1,512 reports of this reaction
1.8% of all RIBOCICLIB reports
#11 most reported adverse reaction
DYSPNOEA is the #11 most commonly reported adverse reaction for RIBOCICLIB, manufactured by Novartis Pharmaceuticals Corporation. There are 1,512 FDA adverse event reports linking RIBOCICLIB to DYSPNOEA. This represents approximately 1.8% 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 dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSPNOEA is a less commonly reported adverse event for RIBOCICLIB, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for RIBOCICLIB:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 1,512 FDA reports for RIBOCICLIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 1.8% of all adverse event reports for RIBOCICLIB, making it a notable side effect.
If you experience dyspnoea 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.