22,090 reports of this reaction
1.6% of all ETANERCEPT reports
#14 most reported adverse reaction
INJECTION SITE PRURITUS is the #14 most commonly reported adverse reaction for ETANERCEPT, manufactured by Immunex Corporation. There are 22,090 FDA adverse event reports linking ETANERCEPT to INJECTION SITE PRURITUS. This represents approximately 1.6% of all 1,356,881 adverse event reports for this drug.
Patients taking ETANERCEPT who experience injection site 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.
INJECTION SITE PRURITUS is a less commonly reported adverse event for ETANERCEPT, but still significant enough to appear in the safety profile.
In addition to injection site pruritus, the following adverse reactions have been reported for ETANERCEPT:
The following drugs have also been linked to injection site pruritus in FDA adverse event reports:
INJECTION SITE PRURITUS has been reported as an adverse event in 22,090 FDA reports for ETANERCEPT. This does not prove causation, but indicates an association observed in post-market surveillance data.
INJECTION SITE PRURITUS accounts for approximately 1.6% of all adverse event reports for ETANERCEPT, making it a notable side effect.
If you experience injection site pruritus while taking ETANERCEPT, 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.