1,259 reports of this reaction
7.6% of all PREDNISOLONE ACETATE reports
#1 most reported adverse reaction
TREATMENT FAILURE is the #1 most commonly reported adverse reaction for PREDNISOLONE ACETATE, manufactured by Allergan, Inc.. There are 1,259 FDA adverse event reports linking PREDNISOLONE ACETATE to TREATMENT FAILURE. This represents approximately 7.6% of all 16,640 adverse event reports for this drug.
Patients taking PREDNISOLONE ACETATE who experience treatment failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
TREATMENT FAILURE is moderately reported among PREDNISOLONE ACETATE users, representing a notable but not dominant share of adverse events.
In addition to treatment failure, the following adverse reactions have been reported for PREDNISOLONE ACETATE:
The following drugs have also been linked to treatment failure in FDA adverse event reports:
TREATMENT FAILURE has been reported as an adverse event in 1,259 FDA reports for PREDNISOLONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
TREATMENT FAILURE accounts for approximately 7.6% of all adverse event reports for PREDNISOLONE ACETATE, making it one of the most commonly reported side effect.
If you experience treatment failure while taking PREDNISOLONE 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.