Adverse Event Profile: Potassium
Adverse Event Profile: Potassium
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 36 Serious Events: 14 Date Range: 20081104 to 20250422
Top Reported Reactions
- CHOKING: 4
- SWOLLEN TONGUE: 3
- HYPERSENSITIVITY: 2
- Pulmonary embolism: 2
- DYSPNOEA: 2
- FALL: 2
- BLOOD PRESSURE INCREASED: 2
- Foreign body: 2
- Blood pressure increased: 2
- Diarrhoea: 2
- Dyspnoea: 2
- ASTHENIA: 2
- DIZZINESS: 2
- APHASIA: 1
- LIP SWELLING: 1
- SWELLING FACE: 1
- DYSPHAGIA: 1
- COLONOSCOPY ABNORMAL: 1
- DIVERTICULUM: 1
- ENDOSCOPY GASTROINTESTINAL ABNORMAL: 1
Outcomes
- Other Serious or Important Medical Event: 23
- Hospitalization: 11
- Visited Emergency Room: 7
- Visited a Health Care Provider: 7
- Other Serious Outcome: 5
- Other Outcome: 3
- Life Threatening: 2
- Disability: 1
Products Involved (15 unique)
- ACESULFAME POTASSIUM
- CVS HEALTH POTASSIUM GLUCONATE
- MICRO K (POTASSIUM CHLORIDE)
- Nature Made potassium
- POTASSIUM
- POTASSIUM (POTASSIUM [POTASSIUM])
- POTASSIUM CHLORIDE
- POTASSIUM GLUCONATE
- POTASSIUM LIQUID
- POTASSIUM SUPPLEMENT
- PURITAN'S PRIDE POTASSIUM
- PURITANS PRIDE POTASSIUM
- Potassium
- Potassium Gluconate
- potassium
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.