Does GOLD THIOMALATE Cause Intentional product use issue? 841 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 841 reports of Intentional product use issue have been filed in association with GOLD THIOMALATE. This represents 18.8% of all adverse event reports for GOLD THIOMALATE.
841
Reports of Intentional product use issue with GOLD THIOMALATE
18.8%
of all GOLD THIOMALATE reports
653
Deaths
670
Hospitalizations
How Dangerous Is Intentional product use issue From GOLD THIOMALATE?
Of the 841 reports, 653 (77.6%) resulted in death, 670 (79.7%) required hospitalization, and 613 (72.9%) were considered life-threatening.
Is Intentional 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, 841 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which GOLD THIOMALATE Alternatives Have Lower Intentional 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