Does SODIUM AUROTIOSULFATE Cause Hepatitis? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Hepatitis have been filed in association with SODIUM AUROTIOSULFATE. This represents 21.2% of all adverse event reports for SODIUM AUROTIOSULFATE.
21
Reports of Hepatitis with SODIUM AUROTIOSULFATE
21.2%
of all SODIUM AUROTIOSULFATE reports
21
Deaths
21
Hospitalizations
How Dangerous Is Hepatitis From SODIUM AUROTIOSULFATE?
Of the 21 reports, 21 (100.0%) resulted in death, 21 (100.0%) required hospitalization, and 21 (100.0%) were considered life-threatening.
Is Hepatitis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 21 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 Hepatitis?
METHOTREXATE (1,835)
ACETAMINOPHEN (1,450)
TOCILIZUMAB (1,184)
HYDROXYCHLOROQUINE (1,133)
ADALIMUMAB (1,096)
RITUXIMAB (1,017)
ETANERCEPT (1,013)
LEFLUNOMIDE (997)
PEMBROLIZUMAB (935)
NIVOLUMAB (930)