7,667 reports of this reaction
6.5% of all ENZALUTAMIDE reports
#2 most reported adverse reaction
DEATH is the #2 most commonly reported adverse reaction for ENZALUTAMIDE, manufactured by Astellas Pharma US, Inc.. There are 7,667 FDA adverse event reports linking ENZALUTAMIDE to DEATH. This represents approximately 6.5% of all 117,902 adverse event reports for this drug.
Patients taking ENZALUTAMIDE 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 ENZALUTAMIDE users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for ENZALUTAMIDE:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 7,667 FDA reports for ENZALUTAMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 6.5% of all adverse event reports for ENZALUTAMIDE, making it one of the most commonly reported side effect.
If you experience death while taking ENZALUTAMIDE, 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.