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Milnacipran Hydrochloride in the Treatment of Fibromyalgia Syndrome: Safety, Efficacy and Tolerability

机译:盐酸米那普仑治疗纤维肌痛综合征:安全性,有效性和耐受性

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Fibromyalgia is a central sensitization disorder characterized by chronic widespread pain, nonrestorative sleep, fatigue, cognitive dysfunction as well as a number of somatic symptoms; that reduces physical/emotional function/quality of life. Treatment options include: Patients education, behavioral medicine strategies, (eg, cognitive behavioral therapy), physical medicine strategies (eg, exercise/aerobic and strength training), and pharmacologic agents. Currently there are three agents approved by the US Federal Drug Administration for the treatment of Fibromyalgia: pregabalin, duloxetine, and milnacipran. Milnacipran is a norepinephrine-serotonin reuptake inhibitor that is only approved in the US for fibromyalgia. It has 3-fold increased selectivity for norepinephrine compared to serotonin. Milnacipran is well absorbed (85% bioavailability), has a half-life of 6–8 hours, and does not undergo cytochrome P450 metabolism. Milnacipran in doses of 50 mg PO BID to 100 mg PO BID has been shown to have efficacy for fibromyalgia. The most common adverse effect is nausea.
机译:纤维肌痛是一种中枢性致敏性疾病,其特征是慢性广泛性疼痛,非恢复性睡眠,疲劳,认知功能障碍以及许多躯体症状。降低身体/情绪功能/生活质量。治疗选择包括:患者教育,行为医学策略(例如认知行为疗法),物理医学策略(例如运动/有氧运动和力量训练)以及药物治疗。目前,美国联邦药物管理局批准了三种治疗纤维肌痛的药物:普瑞巴林,度洛西汀和米那普仑。 Milnacipran是一种去甲肾上腺素5-羟色胺再摄取抑制剂,仅在美国被批准用于纤维肌痛。与5-羟色胺相比,它对去甲肾上腺素的选择性提高了3倍。 Milnacipran被良好吸收(85%生物利用度),半衰期为6–8小时,并且不经历细胞色素P450代谢。已显示50 mg PO BID至100 mg PO BID剂量的米那普仑对纤维肌痛有效。最常见的不良反应是恶心。

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