Does SODIUM AUROTIOSULFATE Cause Hypersensitivity? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Hypersensitivity have been filed in association with SODIUM AUROTIOSULFATE. This represents 29.3% of all adverse event reports for SODIUM AUROTIOSULFATE.
29
Reports of Hypersensitivity with SODIUM AUROTIOSULFATE
29.3%
of all SODIUM AUROTIOSULFATE reports
22
Deaths
29
Hospitalizations
How Dangerous Is Hypersensitivity From SODIUM AUROTIOSULFATE?
Of the 29 reports, 22 (75.9%) resulted in death, 29 (100.0%) required hospitalization, and 22 (75.9%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 29 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 Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)