804 reports of this reaction
5.0% of all ENCORAFENIB reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for ENCORAFENIB, manufactured by Array BioPharma Inc.. There are 804 FDA adverse event reports linking ENCORAFENIB to NAUSEA. This represents approximately 5.0% of all 16,241 adverse event reports for this drug.
Patients taking ENCORAFENIB who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among ENCORAFENIB users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for ENCORAFENIB:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 804 FDA reports for ENCORAFENIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 5.0% of all adverse event reports for ENCORAFENIB, making it one of the most commonly reported side effect.
If you experience nausea while taking ENCORAFENIB, 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.