Ondansetron (Zofran) Dosing Regimen
For optimal management of nausea and vomiting, ondansetron (Zofran) should be dosed at 8 mg orally twice daily or 8 mg IV for most indications, with specific adjustments based on the clinical scenario. 1
Dosing by Administration Route
Oral Administration
Standard oral dose: 8 mg twice daily 1, 2
- First dose 30 minutes before chemotherapy/radiation/trigger
- Second dose 8 hours after first dose
- Continue for 1-2 days after completion of treatment as needed
Oral dissolving tablets/film: 8 mg (equivalent to standard tablets) 3, 4
- Particularly useful for patients with difficulty swallowing
- No water required for administration
Intravenous Administration
- Standard IV dose: 8 mg or 0.15 mg/kg IV 1
- Administered 30 minutes before chemotherapy/radiation/trigger
- Can be given as single dose or divided doses
Dosing by Clinical Scenario
Chemotherapy-Induced Nausea and Vomiting
Highly Emetogenic Chemotherapy
- Oral: 24 mg as a single dose 30 minutes before chemotherapy 2
- IV: 8 mg or 0.15 mg/kg IV 30 minutes before chemotherapy 1
- Combination therapy recommended: Add dexamethasone 12 mg and NK1 receptor antagonist 1
Moderately Emetogenic Chemotherapy
- Oral: 8 mg twice daily 1, 2
- First dose 30 minutes before chemotherapy
- Second dose 8 hours later
- Continue 8 mg twice daily for 1-2 days after completion
- IV: 8 mg IV 30 minutes before chemotherapy 1
- Consider adding: Dexamethasone 8-12 mg 1
Low Emetogenic Chemotherapy
Radiation-Induced Nausea and Vomiting
- Standard dose: 8 mg oral or IV before radiation 1
- For total body irradiation: 8 mg 1.5 hours before each fraction 2
- For fractionated radiotherapy: 8 mg before first daily fraction, then every 8 hours 2
Postoperative Nausea and Vomiting
- Preventive dose: 16 mg oral as single dose 1 hour before anesthesia induction 2
- Treatment dose: 4 mg IV as needed 3
Special Considerations
Refractory Nausea and Vomiting
- Escalated dosing: 8 mg IV followed by continuous infusion of 1 mg/hour for 8 hours 5
- Combination therapy: Add dopamine antagonists (e.g., metoclopramide 5-20 mg) 1, 3
- Alternative 5-HT3 antagonists: Consider granisetron 1-2 mg oral or 1 mg IV 1, 3
Pharmacokinetic Considerations
- Onset of action: 30 minutes to 2 hours after oral administration 6
- Half-life: Approximately 3.8 hours 6
- Bioavailability: ~60% due to first-pass metabolism 6
- Administration with food: Slightly increases bioavailability 6
Common Pitfalls and Caveats
Timing is critical: Administer at least 30 minutes before the emetogenic stimulus for maximum effectiveness 6
QT prolongation risk: Monitor cardiac status in patients with risk factors 3
Common side effects: Headache, constipation, dizziness 3
- Manage with increased fluid intake and mild laxatives as needed
Hepatic impairment: Consider dose reduction in severe hepatic dysfunction 6
Elderly patients: No routine dose adjustment required despite altered pharmacokinetics 6
Three-times-daily dosing: Not recommended for moderately emetogenic chemotherapy despite historical use 2
Alternative formulations: Consider oral dissolving tablets, oral soluble film, or IV formulations for patients with swallowing difficulties 3, 4
By following these evidence-based dosing guidelines, ondansetron can effectively manage nausea and vomiting across various clinical scenarios, significantly improving patient quality of life and reducing morbidity associated with these symptoms.