Does FESOTERODINE Cause Condition aggravated? 100 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Condition aggravated have been filed in association with FESOTERODINE (Toviaz). This represents 3.0% of all adverse event reports for FESOTERODINE.
100
Reports of Condition aggravated with FESOTERODINE
3.0%
of all FESOTERODINE reports
1
Deaths
19
Hospitalizations
How Dangerous Is Condition aggravated From FESOTERODINE?
Of the 100 reports, 1 (1.0%) resulted in death, 19 (19.0%) required hospitalization, and 1 (1.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FESOTERODINE. However, 100 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which FESOTERODINE Alternatives Have Lower Condition aggravated Risk?
FESOTERODINE vs FEXOFENADINE
FESOTERODINE vs FEXOFENADINE OTC
FESOTERODINE vs FEXOFENADINE\FEXOFENADINE
FESOTERODINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FESOTERODINE vs FEZOLINETANT