PRURITUS is the #1 most commonly reported adverse reaction for DUPILUMAB, manufactured by sanofi-aventis U.S. LLC. There are 48,441 FDA adverse event reports linking DUPILUMAB to PRURITUS. This represents approximately 6.2% of all 782,562 adverse event reports for this drug.
Patients taking DUPILUMAB 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.
Reporting Frequency
PRURITUS48,441 of 782,562 reports
PRURITUS is moderately reported among DUPILUMAB users, representing a notable but not dominant share of adverse events.
Other Side Effects of DUPILUMAB
In addition to pruritus, the following adverse reactions have been reported for DUPILUMAB:
PRURITUS has been reported as an adverse event in 48,441 FDA reports for DUPILUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is PRURITUS with DUPILUMAB?
PRURITUS accounts for approximately 6.2% of all adverse event reports for DUPILUMAB, making it one of the most commonly reported side effect.
What should I do if I experience PRURITUS while taking DUPILUMAB?
If you experience pruritus while taking DUPILUMAB, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.