Vorapaxar is a tricyclic himbacine-derived selective inhibitor of protease activated receptor (PAR-1) indicated for reducing the incidence of thrombotic cardiovascular events in patients with a history of myocardial infarction (MI) or with peripheral arterial disease (PAD). By inhibiting PAR-1, a thrombin receptor expressed on platelets, vorapaxar prevents t...
Vorapaxar is indicated for the reduction of thrombotic cardiovascular events in patients with a history of myocardial infarction (MI) or peripheral arterial disease (PAD). It is usually co-administered with acetylsalicylic acid (ASA) and/or clopidogrel, and should therefore be administered as an addition to these medications as it has not been studied alone.
Inova Fairfax Hospital, Falls Church, Virginia, United States
Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria
University of Florida, Jacksonville, Florida, United States
University of Florida, Jacksonville, Florida, United States
Georgetown University Hospital, Georgetown, Maryland, United States
Melbourne Sexual Health Centre, Carlton, Victoria, Australia
Hennepin County Medical Centre, Minneapolis, Minnesota, United States
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