Xagrid

anagrelide · Takeda Pharmaceuticals International AG Ireland
AUTHORISED IN THE EU

What Xagrid is used for

Xagrid 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 ET is defined by one or more of the following features: >60 years of age or; a platelet count >1000 x 109/l or; a history of thrombohaemorrhagic events.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Xagrid
Active substance
anagrelide
Disease area
Thrombocythemia, Essential
Medicine group
Antineoplastic agents
ATC code
L01XX35
Marketing authorisation holder
Takeda Pharmaceuticals International AG Ireland
Authorised in the EU since
2004

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Xagrid used for?

Xagrid 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 ET is defined by one or more of the following features: >60 years of age or; a platelet count >1000 x 109/l or; a history of thrombohaemorrhagic events.

What is the active substance in Xagrid?

Xagrid contains anagrelide.

Who makes Xagrid?

The EU marketing authorisation holder is Takeda Pharmaceuticals International AG Ireland.

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

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