PRURITUS is the #1 most commonly reported adverse reaction for Dupixent, manufactured by Sanofi-Aventis U.S. LLC. There are 52,379 FDA adverse event reports linking Dupixent to PRURITUS. This represents approximately 6.2% of all 838,442 adverse event reports for this drug.
Patients taking Dupixent 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
PRURITUS52,379 of 838,442 reports
PRURITUS is moderately reported among Dupixent users, representing a notable but not dominant share of adverse events.
Other Side Effects of Dupixent
In addition to pruritus, the following adverse reactions have been reported for Dupixent:
PRURITUS has been reported as an adverse event in 52,379 FDA reports for Dupixent. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is PRURITUS with Dupixent?
PRURITUS accounts for approximately 6.2% of all adverse event reports for Dupixent, making it one of the most commonly reported side effect.
What should I do if I experience PRURITUS while taking Dupixent?
If you experience pruritus while taking Dupixent, 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.