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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 CANAKINUMAB Cause Sepsis? 274 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 274 reports of Sepsis have been filed in association with CANAKINUMAB (Ilaris). This represents 2.6% of all adverse event reports for CANAKINUMAB.

274
Reports of Sepsis with CANAKINUMAB
2.6%
of all CANAKINUMAB reports
107
Deaths
210
Hospitalizations

How Dangerous Is Sepsis From CANAKINUMAB?

Of the 274 reports, 107 (39.1%) resulted in death, 210 (76.6%) required hospitalization, and 191 (69.7%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

Yes, Sepsis is listed as a known adverse reaction in the official FDA drug label for CANAKINUMAB.

What Other Side Effects Does CANAKINUMAB Cause?

Pyrexia (1,327) Inappropriate schedule of drug administration (1,238) Drug ineffective (1,078) Inappropriate schedule of product administration (944) Pain (858) Condition aggravated (771) Malaise (684) Off label use (557) Arthralgia (555) Rash (505)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which CANAKINUMAB Alternatives Have Lower Sepsis Risk?

CANAKINUMAB vs CANDESARTAN CANAKINUMAB vs CANDESARTAN CILEXETIL CANAKINUMAB vs CANDESARTAN CILEXETIL\HYDROCHLOROTHIAZIDE CANAKINUMAB vs CANGRELOR CANAKINUMAB vs CANIS LUPUS FAMILIARIS SKIN

Related Pages

CANAKINUMAB Full Profile All Sepsis Reports All Drugs Causing Sepsis CANAKINUMAB Demographics