5,551 reports of this reaction
2.4% of all DIMETHYL FUMARATE reports
#9 most reported adverse reaction
GASTRIC DISORDER is the #9 most commonly reported adverse reaction for DIMETHYL FUMARATE, manufactured by Biogen Inc.. There are 5,551 FDA adverse event reports linking DIMETHYL FUMARATE to GASTRIC DISORDER. This represents approximately 2.4% of all 232,901 adverse event reports for this drug.
Patients taking DIMETHYL FUMARATE who experience gastric disorder should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
GASTRIC DISORDER is a less commonly reported adverse event for DIMETHYL FUMARATE, but still significant enough to appear in the safety profile.
In addition to gastric disorder, the following adverse reactions have been reported for DIMETHYL FUMARATE:
The following drugs have also been linked to gastric disorder in FDA adverse event reports:
GASTRIC DISORDER has been reported as an adverse event in 5,551 FDA reports for DIMETHYL FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
GASTRIC DISORDER accounts for approximately 2.4% of all adverse event reports for DIMETHYL FUMARATE, making it a notable side effect.
If you experience gastric disorder 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.