Adverse Event Profile: Echinacea
Adverse Event Profile: Echinacea
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 9 Serious Events: 5 Date Range: 20070928 to 20240116
Top Reported Reactions
- HEADACHE: 2
- BLOOD ARSENIC INCREASED: 1
- FATIGUE: 1
- PIGMENTATION DISORDER: 1
- POISONING: 1
- SKIN DISCOLOURATION: 1
- ANOSMIA: 1
- ASTHENIA: 1
- CONVULSION: 1
- DECREASED APPETITE: 1
- DYSGEUSIA: 1
- HYPOAESTHESIA: 1
- LOSS OF LIBIDO: 1
- MEMORY IMPAIRMENT: 1
- SEXUAL DYSFUNCTION: 1
- DIZZINESS: 1
- TRANSIENT ISCHAEMIC ATTACK: 1
- VISUAL IMPAIRMENT: 1
- NAUSEA: 1
- REMOVAL OF FOREIGN BODY FROM THROAT: 1
Outcomes
- Other Serious or Important Medical Event: 5
- Hospitalization: 2
- Life Threatening: 2
- Visited a Health Care Provider: 1
- Other Serious Outcome: 1
- Disability: 1
- Required Intervention: 1
- Other Outcome: 1
Products Involved (6 unique)
- BE LIVE ELDERBERRY GUMMIES WITH PROPOLIS AND ECHIN
- ECHINACEA
- ECHINACEA EXTRACT
- NATURE'S BOUNTY ECHINACEA
- NUTRALITE TRIPLE GUARD ECHINACEA SPRAY
- SPRING VALLEY ECHINACEA AND GOLDENSEAL 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.