764 reports of this reaction
3.2% of all VEMURAFENIB reports
#8 most reported adverse reaction
DISEASE PROGRESSION is the #8 most commonly reported adverse reaction for VEMURAFENIB, manufactured by Genentech, Inc.. There are 764 FDA adverse event reports linking VEMURAFENIB to DISEASE PROGRESSION. This represents approximately 3.2% of all 23,551 adverse event reports for this drug.
Patients taking VEMURAFENIB who experience disease 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.
DISEASE PROGRESSION is moderately reported among VEMURAFENIB users, representing a notable but not dominant share of adverse events.
In addition to disease progression, the following adverse reactions have been reported for VEMURAFENIB:
The following drugs have also been linked to disease progression in FDA adverse event reports:
DISEASE PROGRESSION has been reported as an adverse event in 764 FDA reports for VEMURAFENIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DISEASE PROGRESSION accounts for approximately 3.2% of all adverse event reports for VEMURAFENIB, making it a notable side effect.
If you experience disease progression while taking VEMURAFENIB, 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.