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)
Abdominal pain07.01.05.002--
Acute myocardial infarction02.02.02.001; 24.04.04.0010.011559%-
Acute pulmonary oedema02.05.02.004; 22.01.03.0050.000544%-
Acute respiratory distress syndrome10.02.01.067; 22.01.03.001; 24.03.02.0340.000680%
Alveolar proteinosis10.04.04.018; 22.01.02.0090.000952%-
Angina pectoris02.02.02.002; 24.04.04.0020.004052%
Angina unstable02.02.02.004; 24.04.04.0040.003264%-
Angioedema10.01.05.009; 22.04.02.008; 23.04.01.0010.002692%-
Aortic dissection24.02.03.0020.000272%-
Arrhythmia02.03.02.0010.002149%-
Arterial thrombosis24.01.01.0020.000272%-
Arteriosclerosis coronary artery02.02.01.011; 24.04.04.0120.000408%-
Asphyxia12.01.08.011; 22.02.02.0010.009655%-
Asthenia08.01.01.001---
Asthma10.01.03.010; 22.03.01.0020.003372%-
Atrial fibrillation02.03.03.0020.006554%
Atrioventricular block02.03.01.0020.004052%-
Atrioventricular block complete02.03.01.0030.002856%
Atrioventricular block first degree02.03.01.0040.000598%
Atrioventricular block second degree02.03.01.0050.000816%
Back pain15.03.04.005--
Benign prostatic hyperplasia21.04.02.001---
Blood creatinine increased13.13.01.004--
Blood uric acid increased13.02.04.001---
Body temperature increased13.15.01.001---
Bone disorder15.02.04.004---
Bradycardia02.03.02.0020.014713%-
Breath holding19.01.01.002; 22.02.01.0160.000272%-
Bronchospasm10.01.03.012; 22.03.01.0040.005195%
Bundle branch block left02.03.01.0070.000598%-
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ADReCS-Target
Drug Name ADR Term Target
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