4,048 reports of this reaction
7.1% of all ATEZOLIZUMAB reports
#1 most reported adverse reaction
DEATH is the #1 most commonly reported adverse reaction for ATEZOLIZUMAB, manufactured by Genentech, Inc.. There are 4,048 FDA adverse event reports linking ATEZOLIZUMAB to DEATH. This represents approximately 7.1% of all 56,768 adverse event reports for this drug.
Patients taking ATEZOLIZUMAB 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 ATEZOLIZUMAB users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for ATEZOLIZUMAB:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 4,048 FDA reports for ATEZOLIZUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 7.1% of all adverse event reports for ATEZOLIZUMAB, making it one of the most commonly reported side effect.
If you experience death while taking ATEZOLIZUMAB, 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.