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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SODIUM AUROTIOSULFATE Cause Ill-defined disorder? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Ill-defined disorder have been filed in association with SODIUM AUROTIOSULFATE. This represents 9.1% of all adverse event reports for SODIUM AUROTIOSULFATE.

9
Reports of Ill-defined disorder with SODIUM AUROTIOSULFATE
9.1%
of all SODIUM AUROTIOSULFATE reports
9
Deaths
9
Hospitalizations

How Dangerous Is Ill-defined disorder From SODIUM AUROTIOSULFATE?

Of the 9 reports, 9 (100.0%) resulted in death, 9 (100.0%) required hospitalization, and 9 (100.0%) were considered life-threatening.

Is Ill-defined disorder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 9 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 Ill-defined disorder?

ACETAMINOPHEN\OXYCODONE (9,780) ACETAMINOPHEN\HYDROCODONE (6,159) TOCILIZUMAB (4,411) RITUXIMAB (4,220) ETANERCEPT (4,202) METHOTREXATE (4,063) ABATACEPT (3,630) LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600) LEFLUNOMIDE (3,570) CERTOLIZUMAB PEGOL (3,273)

Related Pages

SODIUM AUROTIOSULFATE Full Profile All Ill-defined disorder Reports All Drugs Causing Ill-defined disorder SODIUM AUROTIOSULFATE Demographics