EMA
approval
· 2025-01-21
EMA Authorised: Dabigatran etexilate Teva (previously Dabigatran etexilate Leon Farma) (dabigatran etexilate mesilate) — Teva GmbH
Summary
The EMA authorised Teva's dabigatran etexilate mesilate product for prevention of venous thromboembolism, including after arthroplasty (joint replacement).
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Venous Thromboembolism;Arthroplasty, Replacement. MAH: Teva GmbH. Decision date: 20/01/2025