N/A
Manufactured by Kaz USA, Inc
26 FDA adverse event reports analyzed
Last updated: 2026-04-15
CAMPHOR (SYNTHETIC) is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Kaz USA, Inc. The most commonly reported adverse reactions for CAMPHOR (SYNTHETIC) include AMPHETAMINES POSITIVE, ASPIRATION, CHOKING, COUGH, DIZZINESS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CAMPHOR (SYNTHETIC).
Out of 7 classified reports for CAMPHOR (SYNTHETIC):
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 26 FDA FAERS reports that mention CAMPHOR (SYNTHETIC). Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include AMPHETAMINES POSITIVE, ASPIRATION, CHOKING, COUGH, DIZZINESS, DYSPNOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Kaz USA, Inc in connection with CAMPHOR (SYNTHETIC). Always verify the specific product and NDC with your pharmacist.