Does URIDINE TRIACETATE Cause Complication associated with device? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Complication associated with device have been filed in association with URIDINE TRIACETATE (VISTOGARD). This represents 18.2% of all adverse event reports for URIDINE TRIACETATE.
20
Reports of Complication associated with device with URIDINE TRIACETATE
18.2%
of all URIDINE TRIACETATE reports
2
Deaths
1
Hospitalizations
How Dangerous Is Complication associated with device From URIDINE TRIACETATE?
Of the 20 reports, 2 (10.0%) resulted in death, 1 (5.0%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for URIDINE TRIACETATE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does URIDINE TRIACETATE Cause?
Diarrhoea (19)
Vomiting (19)
Off label use (14)
Thrombocytopenia (10)
Nausea (9)
Neutropenia (9)
Hypokalaemia (8)
Inappropriate schedule of product administration (8)
Mucosal inflammation (7)
Death (6)
What Other Drugs Cause Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which URIDINE TRIACETATE Alternatives Have Lower Complication associated with device Risk?
URIDINE TRIACETATE vs UROFOLLITROPIN
URIDINE TRIACETATE vs URSODIOL
URIDINE TRIACETATE vs USTEKINUMAB
URIDINE TRIACETATE vs USTEKINUMAB-STBA
URIDINE TRIACETATE vs VADADUSTAT