What is the recommended dose of Rantac (ranitidine) for pediatric patients?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: January 19, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Ranitidine Dosing in Pediatric Patients

For pediatric patients aged 1 month to 16 years with GERD or peptic ulcer disease, administer ranitidine at 5-10 mg/kg/day divided into 2-3 doses, with a maximum of 300 mg/day, as recommended by the American Academy of Pediatrics. 1

Standard Oral Dosing by Indication

Treatment of Active Ulcers (Duodenal and Gastric)

  • Administer 2-4 mg/kg twice daily, with a maximum of 300 mg/day 2
  • This dosing is FDA-approved and derived from adult clinical studies combined with pediatric pharmacokinetic data 2

Maintenance of Ulcer Healing

  • Administer 2-4 mg/kg once daily, with a maximum of 150 mg/day 2
  • Single daily dosing improves compliance while maintaining therapeutic efficacy 2

GERD and Erosive Esophagitis

  • Administer 5-10 mg/kg/day divided into 2 doses 1, 2
  • For erosive esophagitis specifically, the adult-equivalent dosing would suggest higher frequency, but pediatric data supports the 2-divided-dose approach 2

Intravenous Dosing for Critically Ill Children

Stress Ulcer Prophylaxis in PICU

  • Administer a minimum of 3 mg/kg/day IV to achieve adequate gastric pH control (pH ≥4) 3
  • The commonly cited 2-4 mg/kg/day range results in poor pH control in 36% of critically ill children 3
  • For optimal prophylaxis, use 1.5 mg/kg IV every 6 hours (6 mg/kg/day total), which maintains gastric pH ≥4 in 80% of high-risk patients 4

Continuous Infusion Alternative

  • Administer 0.1 mg/kg/hour as a continuous infusion for children undergoing cardiopulmonary bypass or other critical illness 5
  • This produces mean gastric pH ≥5.3 within 3 hours and is safer than higher infusion rates 5

Special Populations

Neonates (Term vs Preterm)

  • Preterm infants (<37 weeks): 0.5 mg/kg twice daily 6
  • Term neonates: 1.5 mg/kg three times daily 6
  • Preterm infants have prolonged drug effect and require significantly lower doses than term infants to maintain gastric pH >4 6
  • Note: There is insufficient safety data for neonates <1 month of age to make formal FDA dosing recommendations 2

Anaphylaxis (Second-Line Therapy)

  • Administer 1 mg/kg IM (maximum 50 mg) in combination with diphenhydramine 1, 7
  • For IV administration: dilute in 20 mL D5W and administer over 5 minutes 1
  • This is second-line therapy only; never administer as monotherapy for anaphylaxis 7

Renal Impairment

  • For creatinine clearance <50 mL/min: reduce to 150 mg every 24 hours 2
  • May increase frequency to every 12 hours if clinically necessary, but use caution 2
  • Time dosing to coincide with end of hemodialysis when applicable 2

Formulation Considerations

  • Ranitidine effervescent tablets (25 mg dissolved in 5 mL water) are preferred over peppermint-flavored syrup (15 mg/mL) based on taste acceptance studies 1, 8
  • 71% of children aged 4-8 years preferred the effervescent formulation, which may improve compliance 8

Critical Pitfalls to Avoid

  • Do not use the lower end of 2 mg/kg/day in critically ill children—this results in treatment failure in the majority of PICU patients 3
  • Do not assume adult dosing translates to pediatric patients—neonates, particularly preterm infants, require dramatically different dosing due to altered pharmacokinetics 6
  • Ranitidine develops tachyphylaxis within 6 weeks of continuous use and is less effective than PPIs for healing erosive esophagitis 1
  • Monitor for decreased efficacy with continuous use and consider switching to PPI therapy if symptoms persist beyond 6 weeks 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.