8,956 reports of this reaction
3.8% of all DIMETHYL FUMARATE reports
#2 most reported adverse reaction
NAUSEA is the #2 most commonly reported adverse reaction for DIMETHYL FUMARATE, manufactured by Biogen Inc.. There are 8,956 FDA adverse event reports linking DIMETHYL FUMARATE to NAUSEA. This represents approximately 3.8% of all 232,901 adverse event reports for this drug.
Patients taking DIMETHYL FUMARATE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among DIMETHYL FUMARATE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for DIMETHYL FUMARATE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 8,956 FDA reports for DIMETHYL FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.8% of all adverse event reports for DIMETHYL FUMARATE, making it one of the most commonly reported side effect.
If you experience nausea 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.