Does GOLIMUMAB Cause Device failure? 487 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 487 reports of Device failure have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.7% of all adverse event reports for GOLIMUMAB.
487
Reports of Device failure with GOLIMUMAB
0.7%
of all GOLIMUMAB reports
1
Deaths
3
Hospitalizations
How Dangerous Is Device failure From GOLIMUMAB?
Of the 487 reports, 1 (0.2%) resulted in death, 3 (0.6%) required hospitalization.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 487 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 failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
LEVONORGESTREL (332)
ACLIDINIUM (304)
INSULIN ASPART (271)
Which GOLIMUMAB Alternatives Have Lower Device failure Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN