Following non-submission
AWMSG advice |
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Status: Not endorsed (Statement of Advice) | ||
In the absence of a submission from the holder of the marketing authorisation, vorapaxar (Zontivity®) cannot be endorsed for use within NHS Wales co-administered with acetylsalicylic acid and, where appropriate, clopidogrel, for the reduction of atherothrombotic events in adult patients with a history of myocardial infarction (MI); or symptomatic peripheral arterial disease (PAD). This product is currently not marketed in the UK. |
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Medicine details |
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Medicine name | vorapaxar (Zontivity®) | |
Formulation | 2 mg film-coated tablet | |
Reference number | 1034 | |
Indication | co-administered with acetylsalicylic acid and, where appropriate, clopidogrel, for the reduction of atherothrombotic events in adult patients with a history of myocardial infarction (MI); or symptomatic peripheral arterial disease (PAD). This product is currently not marketed in the UK. |
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Company | Merck Sharp & Dohme Ltd | |
BNF chapter | Cardiovascular system | |
Submission type | Non-submission | |
Status | Not endorsed (Statement of Advice) | |
Ratification by Welsh Government | 15/05/2015 | |
Date of issue | 20/05/2015 |