909 reports of this reaction
1.4% of all LENVATINIB reports
#20 most reported adverse reaction
STOMATITIS is the #20 most commonly reported adverse reaction for LENVATINIB, manufactured by Eisai Inc.. There are 909 FDA adverse event reports linking LENVATINIB to STOMATITIS. This represents approximately 1.4% of all 64,104 adverse event reports for this drug.
Patients taking LENVATINIB who experience stomatitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
STOMATITIS is a less commonly reported adverse event for LENVATINIB, but still significant enough to appear in the safety profile.
In addition to stomatitis, the following adverse reactions have been reported for LENVATINIB:
The following drugs have also been linked to stomatitis in FDA adverse event reports:
STOMATITIS has been reported as an adverse event in 909 FDA reports for LENVATINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
STOMATITIS accounts for approximately 1.4% of all adverse event reports for LENVATINIB, making it a notable side effect.
If you experience stomatitis while taking LENVATINIB, 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.