What is the correct ondansetron (Zofran) dose, route, and dosing interval for a 10‑year‑old child weighing 69 lb (≈31 kg)?

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Ondansetron Dosing for a 10-Year-Old Child Weighing 69 lb (31 kg)

Administer ondansetron 0.15 mg/kg per dose, which equals 4.65 mg (can be rounded to 4.5 mg for practical administration using available formulations), with a maximum single dose of 16 mg. 1, 2

Weight-Based Calculation

  • The child weighs 69 lb = 31.3 kg 1
  • Standard pediatric dose: 0.15 mg/kg per dose 1, 2, 3
  • Calculated dose: 31.3 kg × 0.15 mg/kg = 4.7 mg per dose 1
  • Doses must be calculated exactly according to weight; rounding beyond the precise 0.15 mg/kg calculation is discouraged to avoid under- or overdosing 1

Route of Administration

The route depends on clinical context and severity of symptoms:

Oral Administration

  • Preferred for mild to moderate nausea/vomiting when the child can tolerate oral intake 1, 4
  • Ondansetron oral suspension (6 mg/mL concentration): for a 4.5–4.7 mg dose, administer approximately 0.75–0.78 mL 2
  • Can be given without regard to meals, though co-administration with food may improve gastrointestinal tolerability 1
  • Peak plasma concentration occurs 0.5–2 hours after oral ingestion 5

Intravenous/Intramuscular Administration

  • Use for moderate to severe vomiting or when oral route is not feasible 1, 2
  • Same dose: 0.15 mg/kg (4.7 mg) IV or IM 1, 2, 3
  • IV administration should be given over 2–5 minutes for postoperative nausea or over 15 minutes for chemotherapy-induced nausea 3

Dosing Interval

  • Single dose is often sufficient for acute vomiting episodes 1, 4
  • If repeat dosing is needed: every 8 hours as necessary 1
  • Maximum: 2–3 doses in 24 hours for most indications 1
  • For chemotherapy-induced nausea: administer 30 minutes before chemotherapy, then repeat at 4 and 8 hours after the first dose 1, 3

Context-Specific Considerations

Acute Gastroenteritis

  • Single oral dose of 4.5–4.7 mg reduces risk of recurrent vomiting, need for IV fluids, and hospital admissions 6
  • The American Academy of Pediatrics recommends ondansetron for children >4 years with acute gastroenteritis and vomiting 4
  • Do not use as a substitute for appropriate fluid and electrolyte therapy; oral rehydration solution remains first-line treatment 2, 4

Chemotherapy-Induced Nausea/Vomiting

  • For high-emetic-risk chemotherapy: combine ondansetron with dexamethasone and aprepitant for optimal efficacy 1, 2
  • For moderate-emetic-risk chemotherapy: combine ondansetron with dexamethasone 1, 2
  • For low-emetic-risk chemotherapy: ondansetron monotherapy is sufficient 1, 2
  • Adding dexamethasone significantly improves antiemetic efficacy compared to ondansetron alone 1, 2, 7

Postoperative Nausea/Vomiting

  • Single dose of 4 mg IV (or weight-based 0.15 mg/kg) given immediately before induction of anesthesia 3
  • In pediatric surgical patients, ondansetron 0.1–0.15 mg/kg was superior to droperidol or metoclopramide 7

Critical Safety Warnings

QT Interval Prolongation

  • Ondansetron can prolong the QT interval in a dose-dependent manner 1, 2
  • Exercise special caution in children with congenital long QT syndrome, heart disease, or electrolyte abnormalities (hypokalemia, hypomagnesemia) 1, 2
  • Avoid concurrent use with other QT-prolonging medications (certain antibiotics, antiarrhythmics) 2
  • The pediatric dose of 0.15 mg/kg with a 16 mg maximum provides an appropriate safety margin 1

Common Side Effects

  • Headache is the most frequently reported adverse event 7, 8
  • Ondansetron may increase diarrhea frequency as a side effect, but this does not worsen clinical outcomes 4
  • Constipation may occur, particularly with repeated dosing 7

Contraindications and Precautions

  • Avoid if the child has bloody diarrhea or high fever suggesting inflammatory/invasive diarrhea 4
  • Do not use in infants <6 months of age due to limited safety data 1, 2
  • In overdose (particularly in infants), severe toxicity including seizures, obtundation, and serotonin syndrome has been reported 9

Practical Administration Tips

  • Oral disintegrating tablets (ODT) are available and may be preferred for children who have difficulty swallowing 1
  • For oral suspension: use an accurate measuring device (oral syringe) rather than household spoons 1
  • Administer at least 30 minutes before chemotherapy if used for chemotherapy-induced nausea 3, 5
  • Ondansetron is significantly more effective than metoclopramide and has a more favorable tolerability profile, particularly lower risk of extrapyramidal reactions 2, 7

Efficacy Data

  • In pediatric patients receiving chemotherapy, 58–59% had complete response (no emetic episodes) on Day 1 with ondansetron 3
  • For acute gastroenteritis, single-dose ondansetron produces a 41% higher chance of vomiting cessation within 8 hours compared to placebo 2
  • Ondansetron reduces oral rehydration therapy failure by 57% and IV hydration needs by 56% 2

References

Guideline

Ondansetron Dosing Guidelines for Pediatric Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Ondansetron Dosing in Pediatric Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Ondansetron Dosing and Rehydration for Pediatric Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Ondansetron clinical pharmacokinetics.

Clinical pharmacokinetics, 1995

Research

Antiemetic Drug Use in Children: What the Clinician Needs to Know.

Journal of pediatric gastroenterology and nutrition, 2019

Research

Ondansetron: a novel antiemetic agent.

Southern medical journal, 1993

Research

Obtundation and seizure following ondansetron overdose in an infant.

Clinical toxicology (Philadelphia, Pa.), 2008

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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