745 reports of this reaction
3.4% of all BUSPIRONE HYDROCHLORIDE reports
#2 most reported adverse reaction
NAUSEA is the #2 most commonly reported adverse reaction for BUSPIRONE HYDROCHLORIDE, manufactured by Advagen Pharma Ltd. There are 745 FDA adverse event reports linking BUSPIRONE HYDROCHLORIDE to NAUSEA. This represents approximately 3.4% of all 22,107 adverse event reports for this drug.
Patients taking BUSPIRONE 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 BUSPIRONE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for BUSPIRONE HYDROCHLORIDE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 745 FDA reports for BUSPIRONE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.4% of all adverse event reports for BUSPIRONE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience nausea while taking BUSPIRONE 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.