Does SODIUM AUROTIOSULFATE Cause Contraindicated product administered? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Contraindicated product administered have been filed in association with SODIUM AUROTIOSULFATE. This represents 65.7% of all adverse event reports for SODIUM AUROTIOSULFATE.
65
Reports of Contraindicated product administered with SODIUM AUROTIOSULFATE
65.7%
of all SODIUM AUROTIOSULFATE reports
58
Deaths
42
Hospitalizations
How Dangerous Is Contraindicated product administered From SODIUM AUROTIOSULFATE?
Of the 65 reports, 58 (89.2%) resulted in death, 42 (64.6%) required hospitalization, and 35 (53.8%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 65 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)
Product use in unapproved indication (65)
Vomiting (65)
Abdominal discomfort (64)
What Other Drugs Cause Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)