600 reports of this reaction
4.3% of all TRANEXAMIC ACID reports
#1 most reported adverse reaction
OFF LABEL USE is the #1 most commonly reported adverse reaction for TRANEXAMIC ACID, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 600 FDA adverse event reports linking TRANEXAMIC ACID to OFF LABEL USE. This represents approximately 4.3% of all 13,960 adverse event reports for this drug.
Patients taking TRANEXAMIC ACID 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 TRANEXAMIC ACID 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 TRANEXAMIC ACID:
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 600 FDA reports for TRANEXAMIC ACID. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 4.3% of all adverse event reports for TRANEXAMIC ACID, making it one of the most commonly reported side effect.
If you experience off label use while taking TRANEXAMIC ACID, 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.