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EMA Product

Efient

Product approved by European Medicines Agency (EU)

Basic Information

Efient

Regulatory Information

EMEA/H/C/000984

Authorised

February 24, 2009

December 18, 2008

27

September 4, 2024

Company Information

France

24 rue Erlanger 75016 Paris

SUBSTIPHARM

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Efient, co-administered with acetylsalicylic acid (ASA), is indicated for the prevention of atherothrombotic events in patients with acute coronary syndrome (i.e. unstable angina, non-ST-segment-elevation myocardial infarction \[UA / NSTEMI\] or ST-segment-elevation myocardial infarction \[STEMI\]) undergoing primary or delayed percutaneous coronary intervention (PCI).

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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