Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tamsulosin
Drug ID BADD_D02113
Description Tamsulosin is a selective alpha-1A and alpha-1B adrenoceptor antagonist that exerts its greatest effect in the prostate and bladder, where these receptors are most common.[Label] It is indicated for the treatment of signs and symptoms of benign prostatic hypertrophy.[Label] Antagonism of these receptors leads to relaxation of smooth muscle in the prostate and detrusor muscles in the bladder, allowing for better urinary flow.[Label] Other alpha-1 adrenoceptor antagonists developed in the 1980s were less selective and more likely to act on the smooth muscle of blood vessels, resulting in hypotension.[A178351] Tamsulosin was first approved by the FDA on April 15, 1997.[L6238]
Indications and Usage Tamsulosin is indicated for the treatment of signs and symptoms of benign prostatic hyperplasia.[Label] Tamsulosin is also used off label for the treatment of ureteral stones, prostatitis, and female voiding dysfunction.[A178339,L6259]
Marketing Status approved; investigational
ATC Code G04CA02
DrugBank ID DB00706
KEGG ID D08560
MeSH ID D000077409
PubChem ID 60147
TTD Drug ID D05MBZ
NDC Product Code Not Available
UNII G3P28OML5I
Synonyms Tamsulosin | LY 253352 | LY-253352 | Tamsulosin Hydrochloride | 5-(2-((2-(2-Ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide | Flomax | YM 617 | YM-617
Chemical Information
Molecular Formula C20H28N2O5S
CAS Registry Number 106138-88-9
SMILES CCOC1=CC=CC=C1OCCNC(C)CC2=CC(=C(C=C2)OC)S(=O)(=O)N
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)
Bradycardia02.03.02.0020.000047%Not Available
Cardiac failure02.05.01.0010.000019%
Cataract06.06.01.0010.000134%
Cerebral haemorrhage24.07.04.001; 17.08.01.0030.000019%Not Available
Chest discomfort08.01.08.019; 02.02.02.009; 22.12.02.0020.000079%Not Available
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.011--Not Available
Chills15.05.03.016; 08.01.09.0010.000042%
Cholestasis09.01.01.0010.000019%Not Available
Choroidal detachment06.09.01.003; 12.01.04.0060.000019%Not Available
Chromaturia20.02.01.0020.000028%
Chronic obstructive pulmonary disease22.03.01.0070.000019%Not Available
Circulatory collapse24.06.02.0010.000028%Not Available
Cold sweat23.02.03.002; 08.01.03.0240.000019%Not Available
Condition aggravated08.01.03.0040.000185%Not Available
Constipation07.02.02.0010.000134%
Cough22.02.03.001--
Depressed level of consciousness17.02.04.0020.000028%
Dermatitis23.03.04.002--Not Available
Dermatitis exfoliative10.01.01.004; 23.03.07.001--
Diarrhoea07.02.01.001--
Discomfort08.01.08.0030.000042%Not Available
Disorientation19.13.01.002; 17.02.05.015--Not Available
Dizziness17.02.05.003; 02.11.04.006; 24.06.02.0070.000533%
Dizziness postural02.11.04.008; 24.06.02.008; 17.02.05.004--Not Available
Drug hypersensitivity10.01.01.0010.000261%Not Available
Drug ineffective08.06.01.0060.000839%Not Available
Drug interaction08.06.03.0010.000093%Not Available
Dry mouth07.06.01.002--
Dupuytren's contracture15.03.05.010--Not Available
Dyspepsia07.01.02.001--
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