402 reports of this reaction
1.6% of all AVAPRITINIB reports
#16 most reported adverse reaction
DECREASED APPETITE is the #16 most commonly reported adverse reaction for AVAPRITINIB, manufactured by Blueprint Medicines Corporation. There are 402 FDA adverse event reports linking AVAPRITINIB to DECREASED APPETITE. This represents approximately 1.6% of all 25,335 adverse event reports for this drug.
Patients taking AVAPRITINIB 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 AVAPRITINIB, but still significant enough to appear in the safety profile.
In addition to decreased appetite, the following adverse reactions have been reported for AVAPRITINIB:
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 402 FDA reports for AVAPRITINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DECREASED APPETITE accounts for approximately 1.6% of all adverse event reports for AVAPRITINIB, making it a notable side effect.
If you experience decreased appetite while taking AVAPRITINIB, 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.