Adverse Event Profile: Choline
Adverse Event Profile: Choline
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 7 Serious Events: 1 Date Range: 20121205 to 20250925
Top Reported Reactions
- GASTROINTESTINAL PAIN: 1
- RECTAL HAEMORRHAGE: 1
- TOOTH INJURY: 1
- Pulmonary oedema: 1
- Rash pruritic: 1
- Throat tightness: 1
- Urticaria: 1
- ABORTION SPONTANEOUS: 1
- DRUG EXPOSURE DURING PREGNANCY: 1
- VAGINAL HAEMORRHAGE: 1
- Abortion spontaneous: 1
- Adverse event: 1
- CEREBROVASCULAR ACCIDENT: 1
- FEELING ABNORMAL: 1
- NERVOUS SYSTEM DISORDER: 1
- VERTIGO: 1
- Dyspnoea: 1
- Nasal congestion: 1
- Sinusitis: 1
Outcomes
- Other Serious or Important Medical Event: 6
- Other Serious Outcome: 1
- Disability: 1
Products Involved (7 unique)
- CITICHOLINE
- Choline
- FLINSTONES GUMMIES (MULTIVITAMINS, MINERALS, CHOLI
- FLINTSTONES GUMMIES (MULTIVITAMINS, MINERALS, CHOL
- NATUREMADE CHOLINE EXTRA STRENGTH DOSAGE
- ONE A DAY VITACRAVES GUMMIES MULTIVITAMINS MINERAL
- ONE A DAY VITACRAVES GUMMIES MULTIVITAMINS, MINERA
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.