Tabs

Documento actualizado - 01/09/2010

American Society of Health-System Pharmacists, Inc. Clausula de Proteccion

AHFS ® Patient Medication Information. © Copyright, 2016. The American Society of Health-System Pharmacists, Inc. 7272 Wisconsin Avenue, Bethesda, Maryland. Todos los derechos reservados. La duplicacion de este documento para su uso comercial, debera ser autorizada por ASHP. Traducido del ingles por GraciasDoctor.

Procytox, Procytox

Cyclophosphamide

Brand Names: Canada

What is this drug used for?

It is used to treat cancer.

It is used to treat nephrotic syndrome.

It may be given to you for other reasons. Talk with the doctor.

What do I need to tell my doctor BEFORE I take this drug?

If you have an allergy to cyclophosphamide or any other part of this drug.

If you are allergic to any drugs like this one, any other drugs, foods, or other substances. Tell your doctor about the allergy and what signs you had, like rash; hives; itching; shortness of breath; wheezing; cough; swelling of face, lips, tongue, or throat; or any other signs.

If you have any of these health problems: Bone marrow disease or urinary tract block.

If you are breast-feeding or plan to breast-feed.

This is not a list of all drugs or health problems that interact with this drug. Tell your doctor and pharmacist about all of your drugs (prescription or OTC, natural products, vitamins) and health problems. You must check to make sure that it is safe for you to take this drug with all of your drugs and health problems. Do not start, stop, or change the dose of any drug without checking with your doctor.

What are some things I need to know or do while I take this drug?

Tell all of your health care providers that you take this drug. This includes your doctors, nurses, pharmacists, and dentists.

Avoid driving and doing other tasks or actions that call for you to be alert or have clear eyesight until you see how this drug affects you.

Very bad and sometimes deadly allergic side effects have rarely happened. Talk with your doctor.

Have blood work checked as you have been told by the doctor. Talk with the doctor.

Talk with your doctor before getting any vaccines. Use with this drug may either raise the chance of an infection or make the vaccine not work as well.

You may bleed more easily. Be careful and avoid injury. Use a soft toothbrush and an electric razor.

Very bad and sometimes deadly infections have happened in patients who take this drug. If you have any infection, are taking antibiotics now or in the recent past, or have had many infections, talk with your doctor.

You may have more chance of getting an infection. Wash hands often. Stay away from people with infections, colds, or flu.

Very bad and sometimes deadly heart problems like heart failure have happened with this drug. Talk with the doctor.

Other types of cancer may rarely happen later in life.

This drug may affect how much of some other drugs are in your body. If you are taking other drugs, talk with your doctor. You may need to have your blood work checked more closely while taking this drug with your other drugs.

Lung problems have happened with this drug. Call your doctor right away if you have lung or breathing problems like trouble breathing, shortness of breath, or a cough that is new or worse.

If you are 65 or older, use this drug with care. You could have more side effects.

If you are a man and have sex with a female who could get pregnant, protect her from pregnancy during care and for at least 4 months after stopping this drug. Use birth control that you can trust.

If you are a man and your sex partner gets pregnant while you take this drug or within 4 months after your last dose, call your doctor right away.

This drug may affect fertility. Fertility problems may lead to not being able to get pregnant or father a child. In both men and women, this may go back to normal but sometimes it may not. Talk with your doctor.

This drug may cause harm to the unborn baby if you take it while you are pregnant.

Use birth control that you can trust to prevent pregnancy while taking this drug and for up to 12 months after this drug.

If you get pregnant while taking this drug or within 12 months after your last dose, call your doctor right away.

What are some side effects that I need to call my doctor about right away?

WARNING/CAUTION: Even though it may be rare, some people may have very bad and sometimes deadly side effects when taking a drug. Tell your doctor or get medical help right away if you have any of the following signs or symptoms that may be related to a very bad side effect:

Signs of an allergic reaction, like rash; hives; itching; red, swollen, blistered, or peeling skin with or without fever; wheezing; tightness in the chest or throat; trouble breathing or talking; unusual hoarseness; or swelling of the mouth, face, lips, tongue, or throat.

Signs of infection like fever, chills, very bad sore throat, ear or sinus pain, cough, more sputum or change in color of sputum, pain with passing urine, mouth sores, or wound that will not heal.

Signs of bleeding like throwing up blood or throw up that looks like coffee grounds; coughing up blood; blood in the urine; black, red, or tarry stools; bleeding from the gums; vaginal bleeding that is not normal; bruises without a reason or that get bigger; or any bleeding that is very bad or that you cannot stop.

Signs of low sodium levels like headache, trouble focusing, memory problems, feeling confused, weakness, seizures, or change in balance.

Feeling very tired or weak.

Shortness of breath, a big weight gain, swelling in the arms or legs.

Very bad dizziness or passing out.

A heartbeat that does not feel normal.

A wound that does not heal.

Not able to pass urine or change in how much urine is passed.

Very bad and sometimes deadly urinary tract problems like hemorrhagic cystitis have happened with this drug. Call your doctor right away if you have blood in the urine or pain when passing urine.

Very bad and sometimes deadly liver problems have happened with this drug. Call your doctor right away if you have signs of liver problems like dark urine, feeling tired, not hungry, upset stomach or stomach pain, light-colored stools, throwing up, or yellow skin or eyes.

What are some other side effects of this drug?

All drugs may cause side effects. However, many people have no side effects or only have minor side effects. Call your doctor or get medical help if any of these side effects or any other side effects bother you or do not go away:

Not hungry.

Loose stools (diarrhea).

Hair loss.

Upset stomach or throwing up.

Belly pain.

Change in color of skin.

Change in nails.

These are not all of the side effects that may occur. If you have questions about side effects, call your doctor. Call your doctor for medical advice about side effects. You may report side effects to your national health agency.

How is this drug best taken?

Use this drug as ordered by your doctor. Read all information given to you. Follow all instructions closely.

All products:

Pass urine often. You need to empty your bladder often. Drinking lots of liquids will help.

Drink lots of noncaffeine liquids unless told to drink less liquid by your doctor.

If you have upset stomach, throwing up, loose stools (diarrhea), or are not hungry, talk with your doctor. There may be ways to lower these side effects.

All oral products:

Take with or without food.

If you are taking this drug once a day, take it in the morning. Do not take it at night unless told to do so by your doctor.

Wear gloves when touching this drug.

Swallow whole. Do not chew, break, or crush.

Capsule:

Do not open the capsules.

If the capsule is opened or broken, do not touch the contents. If the contents are touched or they get in the eyes, wash hands or eyes right away.

Tablet:

If the tablet is crushed or broken, do not touch the contents. If you do touch the contents or get it in your eyes, wash hands or eyes right away.

Injection:

It is given as an infusion into a vein over a period of time.

What do I do if I miss a dose?

All oral products:

Take a missed dose as soon as you think about it.

If it is close to the time for your next dose, skip the missed dose and go back to your normal time.

Do not take 2 doses at the same time or extra doses.

Injection:

Call your doctor to find out what to do.

How do I store and/or throw out this drug?

All oral products:

Store at room temperature.

Store in a dry place. Do not store in a bathroom.

Injection:

If you need to store this drug at home, talk with your doctor, nurse, or pharmacist about how to store it.

All products:

Keep all drugs in a safe place. Keep all drugs out of the reach of children and pets.

Check with your pharmacist about how to throw out unused drugs.

General drug facts

If your symptoms or health problems do not get better or if they become worse, call your doctor.

Do not share your drugs with others and do not take anyone else’s drugs.

Keep a list of all your drugs (prescription, natural products, vitamins, OTC) with you. Give this list to your doctor.

Talk with the doctor before starting any new drug, including prescription or OTC, natural products, or vitamins.

Some drugs may have another patient information leaflet. If you have any questions about this drug, please talk with your doctor, nurse, pharmacist, or other health care provider.

If you think there has been an overdose, call your poison control center or get medical care right away. Be ready to tell or show what was taken, how much, and when it happened.

Consumer Information Use and Disclaimer

This information should not be used to decide whether or not to take this medicine or any other medicine. Only the healthcare provider has the knowledge and training to decide which medicines are right for a specific patient. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from the healthcare provider. You must talk with the healthcare provider for complete information about the risks and benefits of using this medicine.

Last Reviewed Date

Copyright

© 2016 Wolters Kluwer Clinical Drug Information, Inc. and its affiliates and/or licensors. All rights reserved.

If you have any questions or concerns, contact a member of your healthcare team directly or call 212-639-2000 for help.

If you have any questions or concerns, talk with a member of your healthcare team. You can reach them Monday through Friday from 9:00 am to 5:00 pm at ____________________. After 5:00 pm. during the weekend, and on holidays, please call____________________. If there’s no number listed, or you’re not sure, call 212-639-2000 .

©2016 Memorial Sloan Kettering Cancer Center - Generated on September 15, 2016

Afungil Price Compare, Afungil

Afungil

What is Afungil?

Afungil is an antifungal medicine. Afungil is used to treat infections caused by fungus, which can invade any part of the body including the mouth, throat, esophagus, lungs, bladder, genital area, and the blood. Afungil is also used to prevent fungal infection in people with weak immune systems caused by cancer treatment, bone marrow transplant, or diseases such as AIDS. Afungil may also be used for purposes not listed in Afungil guide.

What should I avoid while taking Afungil?

Follow your doctor's instructions about any restrictions on food, beverages, or activity. This medicine may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Afungil side effects

Get emergency medical help if you have any of these signs of an allergic reaction . hives; difficult breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have:

headache with chest pain and severe dizziness, fainting, fast or pounding heartbeats;

fever, chills, body aches, flu symptoms;

easy bruising or bleeding, unusual weakness;

seizure (convulsions);

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

skin rash or skin lesions; 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 side effects may include:

stomach pain, diarrhea, upset stomach;

headache;

dizziness; or

changes in your sense of taste.

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. See also: Side effects (in more detail)

What other drugs will affect Afungil?

Certain other drugs can cause unwanted or dangerous effects when used with Afungil. Your doctor may need to change your treatment plan if you use any of the following drugs:

halofantrine;

prednisone;

theophylline;

tofacitinib;

vitamin A;

an antidepressant--amitriptyline, nortriptyline;

other antifungal medicine--amphotericin B or voriconazole;

blood pressure medicine--hydrochlorothiazide (HCTZ), losartan, amlodipine, felodipine, nifedipine, verapamil;

a blood thinner (warfarin, Coumadin, Jantoven);

cancer medicine--cyclophosphamide, vincristine, vinblastine;

cholesterol medicine--atorvastatin, simvastatin, fluvastatin;

HIV/AIDS medicine--saquinavir, zidovudine, and others;

medicine to prevent organ transplant rejection--cyclosporine, tacrolimus or sirolimus;

narcotic medicine--fentanyl, alfentanil, methadone;

NSAIDs (nonsteroidal anti-inflammatory drugs)--celecoxib, ibuprofen, naproxen;

oral diabetes medicine--glyburide, tolbutamide, glipizide;

seizure medicine--carbamazepine, phenytoin; or

tuberculosis medication--rifampin, rifabutin.

This list is not complete and many other drugs can interact with Afungil. This includes prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in Afungil guide. Tell your doctor about all your medications and any you start or stop using during treatment with Afungil. Give a list of all your medicines to any healthcare provider who treats you.

Step 3: Select the most affordable brand or generic drugs

Burana, Burana

Burana

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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Divina - Definition Of Divina By The Free Dictionary, Divina

divine

divine

1. of or belonging to God or a god. divine wisdom. goddelik ????? ??????? божествен divino bozi gottlich guddommelig ?????. ?????? divino jumalik ????? ????? jumalallinen divin ???????? ???????, ????????, ?????? bozanski isteni ilahi gu?domlegur divino ?? ?? dieviskas dieviskigs tuhan goddelijk guddommelig boski ??????? ????? ??????? ?????? ???? ??? divino divin божественный bozi bozanski, bozji bozanski gudomlig ???????????????? kutsal. tanr?sal ?? божий; небесний ??? ?? ????? ?? th?n thanh ??

2. very good or excellent. What divine weather! hemels, fantasties, ongelooflik, wonderlik ????? прекрасен divino bozsky himmlisch himmelsk ????????? divino. precioso jumalik, oivaline ????? ???? ????? hyva divin. admirable ???? ??????? izvrstan pompas bagus himneskur, frab?r magnifico ????? ?? dieviskas briniskigs; lielisks sangat baik heerlijk vidunderlig. skjonn boski. wspanialy ???? ?? divino superb, minunat дивный bozsky cudovit divan gudomlig, harlig, underbar ????????? sahane. muhtesem. enfes ??? божественний; чудовий ??? ??? tuy?t di?u ????

to find out by keen understanding. I managed to divine the truth. vermoed ??????????? ??????? предвиждам adivinhar uhadnout weissagen gisne; ane; g?tte ??????? adivinar ara arvama ???????? ??? ???? aavistaa deviner ??????? ??? ????? spoznati na bozanski nacin megjosol menemukan segja fyrir um; giska a predire. indovinare ??? ???? ispeti paredzet; nojaust mengagak gissen spa. ane intuitivt, gjette odgadywac ?????? adivinhar a ghici предугадывать uhadnut uganiti spoznati ana (gissa) sig till ???????? tahmin etmek. onceden bilmek ?? вгадувати ???? ??? ???? ??? ?? ??? ?? ?????? tien doan ??

?divi?nation ( divi - ) noun

geestelike ???????? ???????? гадаене adivinhacao vestba die Weissagung spadomskunst ??????? adivinacion ennustamine ???????? ??? ???? ennustaminen divination ??????? ????????? ?????? ???, ????, ????? bozanstvenost megerzes, jovendoles penemuan spakleg agiskun; spadomur predizione. divinazione ?? ?, ?? spejimas, numatymas paredzesana; nojausana peramalan gissing spaing. spadom wrozenie ??? ????? ????? ??? ????? ??????? adivinhacao prorocire гадание ; прорицание vestba predvidevanje spoznaja spadom, forutsagelse, aning ???????? kehanet. tahmin ?? віщування; прогноз ???? ???? ?? ???? s? boi toan ??

a person who has or claims a special ability to find hidden water or metals. wiggelaar ??????????? ??????? ?????????? човeк, който открива подпочвена вода/подземни богатства adivinho vestec, hadac, proutkar der Wunschelrutenganger (mineral-)soger ??????. ??????????? zahori kaevutark ??? ?? kaivonkatsoja devin. devineresse. sourcier/-iere ????????, ??????? ????? ?????????? ??????????? vrac, gatalac varazsvesszos forraskutato ahli nujum spama?ur rabdomante ????? ???, ??? vandens/metalu ieskotojas rikstnieks peramal wichelaar vannleter ; malmleter rozdzkarz ??? ?????: ?????? adivinho ghicitor, proroc лозоискатель vestec, - kyna, prorok; prutikar bajalec rasljar slagruteman ??????????? gizli su ve maden yataklar?n? bulma yetenegi olan kimse, kahin ??? той, хто шукає воду чи руду ??? ??? ngu?i do nu?c ???

discovering the presence of underground water, metal etc by holding a di?vining-rod which moves when held directly above the water etc . water-divining. aanwysing ???? ????????????: ??????????? ??? ????? ????? ?? ????????? ?????? ?????? ?????? пръчка за откриване на подпочвена вода adivinhacao hledani pomoci proutku das Wunschelrutengehen (mineral-)sogning ??????????? adivinacion veesoonte otsimine ??? ????? ???????? kaivonkatsonta radiesthesie ??????? ????? ????-?????????? ????? ???? ?????? ????? ?? ???? ?? ???? ????, ???? ??????? ?? ??? ????? otkrivati vodu rasljama varazsvesszos forraskutatas tongkat yang digunakan untuk menemukan sumber air visa a vatn e?a malma me? spakvisti rabdomanzia ???? ?? ??, ? vandens/metalo ie?kojimas rikstnieciba tongkat yang digunakan untuk menemukan sumber air het wichelen leting med onskekvist rozdzkarstwo ? ???? ????? ?????? ????? adivinhacao radieste­zie поиск воды, руды с помощью ивового прута hladanie vody alebo loziska rudy pomocou prutika bajanje raslje slagrutesokning; slagruta ????? yer alt?nda maden ve su bulma ??????????????? “чарівна лозина” ???? ?? ???? ???? ?? ???? ?? ??????? ?? ??? ????? s? do nu?c b?ng que do nu?c ??????????????????

di?vinity ( - ?vi - ) – plural di?vinities – noun

1. religious studies. godsdiens ??????? ??????? богословие teologia bohoslovi die Theologie teologi ???????? teologia usuteadus ?????? teologia theologie ????????? ???? ??????? bogoslovlje hittudomany teologi gu?fr??i teologia ?? ?? teologija teologija belajar ketuhanan godgeleerdheid teologi teologia ??????? ??????? ? ????? teologia teologie богословие bohoslovie bogoslovstvo teologija teologi, religionskunskap ???????????????? ilahiyat, teoloji ?? богослов'я ?????? khoa th?n h?c ??

2. a god or goddess. The ancient Greeks worshipped many divinities. goddelikhede, afgode ??? ?? ???? божество divindade bozstvo die Gottheit guddom ??????? divinidad jumalus ????? ?????? jumaluus divinite ????????? ?????? bozanstvo istenseg dewata gu? e?a gy?ja divinita ? ? dievybe, dievaitis dievs; dieviba ketuhanan godheid guddom. gud bostwo, bog ?? ????????? ?? ??? divindade divinitate божество bozstvo bozanstvo bozanstvo gud, gudinna ??????? tanr? ya da tanr?ca ?,?? божество ???? ?? ????? v? th?n ?,??

3. the state of being divine. the divinity of God. Goddelikheid ??????? божественост divindade bozstvi die Gottlichkeit guddommelighed ???? ???? divinidad jumalikkus ??????? ?????? jumalallisuus divinite ??????, ????? ????? bozansko istenseg keagungan gu?domleiki divinita ?? ?? dieviskumas dieviskiba bersifat ketuhanan godheid guddommelighet boskosc ??????? divindade caracter divin божественность bozska podstata bozanskost bozanstvenost gudomlighet ???????????????? ilahilik, tanr?l?k ?? божественність ????????? ????? ngu?i du?c ton sung ??

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Disease relevance of Casodex

Treatment of androgen sensitive, non-metastatic LNCaP human prostate cancer cells with 0-100 microM Casodex or 0-10 ng/ml TNF-alpha induces cell death in 20-60% of the cells by 48 h in a dose-dependent manner [1] .

Re: A prospective, placebo-controlled study of the antiandrogen Casodex as treatment for patients with benign prostatic hyperplasia [2] .

Inclusion was discontinued at 30 patients after report of liver toxicity when Casodex was given long-term at high doses to mice [3] .

In rats bearing Dunning R3327-G prostate carcinomas casodex exerted a strong antitumour effect at the beginning of therapy [4] .

Casodex has the potential to become an important drug for treatment of prostatic diseases [5] .

Psychiatry related information on Casodex

Even if all patients had side effects, mostly mild, Casodex was well tolerated and patient compliance was excellent [3] .

High impact information on Casodex

The antiandrogen Casodex and specific inhibitors of Src and PI3-kinase prevent both hormonal effects, DNA synthesis and cytoskeletal changes [6] .

We solved the x-ray crystal structure of the mutant W741L AR ligand-binding domain bound to R-bicalutamide at 1.8-A resolution [7] .

The antiandrogen Casodex blocked the effect of androgen. implicating the androgen receptor in regulation of ABCA1 expression by androgens [8] .

In contrast, transcription through the PSA P/E promoter, a prototypical AR-dependent promoter directly activated by agonist, was obliterated only by Casodex [9] .

We show that expression of RasN17 in the hormone-refractory C4-2 cell line enhances in vitro sensitivity to the growth-inhibitory action of the antiandrogen Casodex and inhibits anchorage-independent cell growth [10] .

Chemical compound and disease context of Casodex

Flutamide (89) and its derivatives, Casodex (108) and Anandron (114), are highly effective in the treatment of prostate cancer [11] .

Bicalutamide (Casodex ) is a competitive androgen receptor antagonist that inactivates androgen - regulated prostate cell growth and function, leading to cell apoptosis and inhibition of prostate cancer growth [12] .

Pure antiandrogen casodex in a dose used in humans for treatment of prostate cancer decreased the weight of seminal vesicles. organ which is highly sensitive to the androgenic effect, increased insignificantly the concentration of LH and of testosterone. but did not have any effect on bone density or mineral content of bone [13] .

A controlled trial of Casodex (bicalutamide ) vs. flutamide. each in combination with luteinising hormone-releasing hormone analogue therapy in patients with advanced prostate cancer. Casodex Combination Study Group [14] .

A controlled trial of bicalutamide versus flutamide. each in combination with luteinizing hormone - releasing hormone analogue therapy, in patients with advanced prostate cancer. Casodex Combination Study Group [15] .

Biological context of Casodex

Taken together, these data support the hypothesis that Casodex induces cell death by a pathway that is independent of changes in DeltaPsim and Bcl-2 actions and results in an extended lag phase of cell survival that may promote the induction of an invasive phenotype after treatment [1] .

In contrast, cells treated with Casodex display loss of cell adhesion. but sustained mitochondrial dehydrogenase activity [1] .

Additionally, we demonstrated that R-bicalutamide stimulates transcriptional activation in AR harboring the M895T point mutation [16] .

Microarrays revealed downregulation of eight genes in cells prevented from entering into S phase by Casodex [17] .

Expression of cell-cycle regulatory genes in S phase control cells versus Casodex - treated cells that fail to enter S phase was studied using a microarray containing cDNA probes for 111 cell-cycle specific genes [17] .

Anatomical context of Casodex

Overexpression of Bcl-2 in LNCaP cells attenuates the induction of cell death by TNF-alpha but not Casodex. suggesting that mitochondria depolarization is not required for the induction of cell death by Casodex [1] .

These data, together with known physicochemical properties of Casodex suggest that a blood-brain barrier exists for the drug which results in exclusion of this antiandrogen from central sites of androgen negative feedback and that this accounts for its peripherally selective antihormonal profile [18] .

Androgen receptor localisation and turnover in human prostate epithelium treated with the antiandrogen, casodex [19] .

Androgen receptor (AR) binding assays of rat ventral prostate gland cytosols revealed a relative binding affinity (RBA) for the AR of 0.267 and a k1 of 1.25 x 10(-7) M for Casodex [18] .

We evaluated the endocrine effects of Casodex 150 mg daily given in monotherapy as primary treatment for patients with prostate cancer [20] .

Associations of Casodex with other chemical compounds

The three-dimensional structure demonstrates that the B ring of R-bicalutamide in the W741L mutant is accommodated at the location of the indole ring of Trp-741 in the WT AR bound to dihydrotestosterone [7] .

This activation can be blocked by an anti-androgen drug bicalutamide (Casodex ), implicating the involvement of androgen receptor in this process [21] .

Agonist-bound AR was required because the AR antagonists casodex and hydroxyflutamide failed to translocate beta-catenin [22] .

The c-Met expression is also positively controlled by testosterone. which induces a significant increase in its mRNA level that is abolished by an anti-androgen, casodex [23] .

These antiproliferative effects of 1,25-(OH)2D3 and 9-cis RA, alone or in combination, were blocked by the pure AR antagonist, Casodex [24] .

Gene context of Casodex

Like Cdc6. the levels of both cyclins A and B were attenuated in Casodex - treated cells [17] .

The anti-androgen Casodex enhances the growth-inhibitory action of PTEN and this effect is independent of Akt phosphorylation [25] .

RT-PCR based analysis demonstrates that in LNCaP cells Casodex coordinately alters the expression of steady-state level of mRNAs of several matrix metalloproteases and their cognate inhibitors (most notably MMP2 and TIMP1 ) [26] .

We detect binding of SMRT to hAR when treating with the antiandrogen CPA, but not with the antihormones casodex or hydroxyflutamide [27] .

The anti-androgen Casodex reduced 5alpha-DHT-stimulated cell growth but had no effect on EGF-R mediated LNCaP growth or EGF-stimulated activated MAPK activity [28] .

Analytical, diagnostic and therapeutic context of Casodex

Chemoprevention of rat prostate carcinogenesis by use of finasteride or casodex [29] .

In a comparative trial, bicalutamide (Casodex ) was more effective than flutamide (each in combination with an LHRH analogue) in terms of time to treatment failure and produced a significantly lower incidence of diarrhoea [30] .

Bicalutamide (Casodex ) 150 mg/day was administered for 12 months from the day of radiotherapy [31] .

The peripheral selectivity of Casodex in the intact male rat was related to the distribution of radiolabelled antiandrogen following intravenous injection [18] .

METHODS: A total of 1,453 patients with either confirmed metastatic disease (M1), or T3/T4 non-metastatic disease with elevated prostate-specific antigen (M0) were recruited into one of two identical, multicentre, randomised studies to compare 'Casodex ' 150 mg/day with castration [32] .

References

Antiandrogen-induced cell death in LNCaP human prostate cancer cells. Lee, E. C. Zhan, P. Schallhom, R. Packman, K. Tenniswood, M. Cell Death Differ. (2003) [Pubmed ]

Re: A prospective, placebo-controlled study of the antiandrogen Casodex as treatment for patients with benign prostatic hyperplasia. Strutt, K. L. Blackledge, G. R. Kennealey, G. T. J. Urol. (1994) [Pubmed ]

A prospective, placebo-controlled study of the antiandrogen Casodex as treatment for patients with benign prostatic hyperplasia. Eri, L. M. Tveter, K. J. J. Urol. (1993) [Pubmed ]

Antiproliferative activity of casodex (ICI 176.334) in hormone-dependent tumours. Maucher, A. von Angerer, E. J. Cancer Res. Clin. Oncol. (1993) [Pubmed ]

Effects of the nonsteroidal antiandrogen Casodex on lipoproteins, fibrinogen and plasminogen activator inhibitor in patients with benign prostatic hyperplasia. Eri, L. M. Urdal, P. Eur. Urol. (1995) [Pubmed ]

Androgen-stimulated DNA synthesis and cytoskeletal changes in fibroblasts by a nontranscriptional receptor action. Castoria, G. Lombardi, M. Barone, M. V. Bilancio, A. Di Domenico, M. Bottero, D. Vitale, F. Migliaccio, A. Auricchio, F. J. Cell Biol. (2003) [Pubmed ]

Structural basis for antagonism and resistance of bicalutamide in prostate cancer. Bohl, C. E. Gao, W. Miller, D. D. Bell, C. E. Dalton, J. T. Proc. Natl. Acad. Sci. U. S.A. (2005) [Pubmed ]

Androgenic suppression of ATP-binding cassette transporter A1 expression in LNCaP human prostate cancer cells. Fukuchi, J. Hiipakka, R. A. Kokontis, J. M. Hsu, S. Ko, A. L. Fitzgerald, M. L. Liao, S. Cancer Res. (2004) [Pubmed ]

Changes in androgen receptor nongenotropic signaling correlate with transition of LNCaP cells to androgen independence. Unni, E. Sun, S. Nan, B. McPhaul, M. J. Cheskis, B. Mancini, M. A. Marcelli, M. Cancer Res. (2004) [Pubmed ]

Attenuation of Ras signaling restores androgen sensitivity to hormone-refractory C4-2 prostate cancer cells. Bakin, R. E. Gioeli, D. Bissonette, E. A. Weber, M. J. Cancer Res. (2003) [Pubmed ]

Androgen receptor antagonists (antiandrogens): structure-activity relationships. Singh, S. M. Gauthier, S. Labrie, F. Current medicinal chemistry. (2000) [Pubmed ]

Bicalutamide 150mg: a review of its use in the treatment of locally advanced prostate cancer. Wellington, K. Keam, S. J. Drugs (2006) [Pubmed ]

Effect of antiandrogens casodex and epitestosterone on bone composition in mice. Broulik, P. D. Starka, L. Bone (1997) [Pubmed ]

A controlled trial of Casodex (bicalutamide) vs. flutamide, each in combination with luteinising hormone-releasing hormone analogue therapy in patients with advanced prostate cancer. Casodex Combination Study Group. Soloway, M. S. Schellhammer, P. Sharifi, R. Venner, P. Patterson, A. L. Sarosdy, M. Vogelzang, N. Jones, J. Kolvenbag, G. Eur. Urol. (1996) [Pubmed ]

A controlled trial of bicalutamide versus flutamide, each in combination with luteinizing hormone-releasing hormone analogue therapy, in patients with advanced prostate cancer. Casodex Combination Study Group. Schellhammer, P. Sharifi, R. Block, N. Soloway, M. Venner, P. Patterson, A. L. Sarosdy, M. Vogelzang, N. Jones, J. Kolvenbag, G. Urology (1995) [Pubmed ]

Structural basis for accommodation of nonsteroidal ligands in the androgen receptor. Bohl, C. E. Miller, D. D. Chen, J. Bell, C. E. Dalton, J. T. J. Biol. Chem. (2005) [Pubmed ]

Androgen receptor regulates Cdc6 in synchronized LNCaP cells progressing from G1 to S phase. Bai, V. U. Cifuentes, E. Menon, M. Barrack, E. R. Reddy, G. P. J. Cell. Physiol. (2005) [Pubmed ]

A possible explanation for the peripheral selectivity of a novel non-steroidal pure antiandrogen, Casodex (ICI 176,334). Freeman, S. N. Mainwaring, W. I. Furr, B. J. Br. J. Cancer (1989) [Pubmed ]

Androgen receptor localisation and turnover in human prostate epithelium treated with the antiandrogen, casodex. Waller, A. S. Sharrard, R. M. Berthon, P. Maitland, N. J. J. Mol. Endocrinol. (2000) [Pubmed ]

Endocrine profiles during administration of the new non-steroidal anti-androgen Casodex in prostate cancer. Verhelst, J. Denis, L. Van Vliet, P. Van Poppel, H. Braeckman, J. Van Cangh, P. Mattelaer, J. D'Hulster, D. Mahler, C. Clin. Endocrinol. (Oxf) (1994) [Pubmed ]

Identification of human male germ cell-associated kinase, a kinase transcriptionally activated by androgen in prostate cancer cells. Xia, L. Robinson, D. Ma, A. H. Chen, H. C. Wu, F. Qiu, Y. Kung, H. J. J. Biol. Chem. (2002) [Pubmed ]

Liganded androgen receptor interaction with beta-catenin: nuclear co-localization and modulation of transcriptional activity in neuronal cells. Pawlowski, J. E. Ertel, J. R. Allen, M. P. Xu, M. Butler, C. Wilson, E. M. Wierman, M. E. J. Biol. Chem. (2002) [Pubmed ]

Cross-talk between steroid-receptor-mediated and cell-membrane-receptor-mediated signalling pathways results in the in vivo modulation of c-Met and ornithine decarboxylase gene expression in mouse kidney. Dudkowska, M. Stachurska, A. Chmurzyska, W. Grzelakowska-Sztabert, B. Manteuffel-Cymborowska, M. Biochem. J. (2001) [Pubmed ]

Induction of androgen receptor by 1alpha,25-dihydroxyvitamin D3 and 9-cis retinoic acid in LNCaP human prostate cancer cells. Zhao, X. Y. Ly, L. H. Peehl, D. M. Feldman, D. Endocrinology (1999) [Pubmed ]

Conditional expression of PTEN alters the androgen responsiveness of prostate cancer cells. Wu, Z. Conaway, M. Gioeli, D. Weber, M. J. Theodorescu, D. Prostate (2006) [Pubmed ]

Induction of invasive phenotype by Casodex in hormone-sensitive prostate cancer cells. Zhan, P. Lee, E. C. Packman, K. Tenniswood, M. J. Steroid Biochem. Mol. Biol. (2002) [Pubmed ]

The amino terminus of the human AR is target for corepressor action and antihormone agonism. Dotzlaw, H. Moehren, U. Mink, S. Cato, A. C. Iniguez Lluhi, J. A. Baniahmad, A. Mol. Endocrinol. (2002) [Pubmed ]

Effect of an EGF-R selective tyrosine kinase inhibitor and an anti-androgen on LNCaP cells: identification of divergent growth regulatory pathways. Jones, H. E. Barrow, D. Dutkowski, C. M. Goddard, L. Smith, C. Harper, M. E. Nicholson, R. I. Prostate (2001) [Pubmed ]

Chemoprevention of rat prostate carcinogenesis by use of finasteride or casodex. Tsukamoto, S. Akaza, H. Imada, S. Koiso, K. Shirai, T. Ideyama, Y. Kudo, M. J. Natl. Cancer Inst. (1995) [Pubmed ]

Commentary on maximal androgen blockade in prostate cancer: a theory to put into practice? Denis, L. Prostate (1995) [Pubmed ]

Prophylactic breast irradiation with a single dose of electron beam radiotherapy (10 Gy) significantly reduces the incidence of bicalutamide-induced gynecomastia. Tyrrell, C. J. Payne, H. Tammela, T. L. Bakke, A. Lodding, P. Goedhals, L. Van Erps, P. Boon, T. Van De Beek, C. Andersson, S. O. Morris, T. Carroll, K. Int. J. Radiat. Oncol. Biol. Phys. (2004) [Pubmed ]

A randomised comparison of 'Casodex' (bicalutamide) 150 mg monotherapy versus castration in the treatment of metastatic and locally advanced prostate cancer. Tyrrell, C. J. Kaisary, A. V. Iversen, P. Anderson, J. B. Baert, L. Tammela, T. Chamberlain, M. Webster, A. Blackledge, G. Eur. Urol. (1998) [Pubmed ]

Contributions to this collaborative article are from individual authors of WikiGenes or mined by the WikiGenes Data Mining Engine from MEDLINE®/PubMed®, a database of the U. S. National Library of Medicine. About WikiGenes Open Access Licence Privacy Policy Terms of Use apsburg

Bifuroxim, Bifuroxim

Bifuroxim

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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Antibiotics - Bifuroxim (Brand name: ceftin)

Ceftin is used for treating bacterial infections (sinus, skin, lung, urinary tract, ear, and throat). It may also be used to treat Lyme disease and gonorrhea. Ceftin is a cephalosporin antibiotic. It works by interfering with the formation of the bacteria's cell wall so that the wall ruptures, resulting in the death of the bacteria.

Use Ceftin as directed by your doctor.

Take Ceftin by mouth with or without food.

Swallow Ceftin whole. Do not break, crush, or chew before swallowing.

Ceftin works best if it is taken at the same time each day.

To clear up your infection completely, take Ceftin for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Ceftin, 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 Ceftin.

Store Ceftin at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Ceftin out of the reach of children and away from pets.

Active Ingredient: Cefuroxime axetil.

Do NOT use Ceftin if:

you are allergic to any ingredient in Ceftin or to any other cephalosporin antibiotic (eg, cephalexin, cefprozil).

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

Tell your health care provider 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, a stomach or intestinal infection, or a blood clotting problem

if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin antibiotic (eg, amoxicillin) or other beta-lactam antibiotic (eg, imipenem).

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

Aminoglycosides (eg, gentamicin), cyclosporine, diuretics (eg, furosemide, hydrochlorothiazide), or other medicines affecting the kidney because side effects, such as kidney toxicity, may occur

Hormonal contraceptives (eg, birth control pills) because their effectiveness may be decreased by Ceftin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Ceftin 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:

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur during treatment or within several months after treatment with Ceftin. Do not treat diarrhea without first checking with your doctor.

The tablet and oral suspension forms of Ceftin are not equivalent. Do not substitute one for the other.

Ceftin only works against bacteria; it does not treat viral infections (eg, the common cold).

Be sure to use Ceftin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Long-term or repeated use of Ceftin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Diabetes patients - Ceftin may cause the results of some tests for urine glucose to be wrong. Ask your doctor before you change your diet or the dose of your diabetes medicine.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Ceftin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

Lab tests, including liver function, kidney function, and complete blood cell count, may be performed while you use Ceftin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Ceftin should not be used in children younger 3 months; safety and effectiveness in these 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 Ceftin while you are pregnant. Ceftin is found in breast milk. Do not breastfeed while taking Ceftin.

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/loose stools; nausea; 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); bloody stools; change in the amount of urine; dark urine; easy bruising or bleeding; fatigue; fever; seizures; severe diarrhea; stomach cramps/pain; vaginal irritation or discharge; 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.

Ceftin is used for treating bacterial infections (sinus, skin, lung, urinary tract, ear, and throat). It may also be used to treat Lyme disease and gonorrhea. Ceftin is a cephalosporin antibiotic. It works by interfering with the formation of the bacteria's cell wall so that the wall ruptures, resulting in the death of the bacteria.

Use Ceftin as directed by your doctor.

Take Ceftin by mouth with or without food.

Swallow Ceftin whole. Do not break, crush, or chew before swallowing.

Ceftin works best if it is taken at the same time each day.

To clear up your infection completely, take Ceftin for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Ceftin, 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 Ceftin.

Store Ceftin at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Ceftin out of the reach of children and away from pets.

Active Ingredient: Cefuroxime axetil.

Do NOT use Ceftin if:

you are allergic to any ingredient in Ceftin or to any other cephalosporin antibiotic (eg, cephalexin, cefprozil).

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

Tell your health care provider 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, a stomach or intestinal infection, or a blood clotting problem

if you have had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin antibiotic (eg, amoxicillin) or other beta-lactam antibiotic (eg, imipenem).

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

Aminoglycosides (eg, gentamicin), cyclosporine, diuretics (eg, furosemide, hydrochlorothiazide), or other medicines affecting the kidney because side effects, such as kidney toxicity, may occur

Hormonal contraceptives (eg, birth control pills) because their effectiveness may be decreased by Ceftin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Ceftin 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:

Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur during treatment or within several months after treatment with Ceftin. Do not treat diarrhea without first checking with your doctor.

The tablet and oral suspension forms of Ceftin are not equivalent. Do not substitute one for the other.

Ceftin only works against bacteria; it does not treat viral infections (eg, the common cold).

Be sure to use Ceftin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Long-term or repeated use of Ceftin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

Diabetes patients - Ceftin may cause the results of some tests for urine glucose to be wrong. Ask your doctor before you change your diet or the dose of your diabetes medicine.

Hormonal birth control (eg, birth control pills) may not work as well while you are using Ceftin. To prevent pregnancy, use an extra form of birth control (eg, condoms).

Lab tests, including liver function, kidney function, and complete blood cell count, may be performed while you use Ceftin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Ceftin should not be used in children younger 3 months; safety and effectiveness in these 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 Ceftin while you are pregnant. Ceftin is found in breast milk. Do not breastfeed while taking Ceftin.

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/loose stools; nausea; 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); bloody stools; change in the amount of urine; dark urine; easy bruising or bleeding; fatigue; fever; seizures; severe diarrhea; stomach cramps/pain; vaginal irritation or discharge; 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.

Kailasa, Kailasa

Kailasa

but less-ornate images in black stone and of Buddhist bronze icons. Central Indian craftsmen used the softer sandstone. In the peninsula the profusely sculptured rock-cut temples such as the Kailasa at the Ellora Caves, under Calukya and Rashtrakuta patronage, displayed a style of their own. The dominant style in the south was that of Cola sculpture, particularly in bronze. The severe.

built of stone. The Talapurisvara temple at Panamalai is another excellent example. The capital city of Kanchipuram also possesses some fine temples—for example, the Kailasanatha (dating a little later than the Shore Temple), with its stately superstructure and subsidiary shrines attached to the walls. The enclosure wall has a series of small shrines.

ce ) depicting incidents from Hindu mythology in high relief are to be found in the Rameshvara cave; notable among them is a fearsome representation of the dancing Kali, goddess of death. The Kailasa temple ( c. 757–783) has a remarkable group of elephants struggling with lions all around the plinth. Of the several large reliefs, also at Kailasa . the depiction of Ravana shaking.

part of Ellora Caves

The most remarkable of the cave temples is Kailasa ( Kailasa natha; cave 16), named for the mountain in the Kailas Range of the Himalayas where the Hindu god Shiva resides. Unlike other temples at the site, which were first delved horizontally into the rock face, the Kailasa complex was excavated downward from a basaltic slope and is therefore largely exposed to sunlight. Construction of the.

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Then is narrated the ascent on the hills of Kailasa by Bhimasena. his terrific battle with the mighty Yakshas headed by Hanuman ; then the meeting of the Pandavas with Vaisravana Kuvera. and the meeting with Arjuna after he had obtained for the purpose of Yudhishthira many celestial weapons; then Arjuna's terrible encounter with the Nivatakavachas dwelling in Hiranyaparva. and also with the Paulomas. and the Kalakeyas ; their destruction at the hands of Arjuna ; the commencement of the display of the celestial weapons by Arjuna before Yudhishthira. the prevention of the same by Narada ; the descent of the Pandavas from Gandhamadana ; the seizure of Bhima in the forest by a mighty serpent huge as the mountain; his release from the coils of the snake, upon Yudhishthira's answering certain questions; the return of the Pandavas to the Kamyaka woods.

Then those tigers among men, attired in costly dress, entered that mansion at the instance of Purochana like Guhyakas entering the palace of Siva on the Kailasa mount.

It was surrounded with high mansions perfectly white and resembling the cloud-kissing peaks of Kailasa .

Then Valadeva. white and tall as the peak of Kailasa . decked with garlands of wild flowers and attired in blue robes, and proud and intoxicated with drink, said these words: Ye senseless men, what are ye doing, when Janardana sitteth silent?

And the monarch wending to the mountains of Kailasa . devoted himself to asceticism there.

On the north of the Kailasa peak near the mountains of Mainaka. while the Danavas were engaged in a sacrifice on the banks of Vindu lake, I gathered a huge quantity of delightful and variegated vanda a kind of rough materials composed of jewels and gems.

On the north of Kailasa in the mountains of Mainaka. there is a huge peak of gems and jewels called Hiranya-sringa .

Possessing the splendour of the peaks of Kailasa . that mansion eclipses by its own the brilliance of the Moon himself.

Kailasa

Tenders are invited for providing painting work for kerbwall and bamboo design at health arena foot of kailasa hill, visakhapatnam

The Dewarists stage will feature artists/ bands such as Kailasa. Lucky Ali and Noori while Nucleya and Prateek Kuhad ( amongst others) will perform at Eristoff Wolves Den and MTS Other Stage respectively.

It is only past the Himalayas, on Mount Kailasa. in the second part of the poem, that the gander will again reach friendly territory.

a leading software developer and information technology provider for the automotive industry, today announced that Sameer Kailasa of American Heritage School in Plantation, Florida is the recipient of BookItOut's corporate-sponsored National Merit Scholarship for 2013.

Murals from the Kailasa temples at Kanchipuram and at Ellora would also have introduced little-known material and enhanced the reader's understanding of the later developments.

Khailash Kher and Kailasa (Philharmonic Hall, Hope Street).

Magic Sky 10g Simon Du Desert - Kailasa Mrs D J Brown & Lord Daresbury 2U5-502 RPR 127h 147c OR 121h 132c He goes for the Grand Sefton Chase at Aintree on Saturday.

Because the novel's final scene of lovemaking and destruction occurs on top of a mountain which is at once Shiva's Kailasa and Attar's Qaf, Clark reads it as pointing to a hopeful postcataclysmic fate compatible with Hinduism and Sufi mysticism, a fate that is not, however, actually shown.

Tenders are invited for providing 3d show at second floor of sankuchakranamam building on top of kailasa hill

Owen quotes one well-known art historian who went so far as to characterize the Chota ("Little") Kailasa temple, an unfinished Jain rock-cut temple from the early ninth century, as the "anticlimax" of Ellora (p.

Cut in friable volcanic breccia (5) in the 8th century (the dates are debatable and some experts assign it to the 6th century on account of the stylistic form of its pillars, and classify the extant 8th-century inscription in one of the caves as a later addition), the monument of Jogeshwari is in fact, next to the Kailasa temple at Ellora, the largest known rock-cut form in India, with its length extending nearly 80 metres from east to west, and its breadth, including the long south passage, about 65 metres.

So it's no surprise that his band Kailasa is amongst the most respected Indian bands globally.

Sphax Purebdcraft Resource Pack, Spax

Sphax PureBDCraft Resource Pack 1.10.2

Designed by Sphax, compatible with Minecraft 1.10.x, 1.9.x, 1.8.x, 1.7.x and has 1777347 Views

How to Install This Resource Pack.

Download the resource pack.

Press start and type in %appdata%.

Find and open your. minecraft folder.

Locate to your resourcepacks folder.

Drag and Drop the texture. zip file into this folder.

Last Updated: 10 July 2016, 4:52 pm

Sphax PureBDCraft is a beautiful texture pack which, besides graphics, you can expect a lot of jokes. Sphax PureBDCraft is a pack in cartoon style which has a nice cartoon graphics. Custom design of this texture pack will not leave you indifferent.

This pack is “vector based” and is available in all common resolutions from 16?16 to 512?512. However, the recommended resolution will still be 128?128. Use the resolution which fit the “performance” of your computer!

Mobic - Pain Relief, Roxikam

Mobic is used to relieve the pain and stiffness of osteoarthritis and rheumatoid arthritis.

Take Mobic exactly as directed by your physician. It is recommended that you take it with a glass of water and a meal (to avoid an empty stomach).

If you miss a dose of Mobic, then skip it and continue with your regular schedule. However, do not take a double dose to make up for the missed dose.

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

Some of the symptoms of a Mobic overdose include nausea, vomiting, stomach pain and bleeding. In extreme cases, it may lead to a heart attack or even coma. Seek medical attention immediately if you suspect an overdose.

Consult your doctor before starting treatment if you are allergic to aspirin, have asthma or experience difficulty breathing while using Mobic. Do not smoke, have alcohol or take steroidal medications while using this drug. Use only if prescribed.

Do not use Mobic if:

you are allergic to any ingredient in Mobic; you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or a nonsteroidal anti-inflammatory drug (NSAID) (eg, ibuprofen, celecoxib); you have recently had or will be having bypass heart surgery; you have a peptic ulcer; 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.

Important : Do not drive or perform other possibly unsafe tasks until you know how you react to it. Do not take more than the recommended dose or use for longer than prescribed without checking with your doctor. Mobic is an NSAID. Before you start any new medicine, check the label to see if it has an NSAID (eg, 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 Mobic unless your doctor tells you to. Lab tests, including kidney function, complete blood cell counts, and blood pressure, may be performed while you use Mobic. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Use Mobic with caution in the elderly; they may be more sensitive to its effects, especially stomach bleeding and kidney problems. Caution is advised when using Mobic in children; they may be more sensitive to its effects, especially diarrhea, fever, headache, stomach pain, and vomiting. Mobic should be used with extreme caution in children younger than 2 years old; safety and effectiveness in these children have not been determined. Pregnancy and breast-feeding: Mobic may cause harm to the fetus. Do not use 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 using Mobic while you are pregnant. It is not known if Mobic is found in breast milk. Do not breast-feed while taking Mobic.

Possible 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 upset; trouble sleeping. 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; 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.

Mobic is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

Buy Meneklin Clindamycin Online Without Prescriptions, Meneklin

Cleocin is used for treating serious infections caused by certain bacteria. Cleocin is a lincomycin antibiotic. Cleocin kills sensitive bacteria by stopping the production of essential proteins needed by the bacteria to survive.

Use Cleocin as directed by your doctor.

Take Cleocin by mouth with or without food.

Take Cleocin with a full glass of water (8 oz/240 mL).

Cleocin works best if it is taken at the same time each day.

To clear up your infection completely, take Cleocin for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Cleocin, 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 Cleocin.

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

Active Ingredient: Clindamycin hydrochloride.

Do NOT use Cleocin if:

you are allergic to any ingredient in Cleocin or to lincomycin

you have certain intestinal problems (eg, antibiotic-associated colitis, Crohn disease, ulcerative colitis) or meningitis.

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

Some medical conditions may interact with Cleocin. 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, or a history of liver problems or stomach or bowel problems (eg, colitis)

if you are allergic to tartrazine.

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

Nondepolarizing muscle relaxants (eg, vecuronium) or succinylcholine because the risk of their side effects may be increased by Cleocin.

Erythromycin because it may decrease Cleocin's effectiveness.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Cleocin 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:

Cleocin only works against bacteria; it does not treat viral infections (eg, the common cold).

Be sure to use Cleocin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Long-term or repeated use of Cleocin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

This product may contain tartrazine dye. This may cause an allergic reaction in some patients. If you have ever had an allergic reaction to tartrazine, ask your pharmacist if your product has tartrazine in it.

Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

Lab tests, including liver function, kidney function, and complete blood cell counts, may be performed while you use Cleocin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Cleocin with caution in the elderly; they may be more sensitive to its effects, especially diarrhea.

Use Cleocin with extreme caution in children younger 10 years who have diarrhea or an infection of the stomach or bowel.

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

Mild diarrhea; nausea; 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); bloody or tarry stools; decreased urination; joint pain or swelling; red, swollen, blistered, or peeling skin; severe or persistent diarrhea; severe stomach cramps or pain; unusual vaginal discharge, itching, or odor; 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.

Customers who bought this product also bought

Copyright © 2004-2016 All Rights Reserved

Liquiprin Oral Drug Information On Uses, Side Effects, Interactions, And User Reviews On Rxlist, Liq

Liquiprin oral

Liquiprin oral Warnings

Taking too much acetaminophen may cause serious (possibly fatal) liver disease. Adults should not take more than 4000 milligrams (4 grams) of acetaminophen a day. People with liver problems and children should take less acetaminophen. Ask your doctor or pharmacist how much acetaminophen is safe to take.

Do not use with any other drug containing acetaminophen without asking your doctor or pharmacist first. Acetaminophen is in many nonprescription and prescription medications (such as pain/fever drugs or cough-and-cold products). Check the labels on all your medicines to see if they contain acetaminophen, and ask your pharmacist if you are unsure.

Get medical help right away if you take too much acetaminophen (overdose), even if you feel well. Overdose symptoms may include nausea, vomiting, loss of appetite, sweating, stomach/abdominal pain, extreme tiredness, yellowing eyes/skin, and dark urine.

Daily alcohol use, especially when combined with acetaminophen, may damage your liver. Avoid alcohol.

Liquiprin oral Uses

This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.

How to use Liquiprin oral

Take this product by mouth as directed. Follow all directions on the product package. If you are uncertain about any of the information, consult your doctor or pharmacist.

There are many brands and forms of acetaminophen available. Read the dosing instructions carefully for each product because the amount of acetaminophen may be different between products. Do not take more acetaminophen than recommended. (See also Warning section.)

If you are giving acetaminophen to a child, be sure you use a product that is meant for children. Use your child's weight to find the right dose on the product package. If you don't know your child's weight, you can use their age.

For suspensions, shake the medication well before each dose. Some liquids do not need to be shaken before use. Follow all directions on the product package. Measure the liquid medication with the provided dose-measuring spoon/dropper/syringe to make sure you have the correct dose. Do not use a household spoon.

For rapidly-dissolving tablets, chew or allow to dissolve on the tongue, then swallow with or without water. For chewable tablets, chew thoroughly before swallowing.

Do not crush or chew extended-release tablets. Doing so can release all of the drug at once, increasing the risk of side effects. Also, do not split the tablets unless they have a score line and your doctor or pharmacist tells you to do so. Swallow the whole or split tablet without crushing or chewing.

For effervescent tablets, dissolve the dose in the recommended amount of water, then drink.

Pain medications work best if they are used as the first signs of pain occur. If you wait until the symptoms have worsened, the medication may not work as well.

Do not take this medication for fever for more than 3 days unless directed by your doctor. For adults, do not take this product for pain for more than 10 days (5 days in children) unless directed by your doctor. If the child has a sore throat (especially with high fever, headache, or nausea/vomiting), consult the doctor promptly.

Tell your doctor if your condition persists or worsens or if you develop new symptoms. If you think you may have a serious medical problem, get medical help right away.

Liquiprin oral 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: nausea, vomiting, loss of appetite, sweating, stomach/abdominal pain, extreme tiredness, yellowing eyes/skin, dark urine.

Acetaminophen does not cause the stomach and intestinal ulcers that NSAIDs such as aspirin, ibuprofen, and naproxen may cause. However, acetaminophen does not reduce swelling (inflammation) like the NSAIDs do. Consult your doctor for more details and to see which medication might be right for you.

If you are taking this medication on a regular schedule and 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.

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.

Liquiprin oral

Liquiprin oral Warnings

Taking too much acetaminophen may cause serious (possibly fatal) liver disease. Adults should not take more than 4000 milligrams (4 grams) of acetaminophen a day. People with liver problems and children should take less acetaminophen. Ask your doctor or pharmacist how much acetaminophen is safe to take.

Do not use with any other drug containing acetaminophen without asking your doctor or pharmacist first. Acetaminophen is in many nonprescription and prescription medications (such as pain/fever drugs or cough-and-cold products). Check the labels on all your medicines to see if they contain acetaminophen, and ask your pharmacist if you are unsure.

Get medical help right away if you take too much acetaminophen (overdose), even if you feel well. Overdose symptoms may include nausea, vomiting, loss of appetite, sweating, stomach/abdominal pain, extreme tiredness, yellowing eyes/skin, and dark urine.

Daily alcohol use, especially when combined with acetaminophen, may damage your liver. Avoid alcohol.

Liquiprin oral Uses

This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.

How to use Liquiprin oral

Take this product by mouth as directed. Follow all directions on the product package. If you are uncertain about any of the information, consult your doctor or pharmacist.

There are many brands and forms of acetaminophen available. Read the dosing instructions carefully for each product because the amount of acetaminophen may be different between products. Do not take more acetaminophen than recommended. (See also Warning section.)

If you are giving acetaminophen to a child, be sure you use a product that is meant for children. Use your child's weight to find the right dose on the product package. If you don't know your child's weight, you can use their age.

For suspensions, shake the medication well before each dose. Some liquids do not need to be shaken before use. Follow all directions on the product package. Measure the liquid medication with the provided dose-measuring spoon/dropper/syringe to make sure you have the correct dose. Do not use a household spoon.

For rapidly-dissolving tablets, chew or allow to dissolve on the tongue, then swallow with or without water. For chewable tablets, chew thoroughly before swallowing.

Do not crush or chew extended-release tablets. Doing so can release all of the drug at once, increasing the risk of side effects. Also, do not split the tablets unless they have a score line and your doctor or pharmacist tells you to do so. Swallow the whole or split tablet without crushing or chewing.

For effervescent tablets, dissolve the dose in the recommended amount of water, then drink.

Pain medications work best if they are used as the first signs of pain occur. If you wait until the symptoms have worsened, the medication may not work as well.

Do not take this medication for fever for more than 3 days unless directed by your doctor. For adults, do not take this product for pain for more than 10 days (5 days in children) unless directed by your doctor. If the child has a sore throat (especially with high fever, headache, or nausea/vomiting), consult the doctor promptly.

Tell your doctor if your condition persists or worsens or if you develop new symptoms. If you think you may have a serious medical problem, get medical help right away.

Liquiprin oral 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: nausea, vomiting, loss of appetite, sweating, stomach/abdominal pain, extreme tiredness, yellowing eyes/skin, dark urine.

Acetaminophen does not cause the stomach and intestinal ulcers that NSAIDs such as aspirin, ibuprofen, and naproxen may cause. However, acetaminophen does not reduce swelling (inflammation) like the NSAIDs do. Consult your doctor for more details and to see which medication might be right for you.

If you are taking this medication on a regular schedule and 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.

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.

Buy Cortico-Sol Online Without Prescriptions, Cortico-Sol

Prednisolone is used for treating allergies, arthritis, breathing problems (eg, asthma), certain blood disorders, collagen diseases (eg, lupus), certain eye diseases (eg, keratitis), cancer (eg, leukemia), endocrine problems (eg, adrenocortical insufficiency), intestinal problems (eg, ulcerative colitis), swelling due to certain conditions, or skin conditions (eg, psoriasis). Prednisolone is a corticosteroid. It works by modifying the body's immune response to various conditions and decreasing inflammation.

Use Prednisolone as directed by your doctor.

Take Prednisolone by mouth with food.

If you miss a dose of Prednisolone, 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 Prednisolone.

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

Do NOT use Prednisolone if:

you are allergic to any ingredient in Prednisolone

you have a systemic fungal infection, a certain type of malaria, inflammation of the optic nerve, or herpes infection of the eye

you are scheduled to have a live or attenuated live vaccination (eg, smallpox)

you are taking mifepristone.

Contact your doctor right away if any of these apply to you.

Some medical conditions may interact with Prednisolone. 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 a history of heart problems (eg, congestive heart failure), heart attack, high blood pressure, kidney problems, liver problems, diabetes, seizures, an underactive thyroid, adrenal gland problems, fluid retention (eg, swelling of the hands, ankles, or feet), or any mental or mood problems

if you have or have recently had a fungal, bacterial, viral, or other type of infection; herpes infection of the eye; chickenpox; measles; or shingles

if you have HIV infection or tuberculosis (TB) infection, or if you have had ever had a positive TB skin test

if you have any stomach problems (eg, ulcers), intestinal problems (eg, blockage, perforation, or infection; unexplained diarrhea; diverticulitis; ulcerative colitis), recent intestinal surgery, or inflammation of the esophagus

if you have weak bones (eg, osteoporosis) or muscle problems (eg, myasthenia gravis)

if you have had a recent vaccination (eg, smallpox).

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

Clarithromycin, cyclosporine, estrogens (eg, estradiol), oral contraceptives (eg, birth control pills), or ketoconazole because they may increase the risk of Prednisolone's side effects

Barbiturates (eg, phenobarbital), carbamazepine, ephedrine, hydantoins (eg, phenytoin), or rifampin because they may decrease Prednisolone's effectiveness

Anticholinesterases (eg, pyridostigmine), aspirin, diuretics (eg, hydrochlorothiazide, furosemide), methotrexate, mifepristone, quinolone antibiotics (eg, ciprofloxacin), ritodrine, or live or attenuated live vaccines because the risk of their side effects may be increased by Prednisolone

Anticoagulants (eg, warfarin), hydantoins (eg, phenytoin), or killed or inactivated vaccines because their effectiveness may be decreased by Prednisolone.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Prednisolone 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:

Avoid alcohol while you are using Prednisolone.

Prednisolone may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.

If you have not had chickenpox, shingles, or measles, avoid contact with anyone who does.

If you are taking Prednisolone regularly over a long period of time, carry an ID card at all times that says you take Prednisolone.

Do not receive a live vaccine (eg, measles, mumps, smallpox) while you are taking Prednisolone. Talk with your doctor before you receive any vaccine.

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

Diabetes patients - Prednisolone may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Lab tests, including adrenal function tests, may be performed while you use Prednisolone. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Caution is advised when using Prednisolone in children; they may be more sensitive to its effects.

Corticosteroids may affect growth rate in children and teenagers in some cases. They may need regular growth checks while they take Prednisolone.

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

If you are on long-term or high dosage therapy and you suddenly stop taking Prednisolone, you may have withdrawal symptoms, including fever, vomiting, appetite loss, diarrhea, nausea, dizziness, weight loss, weakness, general body discomfort, joint or muscle pain.

Kop Airomet-Aom (Prilosec) Utan Recept, Airomet-Aom

Kopa Airomet-aom (Prilosec) Natet Utan Recept

Airomet-aom (Prilosec) Forklaring

Airomet-aom OVER-the-counter fokusera pa kan vara att avhjalpa samband med gastroesofageal poisson sjukdom (GERD) tillsammans med andra omstandigheter som beror pa den extra magsyra. Dessutom den levereras till aterhamtning av marknaden i samband med erosiv esofagit (skador pa din luftstrupen vackt den av magen syra).

Airomet-aom OVER disk ar faktiskt utfor genom att minska mangden av surhet som tillverkas i sjalva magen. Det ar verkligen protonpumpmotorn hammare (PPI).

Airomet-aom kan ocksa betecknas som Omeprazol, Omez, Protoloc.

Allmant titeln i samband med Airomet-aom OVER-disk ar faktiskt Omeprazol.

Varumarke associerade med Airomet-aom OVER-THE-COUNTER tenderar att vara Airomet-aom liksom Airomet-aom OVER-THE-RAKNARE.

Airomet-aom (Prilosec) Dose

Airomet-aom OVER disk kommer in:

10 mg lagre dos friktion material

20mg Regular Dos friktionsmaterial

40 mg Forbattrad Dos friktionsmaterial

Airomet-aom OVER disk kommer i piller (10 milligram, tjugo milligram, fyrtio mg) samt tabletter.

Du maste fa Airomet-aom OVER disk varje dag med avseende pa tva veckor. Vanligtvis inte far Airomet-aom OVER-the-counter flera tablett varje dag.

Get Airomet-aom OVER disk innan kravande. Vanligtvis inte spricka, slipa eller ens oppna upp fordrojd frisattning.

Dina egna tecken och symtom kan bli mycket battre innan problemet ar helt hanteras.

Get Airomet-aom OVER disk tillsammans med dricksvatten.

Om du vill astadkomma basta resultaten brukar inte sluta med Airomet-aom OVER disk plotsligt.

Airomet-aom (Prilosec) 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.

Airomet-aom (Prilosec) Overdosering

Om du overdoserar Airomet-aom OVER disk och du undviker ocksa stor att du behover kolla din lakare eller ens lakare omedelbart. Tillhorande med Airomet-aom OVER disk overdosering: trotthet, illamaende eller krakningar, snabb hjartrytm, svettningar, torkade munnen omradet, huvudvark, suddig syn, kasta upp.

Airomet-aom (Prilosec) Lagringsutrymme

Shop i rymden temperaturer mellan 10 och 30 nivaer D (59 samt 86 nivaer F) fran fukt, belysning samt temperatur. Starka nagon form av orord medicinering efter utgangen dagen. Behall fran uppna barnen.

Airomet-aom (Prilosec) Negativa effekter

Airomet-aom OVER disk ger de negativa effekterna. Den mest typiska tenderar att vara:

branslefriktionsmaterial

illamaende eller krakningar friktionsmaterial

kastar upp friktionsmaterial

huvudvark friktionsmaterial

magen obehag friktionsmaterial

diarre friktionsmaterial

Mycket mindre typiska och allvarliga negativa effekter i hela anvander Airomet-aom recept COUNTER: allergisk reaktion reaktioner (urtikaria, andas in och andas problem, allergi, samt utbrott)

Negativa effekter indikationer ar beroende av medicin du kanske anvander men dessutom ar beroende av ditt valbefinnande villkor och en annan aspekter.

Airomet-aom (Prilosec) Kontraindikationer

Vanligtvis inte far Airomet-aom OVER disk om du ar kanslig for att Airomet-aom OVER-the-counter element.

Vanligtvis inte far Airomet-aom OVER disk om du vantar annars du tanker ha ett barn, annars ar du verkligen en medicinsk mamma.

Airomet-aom OVER disk inte riktigt utnyttjas for omedelbar lindring i samband med sura uppstotningar symtom.

Vanligtvis inte fa flera piller i samband med Airomet-aom OVER disk varje dag (24 timmar).

Var forsiktig tillsammans med Airomet-aom OVER disk om du drabbas av och har en kort historia i samband med sjukdomar i levern, vekling eller till och med morka barstolar, sura uppstotningar som tar mer an tre manader, vara haftigt sjuk som visas som blodomloppet eller ens espresso skal, regelbundna hjartproblem, sura uppstotningar tillsammans med vasande andning, magen obehag, illamaende / krakningar, problem eller obehag tillsammans med intag, ovanliga viktminskning.

Get Airomet-aom OVER disk noga om du anvander denna typ av mediciner eftersom disulfiram (Antabus), blodomloppet smalare (warfarin (Waran)), takrolimus (Prograf), ciklosporin (Gengraf, Neoral. Sandimmune), fenytoin (Dilantin), ampicillin (Omnipen, Principen), itrakonazol (Sporanox) eller till och med ketokonazol (Nizoral), somnloshet eller ens angest lakemedel (diazepam (Valium), alprazolam (Xanax), lorazepam (Ativan), temazepam ( Restoril), klorazepat (Tranxene), klordiazepoxid), metall (Feosol, Mol-jarn, Fergon, Femiron och aven andra), atazanavir (Reyataz), teofyllin (TheoBid, Theo-Dur, Theochron, Theolair, Elixophyllin, Slo-Phyllin ).

Forhindra alkoholhaltiga drycker.

Vanligtvis inte sluta anvanda Airomet-aom OVER disk plotsligt.

Airomet-aom (Prilosec) Vanliga fragor

Queen: Det ar viktigt Airomet-aom OVER disk info maste jag forsta?

Airomet-aom OVER disk kan vara medicin av hogsta kvalitet, som forbrukas avhjalpa forknippas med gastroesofageal poisson sjukdom (GERD) tillsammans med andra omstandigheter vackt den genom extra magsyra. Dessutom den levereras till aterhamtning av marknaden i samband med erosiv esofagit (skador pa din luftstrupen vackt den av magen syra). Airomet-aom over-the-Counter ar egentligen inte utnyttjas for omedelbar lindring i samband med sura uppstotningar tecken och symtom. Vanligtvis inte fa flera piller i samband med Airomet-aom OVER disk varje dag (24 timmar). Vanligtvis inte far Airomet-aom OVER disk for dem som har en bra allergisk reaktion for denna medicin eller komponenterna. Var forsiktig tillsammans med Airomet-aom OVER disk om du drabbas av och har en kort historia i samband med sjukdomar i levern, vekling eller till och med morka barstolar, sura uppstotningar som tar mer an tre manader, vara haftigt sjuk som visas som blodomloppet eller ens espresso skal, regelbundna hjartproblem, sura uppstotningar tillsammans med vasande andning, magen obehag, illamaende / krakningar, problem eller obehag tillsammans med intag, ovanliga viktminskning. Fa Airomet-aom OVER disk noga om du anvander denna typ av mediciner eftersom disulfiram (Antabus), blodomloppet smalare (warfarin (Waran)), takrolimus (Prograf), ciklosporin (Gengraf, Neoral, Sandimmune), fenytoin (Dilantin ), ampicillin (Omnipen, Principen), itrakonazol (Sporanox) eller till och med ketokonazol (Nizoral), somnloshet eller ens angest lakemedel (diazepam (Valium), alprazolam (Xanax), lorazepam (Ativan), temazepam (Restoril), klorazepat (Tranxene). klordiazepoxid), metall (Feosol, Mol-jarn, Fergon, Femiron och aven andra), atazanavir (Reyataz), teofyllin (TheoBid, Theo-Dur, Theochron, Theolair, Elixophyllin, Slo-Phyllin). Vanligtvis inte sluta dra fordel av denna medicin helt plotsligt. Bare denna medicin fran barn och gor inte detta nagra andra individer. Det ar verkligen oacceptabelt att overvaga Airomet-aom OVER disk om du vantar annars du tanker ha ett barn, annars ar du verkligen en medicinsk mom. A

Queen: Vad exakt ar Airomet-aom recept COUNTER negativa effekter?

Airomet-aom OVER disk erbjuder de typiska negativa effekter for exempelvis bransle, illamaende eller krakningar, kasta upp, huvudvark, magen obehag, diarre. Men i situationen i samband med att bli avvisad i samband med Airomet-aom OVER-the-counter komponenter du har mojlighet att mota mer allvarliga negativa effekter: problem inandning och utandning, inflammation i motet, lapparna, sprak, eller ens tonsiller, hives. A

Queen: Vad exakt ar allmanna och varumarken som forknippas med Airomet-aom OVER disk?

Allman titeln i samband med Airomet-aom OVER-disk ar faktiskt Omeprazol. Varumarken tenderar att vara Airomet-aom och Airomet-aom OTC-COUNTER. A

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