DRUG WARNING: Boceprevir (Victrelis™)

On February 6, 2012, Merck and Co, Inc. in collaboration with the U.S. Food and Drug Administration (FDA) issued a Dear Healthcare Professional letter regarding the potential for lowered drug concentrations when combining certain ritonavir-boosted HIV protease-inhibitors (atazanavir, darunavir, lopinavir) and the hepatitis C protease-inhibitor, boceprevir. Health care providers who are treating patients with this combination are advised to closely monitor patients for HIV viral rebound and hepatitis C treatment response.

Link not available. Boceprevir is no longer marketed in Canada (January 2017)

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The BC-CfE Laboratory is streamlining reporting processes for certain tests in order to simplify distribution and record-keeping, and to ensure completeness of results. Beginning September 2, 2025, results for the ‘Resistance Analysis of HIV-1 Protease and Reverse Transcriptase’ (Protease-RT) and ‘HIV-1 Integrase Resistance Genotype’ tests will be combined into a single ‘HIV-1 Resistance Genotype Report’.
For more details and example reports, please click on the button below