5,293 reports of this reaction
2.6% of all TOPIRAMATE reports
#5 most reported adverse reaction
FATIGUE is the #5 most commonly reported adverse reaction for TOPIRAMATE, manufactured by Janssen Pharmaceuticals, Inc.. There are 5,293 FDA adverse event reports linking TOPIRAMATE to FATIGUE. This represents approximately 2.6% of all 203,737 adverse event reports for this drug.
TOPIRAMATE has an overall safety score of 85 out of 100. Patients taking TOPIRAMATE 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 TOPIRAMATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for TOPIRAMATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 5,293 FDA reports for TOPIRAMATE. 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 TOPIRAMATE, making it a notable side effect.
If you experience fatigue while taking TOPIRAMATE, 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.