Does NIACINAMIDE Cause Product quality issue? 129 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Product quality issue have been filed in association with NIACINAMIDE (PUVIDA SNOW BLEACH). This represents 10.1% of all adverse event reports for NIACINAMIDE.
129
Reports of Product quality issue with NIACINAMIDE
10.1%
of all NIACINAMIDE reports
129
Deaths
128
Hospitalizations
How Dangerous Is Product quality issue From NIACINAMIDE?
Of the 129 reports, 129 (100.0%) resulted in death, 128 (99.2%) required hospitalization, and 128 (99.2%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NIACINAMIDE. However, 129 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which NIACINAMIDE Alternatives Have Lower Product quality issue Risk?
NIACINAMIDE vs NICARDIPINE
NIACINAMIDE vs NICORANDIL
NIACINAMIDE vs NICORETTE OTC
NIACINAMIDE vs NICORETTE OTC, UNSPECIFIED
NIACINAMIDE vs NICOTINE