What are the doses of Ondansetron?

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Ondansetron Dosing Guidelines

For chemotherapy-induced nausea and vomiting, ondansetron is dosed at 16-24 mg PO once daily or 8-12 mg IV (maximum 32 mg/day) for prevention of acute emesis, with oral dosing of 8 mg PO twice daily or 16 mg PO once daily for delayed emesis. 1, 2

Oral Dosing

Highly Emetogenic Chemotherapy

  • Single dose regimen: 24 mg PO once, administered 30 minutes before chemotherapy 3
  • This regimen showed 66% of patients completing 24 hours with no emetic episodes and no rescue medications 3
  • Not recommended: 8 mg PO twice daily or 32 mg PO once daily 3

Moderately Emetogenic Chemotherapy

  • Initial dose: 8 mg PO 30 minutes before chemotherapy
  • Subsequent doses: 8 mg PO 8 hours after first dose
  • Maintenance: 8 mg PO twice daily for 1-2 days after completion of chemotherapy 3
  • Alternative: 16 mg PO once daily 1, 2

Intravenous Dosing

Highly Emetogenic Chemotherapy

  • Dose: 8-12 mg IV (maximum 32 mg/day) 1
  • Administered 30 minutes before chemotherapy

Moderately Emetogenic Chemotherapy

  • Dose: 8 mg IV 2
  • Administered 30 minutes before chemotherapy

Special Populations

Hepatic Impairment

  • For severe hepatic impairment (Child-Pugh score ≥10), maximum daily dose should be limited to 8 mg 3
  • Patients with mild-to-moderate hepatic impairment have a 2-fold reduction in clearance and increased half-life (11.6 hours vs 5.7 hours in healthy subjects) 3

Elderly Patients

  • No specific dose adjustments required despite slightly decreased clearance and increased bioavailability 4

Pharmacokinetic Considerations

  • Oral bioavailability: approximately 60% 4
  • Time to peak concentration: 0.5-2 hours after oral administration 4
  • Elimination half-life: approximately 3.8 hours 4
  • Primarily metabolized by the liver (95%) 4
  • Should be administered at least 30 minutes before chemotherapy to achieve optimal antiemetic effect 4

Combination Therapy

  • For optimal control of chemotherapy-induced nausea and vomiting, ondansetron is often combined with:
    • Dexamethasone (12 mg PO/IV)
    • NK1 antagonist (e.g., aprepitant 125 mg PO day 1,80 mg PO days 2-3) 2

Clinical Efficacy

  • Complete control of vomiting in 69% of patients on day 1 and 60% on days 2-5 in non-cisplatin chemotherapy 5
  • For cisplatin-based regimens, complete response (no emesis) achieved in 60% of patients 6

Ondansetron's efficacy is maintained over multiple chemotherapy cycles, with most patients (80%) preferring it to previous antiemetic regimens for non-cisplatin chemotherapy 5. The most common side effects are headache and constipation, which are generally mild and well-tolerated 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Chemotherapy-Induced Nausea and Vomiting Prophylaxis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Ondansetron clinical pharmacokinetics.

Clinical pharmacokinetics, 1995

Research

Ondansetron: prevention of nausea & vomiting in cisplatin based chemotherapy.

Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1994

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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