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🇪🇺EU · EMAWithdrawnATC: J05AR16

Dutrebis(lamivudine;raltegravir potassium)

HIV Infections

Marketing Authorisation Holder: Merck Sharp Dohme Limited

EMA Authorisation: 26/03/2015

INN: lamivudine;raltegravir potassium

Indication

Dutrebis is indicated in combination with other anti?retroviral medicinal products for the treatment of human immunodeficiency virus (HIV?1) infection in adults, adolescents, and children from the age of 6 years and weighing at least 30 kg without present or past evidence of viral resistance to antiviral agents of the InSTI (Integrase Strand Transfer Inhibitor) and NRTI (Nucleoside Reverse Transcriptase Inhibitor) classes (see sections 4.2, 4.4 and 5.1).

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.