| EMA number | EMEA/H/C/001166 |
| ATC code | B01AC04 |
| Authorisation | 28 July 2009 |
| Withdrawn | 18 January 2017 |
| Revision | 6 |
Clopidogrel is indicated in adults for the prevention of atherothrombotic events in: Patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease Non-ST segment elevation acute coronary syndrome (unstable angina or non-Q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (ASA) ST segment elevation acute myocardial infarction, in combination with ASA in medically treated patients eligible for thrombolytic therapy Patients suffering from acute coronary syndrome.
CLOPIDOGREL — PURACAP LABS BLU, approved 2022-07-27 (ANDA213351).
118,111 reports across the top reactions. These are spontaneously reported events from the FDA Adverse Event Reporting System — they reflect reporting volume, not incidence or frequency, and a report does not mean the drug caused the event.