4.7 Article

Flunarizine in migraine-related headache prevention: results from 200 patients treated in the UK

期刊

EUROPEAN JOURNAL OF NEUROLOGY
卷 25, 期 6, 页码 811-817

出版社

WILEY
DOI: 10.1111/ene.13621

关键词

flunarizine; migraine; migraine prevention; headache; prophylaxis

资金

  1. Allergan
  2. Amgen
  3. Eli-Lilly and Company
  4. eNeura
  5. Ajinomoto Pharmaceuticals Co.
  6. Akita Biomedical
  7. Alder Bio-pharmaceuticals
  8. Autonomic Technologies Inc.
  9. Avanir Pharma
  10. Cipla Ltd
  11. Colucid Pharmaceuticals Ltd
  12. Dr Reddy's Laboratories
  13. Electrocore LLC
  14. Ethicon, United States
  15. W.L. Gore Associates
  16. Heptares Therapeutics
  17. Novartis
  18. Nupathe Inc.
  19. Pfizer Inc.
  20. Promius Pharma
  21. Scion
  22. Teva Pharmaceuticals
  23. Trigemina Inc.
  24. MedicoLegal work
  25. Journal Watch
  26. Up-to-Date
  27. Oxford University Press

向作者/读者索取更多资源

Background and purposeFor over 20 years, as a group we have been using flunarizine in primary headache disorders. Flunarizine is widely used in Europe, but not licensed in the UK. In September 2014, the National Institute for Clinical Excellence published supportive guidelines for flunarizine use in migraine, based on randomized controlled evidence that it is as effective as propranolol and topiramate in adults. MethodsWe reviewed a cohort of adult patients (n = 200) treated with flunarizine from our practice. The clinical information of these patients, i.e. diagnosis, dose, efficacy, side effects and duration of treatment, was collected. ResultsThe most common indication for flunarizine use was chronic migraine, followed by migraine with aura, sporadic hemiplegic migraine, familial hemiplegic migraine and new daily persistent headache with migrainous features. Flunarizine was generally effective, with only 24% (n = 47) of patients reporting no clinical effect. The most common dose used was 10 mg per day. Duration of treatment information was available for 39% (n = 78) of patients. Of these patients, 64% (n = 50) continued treatment for more than 1 year. Doses up to 15 mg were generally well tolerated, with only 10.5% (n = 21) of patients stopping treatment due to adverse effects. The most common adverse events were tiredness, mood change and weight gain. ConclusionThe data provide supportive evidence from tertiary headache practice in the UK for the use of flunarizine in migraine. The data encourages development of future guidance regarding flunarizine use in headache centres in countries where its use is not routine.

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