Recommended Dosage for Vertin (Betahistine)
The standard recommended dosage for Vertin (betahistine) is 48 mg daily, administered for at least 3 months to properly evaluate therapeutic efficacy. 1
Standard Dosing Regimens
For Ménière's Disease and Vestibular Vertigo:
- 48 mg daily is the evidence-based standard dose for maintenance therapy in patients with definite or probable Ménière's disease 1
- This can be administered as either:
- 16 mg three times daily (tid), or
- 24 mg twice daily (bid) 2
- Both dosing schedules provide comparable efficacy and tolerability with no significant difference in clinical outcomes 2
Treatment Duration and Efficacy Assessment
- Minimum treatment duration of 3 months is required before evaluating whether the medication is providing benefit 1
- Clinical studies demonstrate maximum efficacy occurs with doses of 32-36 mg daily over 3-8 weeks of treatment 3
- If no improvement in vertigo symptoms after 6-9 months of treatment, continued betahistine therapy is unlikely to be beneficial and should be discontinued 1
Important Dosing Considerations
Higher doses have not shown additional benefit:
- Doses of 144 mg/day have not demonstrated significant improvement compared to the standard 48 mg/day dose or placebo in high-quality trials 1
- The usual therapeutic dose range spans 8-48 mg daily based on over 40 years of clinical experience 4
Specific dosing for different conditions:
- For classic Ménière's syndrome with severe symptoms: 16 mg three times daily (48 mg total) 5
- For less severe peripheral vertigo: 32 mg daily has shown efficacy 6
Absolute Contraindications
Betahistine is completely contraindicated in:
Use with caution in:
Common Side Effects to Monitor
- Headache (most frequently reported) 1, 7
- Balance disorder 1
- Nausea and upper gastrointestinal symptoms 1, 7
- These side effects typically diminish with continued treatment 2
Key Clinical Pitfall
Do not expect immediate results - betahistine requires sustained use over months to demonstrate benefit, and premature discontinuation before 3 months may lead to incorrect assessment of treatment failure 1