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Abstract

The hepatitis B virus is currently treated either with a single nucleos(t)ide analog or a finite course of pegylated interferon alfa. These therapies have a low potential for drug interactions but are not devoid of interactions. The treatment of hepatitis C virus has rapidly evolved in recent years. Combinations of agents including inhibitors of the nonstructural (NS) viral protein NS5B polymerase, NS5A, and/or NS3 protease with or without the purine nucleoside analog ribavirin achieve cure rates of at least 90% in most patient populations. The NS3 and NS5A inhibitors participate in a number of important drug interactions, while ribavirin and the NS5B inhibitor, sofosbuvir, have a low potential for interactions. This chapter reviews the pharmacokinetic properties and drug interaction potential of agents used in the treatment of hepatitis B and C viruses, as well as pharmacologic considerations on the use of these therapies in patients with renal or hepatic impairment.

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MacBrayne, C.E., Kiser, J.J. (2018). Hepatitis B and Hepatitis C Antiviral Agents. In: Pai, M., Kiser, J., Gubbins, P., Rodvold, K. (eds) Drug Interactions in Infectious Diseases: Antimicrobial Drug Interactions. Infectious Disease. Humana Press, Cham. https://doi.org/10.1007/978-3-319-72416-4_9

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