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Sumatriptanaproxen sodium: A review of its use in adult patients with migraine

机译:舒马普坦/萘普生钠:其在成年偏头痛患者中的使用的评论

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摘要

A fixed-dose combination of sumatriptanaproxen sodium (Treximet ?) has been approved in the US for the acute treatment of migraine in adults. In two randomized trials, sumatriptanaproxen sodium demonstrated significantly better efficacy than sumatriptan alone, naproxen sodium alone, or placebo as late-intervention therapy for a single migraine episode in adults, as assessed by co-primary efficacy endpoints evaluating pain and other migraine-related symptoms, as well as health-related quality of life (HR-QOL) endpoints. In four other randomized trials, the drug combination was also effective as early intervention in adults with migraine (including those with menstrual migraine and dysmenorrhoea, or those with poor response or intolerance to triptan therapy) according to various pain-related primary efficacy and HR-QOL endpoints. Data from longer-term, non-randomized studies support these findings, and the drug combination appears to be beneficial in patients with migraine and cutaneous allodynia. In clinical trials, sumatriptanaproxen sodium was generally well tolerated, with an overall tolerability profile similar to that of sumatriptan. The most common adverse events were in line with those expected for sumatriptan and naproxen sodium. Current data indicate that sumatriptanaproxen sodium is a useful option in the treatment of adult migraine.
机译:舒马曲坦/萘普生钠(Treximet?)的固定剂量组合已在美国获准用于成人偏头痛的急性治疗。在两项随机试验中,舒马普坦/萘普生钠作为单独干预成人偏头痛的晚期干预疗法,其疗效优于单独使用舒马普坦,萘普生钠或安慰剂,其疗效通过评估疼痛和其他偏头痛的共同主要疗效终点进行了评估相关症状,以及与健康相关的生活质量(HR-QOL)终点。在其他四项随机试验中,根据各种与疼痛相关的主要疗效和HR-HR,药物组合也可作为偏头痛成人(包括月经偏头痛和痛经的患者,或对曲普坦疗法反应不良或不耐受的患者)的早期干预药物。 QOL端点。长期,非随机研究的数据支持了这些发现,并且该药物组合对于偏头痛和皮肤异常性疼痛患者似乎是有益的。在临床试验中,舒马普坦/萘普生钠的耐受性一般良好,总体耐受性与舒马普坦相似。最常见的不良事件与舒马普坦和萘普生钠的不良事件一致。当前数据表明舒马曲坦/萘普生钠是治疗成人偏头痛的有用选择。

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