Does CERTOLIZUMAB PEGOL Cause Haemoglobin increased? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Haemoglobin increased have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 0.0% of all adverse event reports for CERTOLIZUMAB PEGOL.
16
Reports of Haemoglobin increased with CERTOLIZUMAB PEGOL
0.0%
of all CERTOLIZUMAB PEGOL reports
10
Deaths
10
Hospitalizations
How Dangerous Is Haemoglobin increased From CERTOLIZUMAB PEGOL?
Of the 16 reports, 10 (62.5%) resulted in death, 10 (62.5%) required hospitalization, and 10 (62.5%) were considered life-threatening.
Is Haemoglobin increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 16 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 Haemoglobin increased?
RUXOLITINIB (332)
TREPROSTINIL (245)
SOTATERCEPT (151)
CLOZAPINE (142)
SOTATERCEPT-CSRK (100)
DARBEPOETIN ALFA (99)
TESTOSTERONE (96)
METFORMIN (93)
VOXELOTOR (86)
ROSUVASTATIN (85)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Haemoglobin increased Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX