| Literature DB >> 25974703 |
J K Hicks1, J R Bishop2, K Sangkuhl3, D J Müller4, Y Ji5, S G Leckband6, J S Leeder7, R L Graham8, D L Chiulli9, A LLerena10, T C Skaar11, S A Scott12, J C Stingl13, T E Klein3, K E Caudle14, A Gaedigk7.
Abstract
Selective serotonin reuptake inhibitors (SSRIs) are primary treatment options for major depressive and anxiety disorders. CYP2D6 and CYP2C19 polymorphisms can influence the metabolism of SSRIs, thereby affecting drug efficacy and safety. We summarize evidence from the published literature supporting these associations and provide dosing recommendations for fluvoxamine, paroxetine, citalopram, escitalopram, and sertraline based on CYP2D6 and/or CYP2C19 genotype (updates at www.pharmgkb.org).Entities:
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Year: 2015 PMID: 25974703 PMCID: PMC4512908 DOI: 10.1002/cpt.147
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875