1,027 reports of this reaction
4.4% of all RASAGILINE MESYLATE reports
#1 most reported adverse reaction
FALL is the #1 most commonly reported adverse reaction for RASAGILINE MESYLATE, manufactured by Teva Neuroscience, Inc.. There are 1,027 FDA adverse event reports linking RASAGILINE MESYLATE to FALL. This represents approximately 4.4% of all 23,100 adverse event reports for this drug.
Patients taking RASAGILINE MESYLATE who experience fall should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FALL is moderately reported among RASAGILINE MESYLATE users, representing a notable but not dominant share of adverse events.
In addition to fall, the following adverse reactions have been reported for RASAGILINE MESYLATE:
The following drugs have also been linked to fall in FDA adverse event reports:
FALL has been reported as an adverse event in 1,027 FDA reports for RASAGILINE MESYLATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FALL accounts for approximately 4.4% of all adverse event reports for RASAGILINE MESYLATE, making it one of the most commonly reported side effect.
If you experience fall while taking RASAGILINE MESYLATE, 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.