Literature DB >> 16440139

Value of postmarketing surveillance studies in achieving a complete picture of antimigraine agents: using almotriptan as an example.

Julio Pascual1, Hans-Christoph Diener, Hélène Massiou.   

Abstract

Randomised controlled trials cannot collect all the data relevant for use in everyday clinical practice because drug exposure is limited, endpoints are restricted and some patient populations are excluded. Postmarketing surveillance (PS) studies can add important information for real-world clinical practice. Acute migraine therapy with almotriptan 12.5 mg was evaluated in 4 PS studies, 2 conducted in Spain, 1 in Germany and 1 in France. Almotriptan was associated with a high rate of treatment response and was well tolerated in all 4 studies. In the Spanish and German studies, 2-hour pain-relief, 2-hour pain-free, and sustained painfree rates were enhanced when patients treated mild pain. Patient satisfaction with almotriptan, assessed in the German and French studies, was high and the majority of patients preferred almotriptan to their previous acute migraine therapy. In conclusion, PS studies augment our knowledge of antimigraine therapy, giving a more complete picture of how such agents work in the general population.

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Year:  2006        PMID: 16440139      PMCID: PMC3451577          DOI: 10.1007/s10194-006-0266-6

Source DB:  PubMed          Journal:  J Headache Pain        ISSN: 1129-2369            Impact factor:   7.277


  4 in total

Review 1.  Clinical and economic comparison of frovatriptan versus other oral triptans in the treatment of acute migraine in the real-world setting.

Authors:  Mario Guidotti; Roberto Ravasio
Journal:  Clin Drug Investig       Date:  2009       Impact factor: 2.859

2.  Effectiveness and safety of an extended-release tablet of sodium valproate for the prophylactic treatment of migraine: Postmarketing surveillance in Japan.

Authors:  Takao Takeshima; Norihiro Suzuki; Yasuhiko Matsumori; Naoki Shimmoto; Yuji Kurihara; Ryoji Gunji; Fumihiko Sakai
Journal:  Neurol Clin Neurosci       Date:  2016-04-26

Review 3.  Pharmacovigilance: reporting requirements throughout a product's lifecycle.

Authors:  Sylvia Lucas; Jessica Ailani; Timothy R Smith; Ahmad Abdrabboh; Fei Xue; Marco S Navetta
Journal:  Ther Adv Drug Saf       Date:  2022-09-27

4.  Clinically significant interactions between antiretroviral and co-prescribed drugs for HIV-infected children: profiling and comparison of two drug databases.

Authors:  Kazeem A Oshikoya; Ibrahim A Oreagba; Olayinka O Ogunleye; Saheed Lawal; Idowu O Senbanjo
Journal:  Ther Clin Risk Manag       Date:  2013-05-14       Impact factor: 2.423

  4 in total

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