3 reports of this reaction
2.0% of all LOTION reports
#9 most reported adverse reaction
PRURITUS is the #9 most commonly reported adverse reaction for LOTION, manufactured by Derma Glove. There are 3 FDA adverse event reports linking LOTION to PRURITUS. This represents approximately 2.0% of all 148 adverse event reports for this drug.
Patients taking LOTION who experience pruritus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRURITUS is a less commonly reported adverse event for LOTION, but still significant enough to appear in the safety profile.
In addition to pruritus, the following adverse reactions have been reported for LOTION:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 3 FDA reports for LOTION. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 2.0% of all adverse event reports for LOTION, making it a notable side effect.
If you experience pruritus 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.