Does CERTOLIZUMAB PEGOL Cause Device issue? 109 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 109 reports of Device issue have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.1% of all adverse event reports for CERTOLIZUMAB PEGOL.
109
Reports of Device issue with CERTOLIZUMAB PEGOL
0.1%
of all CERTOLIZUMAB PEGOL reports
0
Deaths
13
Hospitalizations
How Dangerous Is Device issue From CERTOLIZUMAB PEGOL?
Of the 109 reports, 13 (11.9%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 109 reports have been filed with the FAERS database.
What Other Side Effects Does CERTOLIZUMAB PEGOL Cause?
Drug ineffective (23,838)
Rheumatoid arthritis (17,782)
Pain (13,929)
Fatigue (11,438)
Off label use (10,281)
Rash (9,663)
Alopecia (9,111)
Maternal exposure during pregnancy (9,013)
Arthralgia (8,993)
Abdominal discomfort (8,615)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Device issue Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX