Does UNSPECIFIED INGREDIENT Cause Product use issue? 232 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 232 reports of Product use issue have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.9% of all adverse event reports for UNSPECIFIED INGREDIENT.
232
Reports of Product use issue with UNSPECIFIED INGREDIENT
0.9%
of all UNSPECIFIED INGREDIENT reports
55
Deaths
82
Hospitalizations
How Dangerous Is Product use issue From UNSPECIFIED INGREDIENT?
Of the 232 reports, 55 (23.7%) resulted in death, 82 (35.3%) required hospitalization, and 41 (17.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 232 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 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 UNSPECIFIED INGREDIENT Alternatives Have Lower Product use issue Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN