Does TOLTERODINE Cause Intentional product misuse? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Intentional product misuse have been filed in association with TOLTERODINE (Tolterodine Tartrate). This represents 1.2% of all adverse event reports for TOLTERODINE.
30
Reports of Intentional product misuse with TOLTERODINE
1.2%
of all TOLTERODINE reports
1
Deaths
10
Hospitalizations
How Dangerous Is Intentional product misuse From TOLTERODINE?
Of the 30 reports, 1 (3.3%) resulted in death, 10 (33.3%) required hospitalization, and 1 (3.3%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOLTERODINE. However, 30 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which TOLTERODINE Alternatives Have Lower Intentional product misuse Risk?
TOLTERODINE vs TOLVAPTAN
TOLTERODINE vs TOPAMAX
TOLTERODINE vs TOPIRAMATE
TOLTERODINE vs TOPOTECAN
TOLTERODINE vs TOPOTECAN\TOPOTECAN