Dose-Dependent Alternations in the Pharmacokinetics of Olanzapine During Coadministration of Fluvoxamine in Patients With Schizophrenia

Olanzapine, an atypical antipsychotic agent, is a substrate of the cytochrome P4501A2 (CYP1A2) enzyme. Administration of a potent CYP1A2 inhibitor (eg, fluvoxamine) may alter the pharmacokinetics of olanzapine. This study investigated the pharmacokinetic interactions between olanzapine and fluvoxami...

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Published in:Journal of clinical pharmacology Vol. 44; no. 12; pp. 1385 - 1390
Main Authors: Chiu, Chih-Chiang, Lane, Hsien-Yuan, Huang, Ming-Chyi, Liu, Hui-Ching, Jann, Michael W., Hon, Yuen-Yi, Chang, Wen-Ho, Lu, Mong-Liang
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-12-2004
SAGE Publications
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Summary:Olanzapine, an atypical antipsychotic agent, is a substrate of the cytochrome P4501A2 (CYP1A2) enzyme. Administration of a potent CYP1A2 inhibitor (eg, fluvoxamine) may alter the pharmacokinetics of olanzapine. This study investigated the pharmacokinetic interactions between olanzapine and fluvoxamine in patients with schizophrenia. Ten male smokers were administrated a single dose of olanzapine 10 mg at baseline, followed by 2 weeks of fluvoxamine 50 mg/day and another 2 weeks of fluvoxamine 100 mg/day. Olanzapine 10 mg was given at day 10 during each fluvoxamine treatment. After pretreatment with fluvoxamine, the area under the curve, maximal plasma concentration, and half‐time of olanzapine were significantly increased by 30% to 55%, 12% to 64%, and 25% to 32%, respectively. Volume of distribution and apparent clearance were significantly reduced by 4% to 26% and 26% t O 38%, respectively, after administration of fluvoxamine. Increases in area under the plasma concentration‐time curve from time 0 to infinity appear to be dose dependent. Presumably, altered olanzapine pharmacokinetics are attributed to the inhibition of CYP1A2. Patients treated with the combination of olanzapine and fluvoxamine should be monitored carefully.
Bibliography:ArticleID:JCPH998
ark:/67375/WNG-9FH50KW4-M
istex:6A4672E9676D8E2AE93520D1387A3434EF103B66
Supported by grants NSC 92‐2314‐B‐038–055 and NSC‐92–2314‐B‐109–003 from the National Science Council and Taipei City Government, Taipei, Taiwan
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ISSN:0091-2700
1552-4604
DOI:10.1177/0091270004270291