Does FESOTERODINE Cause Product quality issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product quality issue have been filed in association with FESOTERODINE (Toviaz). This represents 0.2% of all adverse event reports for FESOTERODINE.
8
Reports of Product quality issue with FESOTERODINE
0.2%
of all FESOTERODINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From FESOTERODINE?
Of the 8 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FESOTERODINE. However, 8 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which FESOTERODINE Alternatives Have Lower Product quality issue Risk?
FESOTERODINE vs FEXOFENADINE
FESOTERODINE vs FEXOFENADINE OTC
FESOTERODINE vs FEXOFENADINE\FEXOFENADINE
FESOTERODINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FESOTERODINE vs FEZOLINETANT