2,129 reports of this reaction
2.5% of all FULVESTRANT reports
#7 most reported adverse reaction
NEOPLASM PROGRESSION is the #7 most commonly reported adverse reaction for FULVESTRANT, manufactured by AstraZeneca Pharmaceuticals LP. There are 2,129 FDA adverse event reports linking FULVESTRANT to NEOPLASM PROGRESSION. This represents approximately 2.5% of all 86,552 adverse event reports for this drug.
Patients taking FULVESTRANT who experience neoplasm progression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NEOPLASM PROGRESSION is a less commonly reported adverse event for FULVESTRANT, but still significant enough to appear in the safety profile.
In addition to neoplasm progression, the following adverse reactions have been reported for FULVESTRANT:
The following drugs have also been linked to neoplasm progression in FDA adverse event reports:
NEOPLASM PROGRESSION has been reported as an adverse event in 2,129 FDA reports for FULVESTRANT. This does not prove causation, but indicates an association observed in post-market surveillance data.
NEOPLASM PROGRESSION accounts for approximately 2.5% of all adverse event reports for FULVESTRANT, making it a notable side effect.
If you experience neoplasm progression while taking FULVESTRANT, 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.