Ondansetron (Zofran) Dosing for Nausea and Vomiting Prevention
Ondansetron should be administered at 8 mg IV or 16-24 mg PO approximately 30 minutes before chemotherapy for prevention of chemotherapy-induced nausea and vomiting, with dosing regimens varying based on the emetogenic potential of the chemotherapy. 1, 2
Dosing Based on Emetogenic Potential
Highly Emetogenic Chemotherapy
- Single oral dose of 24 mg administered 30 minutes before chemotherapy 2
- IV dose of 8 mg administered 30-60 minutes before chemotherapy 3, 1
- Note: 8 mg twice daily and 32 mg once daily regimens are not recommended for highly emetogenic chemotherapy 2
Moderately Emetogenic Chemotherapy
- 8 mg oral dose administered 30 minutes before chemotherapy, with a subsequent dose 8 hours later, followed by 8 mg twice daily for 2 days after completion of chemotherapy 2
- 8 mg IV administered 30-60 minutes before chemotherapy 3, 1
- Note: 8 mg three times daily is not a recommended regimen for moderately emetogenic chemotherapy 2
Combination Therapy
For optimal antiemetic effect, especially with highly emetogenic chemotherapy:
- Triple regimen is recommended: 5-HT3 antagonist (ondansetron) + dexamethasone + NK1 antagonist 1
- Ondansetron 8 mg IV or 16-24 mg PO
- Dexamethasone 20 mg IV/PO (reduced to 10 mg if using aprepitant)
- Aprepitant 125 mg PO (for high-risk patients)
Special Considerations
Delayed Nausea and Vomiting (24-120 hours)
- Ondansetron as monotherapy is less effective for delayed emesis 5
- For delayed emesis, consider:
Breakthrough Nausea and Vomiting
- Add dopamine antagonist (e.g., metoclopramide 20-30 mg PO/IV every 6 hours) 1
- Consider lorazepam 1-2 mg PO/IV every 6 hours for anxiety component 1
Pediatric Dosing
- 5 mg/m² 30 minutes before chemotherapy, then 4 mg/m² every 8 hours IV 6
- This regimen showed better efficacy than tropisetron for mild to moderate emetogenic chemotherapy 6
Safety Considerations
- Most common side effects: headache and constipation 1, 5
- Cardiac safety: FDA warning about potential QT prolongation with high doses (32 mg IV) 7
- Dose adjustment: Maximum daily dose of 8 mg recommended for patients with severe hepatic dysfunction (Child-Pugh score ≥10) 1
Administration Routes
- Oral administration: Preferred for routine use 3
- IV administration: Recommended when patient is actively vomiting 1
- Prophylactic administration should occur 30-60 minutes before chemotherapy 3, 1
Ondansetron has proven to be significantly more effective than placebo and conventional antiemetics like metoclopramide for prevention of chemotherapy-induced and postoperative nausea and vomiting, with an excellent safety profile when used at recommended doses 5.