Does CERTOLIZUMAB PEGOL Cause Product prescribing error? 168 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 168 reports of Product prescribing error have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.2% of all adverse event reports for CERTOLIZUMAB PEGOL.
168
Reports of Product prescribing error with CERTOLIZUMAB PEGOL
0.2%
of all CERTOLIZUMAB PEGOL reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product prescribing error From CERTOLIZUMAB PEGOL?
Of the 168 reports, 13 (7.7%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 168 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 error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Product prescribing error Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX