Famotidine: Difference between revisions
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In [[gastroenterology]], '''famotidine''' is a competitive [[Histamine H2 antagonist]]. Its main pharmacodynamic effect is the inhibition of gastric secretion.<ref>{{MeSH}}</ref> | In [[gastroenterology]], '''famotidine''' is a competitive [[Histamine H2 antagonist]]. Its main pharmacodynamic effect is the inhibition of gastric secretion.<ref>{{MeSH}}</ref> | ||
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===Excretion=== | ===Excretion=== | ||
===Toxicity=== | ===Toxicity=== | ||
While no drug can be considered free of [[drug toxicity]], there have been no reports of acute | While no drug can be considered free of [[drug toxicity|toxicity]], there have been no reports of acute poisoning with famotidine in clinical practice. The oral and IV LD<sub>50</sub> of famotidine have been reported to be greater than 3000 and 254–563 mg/kg, respectively, in both mice and rats.<ref>{{citation | ||
| url = http://www.medscape.com/druginfo/monograph?cid=med&drugid=5035&drugname=Famotidine+Oral&monotype=monograph&secid=6 | | url = http://www.medscape.com/druginfo/monograph?cid=med&drugid=5035&drugname=Famotidine+Oral&monotype=monograph&secid=6 | ||
| title = Monograph: famotidine | | title = Monograph: famotidine | ||
Revision as of 15:13, 9 June 2010
In gastroenterology, famotidine is a competitive Histamine H2 antagonist. Its main pharmacodynamic effect is the inhibition of gastric secretion.[1]
History
Pepcid brand of famotidine was approved by the Food and Drug Administration in the United States. It is available as a generic, and also in over-the-counter forms.
Pharmacology
Administration
It is most commonly administered orally, as a tablet or suspension. An intravenous preparation is approved for hospitalized patients.
Distribution
Metabolism
Excretion
Toxicity
While no drug can be considered free of toxicity, there have been no reports of acute poisoning with famotidine in clinical practice. The oral and IV LD50 of famotidine have been reported to be greater than 3000 and 254–563 mg/kg, respectively, in both mice and rats.[2]
Side effects have been reported to include headache, dizziness, diarrhea and constipation.
Drug-drug interactions are less likely with famotidine than with the related drugs cimetidine and ranitidine. It "does not appear to inhibit the metabolism of drugs, including warfarin, theophylline, phenytoin, diazepam, or procainamide, by the hepatic cytochrome P-450 (microsomal) enzyme system. ... minimal effects of the drug on cytochrome P-450 enzymes have been suggested, and additional experience with long-term therapy and with relatively high dosages is necessary to determine the potential, if any, for clinically important effects." [3]
Clinical use
General medicine
Veterinary medicine
Famotidine is useful for gastrointestinal irritation in cats. It is most commonly administered as a tablet, always a challenge in cats. For human use, oral suspensions are approved, but before use in cats, the "inert ingredients" must be checked to ensure that the preparation does not contain xylitol or other sugar alcohols as sweeteners. These are toxic in cats, and cats, in any event, cannot taste sweetness.
The parenteral preparation may also be administered subcutaneously, which may well be less stressful, for home care, both to cat and human.
External links
The most up-to-date information about Famotidine and other drugs can be found at the following sites.
- Famotidine - FDA approved drug information (drug label) from DailyMed (U.S. National Library of Medicine).
- Famotidine - Drug information for consumers from MedlinePlus (U.S. National Library of Medicine).
- Famotidine - Detailed information from DrugBank.
References
- ↑ Anonymous (2024), Famotidine (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ American Society of Health System Pharmacists, Toxicity, Monograph: famotidine, Medscape
- ↑ American Society of Health System Pharmacists, Drug interactions, Monograph: famotidine, Medscape