20,861 reports of this reaction
1.5% of all ETANERCEPT reports
#15 most reported adverse reaction
INJECTION SITE REACTION is the #15 most commonly reported adverse reaction for ETANERCEPT, manufactured by Immunex Corporation. There are 20,861 FDA adverse event reports linking ETANERCEPT to INJECTION SITE REACTION. This represents approximately 1.5% of all 1,356,881 adverse event reports for this drug.
Patients taking ETANERCEPT who experience injection site reaction 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 REACTION is a less commonly reported adverse event for ETANERCEPT, but still significant enough to appear in the safety profile.
In addition to injection site reaction, the following adverse reactions have been reported for ETANERCEPT:
The following drugs have also been linked to injection site reaction in FDA adverse event reports:
INJECTION SITE REACTION has been reported as an adverse event in 20,861 FDA reports for ETANERCEPT. This does not prove causation, but indicates an association observed in post-market surveillance data.
INJECTION SITE REACTION accounts for approximately 1.5% of all adverse event reports for ETANERCEPT, making it a notable side effect.
If you experience injection site reaction 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.