famotidine
H2 receptor antagonist· Brands: Pepcid, PepcidineIVPO
Gastro-oesophageal reflux disease (GERD)
Non-erosive GERD: 20 mg twice daily. Erosive oesophagitis: 40 mg twice daily for up to 12 weeks.
- adult · PO: 20–40 mg twice daily · Non-erosive GERD: 20 mg twice daily. Erosive oesophagitis: 40 mg twice daily for up to 12 weeks.
Duodenal ulcer (active)
Take at bedtime. Treatment usually continued for 4-8 weeks.
- adult · PO: 40 mg once daily · Take at bedtime. Treatment usually continued for 4-8 weeks.
Gastric ulcer (benign)
Take at bedtime. Treatment usually continued for 4-8 weeks.
- adult · PO: 40 mg once daily · Take at bedtime. Treatment usually continued for 4-8 weeks.
Zollinger-Ellison syndrome
Initial dose; adjust based on acid output. Doses up to 480 mg/day may be required.
- adult · PO: 20 mg every 6 hours · Initial dose; adjust based on acid output. Doses up to 480 mg/day may be required.
Stress ulcer prophylaxis in critically ill patientsoff-label
For patients on enteral feeding, oral route may be used. Use is not routine; follow institutional protocol.
- adult · IV: 20 mg every 12 hours · For patients on enteral feeding, oral route may be used. Use is not routine; follow institutional protocol.
- Hypersensitivity to famotidine or other H2-receptor antagonists · Cross-sensitivity may occur.
- Severe renal impairment (creatinine clearance < 30 mL/min) · Dose reduction required; consider alternate H2 blocker.
- Severe hepatic impairment · Use with caution; monitor for adverse effects.
- Adjust dose in renal impairment; reduce to 20 mg once daily or 10 mg twice daily if creatinine clearance < 30 mL/min.
- Use with caution in elderly patients, as confusion and hallucinations are more likely.
- Avoid in pregnancy and breastfeeding unless clearly needed; seek specialist advice.
- May interfere with gastric pH-dependent absorption of drugs such as ketoconazole, atazanavir, and iron salts; monitor effectiveness.
- Monitor patients with a history of gastric ulcer for malignancy before starting therapy, as symptoms may mask gastric cancer.
- Headache
- Dizziness
- Constipation
- Diarrhoea
- Confusionserious
- Hallucinationsserious
- Thrombocytopeniaserious
- Anaphylaxisserious
- eGFR 0–50: Reduce dose to half or increase the dosing interval to 36-48 hours.
- Clinical response (symptom relief) · Periodically, at follow-up
- Renal function (serum creatinine, eGFR) · Before initiation and periodically in patients with renal impairment
- Neurological symptoms (confusion, hallucinations) · In patients with severe renal impairment or high doses
- Pregnancy: Famotidine is generally considered safe during pregnancy; available data do not indicate an increased risk of congenital anomalies. It may be used for GERD or peptic ulcer disease when clinically indicated.
- Toxicity: Overdose may cause hypotension, bradycardia, lethargy, or confusion. · Supportive care; monitor vital signs; consider activated charcoal if recent ingestion; approximately 25-30% is removed by haemodialysis.
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BNF; local formulary