Does CERTOLIZUMAB PEGOL Cause Product prescribing issue? 297 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 297 reports of Product prescribing issue have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.3% of all adverse event reports for CERTOLIZUMAB PEGOL.
297
Reports of Product prescribing issue with CERTOLIZUMAB PEGOL
0.3%
of all CERTOLIZUMAB PEGOL reports
3
Deaths
40
Hospitalizations
How Dangerous Is Product prescribing issue From CERTOLIZUMAB PEGOL?
Of the 297 reports, 3 (1.0%) resulted in death, 40 (13.5%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 297 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 Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CABOZANTINIB S-MALATE (294)
MORPHINE (288)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Product prescribing issue Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX