Does ECULIZUMAB Cause Post procedural haemorrhage? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Post procedural haemorrhage have been filed in association with ECULIZUMAB (SOLIRIS). This represents 0.1% of all adverse event reports for ECULIZUMAB.
55
Reports of Post procedural haemorrhage with ECULIZUMAB
0.1%
of all ECULIZUMAB reports
4
Deaths
24
Hospitalizations
How Dangerous Is Post procedural haemorrhage From ECULIZUMAB?
Of the 55 reports, 4 (7.3%) resulted in death, 24 (43.6%) required hospitalization, and 1 (1.8%) were considered life-threatening.
Is Post procedural haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 55 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 Post procedural haemorrhage?
LEVONORGESTREL (1,106)
RIVAROXABAN (930)
ASPIRIN (618)
APIXABAN (539)
ADALIMUMAB (476)
IBRUTINIB (269)
CLOPIDOGREL BISULFATE (235)
HEPARIN (174)
WARFARIN (170)
DABIGATRAN ETEXILATE (121)
Which ECULIZUMAB Alternatives Have Lower Post procedural haemorrhage Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB