Olver James S, Burrows Graham D, Norman Trevor R
Department of Psychiatry, University of Melbourne, Austin Hospital, Heidelberg, Victoria, Australia.
Hum Psychopharmacol. 2004 Jan;19(1):9-16. doi: 10.1002/hup.551.
Venlafaxine is the first of a group of antidepressants that show dual reuptake inhibition of serotonin and noradrenaline (SNRIs). Originally marketed in an immediate release (IR) formulation a microencapsulated, extended release (XR) formulation is now available. Significant differences exist between these two formulations with respect to pharmacokinetic parameters which have an impact on clinical use. The XR has lower maximum plasma concentrations (Cmax) and achieves these at a later time (higher Tmax). The longer apparent elimination half-life of the drug after single XR doses suggests that it is suitable for once daily dosing compared with the twice daily dosing regimen required by the IR formulation. With respect to antidepressant efficacy the XR formulation is equivalent to other marketed antidepressants and to the IR formulation. Consistent with its pharmacokinetic properties the use of the XR formulation is associated with less nausea and dizziness at the initiation of therapy. While in clinical usage XR might be expected to increase compliance with medication and to reduce discontinuation syndromes there are few comparative studies for which this has been evaluated. The XR formulation of venlafaxine is no worse than the IR form with respect to tolerability and offers some benefits to patients in terms of ease of use. On the other hand there does not appear to be any increase in the efficacy of the active agent.
文拉法辛是一类显示对5-羟色胺和去甲肾上腺素双重再摄取抑制作用的抗抑郁药中的第一种。最初以速释(IR)制剂上市,现在有一种微囊化缓释(XR)制剂。这两种制剂在药代动力学参数方面存在显著差异,而这些参数会影响临床应用。XR制剂的血浆最大浓度(Cmax)较低,且达到该浓度的时间较晚(Tmax较高)。单次服用XR剂量后,药物的表观消除半衰期较长,这表明与IR制剂所需的每日两次给药方案相比,它适合每日一次给药。在抗抑郁疗效方面,XR制剂与其他已上市的抗抑郁药以及IR制剂相当。与其药代动力学特性一致,使用XR制剂在治疗开始时出现恶心和头晕的情况较少。虽然在临床应用中,预计XR制剂可能会提高用药依从性并减少停药综合征,但很少有比较研究对此进行评估。文拉法辛的XR制剂在耐受性方面不比IR制剂差,并且在易用性方面为患者提供了一些益处。另一方面,活性剂的疗效似乎没有任何提高。