Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L01XX35

Anagrelide Viatris (previously Anagrelide Mylan)(anagrelide hydrochloride)

Thrombocythemia, Essential

Marketing Authorisation Holder: Viatris Limited

EMA Authorisation: 15/02/2018

INN: anagrelide

Indication

Anagrelide Viatris is indicated for the reduction of elevated platelet counts in at risk essential thrombocythaemia (ET) patients who are intolerant to their current therapy or whose elevated platelet counts are not reduced to an acceptable level by their current therapy.An at-risk patient An at-risk essential thrombocythaemia patient is defined by one or more of the following features: >60 years of age or a platelet count >1,000 x 10⁹/l or a history of thrombo-haemorrhagic events.

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.