6,937 reports of this reaction
3.0% of all DIMETHYL FUMARATE reports
#5 most reported adverse reaction
FATIGUE is the #5 most commonly reported adverse reaction for DIMETHYL FUMARATE, manufactured by Biogen Inc.. There are 6,937 FDA adverse event reports linking DIMETHYL FUMARATE to FATIGUE. This represents approximately 3.0% of all 232,901 adverse event reports for this drug.
Patients taking DIMETHYL FUMARATE 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 DIMETHYL FUMARATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for DIMETHYL FUMARATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 6,937 FDA reports for DIMETHYL FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 3.0% of all adverse event reports for DIMETHYL FUMARATE, making it a notable side effect.
If you experience fatigue while taking DIMETHYL FUMARATE, 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.