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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ECULIZUMAB Cause Extra dose administered? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Extra dose administered have been filed in association with ECULIZUMAB (SOLIRIS). This represents 0.1% of all adverse event reports for ECULIZUMAB.

21
Reports of Extra dose administered with ECULIZUMAB
0.1%
of all ECULIZUMAB reports
1
Deaths
13
Hospitalizations

How Dangerous Is Extra dose administered From ECULIZUMAB?

Of the 21 reports, 1 (4.8%) resulted in death, 13 (61.9%) required hospitalization, and 2 (9.5%) were considered life-threatening.

Is Extra dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ECULIZUMAB. However, 21 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 Extra dose administered?

TIRZEPATIDE (6,774) DULAGLUTIDE (3,047) LORATADINE (1,556) DUPILUMAB (1,422) FEXOFENADINE (1,413) NAPROXEN (908) POLYETHYLENE GLYCOL 3350 (589) ACETAMINOPHEN (552) DALFAMPRIDINE (519) FLUTICASONE\SALMETEROL (499)

Which ECULIZUMAB Alternatives Have Lower Extra dose administered Risk?

ECULIZUMAB vs EDARAVONE ECULIZUMAB vs EDETATE ECULIZUMAB vs EDOXABAN ECULIZUMAB vs EDOXABAN TOSILATE ECULIZUMAB vs EFALIZUMAB

Related Pages

ECULIZUMAB Full Profile All Extra dose administered Reports All Drugs Causing Extra dose administered ECULIZUMAB Demographics