Does UNSPECIFIED INGREDIENT Cause Intentional product misuse? 280 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 280 reports of Intentional product misuse have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
280
Reports of Intentional product misuse with UNSPECIFIED INGREDIENT
1.1%
of all UNSPECIFIED INGREDIENT reports
127
Deaths
139
Hospitalizations
How Dangerous Is Intentional product misuse From UNSPECIFIED INGREDIENT?
Of the 280 reports, 127 (45.4%) resulted in death, 139 (49.6%) required hospitalization, and 78 (27.9%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 280 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Intentional product misuse Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN