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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NIACINAMIDE Cause Product use issue? 76 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Product use issue have been filed in association with NIACINAMIDE (PUVIDA SNOW BLEACH). This represents 5.9% of all adverse event reports for NIACINAMIDE.

76
Reports of Product use issue with NIACINAMIDE
5.9%
of all NIACINAMIDE reports
75
Deaths
75
Hospitalizations

How Dangerous Is Product use issue From NIACINAMIDE?

Of the 76 reports, 75 (98.7%) resulted in death, 75 (98.7%) required hospitalization, and 75 (98.7%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NIACINAMIDE. However, 76 reports have been filed with the FAERS database.

What Other Side Effects Does NIACINAMIDE Cause?

Off label use (540) Drug ineffective (436) Pain (405) Nausea (380) Infusion related reaction (325) Malaise (324) Gastrooesophageal reflux disease (311) Dyspepsia (310) Headache (283) Condition aggravated (256)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which NIACINAMIDE Alternatives Have Lower Product use issue Risk?

NIACINAMIDE vs NICARDIPINE NIACINAMIDE vs NICORANDIL NIACINAMIDE vs NICORETTE OTC NIACINAMIDE vs NICORETTE OTC, UNSPECIFIED NIACINAMIDE vs NICOTINE

Related Pages

NIACINAMIDE Full Profile All Product use issue Reports All Drugs Causing Product use issue NIACINAMIDE Demographics