498 reports of this reaction
1.4% of all ABEMACICLIB reports
#16 most reported adverse reaction
DEHYDRATION is the #16 most commonly reported adverse reaction for ABEMACICLIB, manufactured by Eli Lilly and Company. There are 498 FDA adverse event reports linking ABEMACICLIB to DEHYDRATION. This represents approximately 1.4% of all 35,479 adverse event reports for this drug.
Patients taking ABEMACICLIB who experience dehydration should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEHYDRATION is a less commonly reported adverse event for ABEMACICLIB, but still significant enough to appear in the safety profile.
In addition to dehydration, the following adverse reactions have been reported for ABEMACICLIB:
The following drugs have also been linked to dehydration in FDA adverse event reports:
DEHYDRATION has been reported as an adverse event in 498 FDA reports for ABEMACICLIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEHYDRATION accounts for approximately 1.4% of all adverse event reports for ABEMACICLIB, making it a notable side effect.
If you experience dehydration while taking ABEMACICLIB, 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.