403 reports of this reaction
3.6% of all DEUTETRABENAZINE reports
#3 most reported adverse reaction
DYSKINESIA is the #3 most commonly reported adverse reaction for DEUTETRABENAZINE, manufactured by Teva Neuroscience, Inc.. There are 403 FDA adverse event reports linking DEUTETRABENAZINE to DYSKINESIA. This represents approximately 3.6% of all 11,218 adverse event reports for this drug.
Patients taking DEUTETRABENAZINE who experience dyskinesia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSKINESIA is moderately reported among DEUTETRABENAZINE users, representing a notable but not dominant share of adverse events.
In addition to dyskinesia, the following adverse reactions have been reported for DEUTETRABENAZINE:
The following drugs have also been linked to dyskinesia in FDA adverse event reports:
DYSKINESIA has been reported as an adverse event in 403 FDA reports for DEUTETRABENAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSKINESIA accounts for approximately 3.6% of all adverse event reports for DEUTETRABENAZINE, making it one of the most commonly reported side effect.
If you experience dyskinesia while taking DEUTETRABENAZINE, 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.