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🇪🇺EU · EMAAuthorisedATC: B01AC30

Clopidogrel / Acetylsalicylic acid Viatris (previously Clopidogrel / Acetylsalicylic acid Mylan)(acetylsalicylic acid;clopidogrel hydrogen sulfate)

Acute Coronary Syndrome;Myocardial Infarction

Marketing Authorisation Holder: Mylan Pharmaceuticals Limited

EMA Authorisation: 09/01/2020

INN: clopidogrel;acetylsalicylic acid

Indication

 Clopidogrel/Acetylsalicylic acid Viatris is indicated for the secondary prevention of atherothrombotic events in adult patients already taking both clopidogrel and acetylsalicylic acid (ASA). Clopidogrel/Acetylsalicylic acid Viatris is a fixed-dose combination medicinal product for continuation of therapy in: - 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 - ST segment elevation acute myocardial infarction in medically treated patients eligible for thrombolytic therapy

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.