N/A
Manufactured by Boiron
2 FDA adverse event reports analyzed
Last updated: 2026-04-15
ZINC VALERATE DIHYDRATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for ZINC VALERATE DIHYDRATE include NASAL POLYPS, SINUS POLYP. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ZINC VALERATE DIHYDRATE.
Out of 1 classified reports for ZINC VALERATE DIHYDRATE:
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.
This profile reflects 2 FDA FAERS reports that mention ZINC VALERATE DIHYDRATE. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include NASAL POLYPS, SINUS POLYP. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Boiron in connection with ZINC VALERATE DIHYDRATE. Always verify the specific product and NDC with your pharmacist.