3,723 reports of this reaction
1.8% of all PALBOCICLIB reports
#9 most reported adverse reaction
ASTHENIA is the #9 most commonly reported adverse reaction for PALBOCICLIB, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 3,723 FDA adverse event reports linking PALBOCICLIB to ASTHENIA. This represents approximately 1.8% of all 205,909 adverse event reports for this drug.
PALBOCICLIB has an overall safety score of 78 out of 100. Patients taking PALBOCICLIB who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHENIA is a less commonly reported adverse event for PALBOCICLIB, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for PALBOCICLIB:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 3,723 FDA reports for PALBOCICLIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 1.8% of all adverse event reports for PALBOCICLIB, making it a notable side effect.
If you experience asthenia while taking PALBOCICLIB, 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.