8,924 reports of this reaction
3.9% of all HYDROCORTISONE CREAM 1% reports
#1 most reported adverse reaction
OFF LABEL USE is the #1 most commonly reported adverse reaction for HYDROCORTISONE CREAM 1%, manufactured by Aldermed Inc.. There are 8,924 FDA adverse event reports linking HYDROCORTISONE CREAM 1% to OFF LABEL USE. This represents approximately 3.9% of all 229,246 adverse event reports for this drug.
Patients taking HYDROCORTISONE CREAM 1% who experience off label use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OFF LABEL USE is moderately reported among HYDROCORTISONE CREAM 1% users, representing a notable but not dominant share of adverse events.
In addition to off label use, the following adverse reactions have been reported for HYDROCORTISONE CREAM 1%:
The following drugs have also been linked to off label use in FDA adverse event reports:
OFF LABEL USE has been reported as an adverse event in 8,924 FDA reports for HYDROCORTISONE CREAM 1%. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 3.9% of all adverse event reports for HYDROCORTISONE CREAM 1%, making it one of the most commonly reported side effect.
If you experience off label use while taking HYDROCORTISONE CREAM 1%, 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.