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. 2007 Feb;51(2):783-6.
doi: 10.1128/AAC.00420-06. Epub 2006 Dec 11.

Pharmacokinetics and safety of indinavir in human immunodeficiency virus-infected pregnant women

Affiliations

Pharmacokinetics and safety of indinavir in human immunodeficiency virus-infected pregnant women

Jashvant D Unadkat et al. Antimicrob Agents Chemother. 2007 Feb.

Abstract

Human immunodeficiency virus-infected women (n=16) received indinavir (800 mg three times a day) plus zidovudine plus lamivudine from 14 to 28 weeks of gestation to 12 weeks postpartum. Two women and eight infants experienced grade 3 or 4 toxicities that were possibly treatment related. Indinavir area under the plasma concentration-time curve was 68% lower antepartum versus postpartum, suggesting increased intestinal and/or hepatic CYP3A activity during pregnancy.

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Figures

FIG. 1.
FIG. 1.
Area under the plasma concentration-time curves (AUC0-8) of indinavir in all but two women were lower antepartum versus postpartum. The horizontal solid line represents the arithmetic mean AUC0-8 values for the antepartum and postpartum periods.

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