Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: J05AR08

Eviplera(emtricitabine;rilpivirine hydrochloride;tenofovir disoproxil fumarate)

HIV Infections

Marketing Authorisation Holder: Gilead Sciences International Ltd

EMA Authorisation: 27/11/2011

INN: emtricitabine;rilpivirine;tenofovir disoproxil

Indication

Eviplera is indicated for the treatment of adults infected with human immunodeficiency virus type 1 (HIV-1) without known mutations associated with resistance to the non-nucleoside reverse transcriptase inhibitor (NNRTI) class, tenofovir or emtricitabine, and with a viral load ? 100,000 HIV-1 RNA copies/mL. As with other antiretroviral medicinal products, genotypic resistance testing and/or historical resistance data should guide the use of Eviplera.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.