What is the recommended dose of ondansetron (Zofran) for a 9-year-old child?

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Ondansetron Dosing for a 9-Year-Old Child

For a 9-year-old child, ondansetron should be dosed at 0.15 mg/kg (maximum 16 mg) per dose, with the specific route and frequency depending on the clinical indication. 1

Weight-Based Dosing Strategy

The standard pediatric dosing is 0.15 mg/kg per dose with a maximum single dose of 16 mg. 1 For a typical 9-year-old weighing approximately 25-40 kg, this translates to:

  • 25 kg child: 3.75 mg per dose
  • 30 kg child: 4.5 mg per dose
  • 35 kg child: 5.25 mg per dose
  • 40 kg child: 6 mg per dose

Route and Frequency by Clinical Context

For Chemotherapy-Induced Nausea/Vomiting

Highly emetogenic chemotherapy: Administer 0.15 mg/kg IV or IM (maximum 16 mg) 30 minutes before chemotherapy, then repeat at 4 and 8 hours after the first dose. 1 For children receiving highly emetogenic chemotherapy, combining ondansetron with dexamethasone significantly improves efficacy. 1

Moderately emetogenic chemotherapy: Use a 5-HT3 receptor antagonist (ondansetron or granisetron) combined with dexamethasone. 1 The FDA label supports oral dosing of 4 mg three times daily for children under 12 years, which showed similar efficacy to 8 mg three times daily in adolescents 12-18 years. 2

For Acute Gastroenteritis/Vomiting

Single oral dose: 0.15 mg/kg (maximum 16 mg) is effective for reducing vomiting episodes and decreasing the need for IV rehydration and hospitalization. 3 Research demonstrates that doses ranging from 0.13-0.26 mg/kg show similar efficacy without increased side effects, supporting the 0.15 mg/kg standard. 4

For Food Protein-Induced Enterocolitis Syndrome (FPIES)

Age restriction applies: Ondansetron should only be used in children ≥6 months of age. 1

  • Mild episodes: Consider 0.15 mg/kg IM (maximum 16 mg) 1
  • Moderate-to-severe episodes: Administer 0.15 mg/kg IV or IM (maximum 16 mg) 1

For Postoperative Nausea/Vomiting

Prophylactic dosing: 0.1-0.15 mg/kg IV (maximum 16 mg) administered before or during anesthesia induction is significantly more effective than placebo, droperidol, or metoclopramide. 5

Practical Formulation Considerations

Oral disintegrating tablets are available in 4 mg and 8 mg strengths, making them practical for children who have difficulty swallowing pills. 2 Round doses to the nearest available tablet strength for ease of administration:

  • For calculated doses of 3-5 mg: use 4 mg tablet
  • For calculated doses of 6-10 mg: use 8 mg tablet
  • For doses >10 mg: use combination of tablets not exceeding 16 mg maximum

Critical Safety Considerations

QTc prolongation: Ondansetron can prolong the QT interval in a dose-dependent manner. 2 The 32 mg single IV dose previously used in adults is no longer recommended due to this risk. 2 The pediatric dose of 0.15 mg/kg with a 16 mg maximum provides an appropriate safety margin.

Age restriction: Do not use ondansetron in infants under 6 months of age for FPIES management. 1 However, research in gastroenteritis has included children as young as 6 months with demonstrated safety. 3

Diarrhea: Ondansetron may increase diarrhea episodes in children with gastroenteritis, though this does not outweigh the benefits of reduced vomiting and decreased need for IV therapy. 3

No dosage adjustment needed for renal impairment or based on age alone. 2

Common Pitfalls to Avoid

Avoid exceeding 16 mg per dose even in larger/older children, as this increases the risk of QTc prolongation without additional efficacy benefit. 1, 2

Do not use the adult 32 mg single-dose regimen in pediatric patients. 2

For severe FPIES reactions, do not delay IV access and fluid resuscitation while attempting to administer ondansetron—give IM if IV access is difficult. 1

Recognize that ondansetron alone may be insufficient for highly emetogenic chemotherapy; combination with dexamethasone or aprepitant significantly improves outcomes. 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.

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