15 reports of this reaction
1.6% of all CARBAMIDE PEROXIDE reports
#13 most reported adverse reaction
HYPOACUSIS is the #13 most commonly reported adverse reaction for CARBAMIDE PEROXIDE, manufactured by Medtech Products Inc.. There are 15 FDA adverse event reports linking CARBAMIDE PEROXIDE to HYPOACUSIS. This represents approximately 1.6% of all 928 adverse event reports for this drug.
Patients taking CARBAMIDE PEROXIDE who experience hypoacusis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOACUSIS is a less commonly reported adverse event for CARBAMIDE PEROXIDE, but still significant enough to appear in the safety profile.
In addition to hypoacusis, the following adverse reactions have been reported for CARBAMIDE PEROXIDE:
The following drugs have also been linked to hypoacusis in FDA adverse event reports:
HYPOACUSIS has been reported as an adverse event in 15 FDA reports for CARBAMIDE PEROXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOACUSIS accounts for approximately 1.6% of all adverse event reports for CARBAMIDE PEROXIDE, making it a notable side effect.
If you experience hypoacusis while taking CARBAMIDE PEROXIDE, 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.