Does GOLD THIOMALATE Cause Product quality issue? 492 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 492 reports of Product quality issue have been filed in association with GOLD THIOMALATE. This represents 11.0% of all adverse event reports for GOLD THIOMALATE.
492
Reports of Product quality issue with GOLD THIOMALATE
11.0%
of all GOLD THIOMALATE reports
492
Deaths
410
Hospitalizations
How Dangerous Is Product quality issue From GOLD THIOMALATE?
Of the 492 reports, 492 (100.0%) resulted in death, 410 (83.3%) required hospitalization, and 424 (86.2%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLD THIOMALATE. However, 492 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which GOLD THIOMALATE Alternatives Have Lower Product quality issue Risk?
GOLD THIOMALATE vs GOLIMUMAB
GOLD THIOMALATE vs GOLODIRSEN
GOLD THIOMALATE vs GONADORELIN
GOLD THIOMALATE vs GONADOTROPHIN, CHORIONIC
GOLD THIOMALATE vs GOSERELIN