What is the recommended dose of atenolol (beta-blocker) for migraine prevention?

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Atenolol Dosing for Migraine Prevention

For migraine prevention, atenolol should be used at a dose of 50 mg once daily, which has been shown to be effective in reducing both frequency and severity of chronic migraine attacks. 1

Recommended Beta-Blockers for Migraine Prevention

  • Propranolol (80-240 mg/day) and timolol (20-30 mg/day) are the beta-blockers with the strongest evidence for migraine prevention and are considered first-line agents 2, 3
  • Atenolol (50 mg/day) has demonstrated efficacy in reducing migraine frequency from 20.1 to 7.1 days per month and severity from 2.3 to 1.4 in intensity after 3 months of treatment 1
  • Beta-blockers without intrinsic sympathomimetic activity (ISA) are effective for migraine prevention, while those with ISA should be avoided 4

Dosing and Administration Guidelines

  • Start with a low dose of atenolol (50 mg daily) and assess response after 1.5 months 1
  • Significant improvement can be seen as early as 1.5 months of treatment, with continued improvement through 3 months 1
  • An adequate trial requires 2-3 months as clinical benefits may not become apparent immediately 3
  • If using propranolol instead, start with a low dose and gradually increase to 80-240 mg daily as needed and tolerated 3, 5

Efficacy and Patient Selection

  • Consider beta-blockers for patients with:

    • Two or more migraine attacks per month with disability lasting 3+ days per month 3
    • Use of acute rescue medications more than twice per week 3
    • Failure of or contraindications to acute migraine treatments 3
  • In one study, 29% of patients with chronic migraine became completely headache-free after 3 months of atenolol treatment 1

  • Propranolol appears more effective for pure migraine, while amitriptyline may be superior for mixed migraine and tension-type headache 3

Side Effects and Monitoring

  • Common adverse effects of beta-blockers include:

    • Fatigue, depression, nausea, dizziness, and insomnia 2, 3
    • These side effects are generally well-tolerated 2
  • Monitor for:

    • Mood changes, particularly depression 3
    • Sleep disturbances 3
    • Bradycardia or heart block (contraindications) 3

Alternative First-Line Options

  • Other first-line agents for migraine prevention include:

    • Amitriptyline (30-150 mg/day) 2, 3
    • Divalproex sodium (500-1,500 mg/day) 2
    • Sodium valproate (800-1,500 mg/day) 2
    • Candesartan or telmisartan (ARBs) are strongly recommended by newer guidelines 2
  • For patients who fail to respond to beta-blockers, newer options include:

    • CGRP monoclonal antibodies (erenumab, fremanezumab, galcanezumab) which are strongly recommended for both episodic and chronic migraine 2
    • Topiramate, which has a weak recommendation for both episodic and chronic migraine 2

Treatment Duration

  • After achieving a period of stability (usually 2-3 months), consideration can be given to tapering or discontinuing the medication 2
  • Continuous assessment of efficacy and side effects is recommended throughout treatment 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Propranolol Dosing for Migraine Prevention

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Beta-blockers and migraine].

Pathologie-biologie, 1992

Research

The dose of propranolol for migraine prophylaxis. Efficacy of low doses.

Cephalalgia : an international journal of headache, 1989

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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