Adverse Event Profile: Quercetin

Adverse Event Profile: Quercetin

Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 2 Serious Events: 0 Date Range: 20111129 to 20161227

Top Reported Reactions

  • DIARRHOEA: 1
  • FOOD POISONING: 1
  • MALAISE: 1
  • PYREXIA: 1
  • VOMITING: 1
  • CHEST DISCOMFORT: 1
  • DYSPNOEA: 1

Outcomes

  • Other Serious or Important Medical Event: 2

Products Involved (2 unique)

  • GNC QUERCETIN 500
  • QUERCETIN

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.