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)
Haemorrhoids24.10.02.002; 07.15.03.0010.000870%
Haemothorax24.07.01.008; 22.05.02.001; 12.01.18.0050.000272%
Headache17.14.01.001--
Hemiparesis17.01.04.0010.000408%
Hemiplegia17.01.04.0020.000408%Not Available
Hiatus hernia22.09.02.004; 07.16.01.0010.000272%Not Available
Hiccups22.12.01.001; 07.01.06.0090.000598%
Hydrocephalus17.07.01.0010.000408%
Hypersensitivity10.01.03.003--
Hypertension24.08.02.001--
Hyperuricaemia14.09.01.003--
Hyperventilation22.02.01.006; 19.01.02.0040.001006%Not Available
Hypervolaemia02.05.04.019; 14.05.06.0030.000734%Not Available
Hypotension24.06.03.0020.005004%
Hypovolaemia14.05.05.0020.000272%Not Available
Hypovolaemic shock24.06.02.017--Not Available
Ileus07.13.01.0010.000408%
Immune system disorder10.02.01.001--Not Available
Increased tendency to bruise23.06.01.009; 01.01.03.005; 24.07.06.012--Not Available
Injection site bruising24.07.06.017; 23.03.11.015; 08.02.03.042; 12.07.03.0420.000925%Not Available
Injection site haemorrhage24.07.01.010; 12.07.03.005; 08.02.03.005--Not Available
Insomnia17.15.03.002; 19.02.01.002--
Intestinal perforation07.04.06.0020.000272%Not Available
Intracranial aneurysm24.02.04.001; 17.08.06.0010.000598%Not Available
Intracranial pressure increased17.07.02.0020.000272%Not Available
Intraventricular haemorrhage24.07.04.008; 17.08.01.0170.000952%Not Available
Iron deficiency anaemia14.13.02.001; 01.03.01.0020.001550%Not Available
Leukaemia16.01.03.001; 01.10.03.0010.000272%
Lip swelling23.04.01.007; 07.05.04.005; 10.01.05.0050.001333%Not Available
Loss of consciousness17.02.04.004--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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