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Manufactured by DNA Labs, Inc.
1,547 FDA adverse event reports analyzed
Last updated: 2026-04-15
SILICON DIOXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by DNA Labs, Inc.. The most commonly reported adverse reactions for SILICON DIOXIDE include PAIN, PAIN IN EXTREMITY, DIARRHOEA, DRUG INEFFECTIVE, FATIGUE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SILICON DIOXIDE.
Out of 580 classified reports for SILICON DIOXIDE:
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 1,547 FDA FAERS reports that mention SILICON DIOXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include PAIN, PAIN IN EXTREMITY, DIARRHOEA, DRUG INEFFECTIVE, FATIGUE, HEADACHE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list DNA Labs, Inc. in connection with SILICON DIOXIDE. Always verify the specific product and NDC with your pharmacist.