198 reports of this reaction
1.2% of all BENZOYL PEROXIDE reports
#15 most reported adverse reaction
UNDERDOSE is the #15 most commonly reported adverse reaction for BENZOYL PEROXIDE, manufactured by Alchemee, LLC. There are 198 FDA adverse event reports linking BENZOYL PEROXIDE to UNDERDOSE. This represents approximately 1.2% of all 15,861 adverse event reports for this drug.
Patients taking BENZOYL PEROXIDE who experience underdose should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
UNDERDOSE is a less commonly reported adverse event for BENZOYL PEROXIDE, but still significant enough to appear in the safety profile.
In addition to underdose, the following adverse reactions have been reported for BENZOYL PEROXIDE:
The following drugs have also been linked to underdose in FDA adverse event reports:
UNDERDOSE has been reported as an adverse event in 198 FDA reports for BENZOYL PEROXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
UNDERDOSE accounts for approximately 1.2% of all adverse event reports for BENZOYL PEROXIDE, making it a notable side effect.
If you experience underdose while taking BENZOYL 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.