Anpheros Search · Treatment

Tenofovir alafenamide

Also known as: Vemlidy

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In short

In the European Union, tenofovir alafenamide is indicated for the treatment of chronic hepatitis B in adults and paediatric patients six years of age and older weighing at least 25 kg. In the United States, it is indicated for the treatment of chronic hepatitis B virus infection in adults and pediatric patients six years of age and older weighing at least 25 kg with compensated liver disease. Tenofovir alafenamide is listed by the cited source as having an approved use for acute hepatitis B.

From: Source: European Medicines Agency (EMA), Vemlidy — EPAR, 17/09/2024. © European Medicines Agency. · Data provided by the U.S. Food and Drug Administration. · Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
1721603 tenofovir alafenamide
EMA
EMEA/H/C/004169

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) Vemlidy

Vemlidy is indicated for the treatment of chronic hepatitis B (CHB) in adults and paediatric patients 6 years of age and older weighing at least 25 kg (see section 5.1).

Source: European Medicines Agency (EMA), Vemlidy — EPAR, 17/09/2024. © European Medicines Agency.

Document date: 17/09/2024 · Official document →

FDA (USA) VEMLIDY

1 INDICATIONS AND USAGE VEMLIDY is indicated for the treatment of chronic hepatitis B virus (HBV) infection in adults and pediatric patients 6 years of age and older and weighing at least 25 kg with compensated liver disease [see Clinical Studies (14) ] . VEMLIDY is a hepatitis B virus (HBV) nucleoside analog reverse transcriptase inhibitor and is indicated for the treatment of chronic hepatitis B virus infection in adults and pediatric patients 6 years of age and older and weighing at least 25 kg with compensated liver disease. ( 1 )

Data provided by the U.S. Food and Drug Administration.

Document date: 20250714 · Official document →

Related terms in the cited sources

Has an official indication for

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External resources

Questions

What is Tenofovir alafenamide approved for in the European Union?

Vemlidy is indicated for the treatment of chronic hepatitis B (CHB) in adults and paediatric patients 6 years of age and older weighing at least 25 kg (see section 5.1). (Source: European Medicines Agency (EMA), Vemlidy — EPAR, 17/09/2024. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • Data provided by the U.S. Food and Drug Administration.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Vemlidy — EPAR, 17/09/2024. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →