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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 Haemorrhage? 28 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Haemorrhage have been filed in association with CANAKINUMAB (Ilaris). This represents 0.3% of all adverse event reports for CANAKINUMAB.

28
Reports of Haemorrhage with CANAKINUMAB
0.3%
of all CANAKINUMAB reports
5
Deaths
24
Hospitalizations

How Dangerous Is Haemorrhage From CANAKINUMAB?

Of the 28 reports, 5 (17.9%) resulted in death, 24 (85.7%) required hospitalization, and 5 (17.9%) were considered life-threatening.

Is Haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CANAKINUMAB. However, 28 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 Haemorrhage?

RIVAROXABAN (6,571) APIXABAN (4,770) EMICIZUMAB-KXWH (3,612) WARFARIN (2,930) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (2,925) ASPIRIN (2,878) ADALIMUMAB (2,681) IBRUTINIB (1,907) CLOPIDOGREL BISULFATE (1,762) INSULIN LISPRO (1,614)

Which CANAKINUMAB Alternatives Have Lower Haemorrhage 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 Haemorrhage Reports All Drugs Causing Haemorrhage CANAKINUMAB Demographics