17,479 reports of this reaction
4.0% of all DULOXETINE HYDROCHLORIDE reports
#1 most reported adverse reaction
NAUSEA is the #1 most commonly reported adverse reaction for DULOXETINE HYDROCHLORIDE, manufactured by Eli Lilly and Company. There are 17,479 FDA adverse event reports linking DULOXETINE HYDROCHLORIDE to NAUSEA. This represents approximately 4.0% of all 434,529 adverse event reports for this drug.
Patients taking DULOXETINE HYDROCHLORIDE 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 DULOXETINE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for DULOXETINE HYDROCHLORIDE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 17,479 FDA reports for DULOXETINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 4.0% of all adverse event reports for DULOXETINE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience nausea while taking DULOXETINE HYDROCHLORIDE, 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.