9,921 reports of this reaction
9.3% of all PIMAVANSERIN TARTRATE reports
#2 most reported adverse reaction
DEATH is the #2 most commonly reported adverse reaction for PIMAVANSERIN TARTRATE, manufactured by Acadia Pharmaceuticals Inc.. There are 9,921 FDA adverse event reports linking PIMAVANSERIN TARTRATE to DEATH. This represents approximately 9.3% of all 106,130 adverse event reports for this drug.
PIMAVANSERIN TARTRATE has an overall safety score of 85 out of 100. Patients taking PIMAVANSERIN TARTRATE 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 PIMAVANSERIN TARTRATE users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for PIMAVANSERIN TARTRATE:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 9,921 FDA reports for PIMAVANSERIN TARTRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 9.3% of all adverse event reports for PIMAVANSERIN TARTRATE, making it one of the most commonly reported side effect.
If you experience death while taking PIMAVANSERIN TARTRATE, 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.