Clinical data | |
---|---|
Trade names | Fesobig , Toviaz |
AHFS/Drugs.com | Monograph |
MedlinePlus | a609021 |
License data |
|
Routes of administration | By mouth |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Bioavailability | 52% (active metabolite) |
Protein binding | 50% (active metabolite) |
Metabolism | Liver (CYP2D6- and 3A4-mediated) |
Elimination half-life | 7–8 hours (active metabolite) |
Excretion | Kidney (70%) and fecal (7%) |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.184.854 |
Chemical and physical data | |
Formula | C26H37NO3 |
Molar mass | 411.586 g·mol−1 |
3D model (JSmol) | |
| |
| |
(what is this?) (verify) |
Fesoterodine (INN, used as the fumarate under the brand name Toviaz) is an antimuscarinic drug developed by Schwarz Pharma AG to treat overactive bladder syndrome (OAB).[2] It was approved by the European Medicines Agency in April 2007,[3] the US Food and Drug Administration on October 31, 2008 [4] and Health Canada on February 9, 2012.[5]
Fesoterodine is a prodrug. It is broken down into its active metabolite, desfesoterodine, by plasma esterases.