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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 Dyspepsia? 20 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Dyspepsia have been filed in association with SODIUM AUROTIOSULFATE. This represents 20.2% of all adverse event reports for SODIUM AUROTIOSULFATE.

20
Reports of Dyspepsia with SODIUM AUROTIOSULFATE
20.2%
of all SODIUM AUROTIOSULFATE reports
20
Deaths
20
Hospitalizations

How Dangerous Is Dyspepsia From SODIUM AUROTIOSULFATE?

Of the 20 reports, 20 (100.0%) resulted in death, 20 (100.0%) required hospitalization, and 20 (100.0%) were considered life-threatening.

Is Dyspepsia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 20 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 Dyspepsia?

ADALIMUMAB (3,586) METHOTREXATE (2,690) RITUXIMAB (2,289) TOFACITINIB (2,264) PREDNISONE (2,224) APREMILAST (2,207) ETANERCEPT (2,100) ESOMEPRAZOLE (2,064) TOCILIZUMAB (2,046) LEFLUNOMIDE (1,981)

Related Pages

SODIUM AUROTIOSULFATE Full Profile All Dyspepsia Reports All Drugs Causing Dyspepsia SODIUM AUROTIOSULFATE Demographics