Does CERTOLIZUMAB PEGOL Cause Product dose omission in error? 226 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 226 reports of Product dose omission in error have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.2% of all adverse event reports for CERTOLIZUMAB PEGOL.
226
Reports of Product dose omission in error with CERTOLIZUMAB PEGOL
0.2%
of all CERTOLIZUMAB PEGOL reports
0
Deaths
21
Hospitalizations
How Dangerous Is Product dose omission in error From CERTOLIZUMAB PEGOL?
Of the 226 reports, 21 (9.3%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 226 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Product dose omission in error Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX