Does TOLTERODINE Cause Product dispensing error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product dispensing error have been filed in association with TOLTERODINE (Tolterodine Tartrate). This represents 0.3% of all adverse event reports for TOLTERODINE.
8
Reports of Product dispensing error with TOLTERODINE
0.3%
of all TOLTERODINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dispensing error From TOLTERODINE?
Of the 8 reports, 1 (12.5%) 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 TOLTERODINE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does TOLTERODINE Cause?
Drug ineffective (435)
Drug hypersensitivity (156)
Dry mouth (149)
Fall (125)
Off label use (107)
Confusional state (94)
Fatigue (88)
Dizziness (85)
Constipation (81)
Urinary tract infection (81)
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 TOLTERODINE Alternatives Have Lower Product dispensing error Risk?
TOLTERODINE vs TOLVAPTAN
TOLTERODINE vs TOPAMAX
TOLTERODINE vs TOPIRAMATE
TOLTERODINE vs TOPOTECAN
TOLTERODINE vs TOPOTECAN\TOPOTECAN