Does GOLD THIOMALATE Cause Condition aggravated? 1,363 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,363 reports of Condition aggravated have been filed in association with GOLD THIOMALATE. This represents 30.5% of all adverse event reports for GOLD THIOMALATE.
1,363
Reports of Condition aggravated with GOLD THIOMALATE
30.5%
of all GOLD THIOMALATE reports
544
Deaths
863
Hospitalizations
How Dangerous Is Condition aggravated From GOLD THIOMALATE?
Of the 1,363 reports, 544 (39.9%) resulted in death, 863 (63.3%) required hospitalization, and 558 (40.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLD THIOMALATE. However, 1,363 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which GOLD THIOMALATE Alternatives Have Lower Condition aggravated Risk?
GOLD THIOMALATE vs GOLIMUMAB
GOLD THIOMALATE vs GOLODIRSEN
GOLD THIOMALATE vs GONADORELIN
GOLD THIOMALATE vs GONADOTROPHIN, CHORIONIC
GOLD THIOMALATE vs GOSERELIN