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Manufactured by ALPHA NUTRITION, LLC
44 FDA adverse event reports analyzed
Last updated: 2026-04-15
HISTAMINE DIHYDROCHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by ALPHA NUTRITION, LLC. The most commonly reported adverse reactions for HISTAMINE DIHYDROCHLORIDE include COLON CANCER METASTATIC, DIARRHOEA, BACK PAIN, DIZZINESS, ACCIDENTAL EXPOSURE TO PRODUCT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for HISTAMINE DIHYDROCHLORIDE.
Out of 10 classified reports for HISTAMINE DIHYDROCHLORIDE:
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 44 FDA FAERS reports that mention HISTAMINE DIHYDROCHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include COLON CANCER METASTATIC, DIARRHOEA, BACK PAIN, DIZZINESS, ACCIDENTAL EXPOSURE TO PRODUCT, ALLERGY TEST POSITIVE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list ALPHA NUTRITION, LLC in connection with HISTAMINE DIHYDROCHLORIDE. Always verify the specific product and NDC with your pharmacist.