Famotidine Dosage
Medically reviewed by Drugs.com. Last updated on Jul 24, 2023.
Applies to the following strengths: 20 mg; 40 mg; 20 mg/50 mL; 40 mg/5 mL; 10 mg/mL; 10 mg; 20 mg/10 mL-NaCl 0.9%; 20 mg/5 mL-NaCl 0.9%
Usual Adult Dose for:
- Duodenal Ulcer
- Peptic Ulcer
- Duodenal Ulcer Prophylaxis
- Duodenal Ulcer Maintenance
- Gastric Ulcer
- Gastroesophageal Reflux Disease
- Erosive Esophagitis
- Zollinger-Ellison Syndrome
- Pathological Hypersecretory Conditions
- Dyspepsia
Usual Pediatric Dose for:
Additional dosage information:
Usual Adult Dose for Duodenal Ulcer
Oral:
- Active duodenal ulcer (DU): 40 mg orally once a day at bedtime OR 20 mg orally 2 times a day
- Duration of therapy: Up to 8 weeks
Parenteral: 20 mg IV every 12 hours
Comments:
- Both 20 mg and 40 mg have demonstrated efficacy treating active DU in clinical trials.
- Most patients who received oral formulations healed within 4 weeks, with few patients requiring treatment for 6 to 8 weeks; there are no safety data for the treatment of uncomplicated active duodenal ulcer beyond 8 weeks.
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Uses:
- Treatment of active DU
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active duodenal ulcers
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for duodenal ulcer maintenance therapy
Usual Adult Dose for Peptic Ulcer
Oral:
- Active duodenal ulcer (DU): 40 mg orally once a day at bedtime OR 20 mg orally 2 times a day
- Duration of therapy: Up to 8 weeks
Parenteral: 20 mg IV every 12 hours
Comments:
- Both 20 mg and 40 mg have demonstrated efficacy treating active DU in clinical trials.
- Most patients who received oral formulations healed within 4 weeks, with few patients requiring treatment for 6 to 8 weeks; there are no safety data for the treatment of uncomplicated active duodenal ulcer beyond 8 weeks.
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Uses:
- Treatment of active DU
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active duodenal ulcers
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for duodenal ulcer maintenance therapy
Usual Adult Dose for Duodenal Ulcer Prophylaxis
Oral: 20 mg orally once a day
- Duration of therapy: 1 year (or as directed)
Parenteral: 20 mg IV every 12 hours
Comments:
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Use: Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of an active ulcer
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active duodenal ulcers
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for duodenal ulcer maintenance therapy
Usual Adult Dose for Duodenal Ulcer Maintenance
Oral: 20 mg orally once a day
- Duration of therapy: 1 year (or as directed)
Parenteral: 20 mg IV every 12 hours
Comments:
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Use: Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of an active ulcer
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active duodenal ulcers
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for duodenal ulcer maintenance therapy
Usual Adult Dose for Gastric Ulcer
Oral:
- Active gastric ulcer (GU): 40 mg orally once a day at bedtime
- Duration of therapy: Up to 8 weeks
Parenteral: 20 mg IV every 12 hours
Comments:
- Most patients who received oral formulations healed within 4 weeks, with few patients requiring treatment for 6 to 8 weeks; there are no safety data for the treatment of active GU beyond 8 weeks.
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Uses:
- Treatment of active GU
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active benign GU
Usual Adult Dose for Gastroesophageal Reflux Disease
Oral: 20 mg orally 2 times day
- Duration of therapy: Up to 6 weeks
Parenteral: 20 mg IV every 12 hours
Comment:
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Uses:
- Treatment of symptomatic nonerosive gastroesophageal reflux disease (GERD)
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for GERD
Usual Adult Dose for Erosive Esophagitis
Oral: 20 to 40 mg orally 2 times a day
- Duration of therapy: Up to 12 weeks
Parenteral: 20 mg IV every 12 hours
Comment:
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
Uses:
- Treatment of erosive esophagitis (EE) due to GERD, including erosive/ulcerative disease diagnosed by endoscopy
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for esophagitis due to GERD
Usual Adult Dose for Zollinger-Ellison Syndrome
Oral:
- Initial dose: 20 mg orally every 6 hours
- Maximum dose: 160 mg orally every 6 hours
Parenteral: 20 mg IV every 6 to 12 hours
Comments:
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
- Dosing should be determined on an individual basis.
- Treatment should be continued for as long as clinically necessary.
Uses:
- Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome and multiple endocrine adenomas
- Some hospitalized patients with pathological hypersecretory conditions
Usual Adult Dose for Pathological Hypersecretory Conditions
Oral:
- Initial dose: 20 mg orally every 6 hours
- Maximum dose: 160 mg orally every 6 hours
Parenteral: 20 mg IV every 6 to 12 hours
Comments:
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
- Dosing should be determined on an individual basis.
- Treatment should be continued for as long as clinically necessary.
Uses:
- Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome and multiple endocrine adenomas
- Some hospitalized patients with pathological hypersecretory conditions
Usual Adult Dose for Dyspepsia
Oral:
Over-the-Counter (OTC) Formulations:
- Treatment dose: 10 to 20 mg orally once
- Symptom prevention: 10 to 20 mg orally once 10 to 60 minutes prior to consuming food/beverages that cause heartburn
- Maximum dose: 2 tablets/day
- Maximum duration of therapy: 14 days
Comments:
- OTC tablet formulations should be taken with a glass of water.
- Chewable tablet formulations should be chewed completely before swallowing.
Uses:
- Relief of heartburn associated with acid indigestion and sour stomach
- Prevention of heartburn associated with acid indigestion and sour stomach brought on by eating/drinking certain foods and beverages
Usual Pediatric Dose for Duodenal Ulcer
Oral:
1 YEAR TO LESS THAN 17 YEARS:
- Initial dose: 0.5 mg/kg orally once a day at bedtime OR 0.25 mg/kg orally 2 times a day; may increase to 1 mg/kg orally once a day at bedtime OR 0.5 mg/kg orally 2 times day
- Maximum dose: 40 mg/day
- Duration of therapy: 8 weeks
Parenteral:
1 YEAR TO 16 YEARS:
- Initial dose: 0.25 mg/kg IV as an injection over at least 2 minutes OR as an infusion over 15 minutes every 12 hours
- Maximum dose: 40 mg/day
17 YEARS AND OLDER:
Oral: 40 mg orally once a day at bedtime OR 20 mg orally 2 times a day
- Duration of therapy: Up to 8 weeks
Parenteral: 20 mg IV every 12 hours
Comments:
- Uncontrolled clinical trials have used oral doses up to 1 mg/kg in patients 1 to 16 years of age.
- Gastric acid suppression occurred at IV doses of 0.5 mg/kg every 12 hours.
Uses:
- Treatment of active DU
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active duodenal ulcers
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for duodenal ulcer maintenance therapy
Usual Pediatric Dose for Peptic Ulcer
Oral:
1 YEAR TO LESS THAN 17 YEARS:
- Initial dose: 0.5 mg/kg orally once a day at bedtime OR 0.25 mg/kg orally 2 times a day; may increase to 1 mg/kg orally once a day at bedtime OR 0.5 mg/kg orally 2 times day
- Maximum dose: 40 mg/day
- Duration of therapy: 8 weeks
Parenteral:
1 YEAR TO 16 YEARS:
- Initial dose: 0.25 mg/kg IV as an injection over at least 2 minutes OR as an infusion over 15 minutes every 12 hours
- Maximum dose: 40 mg/day
17 YEARS AND OLDER:
Oral: 40 mg orally once a day at bedtime OR 20 mg orally 2 times a day
- Duration of therapy: Up to 8 weeks
Parenteral: 20 mg IV every 12 hours
Comments:
- Uncontrolled clinical trials have used oral doses up to 1 mg/kg in patients 1 to 16 years of age.
- Gastric acid suppression occurred at IV doses of 0.5 mg/kg every 12 hours.
Uses:
- Treatment of active DU
- Hospitalized patients with intractable ulcers, or as an alternative to the oral dosage forms for short-term use in patients who are unable to take oral medication for active duodenal ulcers
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for duodenal ulcer maintenance therapy
Usual Pediatric Dose for Gastroesophageal Reflux Disease
BIRTH TO LESS THAN 3 MONTHS:
Oral:
- Initial dose: 0.5 mg/kg orally once a day; may increase to 1 mg/kg orally once a day
- Duration of therapy: Up to 8 weeks
3 MONTHS TO LESS THAN 1 YEAR:
- Initial dose: 0.5 mg/kg orally 2 times a day; may increase to 1 mg/kg orally 2 times a day
- Maximum dose: 40 mg/day
- Duration of therapy: Up to 8 weeks
1 YEAR TO LESS THAN 17 YEARS:
- Initial dose: 0.5 mg/kg orally 2 times a day
- Maximum dose: 80 mg/day
- Duration of therapy: 6 to 12 weeks
Parenteral:
- Initial dose: 0.25 mg/kg IV injected over at least 2 minutes OR infused over 15 minutes every 12 hours
- Maximum dose: 40 mg/day
16 YEARS AND OLDER:
Oral: 20 mg orally 2 times day
- Duration of therapy: Up to 6 weeks
Parenteral: 20 mg IV every 12 hours
Comments:
- The concomitant use of conservative measures (e.g., thickened feedings) should be considered during treatment.
- Parenteral treatment should be limited to patients who cannot tolerate oral formulations.
- Uncontrolled clinical trials have used oral doses up to 2 mg/kg in patients 1 to 16 years of age with GERD with/without esophagitis (including erosions ad ulcerations).
- Oral dissolving tablets may be used in patients 6 years and older, but should be taken as an intact tablet.
Uses:
- Short-term treatment of esophagitis due to gastroesophageal reflux disease, including erosive/ulcerative disease diagnosed by endoscopy
- Alternative to the oral dosage forms for short-term use in specific hospitalized patients who are unable to take oral medication for GERD
Usual Pediatric Dose for Dyspepsia
12 YEARS AND OLDER:
OTC Formulations:
- Treatment dose: 10 to 20 mg orally once
- Symptom prevention: 10 to 20 mg orally once 10 to 60 minutes prior to consuming food/beverages that cause heartburn
- Maximum dose: 2 tablets/day
- Maximum duration of therapy: 14 days
Comments:
- OTC formulations should be taken with a glass of water.
- Chewable tablet formulations should be chewed completely before swallowing.
Uses:
- Relief of heartburn associated with acid indigestion and sour stomach
- Prevention of heartburn associated with acid indigestion and sour stomach brought on by eating/drinking certain foods and beverages
Renal Dose Adjustments
Parenteral:
- Mild renal dysfunction (CrCl 50 to 90 mL/min): No adjustment recommended.
- Moderate (CrCl less than 50 mL/min) to severe renal dysfunction (CrCl less than 10 mL/min): Reduce the dose by 50% and/or prolong the dosing interval to 36 to 48 hours
Oral suspension:
LESS THAN 18 YEARS: Data not available
18 YEARS AND OLDER:
Moderate renal dysfunction (CrCl 30 to 60 mL/min):
- Active DU, GU, EE due to GERD: 20 mg orally once a day OR 40 mg orally every other day
- DU maintenance: 10 mg orally once a day OR 20 mg orally every other day
- Symptomatic, non-erosive GERD: 20 mg orally once a day
- Active DU, GU, symptomatic, non-erosive GERD, and EE due to GERD: 10 mg orally once a day OR 20 mg orally every other day
- DU maintenance: 10 mg orally every other day
Liver Dose Adjustments
Data not available
Dose Adjustments
Older patients: Dose selection should take into account age-related changes in renal function, and additional renal function monitoring may be necessary. Elderly patients with moderate to severe renal function should follow renal dose adjustments.
Precautions
CONTRAINDICATIONS:
- Hypersensitivity to the active component, other H(2)-receptor antagonists, or any of the ingredients
Safety and efficacy of parenteral formulations have not been established in patients younger than 1 year.
Safety and efficacy of over-the-counter formulations have not been established in patients younger than 12 years.
Consult WARNINGS section for additional precautions.
Dialysis
Data not available
Other Comments
Administration advice:
- Patients may use antacids concomitantly with treatment.
- Oral suspension: Patients should shake the oral suspension vigorously for 5 to 10 seconds prior to use.
- Tablets: Patients should avoid chewing tablets during administration.
Storage requirements:
- The manufacturer product information should be consulted.
Reconstitution/preparation techniques:
- The manufacturer product information should be consulted.
IV compatibility:
- The manufacturer product information should be consulted.
General:
- This drug was not found to affect fasting or postprandial gastrin levels, gastric emptying, or exocrine pancreatic function.
- Patients with hypersecretory conditions have used this drug for over 1 year without experiencing tachyphylaxis or significant adverse effects.
Monitoring:
- Renal function, especially in patients with/at risk of renal dysfunction
Patient advice:
- Patients should be told to discard any oral suspension remaining after 30 days.
- Inform patients that this drug may cause dizziness, confusion, or hallucinations, and they should avoid driving or operating machinery until the full effects of the drug are seen.
- Patients should be instructed to contact their healthcare provider if symptoms do not improve or worsen during treatment.
- Advise patients to speak to their healthcare provider if they become pregnant, intend to become pregnant, or are breastfeeding.
Frequently asked questions
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