Does ECULIZUMAB Cause Unevaluable event? 604 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 604 reports of Unevaluable event have been filed in association with ECULIZUMAB (SOLIRIS). This represents 1.4% of all adverse event reports for ECULIZUMAB.
604
Reports of Unevaluable event with ECULIZUMAB
1.4%
of all ECULIZUMAB reports
109
Deaths
525
Hospitalizations
How Dangerous Is Unevaluable event From ECULIZUMAB?
Of the 604 reports, 109 (18.0%) resulted in death, 525 (86.9%) required hospitalization, and 24 (4.0%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 604 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which ECULIZUMAB Alternatives Have Lower Unevaluable event Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB