Does ECULIZUMAB Cause Adverse event? 114 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 114 reports of Adverse event have been filed in association with ECULIZUMAB (SOLIRIS). This represents 0.3% of all adverse event reports for ECULIZUMAB.
114
Reports of Adverse event with ECULIZUMAB
0.3%
of all ECULIZUMAB reports
11
Deaths
33
Hospitalizations
How Dangerous Is Adverse event From ECULIZUMAB?
Of the 114 reports, 11 (9.6%) resulted in death, 33 (28.9%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for ECULIZUMAB.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ECULIZUMAB Alternatives Have Lower Adverse event Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB