Does CERTOLIZUMAB PEGOL Cause Incorrect product administration duration? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Incorrect product administration duration have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.1% of all adverse event reports for CERTOLIZUMAB PEGOL.
80
Reports of Incorrect product administration duration with CERTOLIZUMAB PEGOL
0.1%
of all CERTOLIZUMAB PEGOL reports
62
Deaths
61
Hospitalizations
How Dangerous Is Incorrect product administration duration From CERTOLIZUMAB PEGOL?
Of the 80 reports, 62 (77.5%) resulted in death, 61 (76.3%) required hospitalization, and 61 (76.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 80 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Incorrect product administration duration Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX