Does ECULIZUMAB Cause Condition aggravated? 1,189 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,189 reports of Condition aggravated have been filed in association with ECULIZUMAB (SOLIRIS). This represents 2.7% of all adverse event reports for ECULIZUMAB.
1,189
Reports of Condition aggravated with ECULIZUMAB
2.7%
of all ECULIZUMAB reports
222
Deaths
510
Hospitalizations
How Dangerous Is Condition aggravated From ECULIZUMAB?
Of the 1,189 reports, 222 (18.7%) resulted in death, 510 (42.9%) required hospitalization, and 69 (5.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 1,189 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ECULIZUMAB Alternatives Have Lower Condition aggravated Risk?
ECULIZUMAB vs EDARAVONE
ECULIZUMAB vs EDETATE
ECULIZUMAB vs EDOXABAN
ECULIZUMAB vs EDOXABAN TOSILATE
ECULIZUMAB vs EFALIZUMAB