What is the typical dose of metoclopramide (antiemetic medication) for pediatric use?

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Metoclopramide Dosing in Pediatric Patients

For pediatric patients, metoclopramide dosing varies significantly by indication and age: 0.1 mg/kg every 6 hours for gastroesophageal reflux, 0.1 mg/kg for small bowel intubation in children under 6 years, 2.5-5 mg for ages 6-14 years, and 1-2 mg/kg for chemotherapy-induced nausea and vomiting (CINV).

Standard Dosing by Indication

Gastroesophageal Reflux and Gastroparesis

  • The recommended dose is 0.1 mg/kg every 6 hours enterally, which achieves therapeutic concentrations for gastroesophageal reflux in most pediatric patients 1
  • This dosing regimen was validated in preterm infants (birth weights 790-1,040g) at 0.1 mg/kg/day divided into three doses intravenously, with excellent response and no adverse effects 2
  • Simulations demonstrate that 0.1 mg/kg every 6 hours produces steady-state concentrations within the efficacy range for >75% of patients, though slightly lower exposures occur in children <2 years 1

Small Bowel Intubation

  • For children under 6 years: 0.1 mg/kg metoclopramide base as a single IV dose over 1-2 minutes 3
  • For children 6-14 years: 2.5-5 mg metoclopramide base as a single IV dose 3
  • For children >14 years and adults: 10 mg metoclopramide base as a single IV dose 3

Chemotherapy-Induced Nausea and Vomiting

  • For highly emetogenic chemotherapy (cisplatin, dacarbazine): 2 mg/kg IV over ≥15 minutes, given 30 minutes before chemotherapy, repeated every 2 hours for two doses, then every 3 hours for three doses 3
  • For less emetogenic regimens: 1 mg/kg per dose may be adequate 3
  • A dose-escalation study found that doses <2 mg/kg had minimal toxicity, while doses ≥2 mg/kg resulted in extrapyramidal reactions in 15% and akathisia in 33% of children 4

Critical Safety Considerations

Extrapyramidal Symptoms (EPS)

  • EPS occur in approximately 9% (95% CI 5-17%) of pediatric patients receiving metoclopramide, making this the most common adverse effect 5
  • Prophylactic diphenhydramine should be administered concurrently with high-dose metoclopramide (≥2 mg/kg) to reduce EPS risk 4
  • If acute dystonic reactions occur, administer diphenhydramine 1-2 mg/kg or 25-50 mg parenterally 6, 3
  • Children receiving two consecutive days of metoclopramide have higher EPS frequency 4

Other Common Adverse Effects

  • Diarrhea occurs in 6% (95% CI 4-9%) of patients 5
  • Sedation occurs in 6% (95% CI 3-12%) in multiple-dose studies 5
  • These effects are reversible and of no long-term significance 5

Rare but Serious Adverse Effects

  • Dysrhythmia, respiratory distress/arrest, neuroleptic malignant syndrome, and tardive dyskinesia are rarely associated with metoclopramide use in children 5

Age-Specific Dosing Considerations

Neonates and Infants (<2 years)

  • Neonates are immature children with developing drug elimination pathways, requiring careful dose adjustment 7
  • The 0.1 mg/kg every 6 hours regimen may result in slightly lower exposures in this age group, though still generally within therapeutic range 1
  • Metoclopramide has been safely used in preterm infants as young as 26 weeks gestational age 2

Children (2-12 years)

  • Children ≥2 years are essentially mature and differ from adults only in size, allowing for straightforward weight-based dosing 7
  • Body weight is the primary covariate affecting metoclopramide pharmacokinetics in this population 1

Adolescents (>12 years)

  • Dosing approaches adult regimens, with 10 mg as the standard dose for most indications 3

Administration Guidelines

Route and Timing

  • IV administration should be given slowly over 1-2 minutes for single doses 3
  • For CINV prophylaxis, infuse over ≥15 minutes 3
  • Oral administration is appropriate for less severe symptoms 3

Duration of Therapy

  • Limit duration to ≤5 days when possible, as regulatory agencies caution against prolonged use in children 5
  • For diabetic gastroparesis, IV therapy may be required for up to 10 days before transitioning to oral administration 3

Renal and Hepatic Impairment

  • For creatinine clearance <40 mL/min, initiate therapy at approximately one-half the recommended dosage 3
  • Metoclopramide undergoes minimal hepatic metabolism and can be used safely in advanced liver disease with normal renal function 3

References

Research

Use of metoclopramide in preterm infants.

Developmental pharmacology and therapeutics, 1982

Research

Metoclopramide: dose-related toxicity and preliminary antiemetic studies in children receiving cancer chemotherapy.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 1985

Guideline

Metoclopramide Administration in Pediatric Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

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