Does ECULIZUMAB Cause Complication associated with device? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Complication associated with device have been filed in association with ECULIZUMAB (SOLIRIS). This represents 0.1% of all adverse event reports for ECULIZUMAB.
28
Reports of Complication associated with device with ECULIZUMAB
0.1%
of all ECULIZUMAB reports
3
Deaths
13
Hospitalizations
How Dangerous Is Complication associated with device From ECULIZUMAB?
Of the 28 reports, 3 (10.7%) resulted in death, 13 (46.4%) required hospitalization, and 2 (7.1%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 28 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which ECULIZUMAB Alternatives Have Lower Complication associated with device Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB