1,035 reports of this reaction
2.1% of all CANAGLIFLOZIN reports
#9 most reported adverse reaction
CELLULITIS is the #9 most commonly reported adverse reaction for CANAGLIFLOZIN, manufactured by Janssen Pharmaceuticals, Inc.. There are 1,035 FDA adverse event reports linking CANAGLIFLOZIN to CELLULITIS. This represents approximately 2.1% of all 49,711 adverse event reports for this drug.
Patients taking CANAGLIFLOZIN who experience cellulitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CELLULITIS is a less commonly reported adverse event for CANAGLIFLOZIN, but still significant enough to appear in the safety profile.
In addition to cellulitis, the following adverse reactions have been reported for CANAGLIFLOZIN:
The following drugs have also been linked to cellulitis in FDA adverse event reports:
CELLULITIS has been reported as an adverse event in 1,035 FDA reports for CANAGLIFLOZIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
CELLULITIS accounts for approximately 2.1% of all adverse event reports for CANAGLIFLOZIN, making it a notable side effect.
If you experience cellulitis while taking CANAGLIFLOZIN, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.