2,493 reports of this reaction
10.2% of all SELINEXOR reports
#1 most reported adverse reaction
NAUSEA is the #1 most commonly reported adverse reaction for SELINEXOR, manufactured by Karyopharm Therapeutics Inc.. There are 2,493 FDA adverse event reports linking SELINEXOR to NAUSEA. This represents approximately 10.2% of all 24,395 adverse event reports for this drug.
Patients taking SELINEXOR 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 a frequently reported adverse event for SELINEXOR, accounting for a significant proportion of all reports.
In addition to nausea, the following adverse reactions have been reported for SELINEXOR:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 2,493 FDA reports for SELINEXOR. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 10.2% of all adverse event reports for SELINEXOR, making it one of the most commonly reported side effect.
If you experience nausea while taking SELINEXOR, 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.