Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Propranolol
Drug ID BADD_D01867
Description Propranolol is a racemic mixture of 2 enantiomers where the S(-)-enantiomer has approximately 100 times the binding affinity for beta adrenergic receptors.[L6904] Propranolol is used to treat a number of conditions but most commonly is used for hypertension.[L6901,L6904,L6907] Propranolol was granted FDA approval on 13 November 1967.[L6904]
Indications and Usage Propranolol is indicated to treat hypertension.[L6907,L6904] Propranolol is also indicated to treat angina pectoris due to coronary atherosclerosis, atrial fibrillation, myocardial infarction, migraine, essential tremor, hypertrophic subaortic stenosis, pheochromocytoma, and proliferating infantile hemangioma.[L6904,L6907]
Marketing Status approved; investigational
ATC Code C07AA05
DrugBank ID DB00571
KEGG ID D08443
MeSH ID D011433
PubChem ID 4946
TTD Drug ID D04JEE
NDC Product Code Not Available
UNII 9Y8NXQ24VQ
Synonyms Propranolol | Propanolol | Inderal | Avlocardyl | AY-20694 | AY 20694 | AY20694 | Rexigen | Dexpropranolol | Dociton | Obsidan | Obzidan | Propranolol Hydrochloride | Hydrochloride, Propranolol | Anaprilin | Anapriline | Betadren
Chemical Information
Molecular Formula C16H21NO2
CAS Registry Number 525-66-6
SMILES CC(C)NCC(COC1=CC=CC2=CC=CC=C21)O
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)
Dyspnoea02.11.05.003; 22.02.01.004--
Dystonia17.01.03.0010.000144%Not Available
Ear pain04.03.01.0030.000454%
Eating disorder19.09.01.008; 14.03.01.0080.000144%Not Available
Eczema23.03.04.0060.000363%
Encephalopathy17.13.02.0010.000267%
Eosinophilia01.02.04.0010.000107%
Epilepsy17.12.03.0020.000240%Not Available
Erythema23.03.06.001--Not Available
Erythema multiforme10.01.03.015; 23.03.01.003--
Euphoric mood19.04.02.0060.000214%
Faeces discoloured07.01.03.0020.000299%Not Available
Faeces hard07.01.03.0030.000182%Not Available
Fasciitis15.03.03.0010.000080%Not Available
Fatigue08.01.01.002--
Fear19.06.03.0010.000053%Not Available
Feeling cold08.01.09.0080.000507%Not Available
Fibrosis08.03.01.001--Not Available
Flatulence07.01.04.0020.000727%
Food allergy10.01.01.0120.000182%Not Available
Frequent bowel movements07.02.04.0020.000481%Not Available
Gastrooesophageal reflux disease07.02.02.0030.002655%
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal necrosis24.04.08.006; 07.15.01.0030.000107%
Gastrointestinal pain07.01.05.005--
Generalised tonic-clonic seizure17.12.01.0020.000267%Not Available
Gingival bleeding07.09.07.001; 24.07.02.0100.000053%Not Available
Glaucoma06.03.01.0020.000053%
Glucose tolerance impaired14.06.02.001; 05.06.02.0010.000053%
Haemangioma24.03.06.004; 16.02.01.0020.000577%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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