Adverse Event Profile: Vitamin K
Adverse Event Profile: Vitamin K
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 16 Serious Events: 6 Date Range: 20101122 to 20241231
Top Reported Reactions
- Alopecia: 2
- Nausea: 2
- Vomiting: 2
- CHOKING SENSATION: 1
- COUGH: 1
- DYSPHONIA: 1
- DYSPNOEA: 1
- Anxiety: 1
- Autonomic neuropathy: 1
- Constipation: 1
- Dizziness: 1
- Fatigue: 1
- Feeling cold: 1
- Hypoaesthesia: 1
- Hypotension: 1
- Insomnia: 1
- Rosacea: 1
- Skin burning sensation: 1
- Syncope: 1
- Tremor: 1
Outcomes
- Other Serious or Important Medical Event: 9
- Disability: 3
- Other Outcome: 3
- Visited a Health Care Provider: 3
- Visited Emergency Room: 2
- Hospitalization: 2
- Other Serious Outcome: 2
- Life Threatening: 1
Products Involved (13 unique)
- MELATONIN VITAMIN K
- PURITAN'S PRIDE VITAMIN K
- PURITAN'S PRIDE VITAMIN K 200MCG TABLETS
- QVC VITAMIN WOMEN 50 PLUS COMBO 1V9 3K2 4F1 4H19J0
- VIT K2
- VITAMIN K
- VITAMIN K (PHYTOMENADIONE)
- VITAMIN K2
- VITAMIN K2 MK7 VCAP
- VITAMIN K3
- Vit. K2
- Vitamin K2
- vitamin K
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.