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Manufactured by KROGER COMPANY
21 FDA adverse event reports analyzed
Last updated: 2026-04-15
ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by KROGER COMPANY. The most commonly reported adverse reactions for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE include BURNING SENSATION, CHEST PAIN, CHROMATURIA, DIZZINESS POSTURAL, DRUG INTERACTION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE.
Out of 6 classified reports for ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE:
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 21 FDA FAERS reports that mention ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include BURNING SENSATION, CHEST PAIN, CHROMATURIA, DIZZINESS POSTURAL, DRUG INTERACTION, DYSPNOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list KROGER COMPANY in connection with ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE. Always verify the specific product and NDC with your pharmacist.