1,788 reports of this reaction
2.8% of all ATOMOXETINE HYDROCHLORIDE reports
#3 most reported adverse reaction
FATIGUE is the #3 most commonly reported adverse reaction for ATOMOXETINE HYDROCHLORIDE, manufactured by Eli Lilly and Company. There are 1,788 FDA adverse event reports linking ATOMOXETINE HYDROCHLORIDE to FATIGUE. This represents approximately 2.8% of all 63,960 adverse event reports for this drug.
Patients taking ATOMOXETINE 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 a less commonly reported adverse event for ATOMOXETINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for ATOMOXETINE HYDROCHLORIDE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 1,788 FDA reports for ATOMOXETINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.8% of all adverse event reports for ATOMOXETINE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience fatigue while taking ATOMOXETINE 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.