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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 Fluid retention? 33 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Fluid retention have been filed in association with CANAKINUMAB (Ilaris). This represents 0.3% of all adverse event reports for CANAKINUMAB.

33
Reports of Fluid retention with CANAKINUMAB
0.3%
of all CANAKINUMAB reports
0
Deaths
26
Hospitalizations

How Dangerous Is Fluid retention From CANAKINUMAB?

Of the 33 reports, 26 (78.8%) required hospitalization, and 1 (3.0%) were considered life-threatening.

Is Fluid retention Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CANAKINUMAB. However, 33 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 Fluid retention?

AMBRISENTAN (3,927) TREPROSTINIL (3,804) MACITENTAN (2,861) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,233) SACUBITRIL\VALSARTAN (2,187) ADALIMUMAB (1,193) SELEXIPAG (1,044) FUROSEMIDE (1,020) LENALIDOMIDE (1,007) EPOPROSTENOL (929)

Which CANAKINUMAB Alternatives Have Lower Fluid retention 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 Fluid retention Reports All Drugs Causing Fluid retention CANAKINUMAB Demographics