Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Dabigatran
Drug ID BADD_D00563
Description Dabigatran is the active form of the orally bioavailable prodrug [dabigatran etexilate].
Indications and Usage Dabigatran is indicated for the prevention of venous thromboembolic events in patients who have undergone elective hip or knee replacement surgery (based on RE-NOVATE, RE-MODEL, and RE-MOBILIZE trials). In 2010, it was approved in the US and Canada for prevention of stroke and systemic embolism in patients with atrial fibrillation (approval based on the RE-LY trial). Contraindications: severe renal impairment (CrCL < 30 ml/min); haemorrhagic manifestations, bleeding diathesis or spontaneous or pharmacologic impairment of haemostasis; lesions at risk of clinically significant bleeding (e.g. extensive cerebral infarction (haemorrhagic or ischemic) in the last 6 months, active peptic ulcer disease); concomitant treatment with P-glycoprotein inhibitors (e.g. oral ketoconazole, verapamil); and those with known hypersensitivity to dabigatran, dabigatran etexilate or any ingredient used in the formulation or component of the container. As of December 2012, dabigatran is contraindicated in patients with mechanical prosthetic heart valves.
Marketing Status Prescription
ATC Code B01AE07
DrugBank ID DB14726
KEGG ID D07144
MeSH ID D000069604
PubChem ID 216210
TTD Drug ID D0M7JT
NDC Product Code Not Available
Synonyms Dabigatran | N-((2-(((4-(aminoiminomethyl)phenyl)amino)methyl)-1-methyl-1H-benzimidazol-5-yl)carbonyl)-N-2-pyridinyl-beta-alanine | BIBR 1048 | Pradaxa | Dabigatran Etexilate | Etexilate, Dabigatran | Dabigatran Etexilate Mesylate | Etexilate Mesylate, Dabigatran | Mesylate, Dabigatran Etexilate
Chemical Information
Molecular Formula C25H25N7O3
CAS Registry Number 211914-51-1
SMILES CN1C2=C(C=C(C=C2)C(=O)N(CCC(=O)O)C3=CC=CC=N3)N=C1CNC4=CC=C(C=C4)C(=N)N
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal discomfort07.01.06.001--Not Available
Abdominal pain07.01.05.002--
Abdominal pain upper07.01.05.003--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Angioedema23.04.01.001; 10.01.05.009--Not Available
Cerebral haemorrhage24.07.04.001; 17.08.01.003--Not Available
Compartment syndrome24.04.05.006; 15.05.05.005--Not Available
Dermatitis23.03.04.002--Not Available
Diarrhoea07.02.01.001--
Drug hypersensitivity10.01.01.001--Not Available
Dyspepsia07.01.02.001--
Gastric haemorrhage24.07.02.007; 07.12.01.001--
Gastritis07.08.02.001--
Gastritis haemorrhagic24.07.02.008; 07.08.02.002--Not Available
Gastrooesophageal reflux disease07.02.02.003--
Gastrointestinal haemorrhage24.07.02.009; 07.12.02.001--Not Available
Gastrointestinal pain07.01.05.005--
Haemoglobin13.01.05.018--Not Available
Haemorrhage intracranial24.07.04.003; 17.08.01.008--
Haemorrhagic stroke24.07.04.014; 17.08.01.011--Not Available
Hypersensitivity10.01.03.003--
Hypotension24.06.03.002--
Myocardial infarction24.04.04.009; 02.02.02.007--
Nausea07.01.07.001--
Oesophageal ulcer07.04.05.002--
Oesophagitis07.08.05.001--
Pericardial haemorrhage24.07.01.013; 02.06.01.003--Not Available
Pruritus23.03.12.001--
Rash23.03.13.001--Not Available
Retroperitoneal haemorrhage24.07.01.017; 07.07.02.002--
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