What are the common prescription medications and treatment approaches for managing vomiting in India?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 30, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Common Prescription Medications for Vomiting in India

Ondansetron is the first-line antiemetic medication for vomiting in India due to its superior efficacy and safety profile compared to other antiemetics. 1

Classification of Antiemetic Medications Available in India

5-HT3 Receptor Antagonists (First-line options)

  • Ondansetron: 8 mg PO/IV every 6 hours or 16-24 mg PO daily 1, 2

    • Most widely used and effective antiemetic
    • Available as tablets, oral disintegrating tablets, oral solution, and injection
    • Preferred for both adults and children
  • Granisetron: 1-2 mg PO daily or 1 mg PO twice daily or 0.01 mg/kg IV (maximum 1 mg) 1

    • Available as tablets and injection
    • Also available as transdermal patch (3.1 mg/24 h patch containing 34.3 mg granisetron)
  • Palonosetron: 0.25 mg IV (preferred for chemotherapy-induced vomiting) 1, 3

    • Longer half-life than other 5-HT3 antagonists
    • Usually administered as single dose
  • Ramosetron: Highly effective with RR 0.44 compared to placebo 4

    • Newer 5-HT3 antagonist gaining popularity in India

Dopamine Receptor Antagonists

  • Metoclopramide: 10-20 mg PO/IV every 4-6 hours 1

    • Also improves gastric emptying
    • Risk of extrapyramidal symptoms, especially at higher doses
  • Domperidone: 0.5 mg/kg in children; 10 mg PO three times daily for adults 5

    • Less central nervous system effects than metoclopramide
    • Commonly used in India for gastritis-related vomiting
  • Prochlorperazine: 10 mg PO/IV every 6 hours or 25 mg suppository every 12 hours 1

    • Effective but has risk of sedation and extrapyramidal symptoms

Corticosteroids

  • Dexamethasone: 8-12 mg PO/IV daily 1
    • Often combined with 5-HT3 antagonists for enhanced effect
    • Particularly effective for chemotherapy-induced and postoperative vomiting

NK1 Receptor Antagonists (For specialized use)

  • Aprepitant: 125 mg PO day 1, then 80 mg PO daily days 2-3 1
    • Used primarily for chemotherapy-induced vomiting
    • Often part of combination therapy for highly emetogenic chemotherapy

Antihistamines and Anticholinergics

  • Promethazine: 12.5-25 mg PO/IV every 4-6 hours 1

    • Causes significant sedation
    • Used when sedative effect is desirable
  • Dimenhydrinate: For motion sickness and postoperative vomiting 6

    • Available as tablets and injection

Treatment Approach Based on Cause of Vomiting

Acute Gastroenteritis

  1. First-line: Ondansetron 8 mg PO/IV every 6 hours (adults) or 0.15 mg/kg (children) 5

    • Facilitates oral rehydration therapy
    • Reduces need for IV fluids and hospitalization
  2. Alternative: Domperidone 10 mg PO three times daily (adults) or 0.5 mg/kg (children) 5

    • Less effective than ondansetron (85% vs 95% cessation of vomiting at 24 hours)
    • Better tolerated in some patients

Chemotherapy-Induced Vomiting

For highly emetogenic chemotherapy:

  1. Combination therapy (preferred): 1

    • 5-HT3 antagonist (ondansetron 16-24 mg PO or 8-24 mg IV day 1)
    • PLUS dexamethasone 12 mg PO/IV day 1, then 8 mg daily days 2-4
    • PLUS NK1 antagonist (aprepitant 125 mg PO day 1, then 80 mg daily days 2-3)
  2. Alternative: Palonosetron 0.25 mg IV (preferred 5-HT3 antagonist for chemotherapy) plus dexamethasone 1

Postoperative Nausea and Vomiting

  1. Prophylaxis: 3, 2, 4

    • Ondansetron 4-8 mg IV before end of surgery
    • OR granisetron 1 mg IV
    • Consider adding dexamethasone 4-8 mg IV for high-risk patients
  2. Treatment of established PONV: 1

    • Ondansetron 4 mg IV if not used for prophylaxis
    • OR promethazine 12.5-25 mg IV
    • OR metoclopramide 10 mg IV

Pregnancy-Related Vomiting

  1. First-line: Non-pharmacological approaches (small frequent meals, ginger)
  2. Second-line: Antihistamines (promethazine)
  3. Severe cases: Ondansetron (benefit outweighs theoretical risk)

Breakthrough Vomiting Management

For persistent vomiting despite initial therapy: 1

  1. Add one agent from a different drug class to the current regimen:

    • If using 5-HT3 antagonist, add dexamethasone 12 mg PO/IV
    • If using dopamine antagonist, add ondansetron 8 mg PO/IV
    • Consider olanzapine 5-10 mg PO daily for refractory cases (category 1 evidence)
  2. For continued vomiting:

    • Re-evaluate cause
    • Consider dose adjustments
    • Switch to combination therapy with multiple antiemetic classes

Common Pitfalls and Caveats

  1. QT prolongation risk: Monitor ECG when using ondansetron in patients with cardiac disease or electrolyte abnormalities 1, 7

  2. Extrapyramidal symptoms: Monitor for acute dystonic reactions with metoclopramide and prochlorperazine; treat with diphenhydramine 25-50 mg PO/IV 1

  3. Sedation: Promethazine and other antihistamines cause significant sedation; avoid in outpatients who need to remain alert 1

  4. Olanzapine caution: Use at low doses (2.5 mg) in elderly patients due to black box warning regarding increased mortality in elderly patients with dementia 1, 7

  5. Combination therapy: More effective than monotherapy for severe vomiting but increases risk of adverse effects 1

  6. Non-pharmacological approaches: Always consider dietary modifications (small frequent meals, room temperature food) alongside medications 1

By following these evidence-based approaches to antiemetic therapy, clinicians in India can effectively manage vomiting across various clinical scenarios while minimizing adverse effects.

Related Questions

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.