Does UNSPECIFIED INGREDIENT Cause Intentional product use issue? 128 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 128 reports of Intentional product use issue have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.5% of all adverse event reports for UNSPECIFIED INGREDIENT.
128
Reports of Intentional product use issue with UNSPECIFIED INGREDIENT
0.5%
of all UNSPECIFIED INGREDIENT reports
48
Deaths
67
Hospitalizations
How Dangerous Is Intentional product use issue From UNSPECIFIED INGREDIENT?
Of the 128 reports, 48 (37.5%) resulted in death, 67 (52.3%) required hospitalization, and 33 (25.8%) were considered life-threatening.
Is Intentional 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, 128 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Intentional 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