Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Solifenacin
Drug ID BADD_D02445
Description Solifenacin is a competitive muscarinic receptor antagonist indicated to treat an overactive bladder with urinary incontinence, urgency, and frequency.[L7511] It has a long duration of action as it is usually taken once daily.[L7511] Solifenacin was granted FDA approval on 19 November 2004.[L7511]
Indications and Usage Solifenacin tablets are indicated to treat an overactive bladder with urinary incontinence, urgency, and frequency.[L7511]
Marketing Status approved
ATC Code G04BD08
DrugBank ID DB01591
KEGG ID D08522
MeSH ID D000069464
PubChem ID 154059
TTD Drug ID D0L4YD
NDC Product Code 70771-1604; 47621-301; 65977-0042; 68382-987; 68382-988; 70771-1605
UNII A8910SQJ1U
Synonyms Solifenacin Succinate | Succinate, Solifenacin | Quinuclidin-3'-yl-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate monosuccinate | YM905 | YM 905 | 905, YM | Vesicare | Solifenacin | 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-1-phenyl-,1- azabicyclo(2.2.2)oct-3-yl ester, (R-(R*,S*))-
Chemical Information
Molecular Formula C23H26N2O2
CAS Registry Number 242478-37-1
SMILES C1CN2CCC1C(C2)OC(=O)N3CCC4=CC=CC=C4C3C5=CC=CC=C5
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)
Hot flush08.01.03.027; 21.02.02.001; 24.03.01.0050.000938%
Prostate cancer16.25.01.001; 21.04.02.0020.000608%-
Adverse event08.06.01.0100.001146%-
Bladder disorder20.03.01.0020.000764%-
Limb discomfort15.03.04.014---
Mental disorder19.07.01.0020.000469%-
Motor dysfunction15.05.06.006; 17.01.02.0310.000174%-
Decreased appetite08.01.09.028; 14.03.01.0050.001372%
Erectile dysfunction19.08.04.001; 21.03.01.0070.000347%
Parkinson's disease17.01.05.0100.000608%-
Adverse reaction08.06.01.0180.000469%-
Drug-induced liver injury09.01.07.023; 12.03.01.0440.000174%-
Sinus node dysfunction02.03.03.0170.000260%
Terminal state08.01.03.0790.000174%-
Myasthenia gravis crisis10.04.05.007; 15.05.08.004; 17.05.04.0070.000174%-
Age-related macular degeneration06.09.03.0180.000174%-
Drug ineffective for unapproved indication08.06.01.038; 12.09.02.0020.001268%-
Graves' disease05.02.02.009; 06.09.04.009; 10.04.08.0140.000260%-
Pregnancy on oral contraceptive18.08.01.0050.000174%-
Therapeutic product effect incomplete08.06.01.0520.002084%-
Therapeutic response changed08.06.01.059---
Therapy non-responder08.06.01.0630.000260%-
Treatment noncompliance08.06.01.067; 12.09.02.0060.003716%-
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