Ticagrelor
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Clinical data | |
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Trade names | Brilinta, Brilique, Possia |
Synonyms | AZD-6140 |
MedlinePlus | a611050 |
[[Regulation of therapeutic goods |Template:Engvar data]] |
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Routes of administration | Oral |
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Pharmacokinetic data | |
Bioavailability | 36% |
Protein binding | >99.7% |
Metabolism | Hepatic (CYP3A4) |
Elimination half-life | 7 hrs (ticagrelor), 8.5 hrs (active metabolite AR-C124910XX) |
Excretion | Biliary |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C23H28F2N6O4S |
Molar mass | 522.567 g/mol |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Jesus Rosario Hernandez, M.D. [2]
Synonyms / Brand Names: Lopressor, Toprol XL
Overview
Ticagrelor (trade name Brilinta in the US, Brilique and Possia in the EU) is a platelet aggregation inhibitor produced by AstraZeneca. The drug was approved for use in the European Union by the European Commission on December 3, 2010.[1][2] The drug was approved by the US Food and Drug Administration on July 20, 2011.[3]
Category
P2Y12 platelet inhibitor, platelet aggregation inhibitor
Prescribing Information
Brilinta (ticagrelor) tablet
References
- ↑ "Assessment Report for Brilique" (PDF). European Medicines Agency. January 2011.
- ↑ European Public Assessment Report Possia
- ↑ "FDA approves blood-thinning drug Brilinta to treat acute coronary syndromes". FDA. 20 July 2011.
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