32 reports of this reaction
5.2% of all COLLOIDAL OATMEAL reports
#1 most reported adverse reaction
PRURITUS is the #1 most commonly reported adverse reaction for COLLOIDAL OATMEAL, manufactured by Crown Laboratories, Inc.. There are 32 FDA adverse event reports linking COLLOIDAL OATMEAL to PRURITUS. This represents approximately 5.2% of all 621 adverse event reports for this drug.
Patients taking COLLOIDAL OATMEAL 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 moderately reported among COLLOIDAL OATMEAL users, representing a notable but not dominant share of adverse events.
In addition to pruritus, the following adverse reactions have been reported for COLLOIDAL OATMEAL:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 32 FDA reports for COLLOIDAL OATMEAL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 5.2% of all adverse event reports for COLLOIDAL OATMEAL, making it one of the most commonly reported side effect.
If you experience pruritus while taking COLLOIDAL OATMEAL, 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.