Does CERTOLIZUMAB PEGOL Cause Unevaluable event? 405 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 405 reports of Unevaluable event have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.4% of all adverse event reports for CERTOLIZUMAB PEGOL.
405
Reports of Unevaluable event with CERTOLIZUMAB PEGOL
0.4%
of all CERTOLIZUMAB PEGOL reports
2
Deaths
88
Hospitalizations
How Dangerous Is Unevaluable event From CERTOLIZUMAB PEGOL?
Of the 405 reports, 2 (0.5%) resulted in death, 88 (21.7%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 405 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Unevaluable event Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX