Adverse Event Profile: Vitamin A
Adverse Event Profile: Vitamin A
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 22 Serious Events: 13 Date Range: 20080122 to 20250617
Top Reported Reactions
- Headache: 2
- Vision blurred: 2
- ABDOMINAL PAIN: 2
- FATIGUE: 2
- HEADACHE: 2
- NAUSEA: 2
- VISION BLURRED: 2
- Dysgeusia: 2
- DYSPHAGIA: 2
- Blood pressure increased: 1
- Epistaxis: 1
- Erythema: 1
- Haemorrhoids: 1
- Infrequent bowel movements: 1
- ALOPECIA: 1
- BLOOD CALCIUM INCREASED: 1
- BONE PAIN: 1
- FONTANELLE BULGING: 1
- HYPERVITAMINOSIS A: 1
- INTRACRANIAL PRESSURE INCREASED: 1
Outcomes
- Other Serious or Important Medical Event: 12
- Hospitalization: 8
- Visited Emergency Room: 6
- Other Serious Outcome: 4
- Required Intervention: 3
- Visited a Health Care Provider: 3
- Life Threatening: 2
- Disability: 2
- Congenital Anomaly: 1
- Other Outcome: 1
Products Involved (14 unique)
- BERKLEY AND JENSEN WOMEN'S DAILY MULTIVITAMIN AND
- BIO - AE MULSION FORTE WITH VITAMIN A
- COD LIVER OIL/VITAMIN A
- NUMAQULA VITAMIN AREDS2 FORMULA DIETARY SUPPLEMENT
- NUTRILITE MEN'S SUPPLEMENT PACK DAILY MULTIVITAMIN
- ONE A DAY WOMEN'S MULTIVITAMIN AND MINERAL SUPPLEM
- PRESERVISION EYE VITAMIN AND MINERAL SUPPLEMENT AR
- PURITANS PRIDE BETA CAROTENE PROVITAMIN A
- RETINOL
- VITALITY MULTIVITAMIN AND MINERAL PRENATAL
- VITALITY MULTIVITAMIN AND MINERAL WOMEN
- VITAMIN A
- Vitamin A
- unspecified Vitamin A
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.