COMFREY ROOT

N/A

Manufactured by Boiron

47 FDA adverse event reports analyzed

Last updated: 2026-04-15

About COMFREY ROOT

COMFREY ROOT is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for COMFREY ROOT include DIARRHOEA, MALAISE, MEMORY IMPAIRMENT, ACUTE KIDNEY INJURY, ACUTE RESPIRATORY FAILURE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for COMFREY ROOT.

Top Adverse Reactions

DIARRHOEA2 reports
MALAISE2 reports
MEMORY IMPAIRMENT2 reports
ACUTE KIDNEY INJURY1 reports
ACUTE RESPIRATORY FAILURE1 reports
AFFECTIVE DISORDER1 reports
ASTHENIA1 reports
BUNION OPERATION1 reports
COMA1 reports
CONDITION AGGRAVATED1 reports
COVID 191 reports
DEPRESSION1 reports
DIABETES MELLITUS1 reports
EMOTIONAL DISTRESS1 reports
FEELING ABNORMAL1 reports

Report Outcomes

Out of 9 classified reports for COMFREY ROOT:

Serious 88.9%Non-Serious 11.1%

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

Female9 (100.0%)

Reports by Age

Age 361 reports
Age 371 reports
Age 451 reports
Age 491 reports

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

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.