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Drug ReportsFesoterodine
Toviaz(fesoterodine)
Fesoterodine, Toviaz (fesoterodine) is a small molecule pharmaceutical. Fesoterodine was first approved as Toviaz on 2007-04-20. It is used to treat urge urinary incontinence in the USA. It has been approved in Europe to treat overactive urinary bladder.
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Drug
Target
Variants
Financial
Trends
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YTD
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2Y
5Y
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Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
urogenital diseasesD000091642
signs and symptoms pathological conditionsD013568
Trade Name
FDA
EMA
Fesoterodine, Toviaz (discontinued: Fesoterodine)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Fesoterodine fumarate
Tradename
Company
Number
Date
Products
TOVIAZPfizerN-022030 RX2008-10-31
2 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
fesoterodine fumarateANDA2024-08-30
toviazNew Drug Application2024-03-04
Indications
FDA
EMA
Agency Specific
FDA
EMA
Expiration
Code
FESOTERODINE FUMARATE, TOVIAZ, PFIZER
2024-12-17PED
2024-06-17I-861
Patent Expiration
Patent
Expires
Flag
FDA Information
Fesoterodine Fumarate, Toviaz, Pfizer
78077152027-06-07DPU-913
80883982027-06-07DPU-913
85017232027-06-07DP
ATC Codes
G: Genito urinary system and sex hormones
— G04: Urologicals
— G04B: Urologicals
— G04BD: Drugs for urinary frequency and incontinence
— G04BD11: Fesoterodine
HCPCS
No data
Clinical
Clinical Trials
77 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Overactive urinary bladderD053201EFO_1000781N32.819413151455
Urinary incontinenceD014549HP_0000020R32211318
EnuresisD004775—R32—113—5
Urge urinary incontinenceD053202EFO_0006865N39.411—11—3
InflammationD007249MP_0001845————1—1
Parkinson diseaseD010300EFO_0002508G20———1—1
AdenocarcinomaD000230—————1—1
Urinary bladder neck obstructionD001748EFO_1000840N32.0———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
SyndromeD013577————3——3
Neurogenic urinary bladderD001750HP_0000011N31——2——2
NocturiaD053158—R35.1—11——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Spinal cord injuriesD013119EFO_1001919——1———1
Autonomic dysreflexiaD020211EFO_1001762G90.4—1———1
Cognitive dysfunctionD060825HP_0001268G31.84—1———1
Stress urinary incontinenceD014550HP_0010992——1———1
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients———4————4
MalnutritionD044342EFO_0008572E40-E461————1
Therapeutic equivalencyD013810——1————1
FoodD005502——1————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Iron-deficiency anemiaD018798HP_0001891D50————88
Iron deficienciesD000090463——————88
Drug-related side effects and adverse reactionsD064420—T88.7————11
Drug interactionsD004347——————11
Urologic diseasesD014570—N39.9————11
Urinary bladder diseasesD001745—N32.9————11
DeprescriptionsD000069340——————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameFesoterodine
INNfesoterodine
Description
Fesoterodine is a diarylmethane.
Classification
Small molecule
Drug class—
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Structure (InChI/SMILES or Protein Sequence)
CC(C)C(=O)Oc1ccc(CO)cc1[C@H](CCN(C(C)C)C(C)C)c1ccccc1
Identifiers
PDB—
CAS-ID286930-02-7
RxCUI—
ChEMBL IDCHEMBL1201764
ChEBI ID—
PubChem CID6918558
DrugBankDB06702
UNII ID621G617227 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Toviaz – Pfizer
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Estimated US medical usage
Fesoterodine
Total medical expenditures per year (USD, in millions)
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Number of persons purchased
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Number of purchases
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Refill frequency
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Price per prescription (USD)
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 704 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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7,691 adverse events reported
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