Does GOLD THIOMALATE Cause Maternal exposure timing unspecified? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Maternal exposure timing unspecified have been filed in association with GOLD THIOMALATE. This represents 0.5% of all adverse event reports for GOLD THIOMALATE.
21
Reports of Maternal exposure timing unspecified with GOLD THIOMALATE
0.5%
of all GOLD THIOMALATE reports
21
Deaths
21
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From GOLD THIOMALATE?
Of the 21 reports, 21 (100.0%) resulted in death, 21 (100.0%) required hospitalization, and 21 (100.0%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLD THIOMALATE. However, 21 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which GOLD THIOMALATE Alternatives Have Lower Maternal exposure timing unspecified Risk?
GOLD THIOMALATE vs GOLIMUMAB
GOLD THIOMALATE vs GOLODIRSEN
GOLD THIOMALATE vs GONADORELIN
GOLD THIOMALATE vs GONADOTROPHIN, CHORIONIC
GOLD THIOMALATE vs GOSERELIN