Adverse Event Profile: Black Cohosh
Adverse Event Profile: Black Cohosh
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 3 Serious Events: 1 Date Range: 20040205 to 20210629
Top Reported Reactions
- GAMMA-GLUTAMYLTRANSFERASE INCREASED: 1
- Abdominal pain: 1
- Hepatic enzyme increased: 1
- Hot flush: 1
- Liver injury: 1
- ACTIVITIES OF DAILY LIVING IMPAIRED: 1
- CONFUSIONAL STATE: 1
- SOMNOLENCE: 1
Outcomes
- Visited a Health Care Provider: 1
- Other Serious or Important Medical Event: 1
- Disability: 1
Products Involved (3 unique)
- BLACK COHOSH
- BLACK COHOSH MENOPAUSE COMPLEX NIGHTTIME FORMULA
- NATURE'S WAY BLACK COHOSH ROOT
Disclaimer
This data is from the FDA CAERS database. A report does not mean the supplement caused the adverse event. Reports may be incomplete, duplicated, or unrelated. This is for safety awareness only.