KALI MURIATICUM

About KALI MURIATICUM

KALI MURIATICUM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Bestmade Natural Products. The most commonly reported adverse reactions for KALI MURIATICUM include ANORECTAL CELLULITIS, APLASTIC ANAEMIA, FEBRILE NEUTROPENIA, GLIOBLASTOMA MULTIFORME, HAEMORRHOIDS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for KALI MURIATICUM.

Top Adverse Reactions

Report Outcomes

Out of 2 classified reports for KALI MURIATICUM:

• Serious: 2 reports (100.0%) — includes hospitalization, disability, life-threatening events, or death
• Non-Serious: 0 reports (0.0%)

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 Breakdown

Reports by Sex

Reports by Age

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

How many FDA adverse event reports are associated with KALI MURIATICUM?

This profile reflects 13 FDA FAERS reports that mention KALI MURIATICUM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for KALI MURIATICUM?

Frequently reported terms in FAERS include ANORECTAL CELLULITIS, APLASTIC ANAEMIA, FEBRILE NEUTROPENIA, GLIOBLASTOMA MULTIFORME, HAEMORRHOIDS, LYMPHOPENIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures KALI MURIATICUM?

Labeling and FAERS entries often list Bestmade Natural Products in connection with KALI MURIATICUM. Always verify the specific product and NDC with your pharmacist.