Does ECULIZUMAB Cause Haemoglobinuria? 521 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 521 reports of Haemoglobinuria have been filed in association with ECULIZUMAB (SOLIRIS). This represents 1.2% of all adverse event reports for ECULIZUMAB.
521
Reports of Haemoglobinuria with ECULIZUMAB
1.2%
of all ECULIZUMAB reports
8
Deaths
102
Hospitalizations
How Dangerous Is Haemoglobinuria From ECULIZUMAB?
Of the 521 reports, 8 (1.5%) resulted in death, 102 (19.6%) required hospitalization, and 5 (1.0%) were considered life-threatening.
Is Haemoglobinuria Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 521 reports have been filed with the FAERS database.
What Other Side Effects Does ECULIZUMAB Cause?
Fatigue (4,858)
Off label use (4,228)
Haemoglobin decreased (3,028)
Headache (2,699)
Death (2,221)
Pyrexia (1,948)
Dyspnoea (1,819)
Asthenia (1,732)
Drug ineffective (1,644)
Nausea (1,579)
What Other Drugs Cause Haemoglobinuria?
SOLIRIS (100)
OXALIPLATIN (23)
HUMAN IMMUNOGLOBULIN G (18)
ASPIRIN (13)
IBUPROFEN (11)
RAVULIZUMAB-CWVZ (9)
METFORMIN (8)
METHYLPREDNISOLONE (8)
PEGCETACOPLAN (8)
QUETIAPINE (8)
Which ECULIZUMAB Alternatives Have Lower Haemoglobinuria Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB