Does UNSPECIFIED INGREDIENT Cause Unevaluable event? 438 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 438 reports of Unevaluable event have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.7% of all adverse event reports for UNSPECIFIED INGREDIENT.
438
Reports of Unevaluable event with UNSPECIFIED INGREDIENT
1.7%
of all UNSPECIFIED INGREDIENT reports
101
Deaths
156
Hospitalizations
How Dangerous Is Unevaluable event From UNSPECIFIED INGREDIENT?
Of the 438 reports, 101 (23.1%) resulted in death, 156 (35.6%) required hospitalization, and 8 (1.8%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 438 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Unevaluable event Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN