490 reports of this reaction
2.8% of all DRONABINOL reports
#6 most reported adverse reaction
OFF LABEL USE is the #6 most commonly reported adverse reaction for DRONABINOL, manufactured by ThePharmaNetwork, LLC. There are 490 FDA adverse event reports linking DRONABINOL to OFF LABEL USE. This represents approximately 2.8% of all 17,794 adverse event reports for this drug.
Patients taking DRONABINOL 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 a less commonly reported adverse event for DRONABINOL, but still significant enough to appear in the safety profile.
In addition to off label use, the following adverse reactions have been reported for DRONABINOL:
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 490 FDA reports for DRONABINOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 2.8% of all adverse event reports for DRONABINOL, making it a notable side effect.
If you experience off label use while taking DRONABINOL, 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.