Does CERTOLIZUMAB PEGOL Cause Adverse event? 1,417 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,417 reports of Adverse event have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 1.4% of all adverse event reports for CERTOLIZUMAB PEGOL.
1,417
Reports of Adverse event with CERTOLIZUMAB PEGOL
1.4%
of all CERTOLIZUMAB PEGOL reports
412
Deaths
560
Hospitalizations
How Dangerous Is Adverse event From CERTOLIZUMAB PEGOL?
Of the 1,417 reports, 412 (29.1%) resulted in death, 560 (39.5%) required hospitalization, and 509 (35.9%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for CERTOLIZUMAB PEGOL.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Adverse event Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX