2,430 reports of this reaction
2.8% of all RIBOCICLIB reports
#5 most reported adverse reaction
DEATH is the #5 most commonly reported adverse reaction for RIBOCICLIB, manufactured by Novartis Pharmaceuticals Corporation. There are 2,430 FDA adverse event reports linking RIBOCICLIB to DEATH. This represents approximately 2.8% of all 86,238 adverse event reports for this drug.
RIBOCICLIB has an overall safety score of 85 out of 100. Patients taking RIBOCICLIB 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 a less commonly reported adverse event for RIBOCICLIB, but still significant enough to appear in the safety profile.
In addition to death, the following adverse reactions have been reported for RIBOCICLIB:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 2,430 FDA reports for RIBOCICLIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 2.8% of all adverse event reports for RIBOCICLIB, making it a notable side effect.
If you experience death while taking RIBOCICLIB, 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.