Does CANAKINUMAB Cause Condition aggravated? 771 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 771 reports of Condition aggravated have been filed in association with CANAKINUMAB (Ilaris). This represents 7.4% of all adverse event reports for CANAKINUMAB.
771
Reports of Condition aggravated with CANAKINUMAB
7.4%
of all CANAKINUMAB reports
14
Deaths
182
Hospitalizations
How Dangerous Is Condition aggravated From CANAKINUMAB?
Of the 771 reports, 14 (1.8%) resulted in death, 182 (23.6%) required hospitalization, and 34 (4.4%) 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 CANAKINUMAB. However, 771 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)
Malaise (684)
Off label use (557)
Arthralgia (555)
Rash (505)
Incorrect dose administered (497)
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 CANAKINUMAB Alternatives Have Lower Condition aggravated Risk?
CANAKINUMAB vs CANDESARTAN
CANAKINUMAB vs CANDESARTAN CILEXETIL
CANAKINUMAB vs CANDESARTAN CILEXETIL\HYDROCHLOROTHIAZIDE
CANAKINUMAB vs CANGRELOR
CANAKINUMAB vs CANIS LUPUS FAMILIARIS SKIN