Does GOLIMUMAB Cause Device defective? 539 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 539 reports of Device defective have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.8% of all adverse event reports for GOLIMUMAB.
539
Reports of Device defective with GOLIMUMAB
0.8%
of all GOLIMUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device defective From GOLIMUMAB?
Of the 539 reports, 4 (0.7%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 539 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
BUDESONIDE\FORMOTEROL (378)
Which GOLIMUMAB Alternatives Have Lower Device defective Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN