Does TOLTERODINE Cause Product prescribing error? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Product prescribing error have been filed in association with TOLTERODINE (Tolterodine Tartrate). This represents 0.9% of all adverse event reports for TOLTERODINE.
22
Reports of Product prescribing error with TOLTERODINE
0.9%
of all TOLTERODINE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Product prescribing error From TOLTERODINE?
Of the 22 reports, 11 (50.0%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOLTERODINE. However, 22 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which TOLTERODINE Alternatives Have Lower Product prescribing error Risk?
TOLTERODINE vs TOLVAPTAN
TOLTERODINE vs TOPAMAX
TOLTERODINE vs TOPIRAMATE
TOLTERODINE vs TOPOTECAN
TOLTERODINE vs TOPOTECAN\TOPOTECAN