Does FESOTERODINE Cause Intentional product misuse? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Intentional product misuse have been filed in association with FESOTERODINE (Toviaz). This represents 2.0% of all adverse event reports for FESOTERODINE.
68
Reports of Intentional product misuse with FESOTERODINE
2.0%
of all FESOTERODINE reports
0
Deaths
12
Hospitalizations
How Dangerous Is Intentional product misuse From FESOTERODINE?
Of the 68 reports, 12 (17.6%) required hospitalization, and 1 (1.5%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FESOTERODINE. However, 68 reports have been filed with the FAERS database.
What Other Side Effects Does FESOTERODINE Cause?
Drug ineffective (460)
Dry mouth (315)
Urinary retention (218)
Fall (200)
Off label use (161)
Constipation (153)
Malaise (120)
Pain (112)
Gait disturbance (111)
Dizziness (101)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which FESOTERODINE Alternatives Have Lower Intentional product misuse Risk?
FESOTERODINE vs FEXOFENADINE
FESOTERODINE vs FEXOFENADINE OTC
FESOTERODINE vs FEXOFENADINE\FEXOFENADINE
FESOTERODINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FESOTERODINE vs FEZOLINETANT