Adverse Event Profile: Glucosamine
Adverse Event Profile: Glucosamine
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 49 Serious Events: 20 Date Range: 20080825 to 20240618
Top Reported Reactions
- DYSPNOEA: 4
- HYPERSENSITIVITY: 4
- BLOOD PRESSURE INCREASED: 3
- Choking: 3
- Dyspnoea: 3
- Pain: 3
- Epistaxis: 3
- HEART RATE INCREASED: 3
- ASTHENIA: 2
- CONVULSION: 2
- LOSS OF CONSCIOUSNESS: 2
- VOMITING: 2
- Nausea: 2
- Dysphagia: 2
- FATIGUE: 2
- MUSCLE SPASMS: 2
- NAUSEA: 2
- Blood pressure increased: 2
- Heart rate increased: 2
- FOREIGN BODY TRAUMA: 2
Outcomes
- Other Serious or Important Medical Event: 29
- Visited a Health Care Provider: 9
- Hospitalization: 9
- Visited Emergency Room: 9
- Life Threatening: 7
- Other Serious Outcome: 6
- Other Outcome: 5
- Disability: 3
- Death: 1
Products Involved (37 unique)
- Chondroitin w/ Glucosamine
- GLUCOSAMINE
- GLUCOSAMINE (DIETARY SUPPLEMENT) TABLET
- GLUCOSAMINE AND CHONDROITIN
- GLUCOSAMINE CHODROITIN
- GLUCOSAMINE CHONDROITIN
- GLUCOSAMINE CHONDROITIN MSM
- GLUCOSAMINE CHONDROTIN
- GLUCOSAMINE SULFATE
- GLUCOSAMINE/CHONDROITIN
- Glucosamine
- Glucosamine Chondroitin
- Glucosamine Chondroitin with MSM
- Glucosamine MSM Complex
- Glucosamine chondroitin
- KIRKLAND GLUCOSAMINE HCL WITH MSM
- KIRKLAND SIGNATURE EXTRA STRENGTH GLUCOSAMINE AND
- KIRKLAND SIGNATURE GLUCOSAMINE HCL WITH MSM
- MOVE FREE ADVANCE (GLUCOSAMINE HYDROCHLORIDE, CHON
- NATURE'S BOUNTY GLUCOSAMINE CHONDROITIN
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.