1,071 reports of this reaction
9.3% of all LORLATINIB reports
#1 most reported adverse reaction
DEATH is the #1 most commonly reported adverse reaction for LORLATINIB, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 1,071 FDA adverse event reports linking LORLATINIB to DEATH. This represents approximately 9.3% of all 11,506 adverse event reports for this drug.
Patients taking LORLATINIB 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 LORLATINIB users, representing a notable but not dominant share of adverse events.
In addition to death, the following adverse reactions have been reported for LORLATINIB:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 1,071 FDA reports for LORLATINIB. 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 LORLATINIB, making it one of the most commonly reported side effect.
If you experience death while taking LORLATINIB, 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.