Abstract
Several safe and highly effective direct-acting antiviral (DAA) drugs for chronic hepatitis C virus (HCV) have been developed and greatly increase the number of therapeutic options available to successfully treat HCV infection. However, because treatment regimens contain at least two drugs (e.g., elbasvir and grazoprevir, glecaprevir and pibrentasvir, or sofosbuvir with daclatasvir, simeprevir, ledipasvir, or velpatasvir) and up to five drugs (ombitasvir/paritaprevir/ritonavir plus dasabuvir with or without ribavirin), the potential for drug-drug interactions (DDIs) becomes an important consideration for HCV-infected individuals with comorbidities that require concomitant medications, such as human immunodeficiency virus/HCV coinfection or immunosuppression after liver transplantation. This review details the pharmacokinetics and DDI potential of approved DAAs for the treatment of HCV infection.
Cite
CITATION STYLE
Garrison, K. L., German, P., Mogalian, E., & Mathias, A. (2018, August 1). The drug-drug interaction potential of antiviral agents for the treatment of chronic hepatitis C infection. Drug Metabolism and Disposition. American Society for Pharmacology and Experimental Therapy. https://doi.org/10.1124/dmd.117.079038
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.