47 reports of this reaction
3.5% of all SELEGILINE HYDROCHLORIDE reports
#2 most reported adverse reaction
FALL is the #2 most commonly reported adverse reaction for SELEGILINE HYDROCHLORIDE, manufactured by Bausch Health US, LLC. There are 47 FDA adverse event reports linking SELEGILINE HYDROCHLORIDE to FALL. This represents approximately 3.5% of all 1,332 adverse event reports for this drug.
Patients taking SELEGILINE HYDROCHLORIDE 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 SELEGILINE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to fall, the following adverse reactions have been reported for SELEGILINE HYDROCHLORIDE:
The following drugs have also been linked to fall in FDA adverse event reports:
FALL has been reported as an adverse event in 47 FDA reports for SELEGILINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FALL accounts for approximately 3.5% of all adverse event reports for SELEGILINE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience fall while taking SELEGILINE 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.