653 reports of this reaction
4.3% of all GLECAPREVIR AND PIBRENTASVIR reports
#4 most reported adverse reaction
PRURITUS is the #4 most commonly reported adverse reaction for GLECAPREVIR AND PIBRENTASVIR, manufactured by AbbVie Inc.. There are 653 FDA adverse event reports linking GLECAPREVIR AND PIBRENTASVIR to PRURITUS. This represents approximately 4.3% of all 15,159 adverse event reports for this drug.
Patients taking GLECAPREVIR AND PIBRENTASVIR who experience pruritus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRURITUS is moderately reported among GLECAPREVIR AND PIBRENTASVIR users, representing a notable but not dominant share of adverse events.
In addition to pruritus, the following adverse reactions have been reported for GLECAPREVIR AND PIBRENTASVIR:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 653 FDA reports for GLECAPREVIR AND PIBRENTASVIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 4.3% of all adverse event reports for GLECAPREVIR AND PIBRENTASVIR, making it a notable side effect.
If you experience pruritus while taking GLECAPREVIR AND PIBRENTASVIR, 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.