Does SODIUM AUROTIOSULFATE Cause Off label use? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Off label use have been filed in association with SODIUM AUROTIOSULFATE. This represents 42.4% of all adverse event reports for SODIUM AUROTIOSULFATE.
42
Reports of Off label use with SODIUM AUROTIOSULFATE
42.4%
of all SODIUM AUROTIOSULFATE reports
35
Deaths
42
Hospitalizations
How Dangerous Is Off label use From SODIUM AUROTIOSULFATE?
Of the 42 reports, 35 (83.3%) resulted in death, 42 (100.0%) required hospitalization, and 35 (83.3%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 42 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)