Does GOLD THIOMALATE Cause Adverse event? 341 Reports in FDA Database

Q: Does GOLD THIOMALATE cause Adverse event?

341 reports of Adverse event have been filed with the FDA for GOLD THIOMALATE, representing 7.6% of all GOLD THIOMALATE adverse event reports.

Q: How dangerous is Adverse event from GOLD THIOMALATE?

Of 341 reports, 106 (31.1%) resulted in death and 268 required hospitalization.

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According to the FDA Adverse Event Reporting System (FAERS), 341 reports of Adverse event have been filed in association with GOLD THIOMALATE. This represents 7.6% of all adverse event reports for GOLD THIOMALATE.

341

Reports of Adverse event with GOLD THIOMALATE

7.6%

of all GOLD THIOMALATE reports

106

Deaths

268

Hospitalizations

How Dangerous Is Adverse event From GOLD THIOMALATE?

Of the 341 reports, 106 (31.1%) resulted in death, 268 (78.6%) required hospitalization, and 110 (32.3%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GOLD THIOMALATE. However, 341 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)