Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ticagrelor
Drug ID BADD_D02214
Description Ticagrelor, or AZD6140, was first described in the literature in 2003.[A204170,A2903] Ticagrelor is an ADP derivative developed for its P2Y12 receptor antagonism.[A2903] Unlike [clopidogrel], ticagrelor is not a prodrug.[A2903] It is marketed by Astra Zeneca as Brilinta in the US[L14201] and Brilique or Possia in the EU,[L14207]. Ticagrelor was granted EMA approval on 3 December 2010.[L14207] Ticagrelor was granted FDA approval on 20 July 2011.[L14201]
Indications and Usage 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.[L14201] Ticagrelor is also indicated to reduce the risk of a first myocardial infarction or stroke in high risk patients with coronary artery disease.[L14201]
Marketing Status approved
ATC Code B01AC24
DrugBank ID DB08816
KEGG ID D09017
MeSH ID D000077486
PubChem ID 9871419
TTD Drug ID D0WF7L
NDC Product Code 53747-092; 69037-0007; 76072-1016; 0186-0777; 45941-3055; 50379-0011; 50923-0314; 58623-0131; 69238-1134; 49587-109; 50379-0023; 55154-9618; 15894-0030; 83137-0001; 17228-0776; 49187-0205; 17228-0777; 17228-7777; 62147-0280; 82712-1001; 0186-0776; 55111-969; 65372-1198
UNII GLH0314RVC
Synonyms Ticagrelor | Brilique | AZD 6140 | AZD6140 | AZD-6140 | Brilinta | 3-(7-((2-(3,4-Difluorophenyl)cyclopropyl)amino)-5-(propylthio)-3H-(1-3)-triazolo(4,5-d)pyrimidin-3-yl)-5-(2-hydroxyethoxy)cyclopentane-1,2-diol
Chemical Information
Molecular Formula C23H28F2N6O4S
CAS Registry Number 274693-27-5
SMILES CCCSC1=NC(=C2C(=N1)N(N=N2)C3CC(C(C3O)O)OCCO)NC4CC4C5=CC(=C(C=C5)F)F
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Cardiac arrest02.03.04.0010.006663%
Cardiac failure02.05.01.0010.003943%
Cardiac failure congestive02.05.01.0020.002937%Not Available
Cardiac tamponade02.06.01.0010.000952%
Cardiogenic shock24.06.02.006; 02.05.01.0030.001360%Not Available
Cardiovascular disorder02.11.01.010; 24.03.02.0090.000544%Not Available
Cerebral artery embolism24.01.04.001; 17.08.01.0010.000272%Not Available
Cerebral haemorrhage24.07.04.001; 17.08.01.0030.006663%Not Available
Cerebrovascular accident17.08.01.007; 24.03.05.0010.005439%
Chest discomfort22.12.02.002; 08.01.08.019; 02.02.02.0090.023797%Not Available
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.0110.024042%Not Available
Cheyne-Stokes respiration22.02.01.0240.001006%Not Available
Choking22.12.03.0030.001197%Not Available
Cholecystitis09.03.01.0010.000408%
Cholecystitis acute09.03.01.0030.000952%Not Available
Cholelithiasis09.03.01.0020.001224%Not Available
Chromaturia20.02.01.0020.000408%
Circulatory collapse24.06.02.0010.000408%Not Available
Coagulopathy01.01.02.0010.000870%Not Available
Coma17.02.09.0010.001496%Not Available
Compartment syndrome24.04.05.006; 15.05.05.0050.000544%Not Available
Confusional state19.13.01.001; 17.02.03.005--
Constipation07.02.02.001--
Contrast media reaction10.01.01.011; 12.02.05.0290.000272%Not Available
Coronary artery disease24.04.04.006; 02.02.01.0010.003372%Not Available
Coronary artery occlusion12.02.01.036; 24.04.04.013; 02.02.01.0060.002176%Not Available
Coronary artery stenosis02.02.01.010; 12.02.01.037; 24.04.04.0170.002420%Not Available
Coronary artery thrombosis24.01.05.002; 02.02.01.0070.002312%Not Available
Cough22.02.03.001--
Cystitis haemorrhagic20.03.02.0030.000272%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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