Does FESOTERODINE Cause Intentional dose omission? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional dose omission have been filed in association with FESOTERODINE (Toviaz). This represents 0.2% of all adverse event reports for FESOTERODINE.
5
Reports of Intentional dose omission with FESOTERODINE
0.2%
of all FESOTERODINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional dose omission From FESOTERODINE?
Of the 5 reports.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FESOTERODINE. However, 5 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 dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which FESOTERODINE Alternatives Have Lower Intentional dose omission Risk?
FESOTERODINE vs FEXOFENADINE
FESOTERODINE vs FEXOFENADINE OTC
FESOTERODINE vs FEXOFENADINE\FEXOFENADINE
FESOTERODINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FESOTERODINE vs FEZOLINETANT