Famotidine
فاموتیدین
🍽️ Alimentary Tract And MetabolismH2-receptor antagonist
Market / country: 🇺🇸 USA
Pepcid (US)
🧮 Dose calculator
Peptic ulcer disease · Regimen source: FDA Famotidine susp · 2.2, Table 2
Enter age and weight.
🛡️ Safety & information
Contraindications
- ⛔ History of serious hypersensitivity to famotidine or other H2-receptor antagonists. FDA Famotidine susp · 4
Warnings
- • Central nervous system adverse reactions FDA Famotidine susp · 5.1
- • Symptomatic response does not rule out gastric malignancy FDA Famotidine susp · 5.2
Renal adjustment
- • eGFR < 60: No safe dose established in pediatric renal impairment; adults with CrCl <60 per Table 3. FDA Famotidine susp · 2.3
Formulations
- 40 mg / 5 mL (8 mg/mL) — suspension 🇺🇸 USA FDA Famotidine susp · 3
👥 Special populations
- 🤰 PregnancyUse with caution
Label states no clear risk or has limited data; use only if needed, under medical advice. FDA Famotidine susp · 8.1
“Risk Summary Available data with H 2 -receptor antagonists, including famotidine, in pregnant women are insufficient to establish a drug-associated risk of major birth defects, miscarriage or adverse maternal or fetal outcomes.”
- 🤱 BreastfeedingUse with caution
Label: use with caution while breastfeeding; see the label text. FDA Famotidine susp · 8.2
“Risk Summary There are limited data available on the presence of famotidine in human breast milk.”
- 👶 ChildrenUse with caution
The label has conditions, age limits or notes for children; the label sentence is quoted below. FDA Famotidine susp · 8.4
“Peptic Ulcer Disease and GERD With or Without Esophagitis and Ulcerations Pediatric Patients 1 Year to Less Than 17 Years of Age The safety and effectiveness of famotidine for oral suspension have been established in pediatric patients 1 year to less than 17 years of age for the treatment of peptic ulcer disease and …”
- 👴 Older adultsUse with caution
Label: use with caution in older adults, usually starting at the low end of the dose range. FDA Famotidine susp · 8.5
“In postmarketing experience, CNS adverse reactions have been reported in elderly patients with and without renal impairment receiving famotidine [see Warnings and Precautions (5.1) ] .”
- ⚥ Females & males of reproductive potentialNo data
The source for this drug has no section for this group.
🔗 Reference links
- FDA (approval record)ANDA219091
- DailyMed (FDA label)FDA Famotidine susp
- MedlinePlus (NIH)FamotidineFamotidine Injection
- WHO ATC/DDDA02BA03
- Darooyab (Iran)Famotidine
🇮🇷 Registered in Iran Darooyab · G-2584/Famotidine
Dosage forms with Iranian generic codes, per Darooyab.
- 00527 · FAMOTIDINE 20MG TAB · قرص فاموتیدین ۲۰ میلیگرم
- 00528 · FAMOTIDINE 40MG TAB · قرص فاموتیدین ۴۰ میلیگرم
- 52859 · FAMOTIDINE INJECTION, 10 mg/1m 2 ML AMP · آمپول فاموتیدین ۱۰ میلیگرم / ۱ M ۲ میلیلیتر
- 53011 · FAMOTIDINE POWDER, FOR SUSPENSION ORAL 40 mg/5mL 120M · سوسپانسیون خوراکی فاموتیدین ۴۰ میلیگرم / ۵ میلیلیتر ۱۲۰ M
- 53000 · FAMOTIDINE POWDER, FOR SUSPENSION ORAL 40 mg/5mL 50 mL · سوسپانسیون خوراکی فاموتیدین ۴۰ میلیگرم / ۵ میلیلیتر ۵۰ میلیلیتر
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Famotidine susp · 3FDA Famotidine susp · 2.2, Table 2FDA Famotidine susp · 2.1, Table 1FDA Famotidine susp · 4FDA Famotidine susp · 5.1FDA Famotidine susp · 5.2FDA Famotidine susp · 2.3FDA Famotidine susp · 8.1FDA Famotidine susp · 8.2FDA Famotidine susp · 8.4FDA Famotidine susp · 8.5FDA Famotidine susp · SPL approval / marketing category
- UK SmPC (eMC / MHRA)❌ Not present
- Published guideline❌ Not present
- Licensed reference (medical school)❌ Not present
- Iranian leaflet (IFDA)❌ Not present
- Pharmacy website (secondary, unreliable)✅ PresentDarooyab · G-2584/Famotidine
- Clinical review⚠ Unverified