Does TOLTERODINE Cause Intentional product use issue? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Intentional product use issue have been filed in association with TOLTERODINE (Tolterodine Tartrate). This represents 1.1% of all adverse event reports for TOLTERODINE.
27
Reports of Intentional product use issue with TOLTERODINE
1.1%
of all TOLTERODINE reports
16
Deaths
19
Hospitalizations
How Dangerous Is Intentional product use issue From TOLTERODINE?
Of the 27 reports, 16 (59.3%) resulted in death, 19 (70.4%) required hospitalization, and 16 (59.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOLTERODINE. However, 27 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 use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which TOLTERODINE Alternatives Have Lower Intentional product use issue Risk?
TOLTERODINE vs TOLVAPTAN
TOLTERODINE vs TOPAMAX
TOLTERODINE vs TOPIRAMATE
TOLTERODINE vs TOPOTECAN
TOLTERODINE vs TOPOTECAN\TOPOTECAN