Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: J05AR20

Biktarvy(bictegravir;emtricitabine;tenofovir alafenamide;fumarate)

HIV Infections

Marketing Authorisation Holder: Gilead Sciences Ireland UC

EMA Authorisation: 21/06/2018

INN: bictegravir;emtricitabine;tenofovir alafenamide

Indication

Biktarvy is indicated for the treatment of human immunodeficiency virus 1 (HIV 1) infection in adults and paediatric patients at least 2 years of age and weighing at least 14 kg i without present or past evidence of viral resistance to the integrase inhibitor class, emtricitabine or tenofovir.(see section 5.1)

Official EMA Resources

View on EMA (ema.europa.eu)

AI Drug & Interaction Analysis

Free account required

Ask Prognia AI about Biktarvy — dosing recommendations, drug interactions, and current guideline evidence from ESC, EMA, NICE and more.

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