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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 GOLD AU-198 Cause Treatment failure? 69 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Treatment failure have been filed in association with GOLD AU-198. This represents 75.8% of all adverse event reports for GOLD AU-198.

69
Reports of Treatment failure with GOLD AU-198
75.8%
of all GOLD AU-198 reports
1
Deaths
2
Hospitalizations

How Dangerous Is Treatment failure From GOLD AU-198?

Of the 69 reports, 1 (1.4%) resulted in death, 2 (2.9%) required hospitalization, and 1 (1.4%) were considered life-threatening.

Is Treatment failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLD AU-198. However, 69 reports have been filed with the FAERS database.

What Other Side Effects Does GOLD AU-198 Cause?

Drug ineffective (62) Infection (62) Rheumatoid arthritis (62) Rash (58) Pain (46) Musculoskeletal stiffness (45) Joint stiffness (43) Sleep disorder (41) Nausea (40) Off label use (37)

What Other Drugs Cause Treatment failure?

METHOTREXATE (14,672) ETANERCEPT (11,893) ADALIMUMAB (9,990) ABATACEPT (9,301) RITUXIMAB (9,217) TOCILIZUMAB (9,097) HYDROXYCHLOROQUINE (8,786) LEFLUNOMIDE (8,686) INFLIXIMAB (8,535) SULFASALAZINE (7,423)

Related Pages

GOLD AU-198 Full Profile All Treatment failure Reports All Drugs Causing Treatment failure GOLD AU-198 Demographics