Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: M04AA03

Febuxostat Viatris (previously Febuxostat Mylan)(febuxostat)

Hyperuricemia;Arthritis, Gouty;Gout

Marketing Authorisation Holder: Viatris Limited

EMA Authorisation: 15/06/2017

INN: febuxostat

Indication

Febuxostat Viatris is indicated for the treatment of chronic hyperuricaemia in conditions where urate deposition has already occurred (including a history, or presence of, tophus and/or gouty arthritis). Febuxostat Viatris is indicated for the prevention and treatment of hyperuricaemia in adult patients undergoing chemotherapy for haematologic malignancies at intermediate to high risk of Tumor Lysis Syndrome (TLS).   Febuxostat Viatris is indicated in adults.

Official EMA Resources

View on EMA (ema.europa.eu)

AI Drug & Interaction Analysis

Free account required

Ask Prognia AI about Febuxostat Viatris (previously Febuxostat Mylan) — 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.