Teva pill 5728

If teva pill 5728 are a consumer or patient please visit this version. Famotidine tablets are a histamine-2 H 2 receptor antagonist indicated 1 :. Administration 2. Tablets: 20 mg, 40 mg 3.

We recommend using a newer internet browser, such as Google Chrome or Microsoft Edge, to optimize your browsing experience. Our mission is to be a global leader in generics and biopharmaceuticals, improving the lives of patients around the globe. View the latest press releases, feature stories, and company resources. At Teva we believe that every one of us should have access to quality medicine that helps manage disease, fight infection, or simply improves overall health. Around million people worldwide take one of our medicines every day.

Teva pill 5728

Famotidine tablets are indicated in adults for the: treatment of pathological hypersecretory conditions e. Famotidine tablets are a histamine-2 H 2 receptor antagonist indicated 1 : In adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer DU. In adults for the: treatment of pathological hypersecretory conditions e. Dispense in a well-closed, light-resis tan t container as defined in the USP, with a child-resis tan t closure as required. While we do our best to index pills, there could still be small errors. This tool does not provide medical advice, and is for informational and educational purposes only, and is not a substitute for professional medical advice, treatment or diagnosis. Call your doctor to receive medical advice. If you think you may have a medical emergency, please dial While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Pill Sync. Upload Pill Login to Save Pill. Advertise Voice Search Barcode Scanner. Identify Pill. FDA Reported Adverse Reactions [1] fatigue [2] nausea [3] drug ineffective [4] dyspnoea [5] diarrhoea [6] pain [7] off label use [8] headache [9] dizziness [10] vomiting.

Due to low binding to plasma proteins, famotidine is eliminated by hemodialysis.

The active ingredient in famotidine tablets USP is a histamine H 2 -receptor antagonist. Famotidine, USP is [1-Amino[[[2-[ diaminomethylene amino]thiazolyl]methyl]thio] propylidene] sulfamide and has the following structural formula:. Famotidine, USP is a white to pale yellow crystalline compound that is freely soluble in glacial acetic acid, slightly soluble in methanol, very slightly soluble in water, and practically insoluble in ethanol. Each tablet for oral administration contains either 20 mg or 40 mg of famotidine, USP and has the following inactive ingredients: colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized corn starch, sodium starch glycolate, talc, titanium dioxide, yellow iron oxide. Famotidine is a competitive inhibitor of histamine H 2 -receptors. The primary clinically important pharmacologic activity of famotidine is inhibition of gastric secretion.

We recommend using a newer internet browser, such as Google Chrome or Microsoft Edge, to optimize your browsing experience. Our mission is to be a global leader in generics and biopharmaceuticals, improving the lives of patients around the globe. View the latest press releases, feature stories, and company resources. At Teva we believe that every one of us should have access to quality medicine that helps manage disease, fight infection, or simply improves overall health. Around million people worldwide take one of our medicines every day.

Teva pill 5728

The active ingredient in famotidine tablets USP is a histamine H 2 -receptor antagonist. Famotidine, USP is [1-Amino[[[2-[ diaminomethylene amino]thiazolyl]methyl]thio] propylidene] sulfamide and has the following structural formula:. Famotidine, USP is a white to pale yellow crystalline compound that is freely soluble in glacial acetic acid, slightly soluble in methanol, very slightly soluble in water, and practically insoluble in ethanol. Each tablet for oral administration contains either 20 mg or 40 mg of famotidine, USP and has the following inactive ingredients: colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized corn starch, sodium starch glycolate, talc, titanium dioxide, yellow iron oxide. Famotidine is a competitive inhibitor of histamine H 2 -receptors. The primary clinically important pharmacologic activity of famotidine is inhibition of gastric secretion.

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Prolonged QT interval, in patients with impaired renal function, has been reported very rarely. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The clearance of famotidine is reduced in adults with moderate and severe renal impairment compared to adults with normal renal function [see Clinical Pharmacology Because animal reproductive studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. Famotidine has an elimination half-life of 2. Central nervous system CNS adverse reactions, including confusion, delirium, hallucinations, disorientation, agitation, seizures, and lethargy, have been reported in elderly patients and patients with moderate and severe renal impairment treated with famotidine tablets. Oral doses of 0. The following other adverse reactions have been reported infrequently in clinical trials or since the drug was marketed. These differences were statistically significant. The active ingredient in famotidine tablets USP is a histamine H 2 -receptor antagonist. Famotidine, USP is [1-Amino[[[2-[ diaminomethylene amino]thiazolyl]methyl]thio] propylidene] sulfamide and has the following structural formula:.

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Most adult patients heal within 6 weeks. Based on the comparison of pharmacokinetic parameters for famotidine in adults and pediatric patients, dosage adjustment in pediatric patients with moderate or severe renal insufficiency should be considered. In in vivo studies in mice, with a micronucleus test and a chromosomal aberration test, no evidence of a mutagenic effect was observed. However, no clinically significant interaction with metformin, a substrate for MATE-1, was observed. There are no data on famotidine effects on milk production. In pediatric patients 11 to 15 years of age, oral doses of 0. Table 1: Recommended Dosage and Duration of Famotidine Tablets in Adult and Pediatric Patients 40 kg and Greater with Normal Renal Function Indication Recommended Dosage Recommended Duration Active duodenal ulcer DU 40 mg once daily; or 20 mg twice daily a Up to 8 weeks b,c Active gastric ulcer 40 mg once daily Up to 8 weeks c Symptomatic nonerosive GERD 20 mg twice daily Up to 6 weeks c Erosive esophagitis diagnosed by endoscopy 20 mg twice daily; or 40 mg twice daily a Up to 12 weeks Pathological hypersecretory conditions d Starting dosage: 20 mg every 6 hours; adjust dosage to individual patient needs Maximum dosage mg every 6 hours As clinically indicated Reduction of the risk of DU recurrence d 20 mg once daily 1 year c or as clinically indicated. Use another famotidine formulation for pediatric patients weighing less than 40 kg. Orally administered famotidine was compared to placebo in a U. In the U. Although an intravenous famotidine formulation was available, no patients were treated with intravenous famotidine in this study.