Ticagrelor, or AZD6140, was first described in the literature in 2003. Ticagrelor is an ADP derivative developed for its P2Y receptor antagonism. Unlike clopidogrel, ticagrelor is not a prodrug. It is marketed by Astra Zeneca as Brilinta in the US and Brilique or Possia in the EU,.
Ticagrelor was granted EMA approval on 3 December 2010.
Ticagrelor was granted FDA approval on 20 July 2011.
Ticagrelor is indicated to reduce the risk of cardiovascular death, myocardial infarction, and stroke in patients with acute coronary syndrome or a history of myocardial infarction. Ticagrelor is also indicated to reduce the risk of a first myocardial infarction or stroke in high risk patients with coronary artery disease.
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
Research Site, Berlin, Germany
Cardiology Ward Shiraz University of Medical Sciences, Shiraz, Fars, Iran, Islamic Republic of
professor Kojuroi cardiology clinic, Shiraz, Iran, Islamic Republic of
V.A. Almazov Fnmrc, Saint-petersburg, Russian Federation
National Institute of Cardiovascular Diseases, Karachi, SIndh, Pakistan
the Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China
University of Florida Jacksonville, Jacksonville, Florida, United States
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
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