Does CERTOLIZUMAB PEGOL Cause Product storage error? 583 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 583 reports of Product storage error have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.6% of all adverse event reports for CERTOLIZUMAB PEGOL.
583
Reports of Product storage error with CERTOLIZUMAB PEGOL
0.6%
of all CERTOLIZUMAB PEGOL reports
0
Deaths
47
Hospitalizations
How Dangerous Is Product storage error From CERTOLIZUMAB PEGOL?
Of the 583 reports, 47 (8.1%) required hospitalization, and 2 (0.3%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 583 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Product storage error Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX