Does CERTOLIZUMAB PEGOL Cause Hypokalaemia? 143 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 143 reports of Hypokalaemia have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.1% of all adverse event reports for CERTOLIZUMAB PEGOL.
143
Reports of Hypokalaemia with CERTOLIZUMAB PEGOL
0.1%
of all CERTOLIZUMAB PEGOL reports
14
Deaths
142
Hospitalizations
How Dangerous Is Hypokalaemia From CERTOLIZUMAB PEGOL?
Of the 143 reports, 14 (9.8%) resulted in death, 142 (99.3%) required hospitalization, and 21 (14.7%) were considered life-threatening.
Is Hypokalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 143 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 Hypokalaemia?
FUROSEMIDE (2,503)
HYDROCHLOROTHIAZIDE (1,152)
CARBOPLATIN (1,118)
PREDNISONE (967)
DEXAMETHASONE (876)
CYCLOPHOSPHAMIDE (864)
OMEPRAZOLE (851)
RITUXIMAB (822)
AMLODIPINE (815)
PANTOPRAZOLE (811)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Hypokalaemia Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX