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