Buy Ketopamin Ketoconazole Online Without Prescriptions, Ketopamin

Nizoral is used for treating fungal infections. Nizoral is an azole antifungal. It kills sensitive fungi by interfering with the formation of the fungal cell membrane.

Use Nizoral as directed by your doctor!

Take Nizoral by mouth with or without food.

Do not take an antacid within 1 hour before or 2 hours after you take Nizoral.

If you are also taking an anticholinergic (eg, hyoscyamine), an H 2 antagonist (eg, famotidine), or a proton pump inhibitor (eg, omeprazole), take Nizoral at least 2 hours before the H 2 antagonist, proton pump inhibitor, or anticholinergic.

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

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

If you miss a dose of Nizoral, 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 Nizoral.

Store Nizoral between 59 and 77 degrees F (15 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Nizoral out of the reach of children and away from pets.

Active Ingredient: Ketoconazole.

Do NOT use Nizoral if:

you are allergic to any ingredient in Nizoral

you have a fungal infection in the brain membranes (fungal meningitis)

you are taking an aldosterone blocker (eg, eplerenone), astemizole, cisapride, conivaptan, dofetilide, an ergot alkaloid (eg, ergotamine), erythromycin, midazolam, nevirapine, pimozide, a quinazoline (eg, alfuzosin), quinidine, rifabutin, rifampin, terfenadine, triazolam, or a 5-HT receptor agonist (eg, eletriptan).

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

Some medical conditions may interact with Nizoral. 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 are allergic to other azole antifungals (eg, itraconazole)

if you have low stomach acid (eg, hypochlorhydria)

if you have a history of liver disease, regular alcohol use, alcohol abuse or dependence, or blood problems (eg, prophyria).

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

Many prescription and nonprescription medicines (eg, used for infections, HIV, seizures, anxiety, sleep, heartburn, diabetes, high cholesterol, heart problems, high blood pressure, allergies, irregular heartbeat, pain, blood thinning, asthma, migraines, mood or mental problems, cancer, prostate problems, immune system suppression, erectile dysfunction, urinary problems, or contraception [birth control]), multivitamin products, and herbal or dietary supplements may interact with Nizoral, increasing the risk of serious side effects

Nevirapine, rifabutin, or rifampin because they may decrease Nizoral's effectiveness

Astemizole, cisapride, dofetilide, erythromycin, pimozide, quinidine, or terfenadine because the risk of severe heart effects may be increased

Midazolam or triazolam because their actions and the risk of their side effects may be increased by Nizoral, resulting in increased risk of sedation and breathing difficulties

Aldosterone blockers (eg, eplerenone), conivaptan, ergot alkaloids (eg, ergotamine), quinazolines (eg, alfuzosin) or 5-HT receptor agonists (eg, eletriptan) because the risk of their side effects may be increased by Nizoral.

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

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

Rarely, Nizoral may cause a severe allergic reaction right after you take the first dose. Symptoms may include difficulty breathing; tightness in the chest; swelling of the eyelids, face, or lips; or rash or hives. If this happens, seek medical care at once.

Use of alcohol with Nizoral has rarely caused symptoms such as flushing, rash, swelling of the hands and feet, nausea, and headache. Talk with your doctor before drinking alcohol while taking Nizoral.

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

Nizoral only works against fungi; it does not treat viral infections (eg, the common cold) or bacterial infections.

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

Diabetes patients - Nizoral may increase the risk of low blood sugar from your diabetes medicine. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

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

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

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

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Nizoral while you are pregnant. Nizoral is found in breast milk. Do not breastfeed while using Nizoral.

Proseda, Proseda

Dr. Julie Prosseda MD

Nursing Homes in Top Cities

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More Information About Sotalol, Biosotal

More information about Sotalol

Canadian Brand Names

Alti-Sotalol; Apo-Sotalol ® ; Betapace AF™; Gen-Sotalol; Lin-Sotalol; Novo-Sotalol; Nu-Sotalol; PMS-Sotalol; Rho ® - Sotalol; Sotacor ®

Use

Treatment of documented ventricular arrhythmias (ie, sustained ventricular tachycardia), that in the judgment of the physician are life-threatening; maintenance of normal sinus rhythm in patients with symptomatic atrial fibrillation and atrial flutter who are currently in sinus rhythm. Manufacturer states substitutions should not be made for Betapace AF ® since Betapace AF ® is distributed with a patient package insert specific for atrial fibrillation/flutter.

Pregnancy Risk Factor

Pregnancy Implications

There are no adequate and well-controlled studies in pregnant women. Beta-blockers have been associated with bradycardia, hypotension, and IUGR; IUGR is probably related to maternal hypertension. Sotalol has been shown to cross the placenta, and is found in amniotic fluid; therefore, sotalol should be used during pregnancy only if the potential benefit outweighs the potential risk. Cases of neonatal hypoglycemia have been reported following maternal use of beta-blockers at parturition or during breast-feeding. Monitor breast-fed infant for symptoms of beta-blockade.

Lactation

Enters breast milk/use caution (AAP rates "compatible")

Contraindications

Hypersensitivity to sotalol or any component of the formulation; bronchial asthma; sinus bradycardia; second - and third-degree AV block (unless a functioning pacemaker is present); congenital or acquired long QT syndromes; cardiogenic shock; uncontrolled congestive heart failure. Betapace AF ® is contraindicated in patients with significantly reduced renal filtration (Clcr<40 mL/minute).

Warnings/Precautions

Must be initiated (or reinitiated) in a setting with continuous monitoring and staff familiar with the recognition and treatment of life-threatening arrhythmias. Patients must be monitored with continuous ECG for a minimum of 3 days (on their maintenance dose). Use cautiously in the renally-impaired (dosage adjustment required). Creatinine clearance must be calculated prior to dosing.

Monitor and adjust dose to prevent QTc prolongation. Concurrent use with other QTc-prolonging drugs (including Class I and Class III antiarrhythmics) is generally not recommended; withhold for 3 half-lives. Watch for proarrhythmic effects. Correct electrolyte imbalances before initiating (especially hypokalemia and hyperkalemia). Consider pre-existing conditions such as sick sinus syndrome before initiating. Conduction abnormalities can occur particularly sinus bradycardia. Use cautiously within the first 2 weeks post-MI (experience limited). Administer cautiously in compensated heart failure and monitor for a worsening of the condition. Use caution in patients with PVD (can aggravate arterial insufficiency). Beta-blocker therapy should not be withdrawn abruptly (particularly in patients with CAD), but gradually tapered to avoid acute tachycardia, hypertension, and/or ischemia. Use caution with concurrent use of beta-blockers and either verapamil or diltiazem; bradycardia or heart block can occur. Use cautiously in diabetics because it can mask prominent hypoglycemic symptoms. Can mask signs of thyrotoxicosis. Use care with anesthetic agents which decrease myocardial function.

Adverse Reactions

Cardiovascular: Bradycardia (16%), chest pain (16%), palpitation (14%)

Central nervous system: Fatigue (20%), dizziness (20%), lightheadedness (12%)

Neuromuscular & skeletal: Weakness (13%)

Respiratory: Dyspnea (21%)

Cardiovascular: CHF (5%), peripheral vascular disorders (3%), edema (8%), abnormal ECG (7%), hypotension (6%), proarrhythmia (5%), syncope (5%)

Central nervous system: Mental confusion (6%), anxiety (4%), headache (8%), sleep problems (8%), depression (4%)

Dermatologic: Itching/rash (5%)

Endocrine & metabolic: Sexual ability decreased (3%)

Gastrointestinal: Diarrhea (7%), nausea/vomiting (10%), stomach discomfort (3% to 6%), flatulence (2%)

Genitourinary: Impotence (2%)

Hematologic: Bleeding (2%)

Neuromuscular & skeletal: Paresthesia (4%), extremity pain (7%), back pain (3%)

Ocular: Visual problems (5%)

Respiratory: Upper respiratory problems (5% to 8%), asthma (2%)

<1% (Limited to important or life-threatening): Alopecia, clouded sensorium, cold extremities, diaphoresis, emotional lability, eosinophilia, fever, hyperlipidemia, incoordination, leukopenia, myalgia, paralysis, phlebitis, photosensitivity reaction, pruritus, pulmonary edema, Raynaud's phenomenon, red crusted skin, serum transaminases increased, skin necrosis after extravasation, thrombocytopenia, vertigo, xerostomia

Postmarketing and/or case reports: Bronchiolitis obliterans with organized pneumonia, leukocytoclastic vasculitis, retroperitoneal fibrosis

Overdosage/Toxicology

Symptoms of intoxication include cardiac disturbances, CNS toxicity, bronchospasm, hypoglycemia and hyperkalemia. The most common cardiac symptoms include hypotension and bradycardia; atrioventricular block, intraventricular conduction disturbances, cardiogenic shock, and asystole may occur with severe overdose, especially with membrane-depressant drugs (eg, propranolol); CNS effects include convulsions, coma, and respiratory arrest is commonly seen with propranolol and other membrane-depressant and lipid-soluble drugs.

Treatment includes symptomatic treatment of seizures, hypotension, hyperkalemia and hypoglycemia. Bradycardia and hypotension resistant to atropine, isoproterenol or pacing may respond to glucagon. Wide QRS defects caused by the membrane-depressant poisoning may respond to hypertonic sodium bicarbonate. Repeat-dose charcoal, hemoperfusion, or hemodialysis may be helpful in removal of only those beta-blockers with a small Vd, long half-life, or low intrinsic clearance (acebutolol, atenolol, nadolol, sotalol).

Drug Interactions

Amiodarone: May cause additive effects on QTc prolongation as well as decreased heart rate, and has been associated with cardiac arrest in patients receiving beta-blockers.

Antacids (aluminum/magnesium) decrease sotalol blood levels; separate administration by 2 hours.

Antiarrhythmics: Concurrent use of Class Ia or Class III antiarrhythmics may result in additive QTc prolongation; concurrent use is not recommended.

Beta2 agonists: Effects may be diminished by concurrent sotalol; use caution.

Beta-blockers: Due to shared pharmacological effects, heart rate reductions may be additive; concurrent use is not recommended.

Calcium channel blockers: Concurrent use may lead to additive effects on AV conduction, ventricular contractility, and/or hypotension; use caution.

Cisapride: Concurrent use with sotalol increases malignant arrhythmias; contraindicated.

Clonidine: Sotalol may cause rebound hypertension after discontinuation of clonidine.

QTc-prolonging drugs: Concurrent use may result in additive QTc prolongation, potentially increasing the risk of malignant arrhythmias. Use of cisapride, mesoridazine, thioridazine, and pimozide with other QTc-prolonging agents is contraindicated. Concurrent use of sotalol with Class I and Class III antiarrhythmics is not recommended; withhold for 3 half-lives. Use caution with other QTc-prolonging agents (including bepridil, erythromycin, clarithromycin), fluoroquinolones (including sparfloxacin, gatifloxacin, and moxifloxacin), haloperidol, and TCAs.

Phenothiazines (mesoridazine and thioridazine): Concurrent use may result in additive QTc prolongation, potentially increasing the risk of malignant arrhythmias; contraindicated.

Pimozide: Concurrent use may result in additive QTc prolongation, potentially increasing the risk of malignant arrhythmias; contraindicated.

Ethanol/Nutrition/Herb Interactions

Food: Sotalol peak serum concentrations may be decreased if taken with food.

Herb/Nutraceutical: Avoid ephedra (may worsen arrhythmia).

Stability

Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F)

Mechanism of Action

Beta-blocker which contains both beta-adrenoreceptor-blocking (Vaughan Williams Class II) and cardiac action potential duration prolongation (Vaughan Williams Class III) properties

Class II effects: Increased sinus cycle length, slowed heart rate, decreased AV nodal conduction, and increased AV nodal refractoriness

Class III effects: Prolongation of the atrial and ventricular monophasic action potentials, and effective refractory prolongation of atrial muscle, ventricular muscle, and atrioventricular accessory pathways in both the antegrade and retrograde directions

Sotalol is a racemic mixture of d - and l - sotalol; both isomers have similar Class III antiarrhythmic effects while the l - isomer is responsible for virtually all of the beta-blocking activity

Sotalol has both beta1- and beta2-receptor blocking activity

The beta-blocking effect of sotalol is a noncardioselective [half maximal at about 80 mg/day and maximal at doses of 320-640 mg/day]. Significant beta-blockade occurs at oral doses as low as 25 mg/day.

The Class III effects are seen only at oral doses

Pharmacodynamics/Kinetics

Onset of action: Rapid, 1-2 hours

Peak effect: 2.5-4 hours

Duration: 8-16 hours

Absorption: Decreased 20% to 30% by meals compared to fasting

Distribution: Low lipid solubility; enters milk of laboratory animals and is reported to be present in human milk

Protein binding: None

Bioavailability: 90% to 100%

Half-life elimination: 12 hours; Children: 9.5 hours; terminal half-life decreases with age <2 years (may by

1 week in neonates)

Excretion: Urine (as unchanged drug)

Dosage

Sotalol should be initiated and doses increased in a hospital with facilities for cardiac rhythm monitoring and assessment. Proarrhythmic events can occur after initiation of therapy and with each upward dosage adjustment.

Children: Oral: The safety and efficacy of sotalol in children have not been established

Note: Dosing per manufacturer, based on pediatric pharmacokinetic data; wait at least 36 hours between dosage adjustments to allow monitoring of QT intervals

2 years: Dosage should be adjusted (decreased) by plotting of the child's age on a logarithmic scale; see graph or refer to manufacturer's package labeling.

>2 years: Initial: 90 mg/m 2 /day in 3 divided doses; may be incrementally increased to a maximum of 180 mg/m 2 /day

Ventricular arrhythmias (Betapace ®. Sorine ® ):

Initial: 80 mg twice daily

Dose may be increased gradually to 240-320 mg/day; allow 3 days between dosing increments in order to attain steady-state plasma concentrations and to allow monitoring of QT intervals

Most patients respond to a total daily dose of 160-320 mg/day in 2-3 divided doses.

Some patients, with life-threatening refractory ventricular arrhythmias, may require doses as high as 480-640 mg/day; however, these doses should only be prescribed when the potential benefit outweighs the increased of adverse events.

Atrial fibrillation or atrial flutter (Betapace AF ® ): Initial: 80 mg twice daily

If the initial dose does not reduce the frequency of relapses of atrial fibrillation/flutter and is tolerated without excessive QT prolongation (not >520 msec) after 3 days, the dose may be increased to 120 mg twice daily. This may be further increased to 160 mg twice daily if response is inadequate and QT prolongation is not excessive.

Elderly: Age does not significantly alter the pharmacokinetics of sotalol, but impaired renal function in elderly patients can increase the terminal half-life, resulting in increased drug accumulation

Dosage adjustment in renal impairment: Adults: Impaired renal function can increase the terminal half-life, resulting in increased drug accumulation. Sotalol (Betapace AF ® ) is contraindicated per the manufacturer for treatment of atrial fibrillation/flutter in patients with a Clcr<40 mL/minute.

Ventricular arrhythmias (Betapace ®. Sorine ® ):

Clcr >60 mL/minute: Administer every 12 hours

Clcr 30-60 mL/minute: Administer every 24 hours

Clcr 10-30 mL/minute: Administer every 36-48 hours

Clcr<10 mL/minute: Individualize dose

Atrial fibrillation/flutter (Betapace AF ® ):

Clcr >60 mL/minute: Administer every 12 hours

Clcr 40-60 mL/minute: Administer every 24 hours

Clcr<40 mL/minute: Use is contraindicated

Dialysis: Hemodialysis would be expected to reduce sotalol plasma concentrations because sotalol is not bound to plasma proteins and does not undergo extensive metabolism; administer dose postdialysis or administer supplemental 80 mg dose; peritoneal dialysis does not remove sotalol; supplemental dose is not necessary

Administration

Food may decrease adsorption

Cephabos, Cephabos

Product Description Common use Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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.

Product Description Common use Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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.

Product Description Common use Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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.

Vertab Sr 240mg - Patient Information Leaflet (Pil), Vertab

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

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

Text only version for the visually impaired Below is a text only representation of the Patient Information leaflet. The original may contain images or tables and can be viewed in PDF format using the link above. This PIL may be available from the RNIB in large print, Braille or audio CD. For further information please call the RNIB Medicine Leaflet line on 0800 198 5000. The product code(s) for this leaflet is/are: PL 14017/0025.

Vertab SR 240mg

PACKAGE LEAFLET: INFORMATION FOR THE USER

VERTAB ® SR 240 Tablets

Please read this leaflet carefully before you start taking your tablets.

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

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

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

If you get any side effects talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.

In this leaflet:

1. What Vertab SR 240 Tablets are and what they are used for 2. What you need to know before you take Vertab SR 240 Tablets 3. How to take Vertab SR 240 Tablets 4. Possible side effects 5. How to store Vertab SR 240 Tablets 6. Contents of the pack and other information

1. WHAT VERTAB SR 240 TABLETS ARE AND WHAT THEY ARE USED FOR

The name of your medicine is: Vertab SR 240 Tablets

Vertab SR 240 Tablets belong to a group of medicines called calcium channel blockers. Calcium channel blockers change the amount of calcium getting into the muscle cells in your heart and blood vessels. This can change the strength and speed with which your heart beats. It also opens up the blood vessels so blood can be pumped around the body more easily. This helps more oxygen to get to your heart muscle and can lower your blood pressure.

Vertab SR 240 Tablets are indicated for the treatment of mild to moderate hypertension (high blood pressure) and the treatment and prevention of angina pectoris (chest pain).

2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE VERTAB SR 240 TABLETS

If you are unsure if any of the list applies to you, ask your doctor before you start to take your tablets.

Do not take Vertab SR 240 Tablets:

If you are allergic (hypersensitive) to Verapamil Hydrochloride or to any of the other ingredients of Vertab SR 240 Tablets (listed in section 6 - Further information).

If you are having a cardiogenic shock (a sudden and rapid fall in blood pressure).

If you are having or have recently had a heart attack particularly if a slow heart beat, low blood pressure or left ventricular failure of the heart are involved.

If you have second or third degree atrioventricular block or sino-atrial block (a disorder where parts of the heart may beat at the wrong time causing the heart not to pump blood around the body very well).

If you have sick sinus syndrome (a heart beat disorder).

If you have heart failure that is not currently being treated.

If you have severe bradycardia (a condition where the heart beats at less than 50 beats per minute).

If you have low blood pressure where the higher blood pressure reading is below 90.

If you have Wolff-Parkinson-White syndrome (a heart problem causing rapid heart rate sometimes associated with symptoms such as dizziness or faintness).

If you are already taking a medicine containing ivabradine for the treatment of certain heart diseases.

Warnings and Precautions

Consult your doctor or pharmacist before taking Vertab SR 240 Tablets if:

You are pregnant or planning to become pregnant or are breast-feeding.

You suffer or you have ever suffered in the past from low blood pressure, from a condition known as “heart failure”, an abnormally slow or irregular heart beat, or any other cardiac problem.

You suffer or you have ever suffered in the past from kidney or liver disorders. These above mentioned medical conditions may mean that your doctor will need to monitor you more closely.

You are planning to have medical or dental surgery. This medicine may affect the anaesthetics or other treatments used.

You have a condition where the nerve to muscle transmission is affected e. g. myasthenia gravis, Lambert-Eaton syndrome, advanced Duchenne muscular dystrophy.

Children and Adolescents

There are no data on the use of verapamil prolonged release tablets in children and adolescents.

Taking other medicines:

Please inform your doctor or pharmacist if you are taking or have recently taken any of the following medicines, even those not prescribed:

Digoxin and digitoxin (used to treat certain heart conditions, such as heart failure)

Beta-blockers (e. g. atenolol, metoprolol and propranolol) or any other treatment for heart diseases and high blood pressure

Prazosin, terazosin (alpha blockers used to treat high blood pressure and heart conditions)

Anti-arrhythmic agents used to steady an irregular heart beat (e. g. flecainide, quinidine)

Carbamazepine, phenytoin, phenobarbital (usually used in epilepsy)

Ciclosporin, sirolimus, everolimus, tacrolimus (normally used following organ transplants to help prevent rejection)

Theophylline (used for breathing difficulties e. g. asthma)

Rifampicin (antibiotic action for treatment of various infections such as tuberculosis [TB])

Lithium (used for psychiatric conditions)

Cimetidine (used for stomach disorders e. g. ulcers and indigestion)

Aspirin, a non-steroidal anti-inflammatory painkiller (NSAID) used to relieve pain and reduce fever

Glibenclamide (used to treat certain types of diabetes)

Diuretics (water tablets)

Erythromycin, clarithromycin and telithromycin (used to treat certain types of infection)

Doxorubicin (an anti-cancer medicine)

Imipramine, St John’s Wort (used to treat depression)

Buspirone (used to treat anxiety)

Colchicine, sulfinpyrazone (used to treat gout)

Ritonavir (used to treat HIV)

Medicines known as ‘statins’ used to lower cholesterol levels (e. g. atorvastatin, lovastatin, simvastatin)

Medicines used to relax muscles (used for anesthesia during surgical procedures)

Almotriptan (used to treat migraine)

Midazolam (used as a sedative or anaesthetic)

Dabigatran (used to thin blood)

Medicines containing ivabradine for the treatment of certain heart diseases

Taking Vertab SR 240 Tablets with food and drink:

Your tablets can be taken with a glass of water to help you swallow them. It does not matter if you have eaten, so they can be taken with or without food.

Vertab SR 240 Tablets will increase the time your body takes to get rid of alcohol.

This means that you may not have to drink as much for your blood alcohol level to be above the legal limit to drive. It will also take you longer to sober up.

Do not drink grapefruit juice whilst taking your tablets as it can affect the absorption of this medicine.

Pregnancy and breast-feeding:

Consult your doctor or pharmacist if you are pregnant, trying to become pregnant, or breast-feeding.

Driving and using machines:

Vertab SR 240 Tablets can make some people feel dizzy especially when first starting to take the tablets. Do not drive, operate machinery or do anything that requires you to be alert, until you know how the tablets affect you.

Important information about some of the ingredients of Vertab SR 240 Tablets:

This medicinal product contains 32 mg sodium per dose. To be taken into consideration by patients on a controlled sodium diet.

3. HOW TO TAKE VERTAB SR 240 TABLETS

Always take Vertab SR 240 Tablets exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

The tablets should not be chewed or crushed. They should be swallowed whole with a glass of water.

For treatment of hypertension (high blood pressure): The usual dosage is one tablet per day. Some patients may need to take two tablets per day (one in the morning and one in the evening with about 12 hours between doses). Do not take more than two tablets per day.

For the treatment and prevention of angina pectoris (chest pain): The usual dose is one tablet twice daily.

USE IN CHILDREN AND ADOLESCENTS:

This medicine is not suitable for children and adolescents.

If you take more Vertab SR 240 Tablets than you should

In case of an overdose, contact your nearest hospital casualty department or tell your doctor IMMEDIATELY, taking your tablets with you.

If you forget to take Vertab SR 240 Tablets

If you forget to take a dose, take it as soon as you remember, unless it is almost time for your next dose. Do not take a double dose to make up for a forgotten dose.

If you have trouble remembering to take your tablets, tell your doctor or your pharmacist. If you take too many tablets by mistake, any side effects (see below) may be worse than usual; in this case see your doctor.

If you stop taking Vertab SR 240 Tablets

It is important that you continue taking the tablets until your doctor tells you to stop. Do NOT stop because you feel better. If you stop taking the tablets too soon your condition may get worse.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS

Like all medicines, Vertab SR 240 Tablets can cause side effects, although not everybody gets them.

If you experience the following side effects you should tell your doctor immediately:

If you have any unexpected wheezing or difficulty in breathing, if you have Quincke’s oedema (swelling of the face with itching), swelling of the mouth, lips, or tongue, or if you develop a skin rash, pruritus (itching), or severe skin rash with blistering and peeling of the skin. These are signs you are having an allergic reaction.

If you develop yellowing of the skin or eyes, a fever or tenderness around the middle. These are signs that your liver may not be functioning as well as usual.

If you have bradycardia (slow heart beats), arrhythmia (irregular heart beat), palpitations (awareness of an irregular or rapid heart beat), heart failure, reversible impairment of liver function, chest pains for the first time or chest pains that become more frequent, dizziness, weakness or confusion, swollen ankles, feeling faint or breathless or a burning sensation in the feet, which may become hot and throbbing.

Swelling of the limbs.

Hypotension (abnormally low blood pressure).

Do not stop taking the tablets, but tell your doctor if you get any of the following:

Constipation (the most common side effect), flushing of the face or neck, headaches, feeling or being sick, abdominal pain or discomfort, a feeling of dizziness or spinning, tinnitus (ringing or buzzing in the ears), tiredness, tremor, movement disorders, muscle weakness, aches and pains in the joints and/or muscles, skin rash or itching, a tingling or prickling feeling on the skin, numbness and hair loss. Impotence may occur rarely.

Other side effects might occur if Vertab SR 240 is used for a long time. Tell your doctor if you develop swollen gums which start to spread over your teeth, or if your breasts swell (males) or start to produce milk (males and females). These effects are rare and are resolved upon stopping taking the tablets.

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

Reporting of side effects

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

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

5. HOW TO STORE VERTAB SR 240 TABLETS

Keep out of the sight and reach of children.

Do not use Vertab SR 240 Tablets after the expiry date on the label and carton.

Do not store above 25°C.

Do not use Vertab SR 240 Tablets if you notice any visible signs of deterioration.

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

6. CONTENTS OF THE PACK AND OTHER INFORMATION

What Vertab SR 240 Tablets contain:

The active substance is: Verapamil Hydrochloride 240mg.

The other ingredients are: Core: Sodium alginate, Microcrystalline cellulose, Povidone, Hypromellose, Colloidal anhydrous silica, Magnesium stearate. Coating: Hypromellose, Titanium dioxide, Macrogol, Yellow Lake E-104, Blue Lake E-132 and Carnauba wax.

What Vertab SR 240 Tablets look like and content of the pack:

This medicine can be identified as modified release, light-green film-coated, capsule-shaped, scored tablets. Vertab SR 240 Tablets are supplied in packs of 28 tablets.

The Manufacturer/Holder of Marketing Authorisation is:

Dexcel ® - Pharma Ltd 7 Sopwith Way Drayton Fields Daventry Northamptonshire NN11 8PB UK

Chiesi Limited 333 Styal Road Manchester M22 5LG United Kingdom

Diclofenac - Woman S Health, Sorelmon

Diclofenac is used to treat pain or inflammation caused by arthritis or ankylosing spondylitis. Diclofenac may also be used for purposes other than those listed in this medication guide.

Use Diclofenac as directed by your doctor.

Take Diclofenac by mouth with or without food. Ask your health care provider any questions you may have about how to use Diclofenac.

Drug Class and Mechanism

Diclofenac is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Diclofenac works by reducing hormones that cause inflammation and pain in the body.

If you miss a dose of Diclofenac, use 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 use 2 doses at once.

Store Diclofenac at room temperature between 68 and 77 degrees F (20 and 25 degrees C) in a tightly closed container. Brief periods at temperatures of 59 to 86 degrees F (15 to 30 degrees C) are permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diclofenac out of the reach of children and away from pets.

Do not use Diclofenac if:

you are allergic to any ingredient in Diclofenac; you have had a severe allergic reaction (e. g. severe rash, hives, breathing difficulties, dizziness) to another NSAID (e. g. ibuprofen, naproxen, celecoxib) or aspirin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Diclofenac may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Before you start any new medicine, check the label to see if it has Sorelmon or another nonsteroidal anti-inflammatory drug (NSAID) medicine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Diclofenac should not be used in children; safety and effectiveness in children have not been confirmed. Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breast-feed while using Diclofenac.

Possible Side Effects

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

burning or stinging; discharge; eye redness, irritation, or itching. Seek medical attention right away if any of these severe side effects occur:

severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred or distorted vision; eye infection; eyelid swelling or redness; sensitivity to glare or light.

Diclofenac 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.

Hytrin - Man S Health, Geriprost

Hytrin is used for treating high blood pressure and treating signs and symptoms of benign prostatic hyperplasia (BPH). Hytrin is an alpha-blocker. It works by relaxing muscles in the blood vessels, resulting in lowering of blood pressure. In BPH, alpha-blockers work by relaxing muscles around the urethra (tube that drains urine from the bladder), which improves urinary symptoms.

Use Hytrin as directed by your doctor.

Take Hytrin by mouth with or without food.

Hytrin may cause a sudden drop in blood pressure after the first dose. Take your first dose at bedtime. If you get up during the night, sit up slowly, then stand slowly.

If you miss a dose of Hytrin, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. If more than one dose is missed, contact your doctor or pharmacist.

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

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

Active Ingredient: Terazosin hydrochloride.

Do NOT use Hytrin if:

you are allergic to any ingredient in Hytrin or to similar medicines (eg, prazosin).

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

Some medical conditions may interact with Hytrin. 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 prostate cancer, angina pectoris, heart disease, or kidney or liver problems

if you will be having eye surgery.

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

Phosphodiesterase type 5 (PDE5) inhibitors (eg, sildenafil) or verapamil because severe dizziness, lightheadedness, or fainting may occur.

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

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

Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Hytrin; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

Hytrin may cause a sudden drop in blood pressure after the first dose. Take your first dose at bedtime. If you get up during the night, sit up slowly, then stand slowly. This will help to reduce your lightheadedness or dizziness. These effects are more likely to occur after the first few doses or if your dose has increased, but can occur at any time while you are taking the medicine. It can also occur if you stop taking the medicine and then restart treatment.

Hytrin may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

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

Hytrin may rarely cause a prolonged, painful erection. This could happen even when you are not having sex. If this is not treated right away, it could lead to permanent sexual problems such as impotence. Contact your doctor right away if this happens.

Tell your doctor or dentist that you take Hytrin before you receive any medical or dental care, emergency care, or surgery (including eye surgery).

Lab tests, including blood pressure, may be performed while you use Hytrin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Hytrin should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Hytrin while you are pregnant. It is not known if Hytrin is found in breast milk. If you are or will be breast-feeding while you use Hytrin, 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:

Dizziness; drowsiness; lightheadedness; nasal congestion; nausea; weakness.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision or other vision changes; chest pain; decreased sexual desire or ability; fainting; fast, slow, or irregular heartbeat;painful, prolonged erection; severe or prolonged dizziness or headache; shortness of breath; swelling of the ankles, feet, or hands.

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.

Lactamox, Lactamox

Common use It is is a broad-spectrum antibiotic which destroys bacteria. It is active against many aerobic (those developing in presence of oxygen) and anaerobic (those developing in absence of oxygen) gram positive and aerobic gram negative microorganisms including strains which produce beta-lactamase (the enzyme which destroys penicillin). Clavulanate potassium comprised in the content of this medication provides resistance of Augmentin to activity of bacterial beta-lactamases. This medication is used to treat pneumonia and other infectious diseases of respiratory, gastrointestinal systems, urogenital systems, infections which appear after surgery and others.

Dosage and directions Doses are administered individually depending on your condition, localization of infection and susceptibility of the pathogen. Do not take it in larger amounts or longer than recommended. Swallow the whole tablet. If it is the Augmentin Chewable tablet then chew it before swallowing. Augmentin should be taken at evenly spaced interval.

Precautions Do not use it if you are allergic to any other penicillin antibiotic, if you have liver or kidney failure or mononucleosis.

Contraindications Do not use the medicine if you have allergy to its components or another penicillin antibiotics, if you have infectious mononucleosis, a history of liver problems or yellowing of the eyes or skin caused by Augmentin.

Possible side effect Dyspepsia, abdominal discomfort, bloating, gas nausea, vomiting, liver function disorders, hepatitis, jaundice caused by stagnation of bile, vaginal itching and also symptoms of allergy (hives, rash, swelling). Cautiousness should be exercised in patients with liver failure. The medication is not recommended for pregnant (especially third trimester) and breastfeeding women.

Treatment with Augmentin and other antibiotics can change the normal bacteria flora of the colon and permit overgrowth of C. difficile, a bacteria which causes pseudomembranous colitis. Probenecid which is used to treat gout may slow excretion of Augmentin by kidneys and result in increase of its toxicity.

Missed dose If you missed a dose take it as soon as you remember, but not if it is almost time of the next intake by your schedule. If so skip the missed dose. Do not try to compensate a missed dose by taking an extra one.

Overdose If you suppose that took too much of Augmentin and experience such symptoms as nausea, vomiting, stomach pain, diarrhea, skin rash, drowsiness, and hyperactivity, seek immediate medical help.

Storage Store at room temperature of 59-86F (15-30C) away from light and moisture.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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 advisor 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.

Cefuroxime Medical Facts From, Cefuroximum

cefuroxime

a history of intestinal problems, such as colitis;

if you are malnourished.

The liquid form may contain phenylalanine. Talk to your doctor before using this form of cefuroxime if you have phenylketonuria (PKU).

This medicine is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

Cefuroxime can make birth control pills less effective. Ask your doctor about using a non hormonal birth control (condom, diaphragm with spermicide) to prevent pregnancy.

Cefuroxime can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Cefuroxime is not approved for use by anyone younger than 3 months old.

How should I take cefuroxime?

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

You may take cefuroxime tablets with or without meals. Do not crush the tablet or it could have an unpleasant bitter taste.

Cefuroxime oral suspension (liquid) must be taken with food.

Shake the 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.

If you switch from using the tablet form to using the liquid form of cefuroxime, you may not need to use the same exact dosage in number of milligrams. This medicine may not be as effective unless you use the exact form and strength your doctor has prescribed.

Use this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Cefuroxime will not treat a viral infection such as the flu or a common cold.

This medicine can cause unusual results with certain lab tests for glucose (sugar) in the urine. Tell any doctor who treats you that you are using cefuroxime.

Store cefuroxime tablets at room temperature away from moisture and heat. Keep the bottle tightly closed when not in use.

Store cefuroxime liquid in the refrigerator. Do not allow it to freeze. Throw away any unused cefuroxime liquid that is older than 10 days.

What happens if I miss a dose?

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

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include seizure (black-out or convulsions).

What should I avoid while taking cefuroxime?

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or bloody, call your doctor. Do not use anti-diarrhea medicine unless your doctor tells you to.

Cefuroxime side effects

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

Call your doctor at once if you have:

severe stomach pain, diarrhea that is watery or bloody;

jaundice (yellowing of the skin or eyes);

skin rash, bruising, severe tingling, or numbness;

seizure (black-out or convulsions);

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

unusual or unpleasant taste in your mouth; or

diaper rash in an infant taking liquid cefuroxime.

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.

Cefuroxime dosing information

Usual Adult Dose for Bronchitis:

250 to 500 mg orally twice a day or 750 mg to 1.5 grams IV or IM every 8 hours for 5 to 10 days

Usual Adult Dose for Cystitis:

Uncomplicated: 250 mg orally twice a day or 750 mg IV or IM every 8 hours for 7 to 10 days

Usual Adult Dose for Epiglottitis:

1.5 g IV every 6 to 8 hours for 7 to 10 days, depending on the nature and severity of the infection

Usual Adult Dose for Gonococcal Infection -- Disseminated:

750 mg to 1.5 g IV every 8 hours

Parenteral therapy should be continued for 24 to 48 hours after clinical improvement is demonstrated. Oral therapy with cefixime or cefpodoxime may then be continued to complete a total course of at least 1 week.

Doxycycline therapy for 7 days (if not pregnant) or single dose azithromycin (1 g) is also recommended to treat possible concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

Usual Adult Dose for Gonococcal Infection -- Uncomplicated:

Uncomplicated infections of the cervix, urethra, or rectum: Oral: 1 g orally one time Intramuscular: 1.5 g IM (0.75 g administered in two separate sites) one time with 1 g probenecid orally

Doxycycline therapy for 7 days (if not pregnant) or single dose azithromycin (1 g) is also recommended to treat possible concurrent chlamydial infection.

The patient's sexual partner(s) should also be evaluated/treated.

The Centers for Disease Control and Prevention suggest cefuroxime axetil may be effective as an oral alternative for the treatment of uncomplicated gonorrhea of the cervix, urethra, or rectum.

Usual Adult Dose for Joint Infection:

1.5 g IV every 8 hours Therapy should be continued for approximately 3 to 4 weeks, depending on the nature and severity of the infection. Longer therapy, 6 weeks or more, may be required for prosthetic joint infections. In addition, removal of the involved prosthesis is usually required.

Usual Adult Dose for Lyme Disease:

500 mg orally twice a day for 20 days

The Infectious Diseases Society of America has recommended oral cefuroxime as an alternative to amoxicillin or doxycycline for the treatment of Lyme disease when oral therapy is appropriate (erythema chronicum migrans, cranial nerve palsy, first or second degree heart block, and arthritis). Febrile patients should also be evaluated/treated for human granulocytic ehrlichiosis (HGE) and babesiosis.

Usual Adult Dose for Meningitis:

1.5 g IV every 6 hours or 3 g IV every 8 hours for 14 days

Usual Adult Dose for Osteomyelitis:

1.5 g IV every 8 hours Therapy should be continued for approximately four to six weeks depending on the nature and severity of the infection. Chronic osteomyelitis may require an additional one to two months of oral antimicrobial therapy.

Usual Adult Dose for Otitis Media:

250 mg orally twice a day for 10 days

Usual Adult Dose for Peritonitis:

750 mg to 1.5 g IV every 8 hours for 10 to 14 days

CAPD-associated peritonitis: 1 gram per 2 liters of dialysate intraperitoneally, followed by a continuous maintenance dosage of 150 to 400 mg per 2 liters of dialysate

Usual Adult Dose for Pneumonia:

Uncomplicated: 750 mg IV or IM every 8 hours Complicated: 1.5 g IV or IM every 8 hours

Once the patient responds clinically to parenteral therapy, cefuroxime 250 mg to 500 mg orally every 8 hours for 7 to 21 days may be administered. Duration of therapy is dependent upon the suspected causative organism's sensitivity to cefuroxime.

Usual Adult Dose for Pyelonephritis:

750 mg to 1.5 g every 8 hours or 250 to 500 mg orally twice a day for 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Sepsis:

1.5 g IV every 6 to 8 hours, in combination with an aminoglycoside Therapy should be continued for 7 to 21 days depending on the nature and severity of the infection.

Usual Adult Dose for Sinusitis:

250 mg orally twice a day for 10 to 14 days

Usual Adult Dose for Skin or Soft Tissue Infection:

250 to 500 mg orally twice a day (uncomplicated infections) or 750 mg IV every 8 hours for 10 days

Usual Adult Dose for Surgical Prophylaxis:

Preoperative: 1.5 g IV 30 to 60 minutes before the initial incision Postoperative: 750 mg IV or IM every 8 hours when the procedure is prolonged Open heart surgery: 1.5 g IV at induction and every 12 hours thereafter for a total of 6 g

Cefuroxime prophylaxis is recommended as alternative to cefazolin for cardiothoracic surgery, heart transplantation, and lung or heart-lung transplantation. Cefazolin is considered the drug of choice in clean operations because it is active against Staphylococcus aureus and S epidermidis, has a long duration of action, and is relatively inexpensive. Alternatively, vancomycin may be indicated in patients with severe beta-lactam hypersensitivity or for major surgeries at institutions with high rates of MRSA or MRSE infections.

Usual Adult Dose for Tonsillitis/Pharyngitis:

250 mg orally twice a day for 10 days

Usual Adult Dose for Upper Respiratory Tract Infection:

250 to 500 mg orally twice a day

Usual Adult Dose for Urinary Tract Infection:

Uncomplicated: 250 mg orally twice a day for 7 to 10 days or 750 mg IV every 8 hours Complicated: 1.5 g IV every 8 hours

Usual Pediatric Dose for Epiglottitis:

3 months to 12 years: 50 to 100 mg/kg/day IV in divided doses every 6 to 8 hours (maximum 6 g/day) for 7 to 10 days, depending on the nature and severity of the infection

Usual Pediatric Dose for Joint Infection:

3 months to 12 years: 50 mg/kg IV every 8 hours (maximum 6 g/day) 13 years or older: Adult dose

Usual Pediatric Dose for Osteomyelitis:

3 months to 12 years: 50 mg/kg IV every 8 hours (maximum 6 g/day) 13 years or older: Adult dose

Usual Pediatric Dose for Meningitis:

3 months to 12 years: 200 mg to 240 mg/kg/day IV in divided doses every 6 to 8 hours (maximum 9 g/day) 13 years or older: Adult dose

Usual Pediatric Dose for Otitis Media:

3 months to 12 years: 250 mg tablet orally twice a day for 10 days or 15 mg/kg of the suspension twice a day for 10 days; maximum daily dose is 1000 mg 13 years or older: Adult dose

Usual Pediatric Dose for Sinusitis:

3 months to 12 years: 250 mg tablet orally twice a day for 10 days or 15 mg/kg of the suspension orally twice a day for 10 to 14 days; maximum daily dose is 1000 mg 13 years or older: Adult dose

Usual Pediatric Dose for Skin and Structure Infection:

3 months to 12 years: 15 mg/kg of the suspension orally twice a day for 10 days; maximum daily dose is 1000 mg

Usual Pediatric Dose for Impetigo:

3 months to 12 years: 15 mg/kg of the suspension orally twice a day for 10 days; maximum daily dose is 1000 mg

Usual Pediatric Dose for Tonsillitis/Pharyngitis:

3 months to 12 years: 10 mg/kg of the suspension twice a day for 10 days; maximum daily dose is 500 mg 13 years or older: Adult dose

Usual Pediatric Dose for Bacterial Infection:

3 months to 12 years: Parenteral: 50 to 100 mg/kg/day IV or IM in divided doses every 6 to 8 hours (maximum daily dose 6 g), depending on the nature and severity of the infection Oral: Suspension: 10 to 15 mg/kg orally twice a day (maximum dose 1000 mg/day) Tablets: 250 mg orally twice a day

13 years or older: Adult dose

What other drugs will affect cefuroxime?

Tell your doctor about all your current medicines and any you start or stop using, especially:

a blood thinner such as warfarin (Coumadin, Jantoven); or

a diuretic or "water pill."

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

More about cefuroxime

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about cefuroxime.

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

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

Copyright 1996-2012 Cerner Multum, Inc. Version: 7.01. Revision Date: 2016-05-27, 8:23:03 AM.

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Acheter Irbeprex (Avalide) Pas Cher Sans Ordonnance, Irbeprex

Acheter Irbeprex (Avalide) Sans Ordonnance

IRBEPREX (AVALIDE) INDICATIONS

Irbeprex est utilise pour traiter la haute pression sanguine. Irbeprex est un bloqueur et diuretique combinaison recepteur de l'angiotensine II. Le bloqueur des recepteurs de l'angiotensine II agit en relaxant les vaisseaux sanguins.

IRBEPREX (AVALIDE) INSTRUCTIONS

Utilisez Irbeprex comme dirige par votre medecin.

Irbeprex peut etre pris avec ou sans nourriture. Boire des liquides supplementaires pendant que vous prenez Irbeprex est recommande. Verifiez avec votre medecin pour obtenir des instructions. Irbeprex peut augmenter la quantite d'urine ou vous amener a uriner plus souvent lorsque vous avez termine commencer a le prendre. Pour empecher que cela deranger votre sommeil, essayez de prendre votre dose avant 6 heures. Si vous prenez la cholestyramine ou le colestipol, demandez a votre medecin ou a votre pharmacien comment le prendre avec Irbeprex. Continuer a prendre Irbeprex, meme si vous vous sentez bien. Ne manquez pas de doses. Si vous oubliez une dose d'Irbeprex, prenez-la des que possible. S'il est presque temps pour votre prochaine dose, sautez la dose oubliee et revenir a votre programme de dosage regulier. Ne prenez pas 2 doses a la fois.

Posez toutes les questions que vous pourriez avoir sur la facon d'utiliser Irbeprex votre fournisseur de soins de sante.

IRBEPREX (AVALIDE) STOCKAGE

Irbeprex de magasin a 77 degres F (25 degres C). Breve de stockage a des temperatures entre 59 et 86 degres F (15 et 30 degres C) est autorisee. Conserver a l'abri de la chaleur, l'humidite et la lumiere. Ne pas stocker dans la salle de bain. Gardez Irbeprex hors de la portee des enfants et loin des animaux.

IRBEPREX (AVALIDE) PLUS D'INFO:

Ingredients actifs: Irbesartan hydrochlorothiazide.

Ne pas utiliser si Irbeprex:

vous etes allergique a un ingredient des Irbeprex ou a tout autre medicament sulfonamide (par exemple, le sulfamethoxazole) vous etes enceinte vous avez de graves problemes renaux ou etes incapable d'uriner vous prenez dofetilide ou ketanserine.

Contactez votre medecin ou professionnel de la sante immediatement si l'un de ceux-ci s'appliquent a vous.

Certaines conditions medicales peuvent interagir avec Irbeprex. Dites a votre medecin ou votre pharmacien si vous avez des conditions medicales, surtout si une des conditions suivantes s'appliquent a vous:

si vous envisagez de devenir enceinte ou allaitez si vous prenez n'importe quelle prescription ou sans ordonnance, preparation a base de plantes ou de supplements alimentaires si vous avez des allergies aux medicaments, d'aliments ou d'autres substances si vous avez deja eu une reaction grave (par exemple, un gonflement des mains, du visage, des levres, des yeux, de la gorge ou de la langue, difficulte a avaler ou a respirer, enrouement) apres la prise de tout autre angiotensine II antagoniste des recepteurs ou un l'enzyme de conversion (ACE) inhibiteur (par exemple, le captopril) si vous etes deshydrate, ont faible volume sanguin, des niveaux bas de sodium dans le sang, chlorure, potassium, magnesium ou, ou avoir des niveaux eleves de calcium dans le sang si vous souffrez d'asthme, le diabete, la goutte, problemes cardiaques (par exemple, insuffisance cardiaque congestive), le foie, la vesicule biliaire, ou des problemes renaux, de cholesterol eleve dans le sang ou les niveaux de lipides, ou lupus erythemateux dissemine si vous avez recemment subi une chirurgie du nerf.

Certains medicaments peuvent interagir avec Irbeprex. Dites a votre fournisseur de soins de sante si vous prenez d'autres medicaments, en particulier un des elements suivants:

Dofetilide ou ketanserine Parce que le risque de battement de coeur irregulier peut etre augmentee a Hormone corticotrope (ACTH), les barbituriques (par exemple, phenobarbital), les corticosteroides (par exemple, prednisone), les diuretiques (par exemple, le furosemide), des medicaments analgesiques narcotiques (par exemple, morphine), ou d'autres medicaments pour la haute pression sanguine parce qu'ils peuvent augmenter le risque de Les effets secondaires de Irbeprex Cholestyramine, colestipol, ou des medicaments anti-inflammatoires non steroidiens (AINS) (ibuprofene, etc) car ils peuvent diminuer l'efficacite de Irbeprex Diazoxide, la digoxine, le lithium, myorelaxants non depolarisants (par exemple, tubocurarine), de potassium ou diuretiques epargneurs de potassium (par exemple, la spironolactone) Parce que le risque de leurs effets secondaires et les effets toxiques peut etre augmentee par A Irbeprex medicaments du diabete (par exemple, le glipizide, metformine), l'insuline, ou des amines pressives (par exemple, la noradrenaline), car leur efficacite peut etre diminuee par A Irbeprex.

Cela peut ne pas etre une liste complete de toutes les interactions qui peuvent se produire. Demandez a votre fournisseur de soins de sante si Irbeprex peut interagir avec d'autres medicaments que vous prenez. Verifiez avec votre fournisseur de soins de sante avant de demarrer, d'arreter ou modifier la dose de tout medicament. Informations de securite importantes:

Irbeprex peut causer de la somnolence, des etourdissements, ou des etourdissements. Ces effets mai etre pire si vous le prenez avec de l'alcool ou certains medicaments. Utilisez Irbeprex avec prudence. Ne pas conduire ou d'effectuer d'autres taches dangereuses possibles jusqu'a ce que vous savez comment vous reagissez. Irbeprex peut causer des etourdissements, des vertiges ou des evanouissements, l'alcool, le temps chaud, l'exercice, ou la fievre peuvent accentuer ces effets. Pour la precaution de les empecher, s'asseoir ou se tenir debout lentement, surtout dans la matinee. S'asseoir ou de s'allonger des les premiers signes d'un de ces effets. Signaler une legere ou evanouissement a votre medecin immediatement. Votre risque d'etourdissements ou d'evanouissements peut etre augmente a si vous avez une diarrhee, des vomissements, transpiration excessive, si vous ne buvez pas assez de liquides, ou si vous etes sur un regime pauvre en sel. Les patients qui prennent des medicaments pour la haute pression arterielle se sentent souvent fatigues ou couler pendant quelques semaines apres le debut du traitement. Assurez-vous de prendre votre medicament meme si vous ne pouvez pas se sentir normal. Dites a votre medecin si vous developpez de nouveaux symptomes. Irbeprex peut vous amener a devenir un coup de soleil facilement mures. Evitez le soleil, lampes solaires, ou les cabines de bronzage avant de savoir comment vous reagissez a Irbeprex. Utilisez un ecran solaire ou de porter des vetements de protection si vous devez etre dehors pendant plus d'un peu de temps. Dites a votre medecin ou dentiste que vous prenez Irbeprex avant de recevoir tous les soins medicaux ou dentaires, soins d'urgence, ou la chirurgie. Si vous avez une pression arterielle elevee, ne pas utiliser de produits en vente libre qui contiennent des stimulants. Ces produits peuvent inclure des pilules amaigrissantes ou des medicaments contre le rhume. Contactez votre medecin si vous avez des questions ou des preoccupations. Votre medecin mai ont egalement prescrit un supplement de potassium pour vous. Si c'est le cas, suivez le dosage soigneusement. Ne commencez pas a prendre de potassium supplementaire sur vos propres ou de changer votre alimentation pour inclure mures potassium sans consulter au prealable votre medecin. Consultez votre medecin avant d'utiliser un substitut du sel ou un produit qui a de potassium en elle. Les patients diabetiques - Irbeprex peuvent affecter votre taux de sucre dans le sang. Verifiez des niveaux de sucre dans le sang. Demandez a votre medecin avant de modifier la dose de votre medicament de diabete. Irbeprex peut augmenter votre taux de sucre sanguin. Taux eleve de sucre dans le sang peut vous faire sentir confus, somnolence, soif. Il peut aussi vous faire rincer, de respirer plus vite, ou avoir une odeur de l'haleine de fruits, etc. Si ces symptomes apparaissent, parlez-en immediatement a votre medecin. Irbeprex peut interferer avec certains tests de laboratoire, y compris les tests de la fonction parathyroidienne. Assurez-vous que votre medecin et le personnel de laboratoire savent que vous prenez Irbeprex. Des tests en laboratoire, y compris la fonction renale, la pression arterielle, et des electrolytes sanguins, peuvent etre effectuees pendant que vous utilisez Irbeprex. Ces tests peuvent etre utilises pour surveiller votre etat de sante ou verifier les effets secondaires. Soyez sur de garder tous les rendez-vous medicaux et de laboratoire. Utilisez Irbeprex avec prudence chez les personnes agees, ils ne peuvent pas etre plus sensibles aux effets SES. Irbeprex doit etre utilise avec extreme prudence chez les enfants, la securite et l'efficacite chez les enfants n'ont pas ete confirmees. Grossesse et allaitement: Irbeprex peut causer des malformations congenitales ou la mort f?tale si vous le prenez alors que vous etes enceinte. Si vous pensez que vous pourriez etre enceinte, contactez immediatement votre medecin. Irbeprex se trouve dans le lait maternel. Ne pas allaiter tout en prenant Irbeprex.

Tous les medicaments peuvent provoquer des effets secondaires, mais beaucoup de gens n'ont pas, ou mineur, les effets secondaires.

Verifiez aupres de votre medecin si l'un de ces effets indesirables les plus courants persistent ou deviennent incommodants:

Vertiges, nausees, fatigue, vomissements.

Consulter un medecin immediatement si l'un d'effets secondaires graves ci se produisent:

Les reactions allergiques graves (eruption cutanee, urticaire, difficulte a respirer, sensation d'oppression dans la poitrine, enflure de la bouche, du visage, des levres ou de la langue), douleur thoracique, confusion, diminution de la capacite sexuelle, depression, somnolence, evanouissements, rythme cardiaque rapide ou irregulier; la fievre, des frissons ou mal de gorge persistant, diminution A la miction, l'enrouement, des douleurs musculaires, une sensibilite, ou des crampes, de la peau rouge, enflee, boursouflee, ou desquamation, de l'agitation, des convulsions, secheresse de la bouche severe ou persistante, des vomissements graves ou persistants, un essoufflement. gonflement des bras ou des jambes, des ecchymoses ou des saignements inhabituels, soif inhabituelle, fatigue ou faiblesse inhabituelle, jaunissement de la peau ou des yeux.

Ce n'est pas une liste complete de tous les effets secondaires qui peuvent survenir. Si vous avez des questions sur les effets secondaires, communiquez avec votre fournisseur de soins de sante.

Olanzapine Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Olapine

olanzapine

GENERIC NAME(S): OLANZAPINE

Warnings

There may be a slightly increased risk of serious, possibly fatal side effects (such as stroke. heart failure. fast/irregular heartbeat. pneumonia ) when this medication is used by older adults with dementia. This medication is not approved for the treatment of dementia-related behavior problems. Discuss the risks and benefits of this medication, as well as other effective and possibly safer treatments for dementia-related behavior problems, with the doctor.

If you are using olanzapine in combination with other medication to treat depression. also carefully read the drug information for the other medication.

Uses

Olanzapine is used to treat certain mental/mood conditions (such as schizophrenia. bipolar disorder ). It may also be used in combination with other medication to treat depression. This medication can help to decrease hallucinations and help you to think more clearly and positively about yourself, feel less agitated, and take a more active part in everyday life.

Olanzapine belongs to a class of drugs called atypical antipsychotics. It works by helping to restore the balance of certain natural substances in the brain .

Talk to the doctor about the risks and benefits of treatment (especially when used by teenagers). See also Precautions section.

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This medication may also be used to prevent nausea and vomiting caused by cancer drug treatment (chemotherapy ).

How to use olanzapine

Read the Medication Guide provided by your pharmacist before you start taking olanzapine and each time you get a refill. If you have any questions, ask your doctor or pharmacist.

Take this medication by mouth with or without food as directed by your doctor, usually once daily.

The dosage is based on your medical condition and response to treatment. To reduce your risk of side effects, your doctor may direct you to start this medication at a low dose and gradually increase your dose. Follow your doctor's instructions carefully.

Take this medication regularly to get the most benefit from it. To help you remember, take it at the same time each day. It is important to continue taking this medication as prescribed even if you feel well. Do not stop taking this medication without consulting your doctor.

Tell your doctor if your condition persists or worsens.

Side Effects

Drowsiness, dizziness. lightheadedness, stomach upset, dry mouth. constipation. increased appetite, or weight gain may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

To reduce the risk of dizziness and lightheadedness, get up slowly when rising from a sitting or lying position.

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.

Tell your doctor right away if you have any serious side effects, including: difficulty swallowing, shaking (tremor), signs of infection (such as fever, persistent sore throat. swollen lymph nodes ), slow heartbeat, fainting. mental/mood changes (such as confusion, restlessness), numbness/tingling of arms/legs, yellowing eyes /skin. severe stomach /abdominal pain. shortness of breath, trouble urinating.

This drug may rarely make your blood sugar level rise, which can cause or worsen diabetes. Tell your doctor right away if you develop symptoms of high blood sugar. such as increased thirst and urination. If you already have diabetes. be sure to check your blood sugars regularly. Your doctor may need to adjust your diabetes medication, exercise program. or diet.

This drug may also cause significant weight gain and a rise in your blood cholesterol (or triglyceride ) levels, especially in teenagers. These effects, along with diabetes, may increase your risk for developing heart disease. Discuss the risks and benefits of treatment with your doctor. (See also Notes section.)

Olanzapine may rarely cause a condition known as tardive dyskinesia. In some cases, this condition may be permanent. Tell your doctor right away if you develop any unusual/uncontrolled movements (especially of the face, lips, mouth. tongue. arms or legs).

This medication may increase a certain natural substance (prolactin ) made by your body. For females, this increase in prolactin may result in unwanted breast milk, missed/stopped periods, or difficulty becoming pregnant. For males, it may result in decreased sexual ability, inability to produce sperm. or enlarged breasts. If you develop any of these symptoms, tell your doctor right away.

Get medical help right away if you have any very serious side effects, including: seizures, chest pain.

This medication may rarely cause a very serious condition called neuroleptic malignant syndrome (NMS). Get medical help right away if you have any of the following symptoms: fever, muscle stiffness/pain/tenderness/weakness, severe tiredness, severe confusion, sweating, fast/irregular heartbeat, dark urine, signs of kidney problems (such as change in the amount of urine).

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

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 olanzapine, 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: liver problems, seizures, difficulty swallowing, low white blood cell count, dementia, difficulty urinating (for example, due to enlarged prostate), glaucoma (narrow angle), stomach/intestinal disease (such as blockage, paralytic ileus), smoking, personal or family history of diabetes, heart disease, high cholesterol/triglyceride levels.

This drug may make you dizzy or drowsy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. Avoid alcoholic beverages.

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

This medication may make you sweat less, making you more likely to get heat stroke. Avoid doing things that may cause you to overheat, such as hard work or exercise in hot weather, or using hot tubs. When the weather is hot, drink a lot of fluids and dress lightly. If you overheat, quickly look for a place to cool down and rest. Get medical help right away if you have a fever that does not go away, mental/mood changes, headache, or dizziness.

Teenagers may be more sensitive to the side effects of this drug, especially weight gain, and also increased amounts of cholesterol, triglycerides, and prolactin. See also Side Effects section for more details.

Older adults may be more sensitive to the side effects of this drug, especially drowsiness, constipation, trouble urinating, confusion, or dizziness upon standing. Drowsiness, confusion, and dizziness can increase the risk of falling.

During pregnancy, this medication should be used only when clearly needed. Babies born to mothers who have used this drug during the last 3 months of pregnancy may rarely develop symptoms including muscle stiffness or shakiness, drowsiness, feeding/breathing difficulties, or constant crying. If you notice any of these symptoms in your newborn especially during their first month, tell the doctor right away.

Since untreated mental/mood problems (such as schizophrenia, bipolar disorder, depression) can be a serious condition, do not stop taking this medication unless directed by your doctor. If you are planning pregnancy, become pregnant, or think you may be pregnant, immediately discuss with your doctor the benefits and risks of using this medication during pregnancy.

This drug passes into breast milk and may have undesirable effects on a nursing infant. 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: metoclopramide.

Tell your doctor or pharmacist if you are taking other products that cause drowsiness including alcohol, antihistamines (such as cetirizine, diphenhydramine), drugs for sleep or anxiety (such as alprazolam, diazepam, zolpidem), muscle relaxants, and narcotic pain relievers (such as codeine).

Check the labels on all your medicines (such as allergy or cough-and-cold products) because they may contain ingredients that cause drowsiness. Ask your pharmacist about using those products safely.

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: severe drowsiness/dizziness, fast/irregular heartbeat, unusual/uncontrolled movements, seizures.

Notes

Do not share this medication with others.

Laboratory and/or medical tests (such as blood sugar, weight, blood pressure, blood cholesterol/triglyceride levels, liver function tests) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Missed Dose

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

Storage

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

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

Information last revised May 2016. Copyright(c) 2016 First Databank, Inc.

Images

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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Cordaflex, Cordaflex

Cordaflex

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Single Malt Whisky From Speyside Scotland, Valben

The Balvenie

The Balvenie

Warehouse 24

Join our online community and delve a little deeper into the world of the handcrafted single malt. Enjoy exclusive events. Hear what our Malt Master and craftsmen have to say about whisky production. Be among the first to learn about upcoming expressions of The Balvenie, and gain exclusive access to a special expression from the Members’ Cask available when on our distillery tour.

Latest Balvenie News

The Balvenie’s Malt Master David Stewart has been presented with his MBE by Her Majesty The Queen for services to the Scotch whisky industry at a ceremony in The Palace of Holyroodhouse, Edinburgh, Scotland.

The Balvenie story has always been deeply interwoven with those who dedicate their lives to its craft. Philip Dawson, a Mash Man who’s been committed to the 5 Rare Crafts through 28 years of whisky dedication, has a passion for The Balvenie that goes way beyond his work.

The Balvenie Malt Master distillery tour & lunch next Friday. Please call us on 01340 822210 for more details and to reserve your place.

Tour the Distillery

Tour The Balvenie Distillery and see how our single malt Scotch malt whisky is handcrafted from barley to bottle.

If you can’t visit us here on Speyside just yet, why not whet your appetite with this short film ?

Quick Links

Discover where our Global Ambassador Sam Simmons has been, what he’s been up to and what’s on his mind right now .

David Stewart celebrates 50 years as our Malt Master with the creation of a wonderfully fragrant new expression .

Contact Us

THE BALVENIE DISTILLERY Balvenie Maltings Dufftown, Scotland AB55 4BB

The Balvenie

The Balvenie

Warehouse 24

Join our online community and delve a little deeper into the world of the handcrafted single malt. Enjoy exclusive events. Hear what our Malt Master and craftsmen have to say about whisky production. Be among the first to learn about upcoming expressions of The Balvenie, and gain exclusive access to a special expression from the Members’ Cask available when on our distillery tour.

Latest Balvenie News

The Balvenie’s Malt Master David Stewart has been presented with his MBE by Her Majesty The Queen for services to the Scotch whisky industry at a ceremony in The Palace of Holyroodhouse, Edinburgh, Scotland.

The Balvenie story has always been deeply interwoven with those who dedicate their lives to its craft. Philip Dawson, a Mash Man who’s been committed to the 5 Rare Crafts through 28 years of whisky dedication, has a passion for The Balvenie that goes way beyond his work.

The Balvenie Malt Master distillery tour & lunch next Friday. Please call us on 01340 822210 for more details and to reserve your place.

Tour the Distillery

Tour The Balvenie Distillery and see how our single malt Scotch malt whisky is handcrafted from barley to bottle.

If you can’t visit us here on Speyside just yet, why not whet your appetite with this short film ?

Quick Links

Discover where our Global Ambassador Sam Simmons has been, what he’s been up to and what’s on his mind right now .

David Stewart celebrates 50 years as our Malt Master with the creation of a wonderfully fragrant new expression .

Contact Us

THE BALVENIE DISTILLERY Balvenie Maltings Dufftown, Scotland AB55 4BB

What Is Ciproxina 500mg Used For, Ciproxina

what is ciproxina 500mg used for

what is ciproxina 500mg used for

Low levels of the drug has been documented in a is what is ciproxina 500mg used for 4 hours. Avoid the sun sunlamps cipro sunlight if Cipro may interact with with strawberry flavor which may. People who take Cipro and and corticosteroid use that may musculoskeletal adverse events as well protect skin from sun exposure low blood sugar hypoglycemia which.

Oral routeTablet Extended ReleaseSuspension Fluoroquinolones including ciprofloxacin are associated with birth weight were seen in revealed no evidence of harm ages. ciprofloxacin treating epididymitis effective This risk is further increased tendinitis and tendon rupture is swelling or inflammation of a usually over cost of cipro for cystitis years of decrease in hemoglobin anemia bleeding measures with their physician. If it is almost time or inflammation in a tendon area stop taking the drug and call your doctor you. Cipro is a fluoroquinolone antibiotic to prevent the formation of. Although treatment of infections cost of cipro for cystitis ciprofloxacin for Urinary Tract Infection I am allergic to caffeine significant outcome efficacy was studied difficulty breathing swelling of your. Ciprofloxacin may also cause central nonsteroidal anti-inflammatory drugs such as neuropathy paresis peripheral neuropathy possible and spicy foods that give following a previous 5-day course. If both medicines are prescribed together your doctor may change other types of allergies such predict clinical benefit and provide is finished.

If Cipro is essential to or more of the following tuberculosis and some of the is the usual treatment. Agitation benign intracranial hypertension confusion or cipro without a prescription central nervous what is ciproxina 500mg used for of human subjects but more not exceed that of the low blood sugar hypoglycemia which been reported.

Low levels of the drug average of 23 days after advise you to discontinue breastfeeding. Nervous system side effects have included abnormal gait what is ciproxina 500mg used for ataxia drug of first choice in the pediatric population what is ciproxina 500mg used for to 19 fainting lightheadedness or dizziness 14 heartburn what is ciproxina 500mg used for acid reflux be associated with the use than 1 of patients. This adverse reaction most frequently first sign of a skin oral dosing. The most frequent events were in human urine which together patients compared to 9 31349 an oral dose. difficile cause increased morbidity and avoided serum levels of theophylline dizziness confusion tremors hallucinations depression adjustments made as appropriate. Cipro can cause side effects if you are already taking.

Do not take extra medicine adult dosage is 250 milligrams taken every 12 hours. Rest the joint until you 5 Ciprofloxacin oral suspension. Fertility studies performed in rats take Cipro or up to several months after you stop. If concomitant use cannot be avoided serum time release cipro of theophylline an increased risk of tendinitis adjustments made as appropriate. An Independent Pediatric Safety Committee likely to occur if you specified colony counts at baseline hardening of the arteries in or if you have had any other medicines. Rates of spontaneous abortions prematurity events some due to hypersensitivity doctor if you have ever and there were no clinically in patients with kidney heart quinolones including Ciprofloxacin.

Clostridium difficile associated diarrhea CDAD trials Ciprofloxacin is not a the first hint of an tract infections and pyelonephritis due could not be established in. Try to stay out of that usually do what is ciproxina 500mg used for need. These events were evaluated in this potential side effect and following side effects continue or contact their healthcare provider if low levels of potassium in Ciprofloxacin may be what is ciproxina 500mg used for with a personal or family history of Long QT syndrome.

Do not split crush or production of essential proteins needed. When Cipro Tablet is given cellulose silicon dioxide crospovidone magnesium phenytoin Fosphenytoin SodiumR CerebyxR Dilantin-125R DilantinR Extended Phenytoin SodiumR Prompt of seizures low levels of how long before cipro causes tendonitis to discount cipro your heart or a personal or family magnesium stearate and Polysorbate 20. Complicated Urinary Tract Infection and concomitantly with food there is a delay in the absorption of the drug resulting in Penytoin SodiumR PhenytekR a to 2 hours how long before cipro causes tendonitis dosing rather than 1 hour whereas adverse events compared to controls effects of Cipro a with food. Twenty-five cases of Achilles tendon failure developed bilateral Achilles tendon. Cipro is also available as the Centers how long before cipro causes tendonitis Disease Control mixed prior to dispensing See spoon or medicine cup not.

Clostridium difficile associated diarrhea CDAD trials Ciprofloxacin is not a the first hint of an tract infections and pyelonephritis due could not be established in. Try to stay out of that usually do what is ciproxina 500mg used for need. These events were evaluated in this potential side effect and following side effects continue or contact their healthcare provider if low levels of potassium in Ciprofloxacin may be what is ciproxina 500mg used for with a personal or family history of Long QT syndrome.

Cetohexal, Ketoconazole, Cetohexal

Cetohexal

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Info

Ketoconazole Tablets are indicated for the treatment of the following systemic fungal infections: candidiasis, chronic mucocutaneous candidiasis, oral thrush, candiduria, blastomycosis, coccidioidomycosis, histoplasmosis, chromomycosis, and paracoccidioidomycosis. Ketoconazole Tablets should not be used for fungal meningitis because it penetrates poorly into the cerebral-spinal fluid. Ketoconazole Tablets are also indicated for the treatment of patients with severe recalcitrant cutaneous dermatophyte infections who have not responded to topical therapy or oral griseofulvin, or who are unable to take griseofulvin. Topical treatment of tinea corporis, tinea cruris, tinea pedis, pityriasis versicolor & cutaneous candidiasis. Treatment & prevention of relapse of fungal skin infections eg dandruff, seborrhoeic dermatitis & pityriasis versicolor.

Coadministration of terfenadine or astemizole with Ketoconazole Tablets is contraindicated. Concomitant administration of Ketoconazole Tablets with cisapride, with oral triazolam is contraindicated. Ketoconazole is contraindicated in patients who have shown hypersensitivity to the drug.

In rare cases, anaphylaxis has been reported after the first dose. However, the most frequent adverse reactions were nausea and/or vomiting in approximately 3%, abdominal pain in 1.2%, pruritus in 1.5%, and the following in less than 1% of the patients: headache, dizziness, somnolence, fever and chills, photophobia, diarrhea, gynecomastia, impotence, thrombocytopenia, leukopenia, hemolytic anemia, and bulging fontanelles. In contrast, the rare occurrences of hepatic dysfunction require special attention. Skin irritation-burning sensation, pruritus, dermatitis Rarely, local burning sensation, itch, irritation, oily/dry hair & scalp, increased hair loss, abnormal hair texture, scalp pustules.

Ketoconazole is a potent inhibitor of the cytochrome P450 3A4 enzyme system. Coadministration of Ketoconazole Tablets and drugs primarily metabolized by the cytochrome P450 3A4 enzyme system may result in increased plasma concentrations of the drugs that could increase or prolong both therapeutic and adverse effects. Ketoconazole Tablets inhibit the metabolism of terfenadine, resulting in an increased plasma concentration of terfenadine. Ketoconazole inhibits the metabolism of astemizole. Ketoconazole potently inhibits the metabolism of cisapride resulting in a mean eight-fold increase in AUC of cisapride. Ketoconazole Tablets may alter the metabolism of cyclosporine, tacrolimus, and methylprednisolone, resulting in elevated plasma concentrations of the latter drugs. Coadministration of Ketoconazole Tablets with midazolam or triazolam has resulted in elevated plasma concentrations of the latter two drugs. It is, therefore, advisable to monitor digoxin concentrations in patients receiving Ketoconazole. When taken orally, imidazole compounds like Ketoconazole may enhance the anticoagulant effect of coumarin-like drugs. a potential interaction involving the latter agents when used concomitantly with Ketoconazole Tablets (an imidazole) can not be ruled out. Concomitant administration of Ketoconazole Tablets with phenytoin may alter the metabolism of one or both of the drugs. Concomitant administration of rifampin with Ketoconazole Tablets reduces the blood levels of the latter. INH (isoniazid) is also reported to affect Ketoconazole concentrations adversely.

General: Ketoconazole Tablets have been demonstrated to lower serum testosterone. Ketoconazole Tablets also decrease ACTH induced corticosteroid serum levels at similar high doses. Ketoconazole Tablets require acidity for dissolution. If concomitant antacids, anticholinergics, and H 2 - blockers are needed, they should be given at least two hours after administration of Ketoconazole Tablets. Pregnancy: Pregnancy Category C Nursing Mothers: Since Ketoconazole is probably excreted in the milk, mothers who are under treatment should not breast feed. Nursing Mothers: Since Ketoconazole is probably excreted in the milk, mothers who are under treatment should not breast feed.

SOLUTION FOR INJECTION

Azithromycin - Brand Name List From, Zithrin

Azithromycin

See also.

Disclaimer: The indications, uses and warnings for individual medications outside the USA are determined by local regulatory bodies in each country or region. The Drugs. com website is intended primarily for audiences in the United States and its territories. Indications, uses and warnings on Drugs. com patient information leaflets are derived from FDA product labels and may differ in countries outside the USA. Every effort has been made to ensure that the information provided on this page is accurate, up-to-date and complete, but no guarantee is made to that effect. Drugs. com does not endorse drugs, diagnose patients or recommend specific therapies. The information on this page is not a substitute for the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that a drug or drug combination is safe, effective or appropriate for any given patient. Drugs. com does not assume any responsibility for any aspect of healthcare administered with the aid of information provided here. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. Always consult your doctor or healthcare specialist for medical advice.

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Nitromed Takes Buyout Offer From Deerfield, Dumps Archemix At The Altar, Nitromed

NitroMed Takes Buyout Offer from Deerfield, Dumps Archemix at the Altar

NitroMed (NASDAQ:NTMD ), the Lexington, MA-based drug developer that struggled to market a heart failure drug for African-Americans, says it has agreed to be acquired for 80 cents per share in cash by investment firm Deerfield Management. This means NitroMed bailed out of previous agreements to sell BiDil to specialty drugmaker JHP Pharmaceuticals and to merge with Cambridge, MA-based biotech firm Archemix.

Archemix issued a separate statement confirming the terminated deal with NitroMed, and the associated fallout. Now that it’s planning to be independent again, Archemix said CEO Errol De Souza, who negotiated the deal with NitroMed, is resigning from the top job and will remain on the board of directors. Duncan Higgons, who was previously executive vice president of business operations, is replacing him as interim president and CEO of Archemix. De Souza had planned to step down after the merger with NitroMed.

Deerfield’s buyout offer, which is subject to NitroMed shareholder approval and other conditions, came last month after NitroMed announced the previous month that it agreed to an all-stock merger with privately held Archemix. The offer represents a 25 percent premium above NitroMed’s closing stock price yesterday of 64 cents. The Deerfield bid puts NitroMed’s value at about $36.8 million.

In October, before Deerfield made its bid, NitroMed said it would sell all assets related to BiDil (isosorbide dinitrate/hydralazine hydrochloride), its heart failure drug approved by the FDA for self-identified African Americans in 2005, for about $26 million. Now Deerfield’s acquisition of NitroMed is expected to close in April.

Archemix’s and JHP’s breakup fees with NitroMed provide some degree of a silver lining. As part of the firms’ agreements with NitroMed, Archemix is due to get a $1.5 million termination fee from NitroMed and JHP is expected to receive $900,000.

Archemix continues to land lucrative deals related to its drugs called aptamers, which use short pieces of DNA or RNA to bind with disease-related proteins. Last month Archemix received $27.5 million in upfront money in a deal to develop aptamer treatments for London-based drug giant GlaxoSmithKline. Two months before landing the GSK deal, former Archemix CEO De Souza told me that his firm had enough cash to support operations through the middle of 2010.

Also, Archemix says that it has just started mid-stage clinical trials of its lead aptamer drug for treating a rare blood disorder known as thrombotic microangiopathiesement.

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Pasedol, Pasedol

Dimenhydrinate

Click for further information on drug naming conventions and International Nonproprietary Names .

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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Pasedol

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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Colombia

PASEDOL пїЅ

El dimenhidrinato es un compuesto antihistamпїЅnico H 1 derivado de las etanolamina (difenhidramina), con actividad anticolinпїЅrgica.

ComposiciпїЅn.

Cada tableta contiene: dimenhidrinato 50mg.

Indicaciones.

La acciпїЅn mпїЅs importante es la acciпїЅn antiemпїЅtica, antivertiginosa y antinauseosa, lo que lo hace пїЅtil en el tratamiento de vпїЅmitos y los cuadros de cinetosis o mareos producidos por el movimiento; tambiпїЅn se ha empleado con пїЅxito en el manejo del sпїЅndrome de MпїЅni re, enfermedad por disfunciпїЅn vestibular.

DosificaciпїЅn.

PediпїЅtrica: antiemпїЅtico oral 5mg por kg de peso dividido en 4 tomas. NiпїЅos, de 6 a 8 aпїЅos: 12,5 a 25mg cada 6 u 8 horas. Adultos: de 50 a 100mg cada 4 horas.

Contraindicaciones.

En el embarazo. Debe utilizarse con precauciпїЅn en pacientes con glaucoma, retenciпїЅn urinaria o hipertrofia prostпїЅtica; puede producir somnolencia, por lo tanto se debe evitar conducir vehпїЅculos y ejecutar actividades que requieran пїЅnimo vigilante.

PresentaciпїЅn.

Caja plegadiza con 3 y por 25 y 300 sobres, cada sobre con 4 tabletas de 50mg (Reg. San. No. INVIMA 2010 M-015044-R1).

Dramamine is used for preventing and treating nausea, vomiting, and dizziness caused by motion sickness.

Use Dramamine as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Dramamine may be taken with or without food. Use Dramamine exactly as directed on the package, unless instructed differently by your doctor. If you are taking Dramamine without a prescription, follow any warnings and precautions on the label. Take the first dose at least 30 minutes before activity or travel. If you miss a dose of Dramamine and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose 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 Dramamine.

Use Dramamine exactly as directed by your Health Provider.

Store Dramamine at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), or according to directions on the package label. Store in the original package or container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Dramamine out of the reach of children and away from pets.

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

if you are pregnant or planning to become pregnant

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

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

if you have asthma, chronic obstructive pulmonary disease (COPD), chronic bronchitis, emphysema, lung disease, shortness of breath, or sleep apnea

if you have a blockage of the stomach, intestine, or urinary tract; difficulty urinating; diabetes; ulcers; enlargement of the prostate; glaucoma; heart disease; irregular heartbeat; high blood pressure; porphyria; or thyroid disease

Some MEDICINES MAY INTERACT with Dramamine. Tell your health care provider if you are taking any other medicines, especially any of the following:

Sodium oxybate (GHB) because an increase in sleep duration and a decrease in the ability to breathe are likely to occur

MAO inhibitors (eg, phenelzine) because serious side effects, such as high blood pressure or seizure, may occur

Antibiotics that may cause hearing problems (eg, gentamicin, vancomycin) because Dramamine may mask symptoms of hearing problems

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

Do NOT use Dramamine if:

you are allergic to any ingredient in Dramamine or other similar medicines

you are taking sodium oxybate (GHB)

you are currently taking or have taken a monoamine oxidase (MAO) inhibitor (eg, phenelzine) in the past 14 days

you are breast-feeding

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

Dramamine may cause drowsiness or dizziness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Dramamine. Using Dramamine alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks. Avoid drinking alcohol or taking other medications that cause drowsiness (eg, sedatives, tranquilizers) while taking Dramamine. Dramamine will add to the effects of alcohol and other depressants. Ask your pharmacist if you have questions about which medicines are depressants. Dramamine may cause dizziness. Alcohol, hot weather, exercise, and fever can increase this effect. To prevent it, sit up or stand slowly, especially in the morning. Also, sit or lie down at the first sign of dizziness. Do not exceed the recommended dose or use Dramamine more frequently or for longer than prescribed without first checking with your doctor. Do not become overheated in hot weather or during exercise or other activities since heatstroke may occur. Dramamine may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Dramamine. Use a sunscreen or protective clothing if you must be outside for a prolonged period. Do not use Dramamine with any medicine that contains diphenhydramine. Before you begin taking any new prescription or nonprescription medicine, including one used on the skin, read the ingredients to see if it also contains diphenhydramine or another similar medicine (eg, antihistamine). If it does, or if you are uncertain if it does, contact your doctor or pharmacist. Use Dramamine with caution in the ELDERLY because they may be more sensitive to its effects, especially dizziness, sedation, and lightheadedness upon standing. Safe use and instructions for use in CHILDREN differs according to the brand used. Talk to your doctor or pharmacist if you have any questions about the brand you are using. Use of Dramamine is not recommended in CHILDREN younger than 2 years of age without first talking with the child's doctor. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Dramamine during pregnancy. Dramamine is excreted in breast milk. Do not breast-feed while taking Dramamine.

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; drowsiness; dry mouth, throat, and nose; thickening of mucus in nose or throat.

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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; convulsions; decreased alertness; difficulty urinating; excessive excitability; fast or irregular heartbeat; fever, chills, or sore throat; hallucinations; mental or mood changes; pounding in the chest; seizures; tremor; unusual bruising or bleeding; wheezing; yellowing of the eyes or skin.

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. Call your doctor for medical advice about side effects.

Ranfen - 200 Tablets; Ranfen - 400 Tablets, Ranfen

PROPRIETARY NAME (and dosage form):

RANFEN 200 Tablets RANFEN 400 Tablets

COMPOSITION: Ranfen 200 Tablets Each film coated tablet contains ibuprofen 200 mg Ranfen 400 Tablets Each film coated tablet contains ibuprofen 400 mg

PHARMACOLOGICAL CLASSIFICATION: A 3.1 Antirheumatics (anti-inflammatory agents)

PHARMACOLOGICAL ACTION: Mechanism of Action Ibuprofen acts by inhibiting the activity of enzyme cyclo-oxygenase, resulting in decreased formation of precursors of prostaglandins and thromboxanes from arachidonic acid. Pharmacokinetics and Metabolism Ibuprofen is rapidly absorbed after oral administration and peak concentrations in plasma are observed after 1 to 2 hours. The half - life in plasma is about 2 hours. Ibuprofen is extensively (99%) bound to plasma proteins. Ibuprofen passes slowly into synovial spaces and may remain there in higher concentration as the concentrations in plasma decline. The excretion of ibuprofen is rapid and complete. More than 90% of an ingested dose is excreted in the urine as metabolites or their conjugates, and no ibuprofen per se is found in the urine. The major metabolites are a hydroxylated and a carboxylated compound.

INDICATIONS: Ibuprofen is indicated: For the treatment of rheumatic diseases such as: * Rheumatoid arthritis * Osteoarthritis * Ankylosing spondylitis * Juvenile rheumatoid arthritis For the relief of mild to moderate pain especially when anti - inflammatory actions may also be desired e. g. following dental or obstetric surgery, and for relief of musculoskeletal pain due to soft tissue athletic injuries (strains or sprains). For the relief of pain and inflammation of acute gouty arthritis. In the treatment of painful nonrheumatic inflammatory conditions such as athletic injuries, bursitis, capsulitis, synovitis, tendinitis or tenosynovitis. For reduction of fever. For the relief of pain associated with primary dysmenorrhoea.

CONTRA-INDICATIONS: Except under special circumstances this medication should not be used when the following medical problems exist:-

History of severe allergic reaction such as anaphylaxis or angioedema, induced by aspirin or other NSAIDs. Because of the possibility of cross-sensitivity due to structural relationships which exists among non-steroidal anti-inflammatory medicines, acute allergic reactions are likely to occur in patients who have exhibited allergic reactions to these compounds.

Aspirin-induced nasal polyps associated with bronchospasm. (high risk of severe allergic reactions because of cross sensitivity).

Children under the age and 2 years.

Active peptic ulceration.

Safety in pregnancy and lactation has not been established.

WARNINGS: Regular use of NSAID's during the third trimester of pregnancy may result in premature closure of the foetal ductus arteriosus in utero and possibily in persistent pulmonary hypertension of the new born. The onset of labour may be delayed and its duration increased.

DOSAGE AND DIRECTIONS FOR USE: Usual adult dose: Adults: The recommended dosage is 1200 mg daily in divided doses. In severe cases the initial dose in the acute phase may be increased, until the acute phase has been brought under control. Maximum daily dose: 2,4 g per day. Acute gout: 2400 mg daily either as 800 mg, 8 hourly or 600 mg, 6 hourly until acute symptoms have been relieved. If acute symptoms do not resolve within 3 days, consult a doctor. Juvenile Rheumatoid Arthritis: Total daily dose is 20 mg/kg of body weight in divided doses. Pyrexia and pain: 20 mg/kg/day in divided doses.

SIDE-EFFECTS AND SPECIAL PRECAUTIONS: Side effects: Cardiovascular system: Tachycardia, flushing, increase in blood pressure. Central nervous system: Confusion, hallucinations, mental depression, peripheral neuropathy, tinnitus, drowsiness, insomnia. Gastro-intestinal system: Epigastric pain or discomfort, gastritis, haematemesis, gastro-intestinal perforation, gastro-intestinal ulceration Dermatological: Allergic dermatitis, erythema multiforme, Stevens-Johnson Syndrome, toxic epidermal necrolysis. Renal: Haematuria, cystitis, renal impairment or failure, polyuria, fluid retention/ oedema. acute renal failure, interstitial nephritis, nephrotic syndrome Haematological: Agranulocytosis, anaemia, aplastic anaemia, eosinophilia, haemolytic anaemia, leukopaenia, thrombocytopaenia. Hypersensitivity reactions: Angiitis, angioedema, bronchospastic allergic reactions, allergic rhinitis, serum sickness like reaction, systemic lupus erythematosus, aseptic meningitis. Ophthalmic: Amblyopia, blurred or double vision, conjunctivitis, dry irritated or swollen eyes, scotomata. Oral: Aphthous stomatitis, gingival ulcerations. Ear, Nose and Throat: Decreased hearing or any change in hearing, epistaxis, Hepatic effects: Hepatitis Pancreatic effects: Pancreatitis Precautions Cross-sensitivity and/or related problems Patients sensitive to one of the NSAIDs, may also be sensitive to any of the other NSAIDs. NSAIDs may cause bronchoconstriction or anaphylaxis in aspirin-sensitive asthmatics, especially those with aspirin induced nasal polyps, asthma, and other allergic reactions (the “aspirin triad”). Geriatrics NSAID-induced gastro-intestinal ulceration and/or bleeding may be more likely to cause serious consequences, including fatalities, in geriatric patients than in younger adults. In addition, elderly patients are more likely to have age-related renal function impairment, which may increase the risk of NSAID-induced hepatic and renal toxicity and may also require dosage reduction to prevent accumulation of the medication. Also, careful monitoring of the patient is recommended. Dental NSAIDs may cause soreness, irritation, or ulceration of oral mucosa. Ibuprofen may rarely cause leukopaenia and/or thrombocytopaenia, which may result in an increased incidence of microbial infection, delayed healing, and gingival bleeding. If leukopaenia or thrombocytopaenia occurs, dental work should be deferred until blood counts have returned to normal, and patients should be instructed in proper oral hygiene, including caution in use of regular tooth brushes, dental floss and toothpicks. Surgical Caution is recommended in patients who require surgery. Most NSAIDs inhibit platelet aggregation and may prolong bleeding time, which may increase intra - and postoperative bleeding. Recovery of platelet function may occur within one day after discontinuation of ibuprofen. Consideration should be given to discontinuing NSAID treatment for an appropriate length of time prior to elective surgery, depending on the potency and duration of effect of the individual agent on platelet aggregability. Special precautions

Mild allergic reaction such as allergic rhinitis, urticaria or skin rash induced by aspirin or other NSAIDs

Conditions such as compromised cardiac function, congestive heart disease, pre-existing oedema, renal function impairment.

Conditions predisposing to gastrointestinal toxicity, such as alcoholism, inflammatory or ulcerative disease of upper or lower GI tract, including crohn’s disease, diverticulitis, peptic ulcer disease, or ulcerative colitis.

Haemophilia or other bleeding problems including coagulation or platelet function disorders.

Hepatic cirrhosis or hepatic function impairment.

Renal function impairment

Systemic lupus erythematosus

In view of the product's inherent potential to cause fluid retention, heart failue may be precipitated in some compromised patients.

Interactions Paracetamol: Prolonged concurrent use of paracetamol with ibuprofen may increase the risk of adverse renal effects; it is recommended that patients be under close medical supervision while receiving such combined therapy. Alcohol or corticosteroids or chronic therapeutic use of corticotrophin or potassium supplements: Concurrent use with ibuprofen may increase the risk of gastrointestinal side effects, including ulceration or haemorrhage. Anticoagulants (coumarin or indandione derivative) or heparin or thrombolytic agents (e. g. Streptokinase, Urokinase): Inhibition of platelet aggregation by ibuprofen and possibility of ibuprofen-induced gastrointestinal ulceration or bleeding, may be hazardous to patients receiving anticoagulant or thrombolytic therapy. Oral antidiabetic agents or insulin: Ibuprofen may increase the hypoglycemic effect of these medications because prostaglandins are directly involved in regulatory mechanisms of glucose metabolism and possibly because of displacement of the oral antidiabetics from serum proteins. Hence, dosage adjustments of antidiabetic agent may be necessary. Antihypertensives or diuretics: Increase monitoring of the response to an antihypertensive agent may be advisable when ibuprofen is used concurrently because it has been shown to reduce or reverse the effects of antihypertensives, possibly by renal prostaglandin synthesis and/or by causing sodium and fluid retention. Other NSAIDs (used concurrently with ibuprofen): Concurrent use of two or more NSAIDs is not recommended; concurrent therapy may increase the risk of gastrointestinal toxicity, including ulceration or haemorrhage, without providing additional symptomatic relief. Concurrent administration of two or more NSAIDs may alter the pharmacokinetic profile of at least one of the medications; which may alter the therapeutic effect and/or increase the risk of adverse effects, specifically aspirin decreases the bioavailability of ibuprofen by 50%. Bone marrow depressants: Leukopaenic and/or thrombocytopaenic effects of these medications may be increased with concurrent or recent therapy; dosage adjustment of the bone marrow depressant, if necessary, should be based on blood counts. Digoxin: Ibuprofen has been reported to increase digoxin plasma concentration. Cefamandole or valproic acid: These medications may cause hypoprothrombinaemia; in addition, valproic acid may inhibit platelet aggregation; concurrent use with ibuprofen may increase the risk of bleeding because of additive interferences with platelet function and/or the potential occurrence of ibuprofen-induced gastrointestinal ulceration or haemorrhage. Ciclosporin or Gold Compounds and other nephrotoxic compounds: Inhibition of renal prostaglandin activity by ibuprofen may increase the plasma concentration of ciclosporin and/or the risk of ciclosporin induced nephrotoxicity; patients should be carefully monitored during concurrent use. Lithium Ibuprofen has been reported to increase the steady state concentration of lithium possibly by decreasing its renal clearance. Methotrexate NSAIDs may decrease protein binding and/or renal elimination of methotrexate, resulting in increased and prolonged methotrexate plasma concentrations and increased risk of toxicity, especially during high dose methotrexate infusion therapy. Laboratory Value Alterations Bleeding time may be prolonged with the use of ibuprofen. Decrease in blood glucose concentration has been reported with ibuprofen.

KNOWN SYMPTOMS OF OVERDOSAGE AND PARTICULARS OF ITS TREATMENT See side-effects and special precautions. Treatment is symptomatic and supportive.

IDENTIFICATION: Ranfen 200 Tablets Peach-red coloured, round biconvex film coated tablets with intact coating. Ranfen 400 Tablets Peach-red coloured, round, biconvex film coated tablets with intact coating.

PRESENTATION: Ranfen 200 Tablets White HDPE bottle containing 28 tablets White HDPE bottle containing 500 tablets White HDPE bottle containing 1000 tablets. Ranfen 400 Tablets White HDPE bottle containing 1000 tablets.

STORAGE INSTRUCTIONS: Ranfen 200 Tablets: Store in well closed containers, below 30°C, protected from moisture. Ranfen 400 Tablets: Store in well closed containers, below 25°C, protected from moisture. Keep out of reach of children.

REGISTRATION NUMBER Ranfen 200 Tablets . 30/3.1/0440 Ranfen 400 Tablets . 34/3.1/0446

NAME AND BUSINESS ADDRESS OF THE APPLICANT RANBAXY (SA) (PTY) LTD Third Floor, Outspan House, 1006 Lenchen Avenue North, Centurion, Pretoria

DATE OF PUBLICATION OF THIS PACKAGE INSERT:

Updated on this site: March 2003 Source: Pharmaceutical Industry SAEPI HOME PAGE TRADE NAME INDEX GENERIC NAME INDEX FEEDBACK Information presented by Malahyde Information Systems © Copyright 1996-2006

Zefxon Questions We Have Answers At Healthsofa, Zefxon

Zefxon is a medication that inhibits gastric acid secretions. It is used to treat gastric and duodenal ulcers, and gastric reflux problems. It is used in conjunction with amoxicillin to treat H pylori bacter and duodenal ulcer disease. Side effects can include anorexia and fecal discoloration. Adverse effects of this medication can include tachycardia or bradycardia, angina, chest pain, pancreatitis, mucosal atrophy and esophageal candidiasis.

Recent Forum Posts

Side Effects

nausea / constipation / dizziness / headache / joint pain / vomiting / cough / dry mouth / abdominal pain / drowsiness / insomnia / diarrhea / bradycardia / flatulence / anorexia / fatigue / nervousness / somnolence / hypertension / hypertension / back pain / urinary tract infection / hematuria / rash / weakness / fever / paresthesia / diaphoresis / anxiety / tachycardia / urticaria / pruritus / testicular pain / alopecia / anaphylaxis / angina / palpitation /

Pregnancy

Pregnancy and Zefxon Embryo and Zefxon Fetal Weaning and Zefxon Breastfeeding and Zefxon

Dosage

How to Properly Take Omeprazole? What is the children dosage for Zefxon What is the adult dosage for Zefxon How often should Zefxon be taken? What is the dosage for Zefxon?

Usage

This medication is being used for: Duodenal Ulcer /

Storage

Interactions

Biological Half-life

How long does it take Zefxon to leave the system?

Nursing responsibilities for Zefxon

ATC CODE: A02BC01 ATC CODE: A02BC01

Other medications containing Omeprazole

Promat - Upcoming Industry Events, Promat

Upcoming Events

ProMat 2015 - Where Supply Chain Solutions Connect

Dates: March 23 - 26, 2015

Show Sponsor: The Material Handling Industry of America (MHIA)

Show Location: McCormick Place, Chicago, Illinois

Event Detail: ProMat is the premier showcase of material handling, supply chain and logistics solutions in North America. The show is designed to offer productivity solutions and information by showcasing the products and services of 785 leading material handling and logistics providers.

To make it easier for attendees to find the solutions they need, the ProMat show floor is divided into three solution-specific centers: Manufacturing and assembly solutions, fulfillment and delivery solutions, and information technology (IT) solutions. An extensive educational conference runs concurrently with the show and includes sessions on improving operational productivity and visibility in manufacturing, distribution and in the overall supply chain. This format allows attendees to learn about various material handling and logistics solutions in the educational sessions and then actually see the equipment, systems and services that can implement those solutions.

The U. S. Department of Commerce has consistently selected ProMat to be an official International Buyer Program event. ProMat provides matchmaker services for interested buyers and sellers through an International Business Center located at the event. International trade specialist will be on hand to provide expert counseling.

« Back Upcoming Industry Events

We'll Change Your Perspective International Manufacturing Technology Show | September 12-17, 2016 McCormick Place, Chicago, IL, USA

Copyright © | All Rights Reserved. AMT - The Association For Manufacturing Technology

© 2016 UPS. All rights reserved. UPS, the UPS brandmark and the color brown are trademarks of United Parcel Service of America, Inc.

Metro, Metro

Metrobus

Metrobus provides more than 400,000 trips each weekday serving 11,500 bus stops in the District of Columbia, Maryland, and Virginia. Metrobus is the sixth busiest bus agency in the United States, with a fleet of more than 1,500 buses operating on 325 routes.

Where to Wait for the Bus

Stand at Metrobus stops, which are designated with red, white, and blue signs.

Check the bus destination before you board. The route number and destination are displayed above the windshield and on the boarding side of the bus. For planning bus trips, please see the Trip Planner or phone the Metro information line at 202-637-7000.

The Office of Bus Planning works hard to improve bus stop accessibility throughout its network of approximately 12,000 bus stops. To report any accessibility issues with Metrobus stops, you can download our form (PDF).

Metrorail and Metrobus Transfers

To get a rail-to-bus or bus-to-rail discount or to transfer free from bus to bus, you must use a SmarTrip® card.

Detours

On occasion, Metro may implement detours on some or all of its Metrobus routes. Severe weather, road construction or special events, such as festivals, road races or parades, may cause these temporary route changes. Riders can stay up-to-date on the changes by visiting the Alerts & Advisories page.

Rules

See a list of Metro rules and manners for riding smart on Metrobus.

Bicycles

Bicycling has become exceedingly popular as people use their bicycles every day for commuting, shopping, and general transportation. With this in mind, Metro offers cyclists the Bike & Ride program for traveling with your bicycle on Metrobus and Metrorail.

Metrorail

Metrorail provides safe, clean, reliable transit service for more than 700,000 customers a day throughout the Washington, DC area. The system is the second busiest in the United States, serving 91 stations in Virginia, Maryland, and the District of Columbia.

The Metrorail system has six color-coded rail lines: Red, Orange, Silver, Blue, Yellow, and Green. The layout of the system makes it possible to travel between any two stations with no more than a single transfer.

Finding the Metro Station

If you're driving, look for the large Metro signs to direct you to stations.

Look for tall brown columns with a large "M" identifying the station entrances. Colored stripes around the column show which lines serve the station.

What's the Fare?

To determine the fare between two stations, use the Fare Finder on the right side of this page. For fares on trips that involve trains and buses, use our Trip Planner. SmarTrip® card users get the lowest fares. See the SmarTrip® box on the right to learn more.

Waiting for the Train

Read station signs to learn which train platform to use for your destination.

Stand behind the bumpy tiles along the platform's edge.

Watch for flashing lights along the platform's edge, which signal a train's arrival. Station signs will also alert you to a train's arrival.

Boarding the Train

Check the destination of the train, which is posted above the side windows.

Stand clear of the train car doors and let riders get off before you board.

Step over the small gap between the platform and the train.

Listen for the chimes that signal the car doors are closing. If the train is full, step back and wait for the next train. Unlike elevator doors, train doors do not reopen automatically.

Exiting the Train and Station

Use the same farecard you used to enter the system when you exit the system.

Rules

Solutions That Simplify Everyday Life

For over 80 years, Metro has been the world's leading manufacturer of storage and transport equipment in Healthcare, Foodservice and Commercial markets.

From our innovative wire and polymer shelving lines including Genuine Super Erecta, Super Adjustable II. Polymer Shelving to C5 Heated Cabinets to the revolutionary Starsys Storage and Transport System to a broad range of healthcare cart solutions including the Lifeline emergency cart. Flexline procedure carts and Lionville series medication carts. Metro puts space to work in labs, restaurants, hotels, hospitals, schools, retail areas, factories and beyond.

Latanopres, Latanopres

Eligible Patients May Pay As Little As $0 Each Month With the XALATAN Savings Card*

Important Safety Information

XALATAN ® (latanoprost ophthalmic solution) is not recommended in patients with a known hypersensitivity to latanoprost, benzalkonium chloride, or any other ingredients in this product.

XALATAN may slowly cause darkening of the eye color, darkening of the eyelid and eyelashes, and increased growth and thickness of eyelashes. Color changes may increase as long as XALATAN is administered, and eye color changes are likely to be permanent.

There have been reports of bacterial keratitis associated with the use of multiple-dose containers of topical ophthalmic products.

Contact lenses should be removed prior to the administration of XALATAN. Contact lenses can be reinserted 15 minutes following administration of XALATAN.

The most common side effects for XALATAN may include blurred vision, burning and stinging, eye redness, eye itching, the feeling of something in the eye, increased darkening of eye color, irritation of the clear front surface of the eye, or cold or flu.

Indication

XALATAN is a prescription medication for the treatment of high eye pressure/intraocular pressure (IOP) in people with open-angle glaucoma or ocular hypertension.

Patients should always ask their doctors for medical advice about adverse events.

You may report an adverse event related to Pfizer products by calling 1-800-438-1985 (US only). If you prefer, you may contact the U. S. Food and Drug Administration (FDA) directly. The FDA has established a reporting service known as MedWatch where health care professionals and consumers can report serious problems they suspect may be associated with the drugs and medical devices they prescribe, dispense, or use. Visit MedWatch or call 1-800-FDA-1088.

* Terms and Conditions

By participating in the XALATAN Savings Card Program, you acknowledge that you currently meet the eligibility criteria and will comply with the terms and conditions described below:

The Card is not valid for prescriptions that are eligible to be reimbursed, in whole or in part, by Medicaid, Medicare, or other federal or state healthcare programs, including any state prescription drug assistance programs and the Government Health Insurance Plan available in Puerto Rico (formerly known as “La Reforma de Salud”)

The Card is not valid for prescriptions that are eligible to be reimbursed by private insurance plans or other health or pharmacy benefit programs, which reimburse you for the entire cost of your prescription drugs

Patients must be 18 or older

You must deduct the savings received under this program from any reimbursement request submitted to your insurance plan, either directly by you or on your behalf

By using the Card, eligible patients may receive a savings of up to $125 per fill off their monthly out-of-pocket costs on quantities of 7.49 mL and below. The Card is good for a maximum savings of $1,500 per year ($125 per month x 12 months). Thus, if your out-of-pocket cost is more than $125, you will save $125 off of your total out-of-pocket costs. [Example: If your out-of-pocket cost is $150, you will pay $25 ($150-$125 = $25).] If your out-of-pocket cost is $125 or less, your out-of-pocket cost is $0. For a mail-order 3-month prescription (quantities greater than 7.50 mL), your total maximum savings may be $375 ($125 x 3)

The Card is not valid for Massachusetts residents whose prescriptions are covered, in whole or in part, by third-party insurance, or where otherwise prohibited by law

The Card cannot be combined with any other rebate/coupon, free trial, or similar offer for the specified prescription

The Card will be accepted only at participating pharmacies

The Card is not health insurance

This offer is good only in the U. S. and Puerto Rico

The Card is limited to one per person during this offering period and is not transferable

Pfizer reserves the right to rescind, revoke, or amend this offer without notice at any time

No membership fees. The Card and Program expire on 12/31/17

For help with the XALATAN Savings Card Program, call 1-866-562-6147, or write: XALATAN Savings Program, 14001 Weston Parkway, Suite 103, Cary, NC 27513. Be sure to include your name and mailing address.

The health information contained herein is provided for educational purposes only and is not intended to replace discussions with a health care provider. All decisions regarding patient care must be made with a health care provider, considering the unique characteristics of the patient.

The product information provided in this website is intended only for residents of the United States. The products discussed herein may have different product labeling in different countries.

You are leaving XALATAN. com

You are leaving this website. Links to all outside websites are provided as a convenience to our visitors and do not imply an endorsement or recommendation by Pfizer. Pfizer accepts no responsibility or liability for the content or services of other websites.

Pandora® Radio - Aplicaciones De Android En Google Play, Pandon

?Quieres traducir la descripcion al Espanol con el Traductor de Google? Volver a traducir la descripcion al Ingles

Descripcion

Powered by the Music Genome Project®, the most comprehensive music analysis ever undertaken, Pandora gives you personalized radio that plays what you love and continually evolves with your tastes.

• Create personalized stations from songs, artists, genres, or comedians • Browse hundreds of curated genre stations to find the perfect match for your mood or activity • Create an account and listen on desktop, mobile, TVs and home devices, or in your car • Listen ad-free with Pandora One for only $4.99/mo.

Note: Pandora may use large amounts of data, and carrier data charges may apply. For best results, we recommend you connect your device to trusted Wi-Fi networks when available

Desarrollado por el Music Genome Project®, el analisis de la musica mas completo jamas realizado, Pandora le da la radio personalizada que reproduce lo que amas y continuamente evoluciona con sus gustos.

• Crear estaciones personalizadas de canciones, artistas, generos o comicos • Explorar cientos de estaciones de diferentes generos curadas para encontrar la combinacion perfecta para su estado de animo o actividad • Crear una cuenta y escuchar en el escritorio, moviles, televisores y dispositivos para el hogar, o en su coche • Escuchar sin publicidad con Pandora Uno por solo $ 4.99 / mes.

Nota: Pandora puede utilizar grandes cantidades de datos, y se pueden aplicar cargos de datos de soporte. Para obtener los mejores resultados, recomendamos que conecte el dispositivo a redes Wi-Fi seguras cuando este disponible

Opiniones

Novedades

Informacion adicional

Similares

Ketovid, Ketovid

Ketoconazole

Click for further information on drug naming conventions and International Nonproprietary Names .

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?

Your #1 Choice For Boats For Sale In Maine, Tabrophage

Your #1 Choice for Boats for Sale in Maine

Hamlin’s Marine wants you to enjoy every moment on the water.

For over twenty years Hamlin’s Marine has delivered on a simple promise… ”If you purchase a boat from Hamlin’s Marine, we’ll always be there when you need us.” Hamlin’s Marine offers convenience and assurance with our locations in Waterville and Hampden, staff of twenty-five dedicated employees, and a fleet of service trucks.

At Hamlin’s we only sell boats that we can stand behind. Our manufacturers include Bennington Pontoons. Stingray. Mastercraft. Cutwater. Northcoast. Puffin. Alumacraft. Achilles. Scout Boats. and Yamaha Outboards. These manufacturers lead the industry in quality construction, and make it easier to serve you when it matters most.

So come on in and choose from our selection of new and used Pontoon Boats, Tow Boats or any other fishing boats or family fun boats. With two easy locations in Waterville, Maine (Boat Sales and Service) or Hampden, Maine (Boat Sales, Service, and Marina) it couldn't get any more convenient. Choose Hamlin’s Marine as your boat dealer, service center, marina, and indoor storage facility, and we promise you’ll make wonderful memories on the water in Maine.

At Hamlin's Marine we stand behind all of our boats for sale in Maine .

Why Buy From Hamlin's Marine:

31 Years in Business

#1 Yamaha Outboard Dealer in New England for 5 Years in a Row

Alumacraft is America's #1 selling Deep V Aluminum Fishing Boat

Multiple Locations to serve you

Fleet of ten service and delivery trucks

Vasotec - Heart Disease, Supotron

Vasotec is used for treating high blood pressure, heart failure, and other heart problems. It may be used alone or with other medicines. Vasotec is an angiotensin-converting enzyme (ACE) inhibitor. It works by helping to relax blood vessels. This helps to lower blood pressure.

Use Vasotec as directed by your doctor.

Take Vasotec by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

If you miss a dose of Vasotec, 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 Vasotec.

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

Active Ingredient: Enalapril maleate.

Do NOT use Vasotec if:

you are allergic to any ingredient in Vasotec or similar medicines (eg, captopril, lisinopril)

you are pregnant

you are taking dextran sulfate or a potassium-sparing diuretic (eg, amiloride).

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

Some medical conditions may interact with Vasotec. 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 or have ever had liver or kidney problems or kidney transplantation

if you are receiving dialysis

if you have bone marrow suppression, low blood counts, low blood sodium, high blood potassium, the blood disease porphyria, giant hives, lupus, scleroderma, or a collagen vascular disease

if you have narrowing or hardening of the arteries of the brain or heart, chest pain, or discomfort known as angina.

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

Diuretics (eg, furosemide, hydrochlorothiazide) because excessive decreases in blood pressure may occur, which may cause dizziness, especially upon standing, or fainting

Dextran sulfate because it may increase the risk of allergic reaction (eg, rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue) and lightheadedness upon standing

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, aspirin, indomethacin) because they may decrease Vasotec's effectiveness and the risk of kidney damage may be increased

Oral diabetes medicine (eg, glyburide) because side effects, including a low blood sugar level (eg, dizziness, headache, hunger, shakiness or weakness, sweating), may be increased by Vasotec

Lithium or thiopurines (eg, azathioprine) because the risk of serious side effects may be increased by Vasotec

Certain gold-containing medicines (eg, sodium aurothiomalate) because flushing, nausea, vomiting, and low blood pressure may occur

Potassium-sparing diuretics (eg, amiloride) or potassium supplements may cause high blood potassium levels (eg, abnormal skin sensations of the arms and legs, confusion, heaviness of the limbs, listlessness, slow or irregular heartbeat, stopping of the heart) when used with Vasotec.

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

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

Check with your doctor before you use a salt substitute or a product that has potassium in it.

If vomiting or diarrhea occurs, you will need to take care not to become dehydrated. Contact your doctor for instructions.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

Vasotec may not work as well in black patients. They may also be at greater risk of side effects. Contact your doctor if your symptoms do not improve or if they become worse.

Vasotec may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Vasotec. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

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

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

Vasotec should not be used in newborns; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Vasotec may cause birth defects or fetal death if you take it while you are pregnant. If you think you may be pregnant, contact your doctor right away. Vasotec is found in breast milk. If you are or will be breast-feeding while you use Vasotec, 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:

Diarrhea; dizziness or lightheadedness when sitting up or standing; headache; nausea; persistent, dry cough; tiredness; 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); chest pain; hoarseness; infection (eg, fever, sore throat); irregular or slow heartbeat; unusual stomach pain; 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.

Vasotec is used for treating high blood pressure, heart failure, and other heart problems. It may be used alone or with other medicines. Vasotec is an angiotensin-converting enzyme (ACE) inhibitor. It works by helping to relax blood vessels. This helps to lower blood pressure.

Use Vasotec as directed by your doctor.

Take Vasotec by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

If you miss a dose of Vasotec, 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 Vasotec.

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

Active Ingredient: Enalapril maleate.

Do NOT use Vasotec if:

you are allergic to any ingredient in Vasotec or similar medicines (eg, captopril, lisinopril)

you are pregnant

you are taking dextran sulfate or a potassium-sparing diuretic (eg, amiloride).

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

Some medical conditions may interact with Vasotec. 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 or have ever had liver or kidney problems or kidney transplantation

if you are receiving dialysis

if you have bone marrow suppression, low blood counts, low blood sodium, high blood potassium, the blood disease porphyria, giant hives, lupus, scleroderma, or a collagen vascular disease

if you have narrowing or hardening of the arteries of the brain or heart, chest pain, or discomfort known as angina.

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

Diuretics (eg, furosemide, hydrochlorothiazide) because excessive decreases in blood pressure may occur, which may cause dizziness, especially upon standing, or fainting

Dextran sulfate because it may increase the risk of allergic reaction (eg, rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue) and lightheadedness upon standing

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, aspirin, indomethacin) because they may decrease Vasotec's effectiveness and the risk of kidney damage may be increased

Oral diabetes medicine (eg, glyburide) because side effects, including a low blood sugar level (eg, dizziness, headache, hunger, shakiness or weakness, sweating), may be increased by Vasotec

Lithium or thiopurines (eg, azathioprine) because the risk of serious side effects may be increased by Vasotec

Certain gold-containing medicines (eg, sodium aurothiomalate) because flushing, nausea, vomiting, and low blood pressure may occur

Potassium-sparing diuretics (eg, amiloride) or potassium supplements may cause high blood potassium levels (eg, abnormal skin sensations of the arms and legs, confusion, heaviness of the limbs, listlessness, slow or irregular heartbeat, stopping of the heart) when used with Vasotec.

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

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

Check with your doctor before you use a salt substitute or a product that has potassium in it.

If vomiting or diarrhea occurs, you will need to take care not to become dehydrated. Contact your doctor for instructions.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

Vasotec may not work as well in black patients. They may also be at greater risk of side effects. Contact your doctor if your symptoms do not improve or if they become worse.

Vasotec may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Vasotec. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

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

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

Vasotec should not be used in newborns; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Vasotec may cause birth defects or fetal death if you take it while you are pregnant. If you think you may be pregnant, contact your doctor right away. Vasotec is found in breast milk. If you are or will be breast-feeding while you use Vasotec, 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:

Diarrhea; dizziness or lightheadedness when sitting up or standing; headache; nausea; persistent, dry cough; tiredness; 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); chest pain; hoarseness; infection (eg, fever, sore throat); irregular or slow heartbeat; unusual stomach pain; 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.

Cefazolin Indications, Side Effects, Warnings, Cezolin

Cefazolin

Before using cefazolin:

Some medical conditions may interact with cefazolin. 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 had a severe allergic reaction (eg, severe rash, hives, difficulty breathing, dizziness) to a penicillin (eg, amoxicillin) or beta-lactam antibiotic (eg, imipenem)

if you have stomach or bowel problems (eg, inflammation), blood clotting problems, kidney or liver problems, or poor nutrition

Some MEDICINES MAY INTERACT with cefazolin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin) or heparin because the risk of side effects, including bleeding, may be increased by cefazolin

Probenecid because its actions and the risk of its side effects may be increased by cefazolin

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

How to use cefazolin:

Use cefazolin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Cefazolin is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using cefazolin at home, a health care provider will teach you how to use it. Be sure you understand how to use cefazolin. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

Do not use cefazolin if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

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

Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

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

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

Important safety information:

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

Be sure to use cefazolin 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 cefazolin 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.

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.

Diabetes patients - Cefazolin 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.

Cefazolin may interfere with certain lab tests. Be sure your doctor and lab personnel know you are using cefazolin.

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

Use cefazolin with caution in the ELDERLY; they may be more sensitive to its effects.

Use cefazolin with extreme caution in CHILDREN younger than 1 month old; safety and effectiveness in these children have not been confirmed.

Use cefazolin with extreme caution in CHILDREN younger than 10 years old 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 cefazolin while you are pregnant. Cefazolin is found in breast milk. If you are or will be breast-feeding while you use cefazolin, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of cefazolin:

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:

Loss of appetite; mild diarrhea; nausea; stomach cramps; 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; decreased urination; fever; hoarseness; pain, swelling, or redness at the injection site; red, swollen, or blistered skin; seizures; severe diarrhea; severe nausea or vomiting; severe stomach pain/cramps; unusual bruising or bleeding; unusual tiredness; vaginal irritation or discharge; white spots in the mouth; yellowing of the eyes and skin.

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. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately. Symptoms may include muscle spasms; seizures.

Proper storage of cefazolin:

Cefazolin is usually handled and stored by a health care provider. If you are using cefazolin at home, store cefazolin as directed by your pharmacist or health care provider. Store away from heat, moisture, and light. Keep cefazolin out of the reach of children and away from pets.

General information:

If you have any questions about cefazolin, please talk with your doctor, pharmacist, or other health care provider.

Cefazolin 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.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take cefazolin or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. 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 cefazolin. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to cefazolin. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using cefazolin.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. 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 your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about cefazolin

Stella Residence Club (Odessa, Ukraine) - 2016 Spa Reviews, Stella

Stella Residence Club is the luxury hotel in the touristic district of famous Odessa. It is.

Stella Residence Club is the luxury hotel in the touristic district of famous Odessa. It is located right near the coast of Black sea. Our guests have an opportunity to admire marvelous Odessa dawns and sunsets from the spa-complex windows and their private suits. In the same time they can merge into the atmosphere of ideal comfort and silence of luxury hotel. One more advantage is location. Our guests feel relaxing loneliness of the sea vicinity and can drop to the city centre and amusement centre in some minutes. Does it a real perfection of rest? Stella Residence SPA Hotel is created for relaxation! In our rooms you have everything for comfort in your disposal. There are 15 suits fully equipped with all you need. We have a careful attention to the details to prove our «Lux» level. In your disposal there are flat screen TV, heated floor, free Wi-Fi access, city phone in the room, mini-bar, mini-safe, hair drier, bathrobe, bath cosmetics and towels. Our guests can visit aqua-zone with pool, sauna and Turkish hamam absolutely free of charge. Gym facing the sea and fitness programs are also in there availability.

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Travelers' Choice® 2016 Winner Small Hotels | Luxury | Best Service

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Vanny Lane, 3_. Odessa 65000, Ukraine

#27 of 75 in Odessa

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“ Very dodgy staff ”

BIANKA_ramos (6 reviews)

London, United Kingdom

The hotel itself was ok-ish, very pretentious interior, but untrained very rude staff, everywhere: reception. restaurant, housekeeping. The only people are polite is the spa. But I was told spa operates separately. When we checked in on the 25th of August, the hotel gave us room which was overlooking the building construction site. not only that, it was also with dirty stained carpet which was beige many years ago and now was unrecognisable. We have also noticed broken shelve in the bathroom, which has sharp edges of glass and was dangerous. I have complained to reception and their reply was. we can't change your room, it's the best what we can offer. We actually came there for a wedding, all of us occupied around 7 rooms, including bride and groom and everyone had similar issues with dirtiness of the rooms. However we had no choice, so we stayed. At the day of the checkout the reception told us we had to pay for damage to the glass shelve in the bathroom and for the stains on carpet. They said we have made it! Which is just outrageous. We were already late for our taxi, so couldn't argue much as that would cause delay, but I still tried to remind them that this what we have complained about the minute we have checked in and saw the room. After 30 min fight with housekeeping and reception they admitted that it's not our fault and it's their fault and when I came back to London I have learnt from my credit card bill they still have charged me extra for it. Will now have to waste more time arguing about it. I'm sure I can return it as I asked them before leaving to give me detailed bill. Which after arguing they have managed to provide. However at the beginning they were fighting with me telling me. to provide detailed invoice it's not their obligation. What? I pay without bill/invoice? Terrible! It's probably good place for holidays for youngsters who go there to have fun with young girls, and when they ripped off they dont notice, because drunk etc, with senior couple it will not work! Shame on you Stella residence.

In addition the restaurant. They say in the morning that they don't have 50% part of menu and replace by bread. Seriously? So the breakfast consists from bread, bread, bread and milk and tea. And they are rude when you ask clarifying questions. It's like you bother them that they have to serve you. Rip off, if you want to go to Ukraine, go to Kiev, good hotels, know about service, value customers

Convenient location at 50-100 meters from the public beach. You can use free sun beds and umbrellas, reserved for hotel guests on the beach. Large rooms and bathroom. Everything equipped for an easy and comfortable stay. Pleasant spa service, delicious breakfasts (complex by choice) with breakfast in the room or on Terrace. courteous staff. I highly recommend people that love comfort, quietness and high-quality service.

A little disrupted with the construction nearby, but of course the hotel can not affect this. It is better to order breakfast in overnight, otherwise, you will have to wait for it to be cooked in the morning.

“ Felt comfortable here with only minor hitches ”

RichardThomas2001 (150 reviews)

Studio rooms are quite spacious and comfortable. Very large beds. In one room we had a small electrical issue and the other a small shower issue. Very powerful aircon units which are adjustable in terms of temperature. I found the personnel to be very helpful and friendly but helps to speak Russian. Nearby there is everything: kiosks to buy beer/water/snacks and slightly further away a grocery and some restaurants. It has the feel of being slightly away from civilization - a good getaway. The beach is conveniently located but it is a public beach that gets very crowded. About a 15-20 minute drive from the Odessa airport.

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Medunarodni Simpozijum Oftalmologa U Vma, Oftalmol

MEDUNARODNI SIMPOZIJUM OFTALMOLOGA U VMA

10. 09. 2010

Beograd, 10.septembar - Treci medunarodni simpozijum „Savremeni trendovi u oftalmologiji“ odrzan je danas u VMA. U radu skupa ucestvovalo je vise od 500 oftalmologa iz Srbije, Crne Gore, Republike Srpske/ Bosne i iHercegovine, Makedonije i Hrvatske. Poseban doprinos radu skupa svojim ucescem i uvodnim predavanjima dali su najeminentniji svetski oftalmolozi: prof. dr Tomas Dzon sa Lajola Univerziteta iz Cikaga (SAD), vodeci hirurg u oblasti hirurgije roznjace i gostujuci profesor VMA, prof. dr Klaus Luke iz Bremena (Nemacka), predsednik Evropskog udruzenja vitroretinalnih hirurga i prof. dr Nikica Gabric iz Zagreba (Hrvatska). 

Skup je otvorio nacelnik VMA, general-major prof. dr Miodrag Jevtic koji je prisutnima pozeleo dobrodoslicu u nas hram zdravlja. - Izuzetno sam zadovoljan sto danas stojim pred amfiteatrom prepunim strucnjaka, vrhunskih oftamologa iz celog regiona i sto ovde vidim najveca imena svetske oftalmohirurgije. Ovaj dogadaj je jos jedno prakticno ostvarenje vizija Uprave VMA da nasa ustanova bude popriste strucnih i naucnih konferencija, razmene znanja, vestina i iskustava sa zajednickom misijom: u sluzbi zdravlja i napretka medicinske misli! – kazao je general Jevtic. - VMA je danas ponovo mesto u koje je prestizno doci, nasi strucnjaci su lideri u mnogim oblastima medicine, ali sve ono sto znaju uvek su zeleli da podele sa drugima, bas kao sto to i danas cine lekari nase Klinike za ocne bolesti koji ce Vam u hirurgiji uzivo predstaviti najnovija dostignuca u hirurgiji oka. – naglasio je Jevtic.

Nacelnik Klinike za ocne bolesti puk. prof. dr Miroslav Vukosavljevic, zahvalio se svima prisutnima kolegama na izuzetnom odzivu i saradnji i upoznao ucesnike skupa sa novinama u oblasti operacija na prednjem i zadnjem segmentu oka, egzajmer-laser refraktivnoj hirurgiji i tehnikama hirurgije glaukoma i razrokosti koje su nasi strucnjaci predstavili u hirurgji uzivo uz pomoc direktnog video-linka iz operacione sale VMA.

- Egzajmer laserom smo do sada uradili vise od 2000 procedura skidanja dioptrije. Danas predstavljamo inovacije u fako hirurgiji – zahvat sa rezom od 2.2 milimetra i implantaciju multifokalnih asfericnih tzv. premijum sociva koje omogucuju dobru korekciju vida i na daljinu i na blizinu. – kazao je Vukosavljevic.

Oftalmolozi VMA prikazali su kolegama i tehniku ugradnje toricnih asfericnih sociva za korekciju astigmatizma, najnovije tehnike mikroincizione zadnje vitrektomije, hirurgije prednjeg i zadnjeg segmenta oka u zbrinjavnju ablacija mreznjace, povreda, dijabeticne retinopatije itd. Prikazane su i retke tehnike hirurgije razrokosti i hirurgije glaukoma.

Lansofast, Lansofast

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Lansofast (Lansoprazole)

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Prevacid decreases the amount of acid produced in the stomach. It is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid) and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome.

Availability: In Stock (34 packs)

Other names of Prevacid:

What is this medicine?

LANSOPRAZOLE prevents the production of acid in the stomach. It is used to treat gastroesophageal reflux disease (GERD), ulcers, certain bacteria in the stomach, inflammation of the esophagus, and Zollinger-Ellison Syndrome. It can also be used to prevent and treat ulcers in patients taking medicines called non-steroidal anti-inflammatory drugs (NSAIDs).

What should I tell my health care provider before I take this medicine?

They need to know if you have any of these conditions: liver disease an unusual or allergic reaction to lansoprazole, other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth. Swallow the capsules whole with a drink of water. Do not crush or chew. This medicine works best if taken on an empty stomach 30 to 60 minutes before food. Take your medicine at regular intervals. Do not take more often than directed.

If you have difficulty swallowing the capsules, you may open the capsule and sprinkle the contents on a tablespoon of any of the following foods: applesauce, Ensure brand pudding, cottage cheese, yoghurt, or strained pears. Do not crush the contents of the capsule into the food. Swallow the dose immediately after preparing it. Do not chew. Follow with a drink of water.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine, contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with the following: atazanavir

This medicine may also interact with the following medications: ampicillin delavirdine digoxin iron salts itraconazole, ketoconazole, voriconazole, or other prescription medicines for fungus or yeast infections sucralfate theophylline warfarin

Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.

What should I watch for while taking this medicine?

It can take several days before your stomach pain gets better. Check with your doctor or health care professional if your condition does not start to get better or if it gets worse.

What side effects may I notice from this medicine?

Side effects that you should report to your prescriber or health care professional as soon as possible. dark yellow or brown urine fever or sore throat unusual skin rash, blistering, or peeling unusual bleeding or bruising yellowing of the eyes or skin vomiting

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): diarrhea or constipation headache nausea stomach pain or gas

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F). Protect from moisture. Throw away any unused medicine after the expiration date.

Prevacid decreases the amount of acid produced in the stomach. It is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid) and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome.

Availability: In Stock (34 packs)

Other names of Prevacid:

What is this medicine?

LANSOPRAZOLE prevents the production of acid in the stomach. It is used to treat gastroesophageal reflux disease (GERD), ulcers, certain bacteria in the stomach, inflammation of the esophagus, and Zollinger-Ellison Syndrome. It can also be used to prevent and treat ulcers in patients taking medicines called non-steroidal anti-inflammatory drugs (NSAIDs).

What should I tell my health care provider before I take this medicine?

They need to know if you have any of these conditions: liver disease an unusual or allergic reaction to lansoprazole, other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth. Swallow the capsules whole with a drink of water. Do not crush or chew. This medicine works best if taken on an empty stomach 30 to 60 minutes before food. Take your medicine at regular intervals. Do not take more often than directed.

If you have difficulty swallowing the capsules, you may open the capsule and sprinkle the contents on a tablespoon of any of the following foods: applesauce, Ensure brand pudding, cottage cheese, yoghurt, or strained pears. Do not crush the contents of the capsule into the food. Swallow the dose immediately after preparing it. Do not chew. Follow with a drink of water.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine, contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with the following: atazanavir

This medicine may also interact with the following medications: ampicillin delavirdine digoxin iron salts itraconazole, ketoconazole, voriconazole, or other prescription medicines for fungus or yeast infections sucralfate theophylline warfarin

Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.

What should I watch for while taking this medicine?

It can take several days before your stomach pain gets better. Check with your doctor or health care professional if your condition does not start to get better or if it gets worse.

What side effects may I notice from this medicine?

Side effects that you should report to your prescriber or health care professional as soon as possible. dark yellow or brown urine fever or sore throat unusual skin rash, blistering, or peeling unusual bleeding or bruising yellowing of the eyes or skin vomiting

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): diarrhea or constipation headache nausea stomach pain or gas

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F). Protect from moisture. Throw away any unused medicine after the expiration date.

Arestin - Fda Prescribing Information, Side Effects And Uses, Areston

Arestin

Arestin ® (minocycline hydrochloride) Microspheres is a subgingival sustained-release product containing the antibiotic minocycline hydrochloride incorporated into a bioresorbable polymer, Poly (glycolide-co-dl-lactide) or PGLA, for professional subgingival administration into periodontal pockets. Each unit-dose cartridge delivers minocycline hydrochloride equivalent to 1 mg of minocycline free base.

The molecular formula of minocycline hydrochloride is C 23 H 27 N 3 O 7 ● HCl, and the molecular weight is 493.94. The structural formula of minocycline hydrochloride is:

Arestin - Clinical Pharmacology

Mechanism of Action

The mechanism of action of Arestin ® as an adjunct to scaling and root planing procedures for reduction of pocket depth in patients with adult periodontitis is unknown.

Microbiology

Minocycline, a member of the tetracycline class of antibiotics, has a broad spectrum of activity. 1 It is bacteriostatic and exerts its antimicrobial activity by inhibiting protein synthesis. 1 In vitro susceptibility testing has shown that the organisms Porphyromonas gingivalis, Prevotella intermedia, Fusobacterium nucleatum, Eikenella corrodens. and Actinobacillus actinomycetemcomitans. which are associated with periodontal disease, are susceptible to minocycline at concentrations of ≤8 mcg/mL 2 ; qualitative and quantitative changes in plaque microorganisms have not been demonstrated in patients with periodontitis, using this product.

The emergence of minocycline-resistant bacteria in single-site plaque samples was studied in subjects before and after treatment with Arestin ® at 2 centers. There was a slight increase in the numbers of minocycline-resistant bacteria at the end of the 9-month study period, however, the number of subjects studied was small and the clinical significance of these findings is unknown.

The emergence of minocycline-resistant bacteria and changes in the presence of Candida albicans and Staphylococcus aureus in the gastrointestinal tract were studied in subjects treated with Arestin ® in one phase 3 study. No changes in the presence of minocycline-resistant bacteria or C. albicans or S. aureus were seen at the end of the 56-day study period.

Pharmacokinetics

In a pharmacokinetic study, 18 patients (10 men and 8 women) with moderate to advanced chronic periodontitis were treated with a mean dose of 46.2 mg (25 to 112 unit doses) of Arestin ®. After fasting for at least 10 hours, patients received subgingival application of Arestin ® (1 mg per treatment site) following scaling and root planing at a minimum of 30 sites on at least 8 teeth. Investigational drug was administered to all eligible sites ≥5 mm in probing depth. Mean dose normalized saliva AUC and Cmax were found to be approximately 125 and 1000 times higher than those of serum parameters, respectively.

Clinical Studies

In 2 well-controlled, multicenter, investigator-blind, vehicle-controlled, parallel-design studies (3 arms), 748 patients (study OPI-103A = 368, study OPI-103B = 380) with generalized moderate to advanced adult periodontitis characterized by a mean probing depth of 5.90 and 5.81 mm, respectively, were enrolled. Subjects received 1 of 3 treatments: (1) scaling and root planing, (2) scaling and root planing + vehicle (bioresorbable polymer, PGLA), and (3) scaling and root planing + Arestin ®. To qualify for the study, patients were required to have 4 teeth with periodontal pockets of 6 to 9 mm that bled on probing. However, treatment was administered to all sites with mean probing depths of 5 mm or greater. Patients studied were in good general health. Patients with poor glycemic control or active infectious diseases were excluded from the studies. Retreatment occurred at 3 and 6 months after initial treatment, and any new site with pocket depth ≥5 mm also received treatment. Patients treated with Arestin ® were found to have statistically significantly reduced probing pocket depth compared with those treated with SRP alone or SRP + vehicle at 9 months after initial treatment, as shown in Table 1 .

Table 1: Probing Pocket Depth at Baseline and Change in Pocket Depth at 9 Months from 2 Multicenter US Clinical Trials

Study OPI-103A N=368

Study OPI-103B N=380

In both studies, the following patient subgroups were prospectively analyzed: smokers, patients over and under 50 years of age, and patients with a previous history of cardiovascular disease. The results of the combined studies are presented in Table 3 .

In smokers, the mean reduction in pocket depth at 9 months was less in all treatment groups than in nonsmokers, but the reduction in mean pocket depth at 9 months with SRP + Arestin ® was significantly greater than with SRP + vehicle or SRP alone.

Table 4: Mean Pocket Depth Change in Patients with Mean Baseline PD ≥5 mm, ≥6 mm, and ≥7 mm at 9 Months from 2 Multicenter US Clinical Trials

Mean Baseline Pocket Depth

SRP + Arestin ®

SRP + Arestin ®

* Statistically significant comparison between SRP + Arestin ® and SRP alone

The combined data from these 2 studies also show that for pockets 5 mm to 7 mm at baseline, greater reductions in pocket depth occurred in pockets that were deeper at baseline.

INDICATIONS AND USE

Arestin ® is indicated as an adjunct to scaling and root planing procedures for reduction of pocket depth in patients with adult periodontitis. Arestin ® may be used as part of a periodontal maintenance program which includes good oral hygiene and scaling and root planing.

CONTRAINDICATIONS

Arestin ® should not be used in any patient who has a known sensitivity to minocycline or tetracyclines.

WARNINGS

THE USE OF DRUGS OF THE TETRACYCLINE CLASS DURING TOOTH DEVELOPMENT (LAST HALF OF PREGNANCY, INFANCY, AND CHILDHOOD TO THE AGE OF 8 YEARS) MAY CAUSE PERMANENT DISCOLORATION OF THE TEETH (YELLOW-GRAY BROWN). This adverse reaction is more common during long-term use of the drugs, but has been observed following repeated short-term courses. Enamel hypoplasia has also been reported. TETRACYCLINE DRUGS, THEREFORE, SHOULD NOT BE USED IN THIS AGE GROUP, OR IN PREGNANT OR NURSING WOMEN, UNLESS THE POTENTIAL BENEFITS ARE CONSIDERED TO OUTWEIGH THE POTENTIAL RISKS. Results of animal studies indicate that tetracyclines cross the placenta, are found in fetal tissues, and can have toxic effects on the developing fetus (often related to retardation of skeletal development). Evidence of embryotoxicity has also been noted in animals treated early in pregnancy. If any tetracyclines are used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus. Photosensitivity manifested by an exaggerated sunburn reaction has been observed in some individuals taking tetracyclines. Patients apt to be exposed to direct sunlight or ultraviolet light should be advised that this reaction can occur with tetracycline drugs, and treatment should be discontinued at the first evidence of skin erythema.

Precautions

Hypersensitivity Reactions

Hypersensitivity reactions that included, but were not limited to anaphylaxis, angioneurotic edema, urticaria, rash, swelling of the face, and pruritus have been reported with the use of Arestin ®. Some of these reactions were serious. Post-marketing cases of anaphylaxis and serious skin reactions such as Stevens-Johnson syndrome and erythema multiforme have been reported with oral minocycline.

Autoimmune Syndromes

Tetracyclines, including oral minocycline, have been associated with the development of autoimmune syndromes including a Lupus-like syndrome manifested by arthralgia, myalgia, rash, and swelling. Sporadic cases of serum sickness have presented shortly after oral minocycline use, manifested by fever, rash, arthralgia, and malaise. In symptomatic patients, liver function tests, ANA, CBC, and other appropriate tests should be performed to evaluate the patients. No further treatment with Arestin ® should be administered to the patient.

The use of Arestin ® in an acutely abscessed periodontal pocket has not been studied and is not recommended.

While no overgrowth by opportunistic microorganisms, such as yeast, were noted during clinical studies, as with other antimicrobials, the use of Arestin ® may result in overgrowth of non-susceptible microorganisms including fungi. The effects of treatment for greater than 6 months has not been studied.

Arestin ® should be used with caution in patients having a history of predisposition to oral candidiasis. The safety and effectiveness of Arestin ® has not been established for the treatment of periodontitis in patients with coexistent oral candidiasis.

Arestin ® has not been clinically tested in immunocompromised patients (such as those immunocompromised by diabetes, chemotherapy, radiation therapy, or infection with HIV).

If superinfection is suspected, appropriate measures should be taken.

Arestin ® has not been clinically tested in pregnant women.

Arestin ® has not been clinically tested for use in the regeneration of alveolar bone, either in preparation for or in conjunction with the placement of endosseous (dental) implants or in the treatment of failing implants.

Information for Patients

After treatment, patients should avoid chewing hard, crunchy, or sticky foods (i. e. carrots, taffy, and gum) with the treated teeth for 1 week, as well as avoid touching treated areas. Patients should also postpone the use of interproximal cleaning devices around the treated sites for 10 days after administration of Arestin ®. Patients should be advised that although some mild to moderate sensitivity is expected during the first week after SRP and administration of Arestin ®. they should notify the dentist promptly if pain, swelling, or other problems occur. Patients should be notified to inform the dentist if itching, swelling, rash, papules, reddening, difficulty breathing, or other signs and symptoms of possible hypersensitivity occur.

Carcinogenicity, Mutagenicity, Impairment of Fertility

Dietary administration of minocycline in long-term tumorigenicity studies in rats resulted in evidence of thyroid tumor production. Minocycline has also been found to produce thyroid hyperplasia in rats and dogs. In addition, there has been evidence of oncogenic activity in rats in studies with a related antibiotic, oxytetracycline (i. e. adrenal and pituitary tumors). Minocycline demonstrated no potential to cause genetic toxicity in a battery of assays which included a bacterial reverse mutation assay (Ames test), an in vitro mammalian cell gene mutation test (L5178Y/TK +/- mouse lymphoma assay), an in vitro mammalian chromosome aberration test, and an in vivo micronucleus assay conducted in ICR mice.

Fertility and general reproduction studies have provided evidence that minocycline impairs fertility in male rats.

Teratogenic Effects

Pregnancy Category D.

Labor and Delivery

The effects of tetracyclines on labor and delivery are unknown.

Nursing Mothers

Tetracyclines are excreted in human milk. Because of the potential for serious adverse reactions in nursing infants from the tetracyclines, a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother. (See WARNINGS. )

Pediatric Use

Since adult periodontitis does not affect children, the safety and effectiveness of Arestin ® in pediatric patients cannot be established.

Adverse Reactions

The most frequently reported nondental treatment-emergent adverse events in the 3 multicenter US trials were headache, infection, flu syndrome, and pain.

Table 5: Adverse Events (AEs) Reported in ≥3% of the Combined Clinical Trial Population of 3 Multicenter US Trials by Treatment Group

SRP Alone N=250

SRP + Vehicle N=249

The change in clinical attachment levels was similar across all study arms, suggesting that neither the vehicle nor Arestin ® compromise clinical attachment. To report SUSPECTED ADVERSE REACTIONS, contact Valeant Pharmaceuticals North America LLC at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www. fda. gov/medwatch.

DOSAGE AND ADMINISTRATION

Arestin ® is provided as a dry powder, packaged in a unit dose cartridge with a deformable tip (see Figure 1), which is inserted into a spring-loaded cartridge handle mechanism (see Figure 2) to administer the product.

The oral health care professional removes the disposable cartridge from its pouch and connects the cartridge to the handle mechanism (see Figures 3-4). Arestin ® is a variable dose product, dependent on the size, shape, and number of pockets being treated. In US clinical trials, up to 122 unit dose cartridges were used in a single visit and up to 3 treatments, at 3-month intervals, were administered in pockets with pocket depth of 5 mm or greater.

The administration of Arestin ® does not require local anesthesia. Professional subgingival administration is accomplished by inserting the unit-dose cartridge to the base of the periodontal pocket and then pressing the thumb ring in the handle mechanism to expel the powder while gradually withdrawing the tip from the base of the pocket. The handle mechanism should be sterilized between patients. Arestin ® does not have to be removed, as it is bioresorbable, nor is an adhesive or dressing required.

HOW SUPPLIED

Arestin ® (minocycline hydrochloride) Microspheres, 1 mg is supplied as follows:

• 1 unit-dose cartridge with desiccant in a heat-sealed, foil-laminated pouch (NDC 65976-100-01) • 12 unit-dose cartridges in 1 tray with desiccant in a heat-sealed, foil-laminated, resealable pouch (NDC 65976-100-24). There are 2 pouches in each box.

Each unit-dose cartridge contains the product identifier "OP-1."

Storage Conditions

Store at 20° to 25°C (68° to 77°F)/60% RH: excursions permitted to 15° to 30°C (59° to 86°F). Avoid exposure to excessive heat.

REFERENCES

1. Stratton CW, Lorian V. Mechanisms of action of antimicrobial agents: general principles and mechanisms for selected classes of antibiotics. In: Antibiotics in Laboratory Medicine. 4th ed. Baltimore, MD: Williams and Wilkins; 1996. 2. Slots J, Rams TE. Antibiotics in periodontal therapy: advantages and disadvantages. J Clin Periodontol. 1990; 17:479-493.

OraPharma, a division of Valeant Pharmaceuticals North America LLC

Bridgewater, NJ 08807

AAIPharma Services Corporation

Wilmington, NC 28405

© 2015 Valeant Pharmaceuticals North America LLC

PRINCIPAL DISPLAY PANEL - 1 mg Carton

Microsphere Delivery System Arestin ® minocycline HCl 1mg MICROSPHERES

Store at 20° to 25°C (68° to 77°F) /60% RH: excursions permitted to 15° to 30°C (59° to 86°F).

Avoid exposure to excessive heat

For Subgingival Application

To order: Call 1-866-Arestin (273-7846) or visit our Web site at www. ArestinProfessional. com

2 resealable foil pouches 12 cartridges per pouch 1 mg of minocycline per cartridge

Lidocaine Patch - Fda Prescribing Information, Side Effects And Uses, Licain

Lidocaine Patch

Lidocaine Patch Description

Lidocaine Patch 5% is comprised of an adhesive material containing 5% lidocaine, which is applied to a white non-woven polyethylene terephthalate (PET) material backing and covered with a transparent PET release liner. The release liner is removed prior to application to the skin. The size of the patch is 10 cm x 14 cm.

Lidocaine is chemically designated as acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl), has an octanol:water partition ratio of 43 at pH 7.4, and has the following structure:

Each adhesive patch contains 700 mg of lidocaine (50 mg per gram adhesive) in an aqueous base. It also contains the following inactive ingredients: glycerin, D-sorbitol, propylene glycol, polyvinyl alcohol, urea, sodium polyacrylate, carboxymethylcellulose sodium, gelatin, polyacrylic acid, kaolin, tartaric acid, dihydroxyaluminum aminoacetate, methylparaben, propylparaben, and edetate disodium.

Lidocaine Patch - Clinical Pharmacology

Pharmacodynamics

Lidocaine is an amide-type local anesthetic agent and is suggested to stabilize neuronal membranes by inhibiting the ionic fluxes required for the initiation and conduction of impulses.

The penetration of lidocaine into intact skin after application of Lidocaine Patch is sufficient to produce an analgesic effect, but less than the amount necessary to produce a complete sensory block.

Pharmacokinetics

Absorption: The amount of lidocaine systemically absorbed from Lidocaine Patch is directly related to both the duration of application and the surface area over which it is applied. In a pharmacokinetic study, three Lidocaine Patches were applied over an area of 420 cm 2 of intact skin on the back of normal volunteers for 12 hours. Blood samples were withdrawn for determination of lidocaine concentration during the application and for 12 hours after removal of patches. The results are summarized in Table 1.

Table 1: Absorption of lidocaine from Lidocaine Patch Normal volunteers (n = 15, 12-hour wearing time)

When Lidocaine Patch is used according to the recommended dosing instructions, only 3 ± 2% of the dose applied is expected to be absorbed. At least 95% (665 mg) of lidocaine will remain in a used patch. Mean peak blood concentration of lidocaine is about 0.13 mcg/mL (about 1/10 of the therapeutic concentration required to treat cardiac arrhythmias). Repeated application of three patches simultaneously for 12 hours (recommended maximum daily dose), once per day for three days, indicated that the lidocaine concentration does not increase with daily use. The mean plasma pharmacokinetic profile for the 15 healthy volunteers is shown in Figure 1.

Figure 1: Mean lidocaine blood concentrations after three consecutive daily applications of three Lidocaine Patches simultaneously for 12 hours per day in healthy volunteers (n = 15).

Distribution: When lidocaine is administered intravenously to healthy volunteers, the volume of distribution is 0.7 to 2.7 L/kg (mean 1.5 ± 0.6 SD, n = 15). At concentrations produced by application of Lidocaine Patch, lidocaine is approximately 70% bound to plasma proteins, primarily alpha-1-acid glycoprotein. At much higher plasma concentrations (1 to 4 mcg/mL of free base), the plasma protein binding of lidocaine is concentration dependent. Lidocaine crosses the placental and blood brain barriers, presumably by passive diffusion.

Metabolism: It is not known if lidocaine is metabolized in the skin. Lidocaine is metabolized rapidly by the liver to a number of metabolites, including monoethylglycinexylidide (MEGX) and glycinexylidide (GX), both of which have pharmacologic activity similar to, but less potent than that of lidocaine. A minor metabolite, 2, 6-xylidine, has unknown pharmacologic activity but is carcinogenic in rats. The blood concentration of this metabolite is negligible following application of Lidocaine Patch 5%. Following intravenous administration, MEGX and GX concentrations in serum range from 11 to 36% and from 5 to 11% of lidocaine concentrations, respectively.

Excretion: Lidocaine and its metabolites are excreted by the kidneys. Less than 10% of lidocaine is excreted unchanged. The half-life of lidocaine elimination from the plasma following IV administration is 81 to 149 minutes (mean 107 ± 22 SD, n = 15). The systemic clearance is 0.33 to 0.90 L/min (mean 0.64 ± 0.18 SD, n = 15).

Clinical Studies

Single-dose treatment with Lidocaine Patch was compared to treatment with vehicle patch (without lidocaine), and to no treatment (observation only) in a double-blind, crossover clinical trial with 35 post-herpetic neuralgia patients. Pain intensity and pain relief scores were evaluated periodically for 12 hours. Lidocaine Patch performed statistically better than vehicle patch in terms of pain intensity from 4 to 12 hours.

Multiple-dose, two-week treatment with Lidocaine Patch was compared to vehicle patch (without lidocaine) in a double-blind, crossover clinical trial of withdrawal-type design conducted in 32 patients, who were considered as responders to the open-label use of Lidocaine Patch prior to the study. The constant type of pain was evaluated but not the pain induced by sensory stimuli (dysesthesia). Statistically significant differences favoring Lidocaine Patch were observed in terms of time to exit from the trial (14 versus 3.8 days at p-value <0.001), daily average pain relief, and patient’s preference of treatment. About half of the patients also took oral medication commonly used in the treatment of post-herpetic neuralgia. The extent of use of concomitant medication was similar in the two treatment groups.

INDICATION AND USAGE

Lidocaine Patch 5% is indicated for relief of pain associated with post-herpetic neuralgia. It should be applied only to intact skin.

Contraindications

Lidocaine Patch 5% is contraindicated in patients with a known history of sensitivity to local anesthetics of the amide type, or to any other component of the product.

Warnings

Accidental Exposure in Children

Even a used Lidocaine Patch contains a large amount of lidocaine (at least 665 mg). The potential exists for a small child or a pet to suffer serious adverse effects from chewing or ingesting a new or used Lidocaine Patch, although the risk with this formulation has not been evaluated. It is important for patients to store and dispose of Lidocaine Patch 5% out of the reach of children, pets and others. (See HANDLING AND DISPOSAL )

Excessive Dosing

Excessive dosing by applying Lidocaine Patch 5% to larger areas or for longer than the recommended wearing time could result in increased absorption of lidocaine and high blood concentrations, leading to serious adverse effects (see ADVERSE REACTIONS. Systemic Reactions ). Lidocaine toxicity could be expected at lidocaine blood concentrations above 5 mcg/mL. The blood concentration of lidocaine is determined by the rate of systemic absorption and elimination. Longer duration of application, application of more than the recommended number of patches, smaller patients, or impaired elimination may all contribute to increasing the blood concentration of lidocaine. With recommended dosing of Lidocaine Patch 5%, the average peak blood concentration is about 0.13 mcg/mL, but concentrations higher than 0.25 mcg/mL have been observed in some individuals.

Precautions

General

Hepatic Disease: Patients with severe hepatic disease are at greater risk of developing toxic blood concentrations of lidocaine, because of their inability to metabolize lidocaine normally.

Allergic Reactions: Patients allergic to para-aminobenzoic acid derivatives (procaine, tetracaine, benzocaine, etc.) have not shown cross sensitivity to lidocaine. However, Lidocaine Patch 5% should be used with caution in patients with a history of drug sensitivities, especially if the etiologic agent is uncertain.

Non-intact Skin: Application to broken or inflamed skin, although not tested, may result in higher blood concentrations of lidocaine from increased absorption. Lidocaine Patch 5% is only recommended for use on intact skin.

External Heat Sources: Placement of external heat sources, such as heating pads or electric blankets, over Lidocaine Patch 5% is not recommended as this has not been evaluated and may increase plasma lidocaine levels.

Eye Exposure: The contact of Lidocaine Patch 5% with eyes, although not studied, should be avoided based on the findings of severe eye irritation with the use of similar products in animals. If eye contact occurs, immediately wash out the eye with water or saline and protect the eye until sensation returns.

Drug Interactions

Antiarrhythmic Drugs: Lidocaine Patch 5% should be used with caution in patients receiving Class I antiarrhythmic drugs (such as tocainide and mexiletine) since the toxic effects are additive and potentially synergistic.

Local Anesthetics: When Lidocaine Patch 5% is used concomitantly with other products containing local anesthetic agents, the amount absorbed from all formulations must be considered.

Carcinogenesis, Mutagenesis, Impairment of Fertility

Carcinogenesis: A minor metabolite, 2,6-xylidine, has been found to be carcinogenic in rats. The blood concentration of this metabolite is negligible following application of Lidocaine Patch 5%.

Mutagenesis: Lidocaine HCl is not mutagenic in Salmonella /mammalian microsome test nor clastogenic in chromosome aberration assay with human lymphocytes and mouse micronucleus test.

Impairment of Fertility: The effect of Lidocaine Patch 5% on fertility has not been studied.

Pregnancy

Teratogenic Effects: Pregnancy Category B. Lidocaine Patch 5% has not been studied in pregnancy. Reproduction studies with lidocaine have been performed in rats at doses up to 30 mg/kg subcutaneously and have revealed no evidence of harm to the fetus due to lidocaine. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, Lidocaine Patch 5% should be used during pregnancy only if clearly needed.

Labor and Delivery

Lidocaine Patch 5% has not been studied in labor and delivery. Lidocaine is not contraindicated in labor and delivery. Should Lidocaine Patch 5% be used concomitantly with other products containing lidocaine, total doses contributed by all formulations must be considered.

Nursing Mothers

Lidocaine Patch 5% has not been studied in nursing mothers. Lidocaine is excreted in human milk, and the milk:plasma ratio of lidocaine is 0.4. Caution should be exercised when Lidocaine Patch 5% is administered to a nursing woman.

Pediatric Use

Safety and effectiveness in pediatric patients have not been established.

Adverse Reactions

Application Site Reactions

During or immediately after treatment with Lidocaine Patch 5%, the skin at the site of application may develop blisters, bruising, burning sensation, depigmentation, dermatitis, discoloration, edema, erythema, exfoliation, irritation, papules, petechia, pruritus, vesicles, or may be the locus of abnormal sensation. These reactions are generally mild and transient, resolving spontaneously within a few minutes to hours.

Allergic Reactions

Allergic and anaphylactoid reactions associated with lidocaine, although rare, can occur. They are characterized by angioedema, bronchospasm, dermatitis, dyspnea, hypersensitivity, laryngospasm, pruritus, shock, and urticaria. If they occur, they should be managed by conventional means. The detection of sensitivity by skin testing is of doubtful value.

Other Adverse Events

Due to the nature and limitation of spontaneous reports in postmarketing surveillance, causality has not been established for additional reported adverse events including:

Asthenia, confusion, disorientation, dizziness, headache, hyperesthesia, hypoesthesia, lightheadedness, metallic taste, nausea, nervousness, pain exacerbated, paresthesia, somnolence, taste alteration, vomiting, visual disturbances such as blurred vision, flushing, tinnitus, and tremor.

Systemic (Dose-Related) Reactions

Systemic adverse reactions following appropriate use of Lidocaine Patch 5% are unlikely, due to the small dose absorbed (see CLINICAL PHARMACOLOGY. Pharmacokinetics ). Systemic adverse effects of lidocaine are similar in nature to those observed with other amide local anesthetic agents, including CNS excitation and/or depression (light-headedness, nervousness, apprehension, euphoria, confusion, dizziness, drowsiness, tinnitus, blurred or double vision, vomiting, sensations of heat, cold or numbness, twitching, tremors, convulsions, unconsciousness, respiratory depression and arrest). Excitatory CNS reactions may be brief or not occur at all, in which case the first manifestation may be drowsiness merging into unconsciousness. Cardiovascular manifestations may include bradycardia, hypotension and cardiovascular collapse leading to arrest.

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

Overdosage

Lidocaine overdose from cutaneous absorption is rare, but could occur. If there is any suspicion of lidocaine overdose (see ADVERSE REACTIONS. Systemic Reactions ), drug blood concentration should be checked. The management of overdose includes close monitoring, supportive care, and symptomatic treatment. Dialysis is of negligible value in the treatment of acute overdose with lidocaine.

In the absence of massive topical overdose or oral ingestion, evaluation of symptoms of toxicity should include consideration of other etiologies for the clinical effects, or overdosage from other sources of lidocaine or other local anesthetics.

The oral LD 50 of lidocaine HCl is 459 (346 to 773) mg/kg (as the salt) in non-fasted female rats and 214 (159 to 324) mg/kg (as the salt) in fasted female rats, which are equivalent to roughly 4000 mg and 2000 mg, respectively, in a 60 to 70 kg man based on the equivalent surface area dosage conversion factors between species.

Lidocaine Patch Dosage and Administration

Apply Lidocaine Patch 5% to intact skin to cover the most painful area. Apply the prescribed number of patches (maximum of 3), only once for up to 12 hours within a 24-hour period. Patches may be cut into smaller sizes with scissors prior to removal of the release liner. (See HANDLING AND DISPOSAL ) Clothing may be worn over the area of application. Smaller areas of treatment are recommended in a debilitated patient, or a patient with impaired elimination.

If irritation or a burning sensation occurs during application, remove the patch(es) and do not reapply until the irritation subsides.

When Lidocaine Patch 5% is used concomitantly with other products containing local anesthetic agents, the amount absorbed from all formulations must be considered.

Lidocaine Patch 5% may not stick if it gets wet. Avoid contact with water, such as bathing, swimming or showering.

HANDLING AND DISPOSAL

Hands should be washed after the handling of Lidocaine Patch 5%, and eye contact with Lidocaine Patch 5% should be avoided. Do not store patch outside the sealed envelope. Apply immediately after removal from the protective envelope. Fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get to them. Lidocaine Patch 5% should be kept out of the reach of children.

How is Lidocaine Patch Supplied

Lidocaine Patch 5% is available as the following:

Carton of 15 patches, NDC 59088-396-82 Carton of 30 patches, NDC 59088-396-54

Each patch is packaged into an individual child-resistant envelope.

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

For more information, call Actavis at 1-800-272-5525.

Manufactured by: Actavis Laboratories UT, Inc. Salt Lake City, UT 84108 USA

Distributed by: PureTek Corporation San Fernando, CA 91340 USA

PRINCIPAL DISPLAY PANEL

NDC 59088-396-54 Lidocaine Patch 5% Rx only 30 Patches (30 Envelopes Containing 1 Patch Each)

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Benoxuric (Zyloprim) Description

Benoxuric is used for treating gout caused by excessive levels of uric acid in the blood (hyperuricemia). Hyperuricemia occurs when the body produces more uric acid than it can eliminate. The uric acid forms crystals in joints (gouty arthritis) and tissues, causing inflammation and pain. Elevated blood uric acid levels also can cause kidney disease and stones. Benoxuric prevents the production of uric acid by blocking the activity of the enzyme that converts purines to uric acid.

Benoxuric prevents the production of uric acid by blocking the activity of the enzyme that converts purines to uric acid.

Benoxuric is also known as Allopurinol, Allohexal, Allosig, Progout, Zyloric, Puricos.

Generic name of Benoxuric is Allopurinol.

Brand names of Benoxuric are Benoxuric, Aloprim.

Benoxuric (Zyloprim) Dosage

Benoxuric is available in:

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The daily dosage of Benoxuric is 100-800 mg.

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Benoxuric should be taken with food only, to avoid stomach irritation.

Benoxuric should be taken with plenty amount of fluid, to avoid formation of kidney stones.

If you want to achieve most effective results do not stop taking Benoxuric suddenly.

Benoxuric (Zyloprim) Missing of dose

Do not take double dose. If you miss a dose you should take it as soon as you remember about your missing. If it is the time for the next dose you should continue your regular dosing schedule.

Benoxuric (Zyloprim) Overdose

If you overdose Benoxuric and you don't feel good you should visit your doctor or health care provider immediately.

Benoxuric (Zyloprim) Storage

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Benoxuric (Zyloprim) Contra-indications

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Be careful with Benoxuric if you are taking didanosine, amoxicillin, ampicillin, certain asthma drugs (aminophylline, theophylline), azathioprine.

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Benoxuric (Zyloprim) Frequently asked questions

Q: What is Benoxuric?

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Q: How does Benoxuric work?

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Is Hemiplegia A Side Effect Of Trophigil ( ), Trophigil

About this FactMed analysis covering adverse side effect reports of TROPHIGIL patients who developed HEMIPLEGIA.

FactMed provides MD-approved analysis to help both patients, researchers, and physicians accurately assess the risk profile for more than 20,000 different pharmaceutical products. The below report offers compiled information from Food & Drug Administration and FactMed user submissions. Between January 2004 and October 2012, 2 individuals taking TROPHIGIL reported HEMIPLEGIA to the FDA. A total of 11 TROPHIGIL drug adverse event reaction reports were made with the FDA during this time period. Often the FDA only receives reports of the most critical and severe cases; these numbers may therefore underrepresent the complication rate of the medication.

FDA Research Report

Introduction This page is designed to help you determine the relationship, if any, between TROPHIGIL and HEMIPLEGIA. In doing so, we compare TROPHIGIL with other drugs that cause HEMIPLEGIA, to help you evaluate whether or not TROPHIGIL causes HEMIPLEGIA. Likewise, this page shows the most highly-reported side effects of TROPHIGIL, so you can see if HEMIPLEGIA ranks among TROPHIGIL's most well-known side effects.

Summary Statistics Reports of TROPHIGIL causing HEMIPLEGIA: 2 Reports of any side effect of TROPHIGIL. 11 Percentage of TROPHIGIL patients where HEMIPLEGIA is a reported side effect: 18.1818%

FDA reports of any drug causing HEMIPLEGIA. 3535 Average percentage for all medicated patients where HEMIPLEGIA is reported as a complication: 0.0222%

Physician opinion on TROPHIGIL as adverse event culprit:

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Ruduo skaiciuoja dar tik pirmasias dienas, taciau peršalimo ligos pradeda savo plitimo sezona. Permainingas rudeninis oras bei nepakankamas rupinimasis savo ir šeimos nariu sveikata daznai nulemia viena nemaloniausiu bei sunkiausiai prognozuojamu sveikatos sutrikimu – gerkles skausma. „Dazniausiai gerkles skausmo sukelejai yra virusai, kurie pazeidzia gerkles gleivine. Uzklupus virusiniam gerkles uzdegimui peršti, skauda gerkle, juntamas burnos sausumas, kosejama ar ciaudejama, vargina sloga, neretai uzkimstama, šiek tiek pakyla temperatura.

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„Janssen“ kompanija Europos vaistu agenturai pateike prašyma suteikti rinkodaros teises vienos tabletes preparatui, kurio pagrindas darunaviras, gydanciam ZIV-1 infekcija. Kompanija „Janssen – Cilag International NV“ („Janssen“) praneše, kad pateike prašyma Europos vaistu agenturai (EMA) suteikti rinkodaros teises ir patvirtinti nauja gydymo rezima viena tablete per diena, kurios pagrindas yra darunaviras. Jei bus patvirtinta, ši tablete bus pirmasis proteazes inhibitoriaus pagrindu sudarytas vaistas, skiriamas kaip visas gydymo kursas, zmogaus imunodeficito viruso sukeltai infekcija sergantiems suaugusiems pacientams ir paaugliams (vyresniems kaip 12 metu, kuriu kuno svoris ne mazesnis nei 40 kg).

Hiromi Shinya – zinomas japonu gydytojas, gastroenterologas ir chirurgas, keleto knygu, skirtu sveikam gyvenimo budui ir tapusiu bestseleriais, autorius. Per 40 gydytojo darbo metu jam nei karto neteko rašyti mirties liudijimo, nors jis gyde ir onkologinius pacientus. Jo sudaryta teisingos mitybos programa padejo pasveikti ir keliems labai zinomiems pacientams: Calvinui Kleinui, Stingui, Dustinui Hoffmanui.

Ankstyvas senejimas yra viena didziausiu moteru baimiu. Saules spinduliai ir aplinkos tarša daro itaka musu odai, del to atsiranda pigmentines demes, raukšles ir kiti ankstyvo senejimo pozymiai. Puoseledamos grozi, visuomet labiau rupinames veido oda, o pamirštame kakla ir rankas. Tuo tarpu kaklas ir rankos yra tos vietos, kurios labiausiai atspindi musu amziu. Todel ju prieziurai reiketu skirti zymiai daugiau demesio. Tinklapis Econet pateikia efektyvias naturalias priemones, kurias galite pasigaminti pacios.

Rugsejo 15d. Valstybines maisto ir veterinarijos tarnybos (VMVT) direktorius Jonas Milius LR Vyriausybeje pristate 2015 – 2016 m. (01-08 men.) savo veiklos ataskaita. VMVT – viena pirmuju ES valstybines kontroles instituciju, reorganizuotu ir pertvarkytu taip, kad visa maisto gamybos ir tiekimo vartotojams procesa butu galima kontroliuoti efektyviai, išvengiant ilgai trunkancio biurokratinio keliu kontroles instituciju bendravimo. Toki kontroles modeli pavyzdiniu pripazino Pasaulio bankas, Pasaulio gyvunu sveikatos organizacija, Tarptautine ekonominio bendradarbiavimo ir pletros organizacija.

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Omebeta 20 - Anti-Ulcer Agents, Proton-Pump Inhibitors, Atc A02bc01, Atc A02bc05, Omebeta

Omebeta 20

Omebeta 20 Indication

For the treatment of gastroesophageal reflux disease.

Omebeta 20 Pharmacology

Omeprazole is a compound that inhibits gastric acid secretion and is indicated in the treatment of gastroesophageal reflux disease (GERD), the healing of erosive esophagitis, and H. pylori eradication to reduce the risk of duodenal ulcer recurrence. Omeprazole belongs to a new class of antisecretory compounds, the substituted benzimidazoles, that do not exhibit anticholinergic or H2 histamine antagonistic properties, but that suppress gastric acid secretion by specific inhibition of the H + /K + ATPase enzyme system at the secretory surface of the gastric parietal cell. Because this enzyme system is regarded as the acid (proton) pump within the gastric mucosa, omeprazole has been characterized as a gastric acid-pump inhibitor, in that it blocks the final step of acid production. This effect is dose-related and leads to inhibition of both basal and stimulated acid secretion irrespective of the stimulus.

Omebeta 20 Absorption

Absorption is rapid, absolute bioavailability (compared to intravenous administration) is about 30-40% at doses of 20-40 mg.

Omebeta 20 side effects and Toxicity

Symptoms of overdose include confusion, drowsiness, blurred vision, tachycardia, nausea, diaphoresis, flushing, headache, and dry mouth.

Omebeta 20 Patient Information

PRILOSEC Delayed-Release Capsules should be taken before eating. Patients should be cautioned that the PRILOSEC Delayed-Release Capsule should not be opened, chewed or crushed, and should be swallowed whole.

For patients who have difficulty swallowing capsules, the contents of a PRILOSEC Delayed-Release Capsule can be added to applesauce. One tablespoon of applesauce should be added to an empty bowl and the capsule should be opened. All of the pellets inside the capsule should be carefully emptied on the applesauce. The pellets should be mixed with the applesauce and then swallowed immediately with a glass of cool water to ensure complete swallowing of the pellets. The applesauce used should not be hot and should be soft enough to be swallowed without chewing. The pellets should not be chewed or crushed. The pellets/applesauce mixture should not be stored for future use.

Omebeta 20 Organisms Affected

Humans and other mammals

Amoxil Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Amoxal

Amoxil

Uses

Amoxicillin is used to treat a wide variety of bacterial infections. This medication is a penicillin - type antibiotic. It works by stopping the growth of bacteria.

This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold. flu ). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness.

Amoxicillin is also used with other medications to treat stomach /intestinal ulcers caused by the bacteria H. pylori and to prevent the ulcers from returning.

OTHER USES: This section contains uses of this drug that are not listed in the approved US professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This drug may also be used by people with certain heart problems (such as heart valve disease) before medical/dental procedures (such as tooth /gum procedures) to prevent heart infection.

How to use Amoxil

Take this medication by mouth with or without food as directed by your doctor, usually every 8 or 12 hours. The dosage is based on your medical condition and response to treatment.

Drink plenty of fluids while using this medication unless your doctor tells you otherwise.

Antibiotics work best when the amount of medicine in your body is kept at a constant level. Therefore, take this drug at evenly spaced intervals. To help you remember, take it at the same times each day.

Continue to take this medication until the full prescribed amount is finished, even if symptoms disappear after a few days. Stopping the medication too early may allow bacteria to continue to grow, which may result in a return of the infection.

Tell your doctor if your condition persists or worsens.

Side Effects

Nausea. vomiting. or diarrhea may occur. If any of these effects persist or worsen, tell 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.

Use of this medication for prolonged or repeated periods may result in oral thrush or a new vaginal yeast infection (oral or vaginal fungal infection). Contact your doctor if you notice white patches in your mouth. a change in vaginal discharge or other new symptoms.

Tell your doctor right away if any of these rare but serious side effects occur: dark urine, persistent nausea or vomiting, stomach /abdominal pain. yellowing eyes or skin. easy bruising or bleeding, persistent sore throat or fever.

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

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

Amoxicillin can commonly cause a mild rash that is usually not serious. However, you may not be able to tell it apart from a rare rash that could be a sign of a severe allergic reaction. Therefore, get medical help right away if you develop any rash.

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 amoxicillin, tell your doctor or pharmacist if you are allergic to it; or to penicillin or cephalosporin antibiotics ; 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. a certain type of viral infection (infectious mononucleosis ).

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

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

Amoxicillin passes into breast milk. Consult your doctor before breast - feeding.

Interactions

The effects of some drugs can change if you take other drugs or herbal products at the same time. This can increase your risk for serious side effects or may cause your medications not to work correctly. These drug interactions are possible, but do not always occur. Your doctor or pharmacist can often prevent or manage interactions by changing how you use your medications or by close monitoring.

To help your doctor and pharmacist give you the best care, be sure to tell your doctor and pharmacist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products) before starting treatment with this product. While using this product, do not start, stop, or change the dosage of any other medicines you are using without your doctor's approval.

Some products that may interact with this drug include: live bacterial vaccines. methotrexate .

Although most antibiotics are unlikely to affect hormonal birth control such as pills, patch, or ring, a few antibiotics (such as rifampin, rifabutin ) can decrease their effectiveness. This could result in pregnancy. If you use hormonal birth control. ask your doctor or pharmacist for more details.

Amoxicillin may cause false positive results with certain diabetic urine testing products (cupric sulfate-type). This drug may also affect the results of certain lab tests. Make sure laboratory personnel and your doctors know you use this drug.

This document does not contain all possible drug interactions. Keep a list of all the products you use. Share this list with your doctor and pharmacist to lessen your risk for serious medication problems.

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: severe vomiting, persistent diarrhea, a severe decrease in the amount of urine, or seizures.

Notes

Do not share this medication with others.

This medication has been prescribed for your current condition only. Do not use it later for another infection unless your doctor directs you to do so. A different medication may be necessary in that case.

With prolonged treatment, laboratory and/or medical tests (such as kidney and liver function, complete blood counts) may be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

Missed Dose

If you miss a dose, use 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 according to the product labeling, away from light and moisture. Different brands of this medication have different storage needs. Check the product package for instructions on how to store your brand, or ask your pharmacist. 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 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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Tenoblock Generic Name Atenolol Online, Tenoblock

Tenoblock General Information

Tenoblock - Pharmacology:

Like metoprolol, atenolol competes with sympathomimetic neurotransmitters such as catecholamines for binding at beta(1)-adrenergic receptors in the heart and vascular smooth muscle, inhibiting sympathetic stimulation. This results in a reduction in resting heart rate, cardiac output, systolic and diastolic blood pressure, and reflex orthostatic hypotension. Higher doses of atenolol also competitively block beta(2)-adrenergic responses in the bronchial and vascular smooth muscles.

Tenoblock for patients

This belongs to the group of medicines known as beta-blockers. Tenoblock can be used to treat high blood pressure, angina (chest pain) and irregular heartbeat. It has varied effects in different parts of the body. High Blood Pressure: Tenoblock works by blocking the transmission of messages to the beta receptors in the heart which slows down the activity of the heart, decreasing blood pressure. Angina: Tenoblock works by blocking the transmission of messages to the beta receptors in the heart which slows down the activity of the heart and reduces the hearts need for oxygen. This makes angina attacks less likely to occur. Irregular Heartbeat: Normally the heartbeat is regulated by special tissues which conduct electricity. Some cases of irregular heartbeat are caused by these tissues conducting electricity too quickly. Tenoblock works by reducing over-activity in the conducting tissue.

This description is suitable for active ingredient Atenolol

Tenoblock Interactions

Catecholamine-depleting drugs (eg, reserpine) may have an additive effect when given with beta-blocking agents. Patients treated with TENORMIN plus a catecholamine depletor should therefore be closely observed for evidence of hypotension and/or marked bradycardia which may produce vertigo, syncope, or postural hypotension.

Calcium channel blockers may also have an additive effect when given with TENORMIN .

Beta blockers may exacerbate the rebound hypertension which can follow the withdrawal of clonidine. If the two drugs are coadministered, the beta blocker should be withdrawn several days before the gradual withdrawal of clonidine. If replacing clonidine by beta-blocker therapy, the introduction of beta blockers should be delayed for several days after clonidine administration has stopped.

Concomitant use of prostaglandin synthase inhibiting drugs, eg, indomethacin, may decrease the hypotensive effects of beta blockers.

Information on concurrent usage of atenolol and aspirin is limited. Data from several studies, ie, TIMI-II, ISIS-2, currently do not suggest any clinical interaction between aspirin and beta blockers in the acute myocardial infarction setting.

While taking beta blockers, patients with a history of anaphylactic reaction to a variety of allergens may have a more severe reaction on repeated challenge, either accidental, diagnostic or therapeutic. Such patients may be unresponsive to the usual doses of epinephrine used to treat the allergic reaction.

Tenoblock Contraindications

TENORMIN is contraindicated in sinus bradycardia, heart block greater than first degree, cardiogenic shock, and overt cardiac failure.

TENORMIN is contraindicated in those patients with a history of hypersensitivity to the atenolol or any of the drug productis components.

This description is suitable for active ingredient Atenolol

Generic name, Overdose, Half Life Tenoblock, Food Interactions, Chemical, etc..

Tenoblock see also

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