630 reports of this reaction
2.4% of all BREXPIPRAZOLE reports
#6 most reported adverse reaction
TREMOR is the #6 most commonly reported adverse reaction for BREXPIPRAZOLE, manufactured by Otsuka America Pharmaceutical, Inc.. There are 630 FDA adverse event reports linking BREXPIPRAZOLE to TREMOR. This represents approximately 2.4% of all 26,345 adverse event reports for this drug.
Patients taking BREXPIPRAZOLE who experience tremor should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
TREMOR is a less commonly reported adverse event for BREXPIPRAZOLE, but still significant enough to appear in the safety profile.
In addition to tremor, the following adverse reactions have been reported for BREXPIPRAZOLE:
The following drugs have also been linked to tremor in FDA adverse event reports:
TREMOR has been reported as an adverse event in 630 FDA reports for BREXPIPRAZOLE. This does not prove causation, but indicates an association observed in post-market surveillance data.
TREMOR accounts for approximately 2.4% of all adverse event reports for BREXPIPRAZOLE, making it a notable side effect.
If you experience tremor while taking BREXPIPRAZOLE, 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.