Does DIETARY SUPPLEMENT Cause Intentional product misuse? 99 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 99 reports of Intentional product misuse have been filed in association with DIETARY SUPPLEMENT. This represents 5.1% of all adverse event reports for DIETARY SUPPLEMENT.
99
Reports of Intentional product misuse with DIETARY SUPPLEMENT
5.1%
of all DIETARY SUPPLEMENT reports
73
Deaths
66
Hospitalizations
How Dangerous Is Intentional product misuse From DIETARY SUPPLEMENT?
Of the 99 reports, 73 (73.7%) resulted in death, 66 (66.7%) required hospitalization, and 55 (55.6%) 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 DIETARY SUPPLEMENT. However, 99 reports have been filed with the FAERS database.
What Other Side Effects Does DIETARY SUPPLEMENT Cause?
Off label use (363)
Dyspnoea (357)
Headache (349)
Drug ineffective (347)
Hypertension (328)
Vomiting (322)
Fatigue (312)
Nausea (306)
Condition aggravated (300)
General physical health deterioration (290)
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 DIETARY SUPPLEMENT Alternatives Have Lower Intentional product misuse Risk?
DIETARY SUPPLEMENT vs DIETARY SUPPLEMENT\HERBALS
DIETARY SUPPLEMENT vs DIETARY SUPPLEMENT\MINERALS\VITAMINS
DIETARY SUPPLEMENT vs DIETARY SUPPLEMENT\UBIDECARENONE
DIETARY SUPPLEMENT vs DIFELIKEFALIN
DIETARY SUPPLEMENT vs DIFLUNISAL