1,075 reports of this reaction
2.9% of all AXITINIB reports
#9 most reported adverse reaction
DECREASED APPETITE is the #9 most commonly reported adverse reaction for AXITINIB, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 1,075 FDA adverse event reports linking AXITINIB to DECREASED APPETITE. This represents approximately 2.9% of all 37,114 adverse event reports for this drug.
Patients taking AXITINIB who experience decreased appetite should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DECREASED APPETITE is a less commonly reported adverse event for AXITINIB, but still significant enough to appear in the safety profile.
In addition to decreased appetite, the following adverse reactions have been reported for AXITINIB:
The following drugs have also been linked to decreased appetite in FDA adverse event reports:
DECREASED APPETITE has been reported as an adverse event in 1,075 FDA reports for AXITINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DECREASED APPETITE accounts for approximately 2.9% of all adverse event reports for AXITINIB, making it a notable side effect.
If you experience decreased appetite while taking AXITINIB, 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.