3,151 reports of this reaction
2.6% of all FLUOXETINE reports
#5 most reported adverse reaction
FATIGUE is the #5 most commonly reported adverse reaction for FLUOXETINE, manufactured by Alembic Pharmaceuticals Inc.. There are 3,151 FDA adverse event reports linking FLUOXETINE to FATIGUE. This represents approximately 2.6% of all 120,799 adverse event reports for this drug.
Patients taking FLUOXETINE 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 a less commonly reported adverse event for FLUOXETINE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for FLUOXETINE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 3,151 FDA reports for FLUOXETINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.6% of all adverse event reports for FLUOXETINE, making it a notable side effect.
If you experience fatigue while taking FLUOXETINE, 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.