Adverse Event Profile: Vitamin B6
Adverse Event Profile: Vitamin B6
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 16 Serious Events: 9 Date Range: 20090623 to 20250831
Top Reported Reactions
- NAUSEA: 4
- Neuropathy peripheral: 3
- NEUROPATHY PERIPHERAL: 3
- Hypervitaminosis: 2
- Constipation: 2
- Diarrhoea: 2
- CHEST PAIN: 2
- COLD SWEAT: 2
- GASTROOESOPHAGEAL REFLUX DISEASE: 2
- LIVER FUNCTION TEST ABNORMAL: 2
- HYPOAESTHESIA: 2
- DECREASED APPETITE: 1
- DEHYDRATION: 1
- FALL: 1
- HYPOTENSION: 1
- KETOSIS: 1
- LOSS OF CONSCIOUSNESS: 1
- Chest pain: 1
- Palpitations: 1
- Burning mouth syndrome: 1
Outcomes
- Other Serious or Important Medical Event: 11
- Disability: 5
- Hospitalization: 4
- Visited a Health Care Provider: 3
- Other Serious Outcome: 3
- Visited Emergency Room: 1
Products Involved (10 unique)
- B COMPLEX (B3,B6,B2,B1 HCL)
- B-6
- B6
- CENTRUM WOMEN'S MULTIVITAMIN VITAMIN B6
- FINEST NUTRITION 100MG B6
- NATUREMADE VITAMIN B6
- SAW PALMETTO WITH B6
- SOLGAR VITAMIN B6
- SUNDOWN NATURALS VITAMIN B6
- VITAMIN B6
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.