Enbrel and INJECTION SITE REACTION

20,886 reports of this reaction

1.5% of all Enbrel reports

#15 most reported adverse reaction

Overview

INJECTION SITE REACTION is the #15 most commonly reported adverse reaction for Enbrel, manufactured by Immunex Corporation. There are 20,886 FDA adverse event reports linking Enbrel to INJECTION SITE REACTION. This represents approximately 1.5% of all 1,364,746 adverse event reports for this drug.

Patients taking Enbrel 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.

Reporting Frequency

INJECTION SITE REACTION20,886 of 1,364,746 reports

INJECTION SITE REACTION is a less commonly reported adverse event for Enbrel, but still significant enough to appear in the safety profile.

Other Side Effects of Enbrel

In addition to injection site reaction, the following adverse reactions have been reported for Enbrel:

Other Drugs Associated with INJECTION SITE REACTION

The following drugs have also been linked to injection site reaction in FDA adverse event reports:

ASFOTASE ALFABUPRENORPHINE AND NALOXONEETANERCEPTGALCANEZUMAB GNLMGLATIRAMER ACETATEINTERFERON BETA 1BIXEKIZUMABNALTREXONENITROGENPEGVALIASE PQPZTaltz

Frequently Asked Questions

Does Enbrel cause INJECTION SITE REACTION?

INJECTION SITE REACTION has been reported as an adverse event in 20,886 FDA reports for Enbrel. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is INJECTION SITE REACTION with Enbrel?

INJECTION SITE REACTION accounts for approximately 1.5% of all adverse event reports for Enbrel, making it a notable side effect.

What should I do if I experience INJECTION SITE REACTION while taking Enbrel?

If you experience injection site reaction while taking Enbrel, 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.