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Manufactured by Garam Of Nature
2,059 FDA adverse event reports analyzed
Last updated: 2026-04-15
NIACINAMIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Garam Of Nature. The most commonly reported adverse reactions for NIACINAMIDE include OFF LABEL USE, FATIGUE, DRUG INEFFECTIVE, DIARRHOEA, SOMNOLENCE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for NIACINAMIDE.
Out of 899 classified reports for NIACINAMIDE:
The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.
Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.