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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 AUROTHIOGLUCOSE Cause Contraindicated product administered? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Contraindicated product administered have been filed in association with AUROTHIOGLUCOSE. This represents 37.5% of all adverse event reports for AUROTHIOGLUCOSE.

9
Reports of Contraindicated product administered with AUROTHIOGLUCOSE
37.5%
of all AUROTHIOGLUCOSE reports
2
Deaths
2
Hospitalizations

How Dangerous Is Contraindicated product administered From AUROTHIOGLUCOSE?

Of the 9 reports, 2 (22.2%) resulted in death, 2 (22.2%) required hospitalization, and 2 (22.2%) 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 AUROTHIOGLUCOSE. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does AUROTHIOGLUCOSE Cause?

Drug ineffective (18) Rheumatoid arthritis (12) Drug intolerance (9) Condition aggravated (7) Drug hypersensitivity (7) Arthropathy (6) Infection (6) Pain in extremity (6) Treatment failure (6) Headache (5)

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)

Related Pages

AUROTHIOGLUCOSE Full Profile All Contraindicated product administered Reports All Drugs Causing Contraindicated product administered AUROTHIOGLUCOSE Demographics