Does GOLD THIOMALATE Cause Incorrect product administration duration? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Incorrect product administration duration have been filed in association with GOLD THIOMALATE. This represents 1.3% of all adverse event reports for GOLD THIOMALATE.
59
Reports of Incorrect product administration duration with GOLD THIOMALATE
1.3%
of all GOLD THIOMALATE reports
59
Deaths
58
Hospitalizations
How Dangerous Is Incorrect product administration duration From GOLD THIOMALATE?
Of the 59 reports, 59 (100.0%) resulted in death, 58 (98.3%) required hospitalization, and 58 (98.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLD THIOMALATE. However, 59 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which GOLD THIOMALATE Alternatives Have Lower Incorrect product administration duration Risk?
GOLD THIOMALATE vs GOLIMUMAB
GOLD THIOMALATE vs GOLODIRSEN
GOLD THIOMALATE vs GONADORELIN
GOLD THIOMALATE vs GONADOTROPHIN, CHORIONIC
GOLD THIOMALATE vs GOSERELIN