Pediatric Dosing of Intravenous Ondansetron
The recommended intravenous (IV) dose of ondansetron for pediatric patients is 0.15 mg/kg (maximum 16 mg per dose) for children 6 months of age and older. 1
Dosing Guidelines by Age and Clinical Scenario
General Pediatric Dosing
- For children 6 months and older: 0.15 mg/kg IV (maximum 16 mg per dose) 1
- For infants 1-4 months: Pharmacokinetic studies show a longer half-life due to higher volume of distribution in this age group 2
Dosing by Clinical Scenario
Chemotherapy-induced nausea and vomiting:
Emergency management of vomiting:
Food Protein-Induced Enterocolitis Syndrome (FPIES):
Administration Considerations
- IV administration is preferred in emergency settings or when rapid onset is needed 1
- For patients with severe hepatic impairment, the total daily dose should not exceed 8 mg 2
- No dose adjustment is required for patients with renal impairment 2
Special Considerations
- Monitor patients with congenital long QT syndrome or those taking other medications that prolong the QT interval 1
- Ondansetron is extensively metabolized in the liver, with only 5% of a dose recovered as the parent compound in urine 2
- Pediatric patients generally have higher ondansetron clearance compared to adults, leading to shorter half-lives in most pediatric patients 2
- Studies have shown that within the dose range of 0.13-0.26 mg/kg, higher doses were not superior to lower doses, nor were they associated with increased side effects 5
Efficacy and Safety
- Ondansetron effectively reduces vomiting episodes and decreases the need for IV hydration and hospitalization 1, 6
- A potential side effect is increased diarrhea episodes in the 48 hours following administration 1
- Ondansetron has shown superior efficacy compared to metoclopramide and chlorpromazine in reducing nausea and vomiting in children 1
The evidence strongly supports the use of ondansetron at 0.15 mg/kg IV for pediatric patients, with appropriate maximum dose limits based on the clinical scenario. This dosing regimen has been shown to be both safe and effective across various clinical indications.