2,190 reports of this reaction
1.5% of all TRAMADOL HYDROCHLORIDE reports
#10 most reported adverse reaction
OFF LABEL USE is the #10 most commonly reported adverse reaction for TRAMADOL HYDROCHLORIDE, manufactured by Vertical Pharmaceuticals, LLC. There are 2,190 FDA adverse event reports linking TRAMADOL HYDROCHLORIDE to OFF LABEL USE. This represents approximately 1.5% of all 142,038 adverse event reports for this drug.
TRAMADOL HYDROCHLORIDE has an overall safety score of 85 out of 100. Patients taking TRAMADOL HYDROCHLORIDE 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 TRAMADOL HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to off label use, the following adverse reactions have been reported for TRAMADOL HYDROCHLORIDE:
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 2,190 FDA reports for TRAMADOL HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 1.5% of all adverse event reports for TRAMADOL HYDROCHLORIDE, making it a notable side effect.
If you experience off label use while taking TRAMADOL HYDROCHLORIDE, 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.