Does GOLIMUMAB Cause Device malfunction? 2,293 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,293 reports of Device malfunction have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 3.3% of all adverse event reports for GOLIMUMAB.
2,293
Reports of Device malfunction with GOLIMUMAB
3.3%
of all GOLIMUMAB reports
1
Deaths
56
Hospitalizations
How Dangerous Is Device malfunction From GOLIMUMAB?
Of the 2,293 reports, 1 (0.0%) resulted in death, 56 (2.4%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 2,293 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which GOLIMUMAB Alternatives Have Lower Device malfunction Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN