2,272 reports of this reaction
1.8% of all IBRUTINIB reports
#11 most reported adverse reaction
NAUSEA is the #11 most commonly reported adverse reaction for IBRUTINIB, manufactured by Pharmacyclics LLC. There are 2,272 FDA adverse event reports linking IBRUTINIB to NAUSEA. This represents approximately 1.8% of all 129,122 adverse event reports for this drug.
Patients taking IBRUTINIB 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 IBRUTINIB, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for IBRUTINIB:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 2,272 FDA reports for IBRUTINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 1.8% of all adverse event reports for IBRUTINIB, making it a notable side effect.
If you experience nausea while taking IBRUTINIB, 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.