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.