Does GOLD THIOMALATE Cause Product use issue? 855 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 855 reports of Product use issue have been filed in association with GOLD THIOMALATE. This represents 19.1% of all adverse event reports for GOLD THIOMALATE.
855
Reports of Product use issue with GOLD THIOMALATE
19.1%
of all GOLD THIOMALATE reports
373
Deaths
673
Hospitalizations
How Dangerous Is Product use issue From GOLD THIOMALATE?
Of the 855 reports, 373 (43.6%) resulted in death, 673 (78.7%) required hospitalization, and 336 (39.3%) 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 THIOMALATE. However, 855 reports have been filed with the FAERS database.
What Other Side Effects Does GOLD THIOMALATE Cause?
Drug ineffective (2,904)
Rheumatoid arthritis (2,472)
Off label use (1,909)
Joint swelling (1,804)
Drug hypersensitivity (1,778)
Drug intolerance (1,681)
Pain (1,663)
Contraindicated product administered (1,583)
Treatment failure (1,530)
Arthralgia (1,481)
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)
Which GOLD THIOMALATE Alternatives Have Lower Product use issue Risk?
GOLD THIOMALATE vs GOLIMUMAB
GOLD THIOMALATE vs GOLODIRSEN
GOLD THIOMALATE vs GONADORELIN
GOLD THIOMALATE vs GONADOTROPHIN, CHORIONIC
GOLD THIOMALATE vs GOSERELIN