1,781 reports of this reaction
2.9% of all NALTREXONE reports
#6 most reported adverse reaction
FATIGUE is the #6 most commonly reported adverse reaction for NALTREXONE, manufactured by Alkermes, Inc.. There are 1,781 FDA adverse event reports linking NALTREXONE to FATIGUE. This represents approximately 2.9% of all 60,963 adverse event reports for this drug.
NALTREXONE has an overall safety score of 78 out of 100. Patients taking NALTREXONE 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 NALTREXONE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for NALTREXONE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 1,781 FDA reports for NALTREXONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.9% of all adverse event reports for NALTREXONE, making it a notable side effect.
If you experience fatigue while taking NALTREXONE, 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.