| Literature DB >> 18609433 |
Hikaru Hori1, Reiji Yoshimura, Nobuhisa Ueda, Atsuko Ikenouchi-Sugita, Wakako Umene-Nakano, Jun Nakamura.
Abstract
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.Entities:
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Year: 2009 PMID: 18609433 DOI: 10.1080/15622970802118349
Source DB: PubMed Journal: World J Biol Psychiatry ISSN: 1562-2975 Impact factor: 4.132