19,928 reports of this reaction
7.2% of all DENOSUMAB reports
#2 most reported adverse reaction
DEATH is the #2 most commonly reported adverse reaction for DENOSUMAB, manufactured by Amgen, Inc. There are 19,928 FDA adverse event reports linking DENOSUMAB to DEATH. This represents approximately 7.2% of all 278,448 adverse event reports for this drug.
Patients taking DENOSUMAB 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 DENOSUMAB users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for DENOSUMAB:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 19,928 FDA reports for DENOSUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 7.2% of all adverse event reports for DENOSUMAB, making it one of the most commonly reported side effect.
If you experience death while taking DENOSUMAB, 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.