Does UNSPECIFIED INGREDIENT Cause Ventricular fibrillation? 125 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 125 reports of Ventricular fibrillation have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.5% of all adverse event reports for UNSPECIFIED INGREDIENT.
125
Reports of Ventricular fibrillation with UNSPECIFIED INGREDIENT
0.5%
of all UNSPECIFIED INGREDIENT reports
113
Deaths
89
Hospitalizations
How Dangerous Is Ventricular fibrillation From UNSPECIFIED INGREDIENT?
Of the 125 reports, 113 (90.4%) resulted in death, 89 (71.2%) required hospitalization, and 76 (60.8%) were considered life-threatening.
Is Ventricular fibrillation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 125 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
What Other Drugs Cause Ventricular fibrillation?
AMIODARONE (456)
ONDANSETRON (436)
HEPARIN (268)
ACETAMINOPHEN (266)
LANSOPRAZOLE (254)
METRONIDAZOLE (253)
ALBUTEROL (238)
CEFTRIAXONE (234)
SODIUM (232)
ALLOPURINOL (230)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Ventricular fibrillation Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN