21 reports of this reaction
1.4% of all SILICON DIOXIDE reports
#20 most reported adverse reaction
SKIN LESION is the #20 most commonly reported adverse reaction for SILICON DIOXIDE, manufactured by DNA Labs, Inc.. There are 21 FDA adverse event reports linking SILICON DIOXIDE to SKIN LESION. This represents approximately 1.4% of all 1,547 adverse event reports for this drug.
Patients taking SILICON DIOXIDE who experience skin lesion should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SKIN LESION is a less commonly reported adverse event for SILICON DIOXIDE, but still significant enough to appear in the safety profile.
In addition to skin lesion, the following adverse reactions have been reported for SILICON DIOXIDE:
The following drugs have also been linked to skin lesion in FDA adverse event reports:
SKIN LESION has been reported as an adverse event in 21 FDA reports for SILICON DIOXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SKIN LESION accounts for approximately 1.4% of all adverse event reports for SILICON DIOXIDE, making it a notable side effect.
If you experience skin lesion while taking SILICON DIOXIDE, 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.