2 reports of this reaction
1.4% of all LOTION reports
#12 most reported adverse reaction
ACNE is the #12 most commonly reported adverse reaction for LOTION, manufactured by Derma Glove. There are 2 FDA adverse event reports linking LOTION to ACNE. This represents approximately 1.4% of all 148 adverse event reports for this drug.
Patients taking LOTION who experience acne should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ACNE is a less commonly reported adverse event for LOTION, but still significant enough to appear in the safety profile.
In addition to acne, the following adverse reactions have been reported for LOTION:
The following drugs have also been linked to acne in FDA adverse event reports:
ACNE has been reported as an adverse event in 2 FDA reports for LOTION. This does not prove causation, but indicates an association observed in post-market surveillance data.
ACNE accounts for approximately 1.4% of all adverse event reports for LOTION, making it a notable side effect.
If you experience acne while taking LOTION, 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.