Pharmacokinetics and safety of indinavir in human immunodeficiency virus-infected pregnant women
- PMID: 17158945
- PMCID: PMC1797783
- DOI: 10.1128/AAC.00420-06
Pharmacokinetics and safety of indinavir in human immunodeficiency virus-infected pregnant women
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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