Does DIETARY SUPPLEMENT Cause Product formulation issue? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Product formulation issue have been filed in association with DIETARY SUPPLEMENT. This represents 1.1% of all adverse event reports for DIETARY SUPPLEMENT.
22
Reports of Product formulation issue with DIETARY SUPPLEMENT
1.1%
of all DIETARY SUPPLEMENT reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product formulation issue From DIETARY SUPPLEMENT?
Of the 22 reports, 1 (4.5%) resulted in death, 6 (27.3%) required hospitalization, and 5 (22.7%) were considered life-threatening.
Is Product formulation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIETARY SUPPLEMENT. However, 22 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 Product formulation issue?
MINOXIDIL (1,369)
LEVOTHYROXINE (740)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (174)
OMEPRAZOLE (99)
METHYLPHENIDATE (78)
OXYCODONE (73)
ACETAMINOPHEN\HYDROCODONE (62)
ACETAMINOPHEN\OXYCODONE (61)
ACETAMINOPHEN (59)
BUPROPION (59)
Which DIETARY SUPPLEMENT Alternatives Have Lower Product formulation 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