226 reports of this reaction
2.0% of all BARICITINIB reports
#10 most reported adverse reaction
NAUSEA is the #10 most commonly reported adverse reaction for BARICITINIB, manufactured by Eli Lilly and Company. There are 226 FDA adverse event reports linking BARICITINIB to NAUSEA. This represents approximately 2.0% of all 11,538 adverse event reports for this drug.
Patients taking BARICITINIB 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 less commonly reported adverse event for BARICITINIB, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for BARICITINIB:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 226 FDA reports for BARICITINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.0% of all adverse event reports for BARICITINIB, making it a notable side effect.
If you experience nausea while taking BARICITINIB, 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.