Does TOLTERODINE Cause Condition aggravated? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Condition aggravated have been filed in association with TOLTERODINE (Tolterodine Tartrate). This represents 2.4% of all adverse event reports for TOLTERODINE.
58
Reports of Condition aggravated with TOLTERODINE
2.4%
of all TOLTERODINE reports
1
Deaths
31
Hospitalizations
How Dangerous Is Condition aggravated From TOLTERODINE?
Of the 58 reports, 1 (1.7%) resulted in death, 31 (53.4%) required hospitalization, and 2 (3.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TOLTERODINE. However, 58 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which TOLTERODINE Alternatives Have Lower Condition aggravated Risk?
TOLTERODINE vs TOLVAPTAN
TOLTERODINE vs TOPAMAX
TOLTERODINE vs TOPIRAMATE
TOLTERODINE vs TOPOTECAN
TOLTERODINE vs TOPOTECAN\TOPOTECAN