740 reports of this reaction
4.3% of all VISMODEGIB reports
#5 most reported adverse reaction
DYSGEUSIA is the #5 most commonly reported adverse reaction for VISMODEGIB, manufactured by Genentech, Inc.. There are 740 FDA adverse event reports linking VISMODEGIB to DYSGEUSIA. This represents approximately 4.3% of all 17,013 adverse event reports for this drug.
Patients taking VISMODEGIB who experience dysgeusia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSGEUSIA is moderately reported among VISMODEGIB users, representing a notable but not dominant share of adverse events.
In addition to dysgeusia, the following adverse reactions have been reported for VISMODEGIB:
The following drugs have also been linked to dysgeusia in FDA adverse event reports:
DYSGEUSIA has been reported as an adverse event in 740 FDA reports for VISMODEGIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSGEUSIA accounts for approximately 4.3% of all adverse event reports for VISMODEGIB, making it a notable side effect.
If you experience dysgeusia while taking VISMODEGIB, 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.