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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 Therapy non-responder? 62 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Therapy non-responder have been filed in association with CANAKINUMAB (Ilaris). This represents 0.6% of all adverse event reports for CANAKINUMAB.

62
Reports of Therapy non-responder with CANAKINUMAB
0.6%
of all CANAKINUMAB reports
0
Deaths
6
Hospitalizations

How Dangerous Is Therapy non-responder From CANAKINUMAB?

Of the 62 reports, 6 (9.7%) required hospitalization, and 2 (3.2%) were considered life-threatening.

Is Therapy non-responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CANAKINUMAB. However, 62 reports have been filed with the FAERS database.

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 Therapy non-responder?

ETANERCEPT (3,472) APREMILAST (3,360) METHOTREXATE (2,965) RITUXIMAB (2,731) ADALIMUMAB (2,595) PREDNISONE (2,563) TREPROSTINIL (2,289) INFLIXIMAB (2,122) TOCILIZUMAB (1,775) HYDROXYCHLOROQUINE (1,699)

Which CANAKINUMAB Alternatives Have Lower Therapy non-responder 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 Therapy non-responder Reports All Drugs Causing Therapy non-responder CANAKINUMAB Demographics