Adverse Event Profile: Vitamin E
Adverse Event Profile: Vitamin E
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 69 Serious Events: 30 Date Range: 20040205 to 20250910
Top Reported Reactions
- FOREIGN BODY TRAUMA: 5
- HEADACHE: 4
- CHOKING: 4
- DYSPHAGIA: 4
- DYSPNOEA: 4
- CONSTIPATION: 4
- NAUSEA: 4
- ABDOMINAL PAIN UPPER: 4
- HYPOAESTHESIA: 4
- FATIGUE: 3
- Dizziness: 3
- Diarrhoea: 3
- ABDOMINAL PAIN: 3
- Alopecia: 3
- LOSS OF CONSCIOUSNESS: 3
- HYPERSENSITIVITY: 3
- PULMONARY EMBOLISM: 3
- THROMBOSIS: 3
- BLOOD PRESSURE INCREASED: 2
- Retching: 2
Outcomes
- Other Serious or Important Medical Event: 45
- Visited a Health Care Provider: 20
- Hospitalization: 18
- Visited Emergency Room: 11
- Other Serious Outcome: 10
- Other Outcome: 5
- Disability: 5
- Life Threatening: 5
- Required Intervention: 2
- Death: 2
Products Involved (25 unique)
- NATUREMADE VITAMIN E
- OMEGA 3 (TOCOPHEROL, FISH OIL)
- PURITAN'S PRIDE COMPLETE B B-COMPLEX VITAMIN EASY
- PURITAN'S PRIDE HIGH GAMMA TOCOPHEROL
- PURITAN'S PRIDE VITAMIN E 184MG (400 IU) WITH SELE
- PURITANS PRIDE NATURAL E-400 IU D-ALPHA TOCOPHERYL
- PURITANS PRIDE NATURAL E-400 IU RAPID RELEASE SOFT
- PURITANS PRIDE NATURAL E-4001U MIXED TOCOPHEROLS R
- PURITANS PRIDE NATURAL E-400IU WITH SELENIUM
- SOLGAR NATURALLY SOURCED VITAMIN E
- TOCOPHEROL
- VITAMIN E
- VITAMIN E (SHAKLEE)
- VITAMIN E (TOCOPHEROL)
- VITAMIN E (TOCOPHEROL) CAPSULE, SOFT
- VITAMIN E 400IU
- VITAMIN E DIETARY SUPPLEMENT
- VITAMIN E TOCOPHEROL
- VITAMIN E TOCOPHEROL TOCOPHEROL
- VITAMIN WORLD VITAMIN E-400
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.