Does DIETARY SUPPLEMENT Cause Intentional product use issue? 154 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 154 reports of Intentional product use issue have been filed in association with DIETARY SUPPLEMENT. This represents 7.9% of all adverse event reports for DIETARY SUPPLEMENT.
154
Reports of Intentional product use issue with DIETARY SUPPLEMENT
7.9%
of all DIETARY SUPPLEMENT reports
103
Deaths
116
Hospitalizations
How Dangerous Is Intentional product use issue From DIETARY SUPPLEMENT?
Of the 154 reports, 103 (66.9%) resulted in death, 116 (75.3%) required hospitalization, and 89 (57.8%) 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 DIETARY SUPPLEMENT. However, 154 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 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 DIETARY SUPPLEMENT Alternatives Have Lower Intentional product use issue 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