Tanum L
Department of Psychosomatic and Behavioural Medicine, Rikshospitalet, Oslo, Norway.
Acta Psychiatr Scand Suppl. 2000;402:37-40. doi: 10.1034/j.1600-0447.2000.02606.x.
Since reboxetine acts selectively on the reuptake of noradrenaline, it has a different side-effects profile than drugs acting predominantly on the serotonin reuptake mechanism. Data from patients treated with reboxetine (n = 1503) or placebo/comparator drugs (n = 1027) show that reboxetine has no significant cardiovascular effects, a low potential for drug interactions, causes no significant impairment of cognitive or motor function and no increase in suicidal ideation. In contrast to certain serotonergic drugs, there is no evidence of any withdrawal syndrome upon abrupt discontinuation or tapering of reboxetine treatment. Sexual dysfunction appears in only a small fraction of the patients and mainly with doses higher than 8 mg daily. The rate of discontinuation due to adverse effects with reboxetine was not significantly different from that observed with placebo in short-term studies. The level of efficacy and apparently favourable tolerability profile makes reboxetine an important alternative in the medical treatment of depressive illness.
由于瑞波西汀选择性作用于去甲肾上腺素的再摄取,其副作用特征与主要作用于5-羟色胺再摄取机制的药物不同。接受瑞波西汀治疗的患者(n = 1503)或接受安慰剂/对照药物治疗的患者(n = 1027)的数据表明,瑞波西汀无显著心血管效应,药物相互作用可能性低,不会显著损害认知或运动功能,也不会增加自杀意念。与某些5-羟色胺能药物不同,没有证据表明突然停用或逐渐减少瑞波西汀治疗会出现任何戒断综合征。性功能障碍仅出现在一小部分患者中,且主要出现在每日剂量高于8毫克时。在短期研究中,因瑞波西汀不良反应而停药的发生率与安慰剂观察到的情况无显著差异。疗效水平和明显良好的耐受性使瑞波西汀成为抑郁症药物治疗的重要选择。