Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Silodosin
Drug ID BADD_D02020
Description Silodosin is a selective antagonist of alpha(α)-1 adrenergic receptors that binds to the α1A subtype with the highest affinity. α1-adrenergic receptors regulate smooth muscle tone in the bladder neck, prostate, and prostatic urethra: the α1A subtype accounts for approximately 75% of α1-adrenoceptors in the prostate.[A231159] Silodosin was first approved by the FDA in October 2008 [A231159] and it is also approved in Europe and Canada. Silodosin is available as oral capsules with common trade names Rapaflo and Urorec. It is indicated for the symptomatic treatment of benign prostatic hyperplasia in adults.[L32368] Most commonly affecting males over the age of 40 years, benign prostatic hyperplasia is the non-malignant enlargement of the prostate gland, associated with lower urinary tract symptoms that have a negative impact on the quality of life of patients.[A231159] Silodosin works by binding to α1A-adrenoceptors with high affinity and relaxing the lower urinary tract, thereby improving urinary symptoms and alleviating bladder outlet obstruction.[A231229]
Indications and Usage Treatment for symptomatic relief of benign prostatic hyperplasia
Marketing Status Prescription
ATC Code G04CA04
DrugBank ID DB06207
KEGG ID D01965
MeSH ID C095285
PubChem ID 5312125
TTD Drug ID D0U0VU
NDC Product Code 46708-405; 0023-6142; 42334-001; 59651-100; 0023-6147; 31722-635; 14501-0074; 73005-0002; 60219-1420; 33342-384; 69539-052; 60219-1421; 33342-385; 62332-406; 69238-1421; 68180-740; 65977-0091; 59651-096; 31722-636; 0781-2624; 52544-151; 69539-053; 69238-1420; 72789-090; 46708-406; 72205-009; 72205-010; 27241-145; 59651-095; 42765-005; 27241-144; 0781-2623; 68180-741; 62332-405; 52544-152
Synonyms silodosin | 1-(3-hydroxypropyl)-5-(2-(2-(2-(2,2,2-trifluoroethoxy)phenoxy)ethylamino)propyl)indoline-7-carboxamide | KMD 3213 | KMD-3213 | rapaflo
Chemical Information
Molecular Formula C25H32F3N3O4
CAS Registry Number 160970-54-7
SMILES CC(CC1=CC2=C(C(=C1)C(=O)N)N(CC2)CCCO)NCCOC3=CC=CC=C3OCC(F)(F)F
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 pain07.01.05.002--
Asthenia08.01.01.001--Not Available
Constipation07.02.02.0010.002592%
Death08.04.01.0010.002367%
Dehydration14.05.05.0010.002592%
Dementia19.20.02.001; 17.03.01.0010.002592%Not Available
Dermatitis23.03.04.002--Not Available
Diarrhoea07.02.01.0010.003888%
Disorientation19.13.01.002; 17.02.05.0150.002592%Not Available
Dizziness17.02.05.003; 02.01.02.004; 24.06.02.0070.007776%
Drug eruption23.03.05.001; 10.01.01.005; 08.01.06.015--Not Available
Dry mouth07.06.01.002--
Dyspnoea02.01.03.002; 22.02.01.0040.003888%
Dysuria20.02.02.0020.003888%
Ejaculation failure21.03.01.003--Not Available
Fatigue08.01.01.0020.002592%
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal pain07.01.05.005--
Headache17.14.01.001--
Hepatic function abnormal09.01.02.001--Not Available
Hypersensitivity10.01.03.0030.002592%
Hypotension24.06.03.0020.002592%
Immune system disorder10.02.01.001--Not Available
Insomnia19.02.01.002; 17.15.03.002--
Interstitial lung disease22.01.02.003; 10.02.01.0330.002592%Not Available
Jaundice01.06.04.004; 23.03.03.030; 09.01.01.004--Not Available
Libido decreased21.03.02.005; 19.08.03.001--
Liver function test abnormal13.03.01.013--Not Available
Loss of consciousness17.02.04.0040.011663%Not Available
Nasal congestion22.04.04.0010.002592%
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