Does CERTOLIZUMAB PEGOL Cause Condition aggravated? 5,624 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,624 reports of Condition aggravated have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 5.7% of all adverse event reports for CERTOLIZUMAB PEGOL.
5,624
Reports of Condition aggravated with CERTOLIZUMAB PEGOL
5.7%
of all CERTOLIZUMAB PEGOL reports
1,468
Deaths
2,281
Hospitalizations
How Dangerous Is Condition aggravated From CERTOLIZUMAB PEGOL?
Of the 5,624 reports, 1,468 (26.1%) resulted in death, 2,281 (40.6%) required hospitalization, and 1,696 (30.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 5,624 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Condition aggravated Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX