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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 Contraindicated product administered? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Contraindicated product administered have been filed in association with GOLD AU-198. This represents 37.4% of all adverse event reports for GOLD AU-198.

34
Reports of Contraindicated product administered with GOLD AU-198
37.4%
of all GOLD AU-198 reports
0
Deaths
1
Hospitalizations

How Dangerous Is Contraindicated product administered From GOLD AU-198?

Of the 34 reports, 1 (2.9%) required hospitalization.

Is Contraindicated product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLD AU-198. However, 34 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 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

GOLD AU-198 Full Profile All Contraindicated product administered Reports All Drugs Causing Contraindicated product administered GOLD AU-198 Demographics