πŸ’Š H2-receptor antagonist Β· Acid suppression

Famotidine Dose Calculator

India Β· Paediatric mg/kg & Adult Β· GERD Β· Peptic Ulcer Β· Stress Ulcer Β· Pepcid Β· Topcid Β· Famocid

Oral Β· IV0.5 mg/kg/dose paedsRenal adjustmentBNF Β· IAP aligned

Famotidine Dose Calculator

Recommended Dose
β€”
β€”
Per dose (mg)
β€”
Volume / Tablets
β€”
Daily dose
β€”
Duration
β€”
⚠️

Famotidine Dosing Reference Table β€” Paediatric & Adult

PatientIndicationDoseFrequencyDuration
Child (1 month–16 yr)GERD0.5 mg/kg/dose (max 40 mg)BD (every 12h)4–8 weeks
Child (1 month–16 yr)Peptic ulcer0.5 mg/kg/dose (max 40 mg)OD at bedtime4–8 weeks
Infant ≀ 3 monthsGERD / acid0.5 mg/kg/doseODUp to 8 weeks
AdultGERD20 mgBD6–12 weeks
AdultPeptic ulcer (active)40 mgOD at bedtime4–8 weeks
AdultPeptic ulcer (maintenance)20 mgOD at bedtimeOngoing
Adult / ChildStress ulcer (ICU) β€” IV20 mg (adult) / 0.25–0.5 mg/kgEvery 12h IVICU stay
AdultZollinger-Ellison20 mg 6-hourly (titrate up)QDSOngoing

Famotidine β€” Clinical Guide for Indian Doctors & Nurses

Famotidine is a potent, selective histamine H2-receptor antagonist (H2RA) that reduces basal and stimulated gastric acid secretion. It is approximately 7.5 times more potent than ranitidine (now withdrawn from the Indian and global market due to NDMA contamination concerns) and 20 times more potent than cimetidine. In the post-ranitidine era, famotidine has become the most widely used H2RA in India and is available as Topcid, Famocid, and Pepcid across Indian pharmacies in both tablet and injection form.

In paediatric practice, famotidine is particularly valued because β€” unlike proton pump inhibitors (PPIs) β€” it has a well-established safety profile in infants and young children, does not significantly affect cytochrome P450 enzymes, and is available as a liquid suspension suitable for weight-based dosing in small children. The IAP endorses famotidine as a first-line H2RA for paediatric GERD and peptic ulcer disease.

Paediatric famotidine dosing β€” what Indian doctors need to know

The standard paediatric famotidine dose is 0.5 mg/kg/dose, capped at a maximum of 40 mg per dose. For GERD (the most common indication in children), this is given twice daily (every 12 hours). For peptic ulcer disease, it is given once daily at bedtime. For infants aged 3 months or younger, the dose is the same (0.5 mg/kg) but given only once daily, given immature hepatic and renal metabolism.

The oral suspension 8 mg/ml formulation is the most practical option for children under 5 years or those who cannot swallow tablets. For a 10 kg child at 0.5 mg/kg: 5 mg per dose = 0.625 ml of 8mg/ml suspension. For a 20 kg child: 10 mg per dose = 1.25 ml. Tablet splitting (20 mg tablets) is feasible for older children where the dose is β‰₯ 10 mg, but the suspension provides better accuracy for younger children.

Adult famotidine dosing β€” standard indications

For active peptic ulcer disease (duodenal or gastric), the standard adult dose is famotidine 40 mg once daily at bedtime, or 20 mg twice daily, for 4–8 weeks. Bedtime dosing is preferred because nocturnal acid secretion is the primary driver of ulcer persistence. After healing confirmation (endoscopy or clinical response), maintenance therapy with 20 mg once daily at bedtime can prevent recurrence. For GERD without oesophagitis: 20 mg twice daily for 6–12 weeks. For erosive GERD or oesophagitis, a PPI may offer superior mucosal healing.

Famotidine vs PPIs β€” when to choose which

In India, there is a tendency to over-prescribe PPIs (omeprazole, pantoprazole) for even mild acid-related symptoms. Famotidine is appropriate β€” and preferred β€” for: on-demand acid relief, mild-moderate GERD, peptic ulcer disease (especially in H. pylori-positive patients on eradication therapy), stress ulcer prophylaxis in ICU, and paediatric acid suppression. PPIs are preferred for severe GERD with oesophagitis, Barrett's oesophagus, NSAID-induced ulcer prevention in high-risk patients, and H. pylori eradication regimens. Unlike long-term PPI use, famotidine does not carry the risk of hypomagnesaemia, C. difficile-associated diarrhoea (at lower frequency), or bone density reduction.

ICU stress ulcer prophylaxis

In critically ill patients (ICU, mechanical ventilation, coagulopathy), famotidine 20 mg IV every 12 hours is the standard stress ulcer prophylaxis regimen in India, particularly in centres where IV pantoprazole is unavailable or cost-prohibitive. In paediatric ICU patients, IV famotidine 0.25–0.5 mg/kg every 12 hours is used.

Frequently Asked Questions

What is the famotidine dose for a 15 kg child with GERD?+
For a 15 kg child: 0.5 mg/kg Γ— 15 = 7.5 mg per dose, given every 12 hours. In 8 mg/ml suspension: 7.5 Γ· 8 Γ— 1 ml = 0.94 ml (~1 ml) per dose, twice daily. If using 20 mg tablets (splitting), 7.5 mg is approximately 3/8 of a tablet β€” the suspension is more accurate in this weight range. Maximum dose is 40 mg regardless of weight.
Can famotidine be given to infants under 1 year?+
Yes. Famotidine is one of the few H2RAs with published safety and dosing data in infants. For infants aged 1–3 months: 0.5 mg/kg once daily. For infants aged 3–12 months: 0.5 mg/kg twice daily for GERD. In neonates under 1 month, use only under specialist supervision with careful monitoring. The 8 mg/ml suspension is the preferred formulation for infants.
How does famotidine compare to ranitidine? Is ranitidine still available in India?+
Ranitidine was withdrawn from the Indian market in 2020 by CDSCO following global concerns about NDMA (N-nitrosodimethylamine) contamination β€” a probable human carcinogen. Famotidine is now the standard H2RA replacement. It is more potent (7.5Γ— compared to ranitidine), has a cleaner drug interaction profile, and is available in equivalent formulations across India. Famotidine does not have the NDMA contamination issue.
Does famotidine need dose adjustment in kidney disease?+
Yes. Famotidine is primarily renally excreted (65–70%). For CrCl 30–50 mL/min: halve the dose or double the dosing interval. For CrCl < 30 mL/min: 20 mg every 36–48 hours. In severe renal failure, famotidine accumulation can cause CNS side effects including confusion, agitation, and hallucinations β€” monitor elderly patients carefully.
Is famotidine safe in pregnancy?+
Famotidine is classified as Pregnancy Category B (no evidence of risk in humans in available studies) and is considered one of the safer options for acid suppression during pregnancy. It is preferred over PPIs in the first trimester when the evidence for PPI safety is less certain. Standard doses apply.
⚠️Decision-support tool for trained healthcare professionals. Verify against BNF and current prescribing information. Not a substitute for clinical judgement or professional medical advice.

Related Tools