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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

SODIUM CHONDROITIN: 46 Adverse Event Reports & Safety Profile

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46
Total FAERS Reports
6 (13.0%)
Deaths Reported
27
Hospitalizations
46
As Primary/Secondary Suspect
1
Life-Threatening
2
Disabilities

Active Ingredient: SODIUM CHONDROITIN SULFATE ·

First Report: 201004 · Latest Report: 202004

What Are the Most Common SODIUM CHONDROITIN Side Effects?

#1 Most Reported
Urinary retention
17 reports (37.0%)
#2 Most Reported
Hyponatraemia
17 reports (37.0%)
#3 Most Reported
Hypokalaemia
17 reports (37.0%)

All SODIUM CHONDROITIN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Cognitive disorder 17 37.0% 0 17
Confusional state 17 37.0% 0 17
Hypokalaemia 17 37.0% 0 17
Hyponatraemia 17 37.0% 0 17
Urinary retention 17 37.0% 0 17
Oxygen saturation decreased 16 34.8% 0 16
Atrial fibrillation 15 32.6% 0 11
Liver function test increased 13 28.3% 0 13
Apathy 12 26.1% 0 12
Delirium 12 26.1% 0 12
Head discomfort 12 26.1% 0 12
Nausea 12 26.1% 0 12
Vertigo 12 26.1% 0 12
Anxiety 11 23.9% 0 11
Listless 11 23.9% 0 11
Medication error 11 23.9% 0 11
Fall 10 21.7% 0 10
Hypertension 10 21.7% 0 10
Intentional product misuse 9 19.6% 0 9
Drug abuse 8 17.4% 0 8

Who Reports SODIUM CHONDROITIN Side Effects? Age & Gender Data

Gender: 68.9% female, 31.1% male. Average age: 71.9 years. Most reports from: CZ. View detailed demographics →

Is SODIUM CHONDROITIN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2010 2 0 2
2014 3 0 2
2015 3 0 3
2016 2 0 1
2018 8 0 5
2019 4 3 1
2020 5 2 1

View full timeline →

What Is SODIUM CHONDROITIN Used For?

IndicationReports
Product used for unknown indication 28
Rheumatoid arthritis 6
Osteoarthritis 5

Official FDA Label for SODIUM CHONDROITIN

Official prescribing information from the FDA-approved drug label.