Related Experiment Video
Updated: May 11, 2026

Zika Virus Infectious Cell Culture System and the In Vitro Prophylactic Effect of Interferons
Published on: August 23, 2016
Atazanavir pharmacokinetics, efficacy and safety in pregnancy: a systematic review
Timothy Eley1, Richard Bertz, Hélène Hardy
1Research and Development, Bristol-Myers Squibb, Princeton, NJ, USA. timothy.eley@bms.com
Background:
For some antiretroviral therapies, drug concentrations are reduced during pregnancy, potentially compromising effective virological suppression.
Methods:
Data on atazanavir boosted with ritonavir in pregnancy are reviewed.
Results:
With standard atazanavir/ritonavir 300/100 mg once-daily dosing: atazanavir area-under-the-concentration-time curves were reduced during pregnancy in most studies, but overall interpretation differed according to the data used for comparison; atazanavir concentration 24 h post-dose was maintained >150 ng/ml in 97.6% of women; no instance of mother-to-child transmission occurred in treatment-adherent mothers; and infant hyperbilirubinaemia was not elevated beyond levels expected in the neonatal period.
Conclusions:
With concurrent medications that reduce atazanavir drug concentrations, optimal therapy during pregnancy may require once-daily atazanavir/ritonavir 400/100 mg; however, using this dose during the third trimester doubled maternal grade 3-4 hyperbilirubinaemia rates.
Related Concept Videos
Teratogenicity
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment
Pharmacokinetics: Drug–Food and Drug–Viral Interactions
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion

