10,132 reports of this reaction
3.4% of all HYDROCORTISONE ACETATE reports
#1 most reported adverse reaction
OFF LABEL USE is the #1 most commonly reported adverse reaction for HYDROCORTISONE ACETATE, manufactured by Sun Pharmaceutical Industries, Inc.. There are 10,132 FDA adverse event reports linking HYDROCORTISONE ACETATE to OFF LABEL USE. This represents approximately 3.4% of all 298,939 adverse event reports for this drug.
Patients taking HYDROCORTISONE ACETATE 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 ACETATE 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 ACETATE:
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 10,132 FDA reports for HYDROCORTISONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 3.4% of all adverse event reports for HYDROCORTISONE ACETATE, making it one of the most commonly reported side effect.
If you experience off label use while taking HYDROCORTISONE ACETATE, 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.