Does FESOTERODINE Cause Product dispensing error? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product dispensing error have been filed in association with FESOTERODINE (Toviaz). This represents 0.8% of all adverse event reports for FESOTERODINE.
26
Reports of Product dispensing error with FESOTERODINE
0.8%
of all FESOTERODINE reports
1
Deaths
3
Hospitalizations
How Dangerous Is Product dispensing error From FESOTERODINE?
Of the 26 reports, 1 (3.8%) resulted in death, 3 (11.5%) required hospitalization.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FESOTERODINE. However, 26 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 dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
Which FESOTERODINE Alternatives Have Lower Product dispensing error Risk?
FESOTERODINE vs FEXOFENADINE
FESOTERODINE vs FEXOFENADINE OTC
FESOTERODINE vs FEXOFENADINE\FEXOFENADINE
FESOTERODINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FESOTERODINE vs FEZOLINETANT