30 reports of this reaction
1.9% of all DIMETHICONE reports
#11 most reported adverse reaction
ABDOMINAL DISTENSION is the #11 most commonly reported adverse reaction for DIMETHICONE, manufactured by Kenvue Brands LLC. There are 30 FDA adverse event reports linking DIMETHICONE to ABDOMINAL DISTENSION. This represents approximately 1.9% of all 1,584 adverse event reports for this drug.
Patients taking DIMETHICONE who experience abdominal distension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL DISTENSION is a less commonly reported adverse event for DIMETHICONE, but still significant enough to appear in the safety profile.
In addition to abdominal distension, the following adverse reactions have been reported for DIMETHICONE:
The following drugs have also been linked to abdominal distension in FDA adverse event reports:
ABDOMINAL DISTENSION has been reported as an adverse event in 30 FDA reports for DIMETHICONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISTENSION accounts for approximately 1.9% of all adverse event reports for DIMETHICONE, making it a notable side effect.
If you experience abdominal distension while taking DIMETHICONE, 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.