Adverse Event Profile: Green Tea
Adverse Event Profile: Green Tea
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 15 Serious Events: 9 Date Range: 20081112 to 20240513
Top Reported Reactions
- DIARRHOEA: 3
- LIVER INJURY: 2
- DECREASED APPETITE: 2
- FATIGUE: 2
- ABDOMINAL PAIN UPPER: 2
- Asthenia: 1
- Gastrointestinal haemorrhage: 1
- Haemoptysis: 1
- Hypoacusis: 1
- Memory impairment: 1
- Abdominal pain upper: 1
- Chromaturia: 1
- Fatigue: 1
- Hepatic steatosis: 1
- Hepatitis: 1
- Jaundice: 1
- Transaminases increased: 1
- Viral infection: 1
- Pulmonary embolism: 1
- ALANINE AMINOTRANSFERASE INCREASED: 1
Outcomes
- Other Serious or Important Medical Event: 9
- Hospitalization: 8
- Visited a Health Care Provider: 5
- Visited Emergency Room: 4
- Other Serious Outcome: 3
- Required Intervention: 2
- Life Threatening: 1
Products Involved (12 unique)
- ABH NATURE VEGAN GREEN TEA EXTRACT + EGCG
- GNC ULTRA MEGA GREEN WOMEN'S VITAPAK - GREEN TEA C
- GREEN TEA
- GREEN TEA ELIXIR
- GREEN TEA EXT RACT
- GREEN TEA FAT BURNER
- GREEN TEA TRIPLE FAT BURNER
- MEGA GREEN TEA EXTRACT
- NOW FOODS GREEN TEA EXTRACT
- PURITANS PRIDE GREEN TEA EXTRACT
- PURITY PRODUCTS GREEN TEA CR -PHYTOSOME
- green tea
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.