Does SODIUM AUROTIOSULFATE Cause Intentional product use issue? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Intentional product use issue have been filed in association with SODIUM AUROTIOSULFATE. This represents 67.7% of all adverse event reports for SODIUM AUROTIOSULFATE.
67
Reports of Intentional product use issue with SODIUM AUROTIOSULFATE
67.7%
of all SODIUM AUROTIOSULFATE reports
66
Deaths
43
Hospitalizations
How Dangerous Is Intentional product use issue From SODIUM AUROTIOSULFATE?
Of the 67 reports, 66 (98.5%) resulted in death, 43 (64.2%) required hospitalization, and 42 (62.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 67 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)
Treatment failure (67)
Contraindicated product administered (65)
Product use in unapproved indication (65)
Vomiting (65)
Abdominal discomfort (64)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)