Does SODIUM AUROTIOSULFATE Cause Swollen joint count increased? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Swollen joint count increased have been filed in association with SODIUM AUROTIOSULFATE. This represents 6.1% of all adverse event reports for SODIUM AUROTIOSULFATE.
6
Reports of Swollen joint count increased with SODIUM AUROTIOSULFATE
6.1%
of all SODIUM AUROTIOSULFATE reports
6
Deaths
6
Hospitalizations
How Dangerous Is Swollen joint count increased From SODIUM AUROTIOSULFATE?
Of the 6 reports, 6 (100.0%) resulted in death, 6 (100.0%) required hospitalization, and 6 (100.0%) were considered life-threatening.
Is Swollen joint count increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM AUROTIOSULFATE Cause?
Drug intolerance (76)
Drug ineffective (71)
Synovitis (70)
Hypertension (68)
Product use issue (68)
Intentional product use issue (67)
Treatment failure (67)
Contraindicated product administered (65)
Product use in unapproved indication (65)
Vomiting (65)
What Other Drugs Cause Swollen joint count increased?
METHOTREXATE (2,068)
ABATACEPT (2,032)
TOCILIZUMAB (1,987)
RITUXIMAB (1,973)
ADALIMUMAB (1,933)
DICLOFENAC (1,916)
LEFLUNOMIDE (1,907)
FOLIC ACID (1,898)
PREDNISONE (1,882)
ALENDRONATE (1,880)