Does NIACINAMIDE Cause Incorrect product administration duration? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Incorrect product administration duration have been filed in association with NIACINAMIDE (PUVIDA SNOW BLEACH). This represents 1.5% of all adverse event reports for NIACINAMIDE.
19
Reports of Incorrect product administration duration with NIACINAMIDE
1.5%
of all NIACINAMIDE reports
19
Deaths
19
Hospitalizations
How Dangerous Is Incorrect product administration duration From NIACINAMIDE?
Of the 19 reports, 19 (100.0%) resulted in death, 19 (100.0%) required hospitalization, and 19 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NIACINAMIDE. However, 19 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which NIACINAMIDE Alternatives Have Lower Incorrect product administration duration Risk?
NIACINAMIDE vs NICARDIPINE
NIACINAMIDE vs NICORANDIL
NIACINAMIDE vs NICORETTE OTC
NIACINAMIDE vs NICORETTE OTC, UNSPECIFIED
NIACINAMIDE vs NICOTINE