Does GOLIMUMAB Cause Device mechanical issue? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Device mechanical issue have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.1% of all adverse event reports for GOLIMUMAB.
44
Reports of Device mechanical issue with GOLIMUMAB
0.1%
of all GOLIMUMAB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device mechanical issue From GOLIMUMAB?
Of the 44 reports, 1 (2.3%) required hospitalization.
Is Device mechanical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 44 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 mechanical issue?
SOMATROPIN (6,411)
INSULIN GLARGINE-YFGN (853)
INSULIN GLARGINE (725)
ALBUTEROL (455)
DEVICE (226)
ETANERCEPT (145)
FLUTICASONE\SALMETEROL (127)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
Which GOLIMUMAB Alternatives Have Lower Device mechanical issue Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN