907 reports of this reaction
3.2% of all ROTIGOTINE reports
#4 most reported adverse reaction
DEATH is the #4 most commonly reported adverse reaction for ROTIGOTINE, manufactured by UCB, Inc.. There are 907 FDA adverse event reports linking ROTIGOTINE to DEATH. This represents approximately 3.2% of all 28,260 adverse event reports for this drug.
Patients taking ROTIGOTINE who experience death should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEATH is moderately reported among ROTIGOTINE users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for ROTIGOTINE:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 907 FDA reports for ROTIGOTINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 3.2% of all adverse event reports for ROTIGOTINE, making it a notable side effect.
If you experience death while taking ROTIGOTINE, 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.