Adverse Event Profile: Valerian
Adverse Event Profile: Valerian
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 6 Serious Events: 3 Date Range: 20130628 to 20190717
Top Reported Reactions
- CEREBROVASCULAR ACCIDENT: 1
- CONVULSION: 1
- COORDINATION ABNORMAL: 1
- LOSS OF CONSCIOUSNESS: 1
- VOMITING: 1
- BLOOD PRESSURE INCREASED: 1
- HEART RATE INCREASED: 1
- PALPITATIONS: 1
- Pulmonary oedema: 1
- Rash pruritic: 1
- Throat tightness: 1
- Urticaria: 1
- Vitreous floaters: 1
- Dehydration: 1
- Diarrhoea haemorrhagic: 1
- Feeling abnormal: 1
- Gastric ulcer haemorrhage: 1
- ALANINE AMINOTRANSFERASE INCREASED: 1
- ASPARTATE AMINOTRANSFERASE INCREASED: 1
- BLOOD BILIRUBIN INCREASED: 1
Outcomes
- Visited Emergency Room: 3
- Other Serious or Important Medical Event: 3
- Hospitalization: 2
- Visited a Health Care Provider: 2
- Other Serious Outcome: 1
- Disability: 1
Products Involved (5 unique)
- NUTRILITE VALERIAN AND HOPS
- NUTRILITE VALERIAN AND HOPS 90 TABLETS DIETARY SUP
- SUNDOWN NATURALS VALERIAN ROOT
- VALERIAN ROOT
- Valerian 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.