Literature DB >> 17158945

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

Jashvant D Unadkat1, Diane W Wara, Michael D Hughes, Anita A Mathias, Diane T Holland, Mary E Paul, James Connor, Sharon Huang, Bach-Yen Nguyen, D Heather Watts, Lynne M Mofenson, Elizabeth Smith, Paul Deutsch, Kathleen A Kaiser, Ruth E Tuomala.   

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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Year:  2006        PMID: 17158945      PMCID: PMC1797783          DOI: 10.1128/AAC.00420-06

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  11 in total

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7.  Public Health Service Task Force recommendations for the use of antiretroviral drugs in pregnant women infected with HIV-1 for maternal health and for reducing perinatal HIV-1 transmission in the United States. Centers for Disease Control and Prevention.

Authors: 
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7.  As in humans, pregnancy increases the clearance of the protease inhibitor nelfinavir in the nonhuman primate Macaca nemestrina.

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