Does GOLD Cause Incorrect product administration duration? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Incorrect product administration duration have been filed in association with GOLD (Aurum Met). This represents 1.1% of all adverse event reports for GOLD.
47
Reports of Incorrect product administration duration with GOLD
1.1%
of all GOLD reports
47
Deaths
46
Hospitalizations
How Dangerous Is Incorrect product administration duration From GOLD?
Of the 47 reports, 47 (100.0%) resulted in death, 46 (97.9%) required hospitalization, and 46 (97.9%) 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. However, 47 reports have been filed with the FAERS database.
What Other Side Effects Does GOLD Cause?
Drug ineffective (2,759)
Rheumatoid arthritis (2,220)
Drug intolerance (1,620)
Off label use (1,601)
Joint swelling (1,532)
Arthropathy (1,456)
Drug hypersensitivity (1,405)
Arthralgia (1,328)
Treatment failure (1,271)
Contraindicated product administered (1,252)
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 Alternatives Have Lower Incorrect product administration duration Risk?
GOLD vs GOLD THIOMALATE
GOLD vs GOLIMUMAB
GOLD vs GOLODIRSEN
GOLD vs GONADORELIN
GOLD vs GONADOTROPHIN, CHORIONIC