What are the medications designed to prevent migraines?

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Medications Designed to Prevent Migraines

Medications designed to prevent migraines include beta-blockers (propranolol, timolol, metoprolol), anticonvulsants (topiramate, divalproex sodium, sodium valproate), antidepressants (amitriptyline), CGRP antagonists (erenumab, galcanezumab), and several other drug classes with varying levels of evidence. 1, 2, 3

First-Line Preventive Medications

Beta-Blockers

  • Propranolol: 80-240 mg/day
  • Timolol: 20-30 mg/day
  • Metoprolol: Effective for migraine prevention
  • Atenolol: Limited evidence but may be effective
  • Avoid in patients with asthma, bradycardia, or heart block 1

Anticonvulsants

  • Topiramate: Strong evidence for efficacy
  • Divalproex sodium: 500-1500 mg/day
  • Sodium valproate: 800-1500 mg/day
  • Valproate is contraindicated in women of childbearing potential due to teratogenicity 1

Antidepressants

  • Amitriptyline: 30-150 mg/day
  • Avoid in patients with cardiac conduction disorders or urinary retention 1

CGRP Antagonists

  • Erenumab (Aimovig): FDA-approved for preventive treatment of migraine in adults 2
  • Galcanezumab (Emgality): Reduces monthly migraine headache days by 4.3-4.7 days compared to 2.3-2.8 days with placebo 3

Second-Line Preventive Medications

Calcium Channel Blockers

  • Flunarizine: 10 mg/day (proven efficacy but not available in all countries)
  • Verapamil: Limited evidence of modest effect 4

Angiotensin Pathway Blockers

  • Candesartan: Effective for migraine prevention 1
  • Lisinopril: Limited evidence but may be effective 5

NSAIDs

  • Naproxen: Modest effect on headache prevention
  • Common side effects include gastrointestinal symptoms (3-45% of patients) 4

Serotonergic Agents

  • Methysergide: Strong evidence for efficacy but requires drug holidays due to risk of fibrosis
  • Time-released DHE: Strong support from placebo-controlled trials 4

Nutraceuticals and Supplements

  • Magnesium: Fair evidence for modest efficacy
  • Riboflavin (Vitamin B2): Fair evidence for modest efficacy
  • Coenzyme Q10: Limited evidence but may be effective
  • Feverfew: Fair evidence in certain circumstances 4, 1

Practical Approach to Migraine Prevention

  1. Start preventive treatment when:

    • Migraines occur ≥2 days per month
    • Attacks significantly impact quality of life despite acute treatment 1
  2. Medication initiation:

    • Start with lowest effective dose
    • Titrate slowly to minimize side effects
    • Allow 2-3 months for full clinical benefit 1
  3. Monitoring and follow-up:

    • Assess response within 2-4 weeks of medication changes
    • Monitor for medication overuse headaches
    • Consider tapering or discontinuing after a period of stability 1

Special Considerations

  • Pregnancy planning: Avoid valproate in women of childbearing potential
  • Cardiovascular risk: Monitor blood pressure in patients using certain preventives
  • Comorbidities: Choose preventives that may treat comorbid conditions (e.g., depression, hypertension)
  • Combination therapy: Behavioral therapy with preventive medication may achieve additional improvement 1

Emerging Treatments

  • Botulinum toxin: Demonstrated fair effectiveness for chronic migraine prevention, though further studies are needed 5
  • CGRP pathway antagonists: Newer class of medications specifically designed for migraine prevention with promising efficacy data 2, 3

The choice of preventive medication should be based on efficacy evidence, side effect profile, comorbidities, and patient-specific factors. Regular monitoring and dose adjustments are essential to optimize treatment outcomes.

References

Guideline

Migraine Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Medications for migraine prophylaxis.

American family physician, 2006

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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