Adverse Event Profile: Berberine
Adverse Event Profile: Berberine
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 4 Serious Events: 2 Date Range: 20180109 to 20240911
Top Reported Reactions
- Malaise: 2
- Depression: 1
- Suicidal ideation: 1
- Anxiety: 1
- Blood pressure increased: 1
- Stress: 1
- Chills: 1
- Headache: 1
- Hyperhidrosis: 1
- Muscle spasms: 1
- Vomiting: 1
Outcomes
- Other Serious or Important Medical Event: 2
- Disability: 1
- Hospitalization: 1
- Visited Emergency Room: 1
Products Involved (4 unique)
- BERBERINE AND MICROPQQ ADVANCED
- Berberine
- NATURE 'S WAY BERBERINE
- ZHOU NUTRITION BERBERINE
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.