Does GOLIMUMAB Cause Device leakage? 480 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 480 reports of Device leakage have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.7% of all adverse event reports for GOLIMUMAB.
480
Reports of Device leakage with GOLIMUMAB
0.7%
of all GOLIMUMAB reports
0
Deaths
6
Hospitalizations
How Dangerous Is Device leakage From GOLIMUMAB?
Of the 480 reports, 6 (1.3%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 480 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which GOLIMUMAB Alternatives Have Lower Device leakage Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN