Does GOLIMUMAB Cause Poor quality product administered? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Poor quality product administered have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.0% of all adverse event reports for GOLIMUMAB.
15
Reports of Poor quality product administered with GOLIMUMAB
0.0%
of all GOLIMUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Poor quality product administered From GOLIMUMAB?
Of the 15 reports, 2 (13.3%) required hospitalization.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does GOLIMUMAB Cause?
Drug ineffective (17,959)
Rheumatoid arthritis (12,272)
Pain (11,443)
Fatigue (9,626)
Off label use (8,764)
Alopecia (8,394)
Rash (8,331)
Joint swelling (8,264)
Arthralgia (7,968)
Abdominal discomfort (7,902)
What Other Drugs Cause Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which GOLIMUMAB Alternatives Have Lower Poor quality product administered Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN