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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TOLTERODINE Cause Product use issue? 70 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Product use issue have been filed in association with TOLTERODINE (Tolterodine Tartrate). This represents 2.9% of all adverse event reports for TOLTERODINE.

70
Reports of Product use issue with TOLTERODINE
2.9%
of all TOLTERODINE reports
1
Deaths
9
Hospitalizations

How Dangerous Is Product use issue From TOLTERODINE?

Of the 70 reports, 1 (1.4%) resulted in death, 9 (12.9%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TOLTERODINE. However, 70 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 use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which TOLTERODINE Alternatives Have Lower Product use issue Risk?

TOLTERODINE vs TOLVAPTAN TOLTERODINE vs TOPAMAX TOLTERODINE vs TOPIRAMATE TOLTERODINE vs TOPOTECAN TOLTERODINE vs TOPOTECAN\TOPOTECAN

Related Pages

TOLTERODINE Full Profile All Product use issue Reports All Drugs Causing Product use issue TOLTERODINE Demographics