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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 Product use issue? 30 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Product use issue have been filed in association with GOLD AU-198. This represents 33.0% of all adverse event reports for GOLD AU-198.

30
Reports of Product use issue with GOLD AU-198
33.0%
of all GOLD AU-198 reports
1
Deaths
2
Hospitalizations

How Dangerous Is Product use issue From GOLD AU-198?

Of the 30 reports, 1 (3.3%) resulted in death, 2 (6.7%) required hospitalization, and 1 (3.3%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLD AU-198. However, 30 reports have been filed with the FAERS database.

What Other Side Effects Does GOLD AU-198 Cause?

Treatment failure (69) Drug ineffective (62) Infection (62) Rheumatoid arthritis (62) Rash (58) Pain (46) Musculoskeletal stiffness (45) Joint stiffness (43) Sleep disorder (41) Nausea (40)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

GOLD AU-198 Full Profile All Product use issue Reports All Drugs Causing Product use issue GOLD AU-198 Demographics