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Manufactured by Bionpharma Inc.
8 FDA adverse event reports analyzed
Last updated: 2026-04-15
PAIN RELIEF PATCH is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Bionpharma Inc.. The most commonly reported adverse reactions for PAIN RELIEF PATCH include APPLICATION SITE ERYTHEMA, APPLICATION SITE PRURITUS, APPLICATION SITE SWELLING, APPLICATION SITE WARMTH, MEDICAL DEVICE SITE REACTION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PAIN RELIEF PATCH.
Out of 1 classified reports for PAIN RELIEF PATCH:
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 8 FDA FAERS reports that mention PAIN RELIEF PATCH. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include APPLICATION SITE ERYTHEMA, APPLICATION SITE PRURITUS, APPLICATION SITE SWELLING, APPLICATION SITE WARMTH, MEDICAL DEVICE SITE REACTION, RASH PAPULAR. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Bionpharma Inc. in connection with PAIN RELIEF PATCH. Always verify the specific product and NDC with your pharmacist.