2,253 reports of this reaction
9.8% of all CRIZOTINIB reports
#1 most reported adverse reaction
DEATH is the #1 most commonly reported adverse reaction for CRIZOTINIB, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 2,253 FDA adverse event reports linking CRIZOTINIB to DEATH. This represents approximately 9.8% of all 22,895 adverse event reports for this drug.
Patients taking CRIZOTINIB 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 CRIZOTINIB users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for CRIZOTINIB:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 2,253 FDA reports for CRIZOTINIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 9.8% of all adverse event reports for CRIZOTINIB, making it one of the most commonly reported side effect.
If you experience death while taking CRIZOTINIB, 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.