Does CANAKINUMAB Cause Sinus node dysfunction? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Sinus node dysfunction have been filed in association with CANAKINUMAB (Ilaris). This represents 0.1% of all adverse event reports for CANAKINUMAB.
11
Reports of Sinus node dysfunction with CANAKINUMAB
0.1%
of all CANAKINUMAB reports
1
Deaths
11
Hospitalizations
How Dangerous Is Sinus node dysfunction From CANAKINUMAB?
Of the 11 reports, 1 (9.1%) resulted in death, 11 (100.0%) required hospitalization, and 1 (9.1%) were considered life-threatening.
Is Sinus node dysfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CANAKINUMAB. However, 11 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 Sinus node dysfunction?
AMIODARONE (119)
METOPROLOL (101)
BISOPROLOL (84)
DEXAMETHASONE (69)
APIXABAN (67)
LENALIDOMIDE (66)
LACOSAMIDE (50)
DONEPEZIL (49)
METHOTREXATE (49)
ROSIGLITAZONE (48)
Which CANAKINUMAB Alternatives Have Lower Sinus node dysfunction Risk?
CANAKINUMAB vs CANDESARTAN
CANAKINUMAB vs CANDESARTAN CILEXETIL
CANAKINUMAB vs CANDESARTAN CILEXETIL\HYDROCHLOROTHIAZIDE
CANAKINUMAB vs CANGRELOR
CANAKINUMAB vs CANIS LUPUS FAMILIARIS SKIN