Does SODIUM AUROTIOSULFATE Cause Hypercholesterolaemia? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Hypercholesterolaemia have been filed in association with SODIUM AUROTIOSULFATE. This represents 46.5% of all adverse event reports for SODIUM AUROTIOSULFATE.
46
Reports of Hypercholesterolaemia with SODIUM AUROTIOSULFATE
46.5%
of all SODIUM AUROTIOSULFATE reports
46
Deaths
24
Hospitalizations
How Dangerous Is Hypercholesterolaemia From SODIUM AUROTIOSULFATE?
Of the 46 reports, 46 (100.0%) resulted in death, 24 (52.2%) required hospitalization, and 24 (52.2%) were considered life-threatening.
Is Hypercholesterolaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 46 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 Hypercholesterolaemia?
ALENDRONATE (1,607)
METHOTREXATE (1,547)
TOCILIZUMAB (1,483)
ADALIMUMAB (1,479)
ABATACEPT (1,410)
RITUXIMAB (1,389)
PREDNISONE (1,377)
INFLIXIMAB (1,338)
DICLOFENAC (1,331)
LEFLUNOMIDE (1,322)