242 reports of this reaction
3.5% of all CARBIDOPA reports
#3 most reported adverse reaction
FALL is the #3 most commonly reported adverse reaction for CARBIDOPA, manufactured by Bausch Health US, LLC. There are 242 FDA adverse event reports linking CARBIDOPA to FALL. This represents approximately 3.5% of all 6,903 adverse event reports for this drug.
Patients taking CARBIDOPA 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 CARBIDOPA users, representing a notable but not dominant share of adverse events.
In addition to fall, the following adverse reactions have been reported for CARBIDOPA:
The following drugs have also been linked to fall in FDA adverse event reports:
FALL has been reported as an adverse event in 242 FDA reports for CARBIDOPA. 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 CARBIDOPA, making it one of the most commonly reported side effect.
If you experience fall while taking CARBIDOPA, 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.