1,077 reports of this reaction
2.3% of all IMATINIB MESYLATE reports
#7 most reported adverse reaction
MALAISE is the #7 most commonly reported adverse reaction for IMATINIB MESYLATE, manufactured by Novartis Pharmaceuticals Corporation. There are 1,077 FDA adverse event reports linking IMATINIB MESYLATE to MALAISE. This represents approximately 2.3% of all 47,520 adverse event reports for this drug.
Patients taking IMATINIB MESYLATE who experience malaise should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MALAISE is a less commonly reported adverse event for IMATINIB MESYLATE, but still significant enough to appear in the safety profile.
In addition to malaise, the following adverse reactions have been reported for IMATINIB MESYLATE:
The following drugs have also been linked to malaise in FDA adverse event reports:
MALAISE has been reported as an adverse event in 1,077 FDA reports for IMATINIB MESYLATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MALAISE accounts for approximately 2.3% of all adverse event reports for IMATINIB MESYLATE, making it a notable side effect.
If you experience malaise while taking IMATINIB MESYLATE, 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.