486 reports of this reaction
1.5% of all EVEROLIMUS TABLETS reports
#16 most reported adverse reaction
METASTASES TO LIVER is the #16 most commonly reported adverse reaction for EVEROLIMUS TABLETS, manufactured by Amneal Pharmaceuticals NY LLC. There are 486 FDA adverse event reports linking EVEROLIMUS TABLETS to METASTASES TO LIVER. This represents approximately 1.5% of all 31,530 adverse event reports for this drug.
Patients taking EVEROLIMUS TABLETS who experience metastases to liver should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
METASTASES TO LIVER is a less commonly reported adverse event for EVEROLIMUS TABLETS, but still significant enough to appear in the safety profile.
In addition to metastases to liver, the following adverse reactions have been reported for EVEROLIMUS TABLETS:
The following drugs have also been linked to metastases to liver in FDA adverse event reports:
METASTASES TO LIVER has been reported as an adverse event in 486 FDA reports for EVEROLIMUS TABLETS. This does not prove causation, but indicates an association observed in post-market surveillance data.
METASTASES TO LIVER accounts for approximately 1.5% of all adverse event reports for EVEROLIMUS TABLETS, making it a notable side effect.
If you experience metastases to liver while taking EVEROLIMUS TABLETS, 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.