5 reports of this reaction
3.4% of all LOTION reports
#2 most reported adverse reaction
DRY SKIN is the #2 most commonly reported adverse reaction for LOTION, manufactured by Derma Glove. There are 5 FDA adverse event reports linking LOTION to DRY SKIN. This represents approximately 3.4% of all 148 adverse event reports for this drug.
Patients taking LOTION who experience dry skin should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRY SKIN is moderately reported among LOTION users, representing a notable but not dominant share of adverse events.
In addition to dry skin, the following adverse reactions have been reported for LOTION:
The following drugs have also been linked to dry skin in FDA adverse event reports:
DRY SKIN has been reported as an adverse event in 5 FDA reports for LOTION. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY SKIN accounts for approximately 3.4% of all adverse event reports for LOTION, making it one of the most commonly reported side effect.
If you experience dry skin 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.