Does DIETARY SUPPLEMENT Cause Adverse event? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Adverse event have been filed in association with DIETARY SUPPLEMENT. This represents 5.7% of all adverse event reports for DIETARY SUPPLEMENT.
111
Reports of Adverse event with DIETARY SUPPLEMENT
5.7%
of all DIETARY SUPPLEMENT reports
64
Deaths
89
Hospitalizations
How Dangerous Is Adverse event From DIETARY SUPPLEMENT?
Of the 111 reports, 64 (57.7%) resulted in death, 89 (80.2%) required hospitalization, and 49 (44.1%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIETARY SUPPLEMENT. However, 111 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which DIETARY SUPPLEMENT Alternatives Have Lower Adverse event 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