Adverse Event Profile: Resveratrol

Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 4 Serious Events: 2 Date Range: 20100914 to 20200415

Top Reported Reactions

  • Dizziness: 1
  • Vertigo: 1
  • PARALYSIS: 1
  • POOR PERIPHERAL CIRCULATION: 1
  • THROMBOSIS: 1
  • ABDOMINAL DISTENSION: 1
  • Adverse reaction: 1
  • BURNING SENSATION: 1
  • CONSTIPATION: 1
  • GASTROINTESTINAL DISORDER: 1
  • ULCER: 1
  • Hypersensitivity: 1
  • Lip swelling: 1
  • Local swelling: 1
  • Urticaria: 1

Outcomes

  • Disability: 1
  • Hospitalization: 1
  • Visited Emergency Room: 1
  • Visited a Health Care Provider: 1
  • Other Serious or Important Medical Event: 1

Products Involved (4 unique)

  • HERBADIREKT RESVERATROL
  • NOW FOODS NATURAL RESVERATROL SUPPLEMENT
  • NUTRACHAMPS RESVERATROL
  • RESVERATROL

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.