18,216 reports of this reaction
3.3% of all LENALIDOMIDE reports
#5 most reported adverse reaction
OFF LABEL USE is the #5 most commonly reported adverse reaction for LENALIDOMIDE, manufactured by Celgene Corporation. There are 18,216 FDA adverse event reports linking LENALIDOMIDE to OFF LABEL USE. This represents approximately 3.3% of all 557,894 adverse event reports for this drug.
Patients taking LENALIDOMIDE 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 LENALIDOMIDE 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 LENALIDOMIDE:
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 18,216 FDA reports for LENALIDOMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 3.3% of all adverse event reports for LENALIDOMIDE, making it a notable side effect.
If you experience off label use while taking LENALIDOMIDE, 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.