Does SODIUM AUROTIOSULFATE Cause Adverse event? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Adverse event have been filed in association with SODIUM AUROTIOSULFATE. This represents 6.1% of all adverse event reports for SODIUM AUROTIOSULFATE.
6
Reports of Adverse event with SODIUM AUROTIOSULFATE
6.1%
of all SODIUM AUROTIOSULFATE reports
4
Deaths
6
Hospitalizations
How Dangerous Is Adverse event From SODIUM AUROTIOSULFATE?
Of the 6 reports, 4 (66.7%) resulted in death, 6 (100.0%) required hospitalization, and 4 (66.7%) were considered life-threatening.
Is Adverse event 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)