Department of Psychiatry, University of Occupational and Environmental Health Iseigaoka, Yahatanishi-ku, Kitakyushu, Japan.
World J Biol Psychiatry. 2009;10(4 Pt 2):620-2. doi: 10.1080/15622970802118349.
Selective serotonin reuptake inhibitors (SSRIs) are first line drugs for treating not only depressive disorder but also anxiety disorder. Fluvoxamine, a SSRI, is mainly metabolized by cytochrome P450 (CYP) 2D6 and 1A2. However, paroxetine, an another SSRI is potent inhibitor for CYP 2D6. We report a case with depression whose plasma fluvoxamine level rapidly increased after the addition of paroxetine while switching from fluvoxamine to paroxetine. The case indicates that emerging adverse effects via the pharmacokinetic interaction of these drugs when switching patients from fluvoxamine to paroxetine can occur.
选择性 5-羟色胺再摄取抑制剂(SSRIs)不仅是治疗抑郁症的一线药物,也是治疗焦虑症的一线药物。氟伏沙明是一种 SSRI,主要通过细胞色素 P450(CYP)2D6 和 1A2 代谢。然而,帕罗西汀是另一种 SSRI,是 CYP 2D6 的强效抑制剂。我们报告了一例抑郁症患者,在从氟伏沙明转换为帕罗西汀时,加用帕罗西汀后,其血浆氟伏沙明水平迅速升高。该病例表明,当患者从氟伏沙明转换为帕罗西汀时,这些药物的药代动力学相互作用可能会导致新的不良反应。