Adverse Event Profile: St Johns Wort

Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 3 Serious Events: 1 Date Range: 20140624 to 20200727

Top Reported Reactions

  • Suicidal ideation: 1
  • Pulmonary embolism: 1
  • EXOSTOSIS: 1
  • PAIN: 1
  • PAIN IN JAW: 1
  • STOMATITIS: 1
  • SWELLING: 1

Outcomes

  • Other Serious or Important Medical Event: 2
  • Hospitalization: 1
  • Other Serious Outcome: 1
  • Visited a Health Care Provider: 1

Products Involved (3 unique)

  • PURITAN'S PRIDE ST. JOHN'S WORT
  • PURITANS PRIDE ST JOHNS WORT
  • SPRING VALLEY ST JOHN'S WORT COMPLEX

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.