6,919 reports of this reaction
3.3% of all BUPROPION HYDROCHLORIDE reports
#3 most reported adverse reaction
FATIGUE is the #3 most commonly reported adverse reaction for BUPROPION HYDROCHLORIDE, manufactured by Bausch Health US LLC. There are 6,919 FDA adverse event reports linking BUPROPION HYDROCHLORIDE to FATIGUE. This represents approximately 3.3% of all 208,986 adverse event reports for this drug.
Patients taking BUPROPION HYDROCHLORIDE who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is moderately reported among BUPROPION HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for BUPROPION HYDROCHLORIDE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 6,919 FDA reports for BUPROPION HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 3.3% of all adverse event reports for BUPROPION HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience fatigue while taking BUPROPION 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.