Does FESOTERODINE Cause Product use issue? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Product use issue have been filed in association with FESOTERODINE (Toviaz). This represents 1.5% of all adverse event reports for FESOTERODINE.
49
Reports of Product use issue with FESOTERODINE
1.5%
of all FESOTERODINE reports
2
Deaths
27
Hospitalizations
How Dangerous Is Product use issue From FESOTERODINE?
Of the 49 reports, 2 (4.1%) resulted in death, 27 (55.1%) required hospitalization, and 15 (30.6%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FESOTERODINE. However, 49 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which FESOTERODINE Alternatives Have Lower Product use issue Risk?
FESOTERODINE vs FEXOFENADINE
FESOTERODINE vs FEXOFENADINE OTC
FESOTERODINE vs FEXOFENADINE\FEXOFENADINE
FESOTERODINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FESOTERODINE vs FEZOLINETANT