FDA Warns of Risk of Legionella and Listeria with Enbrel and other TNFa blockers

What are you looking for?

Washington, DC: The Food and Drug Administration (FDA) has notified healthcare professionals that the Boxed Warning for the entire class of Tumor Necrosis Factor-alpha (TNFa) blockers including Enbrel (etanercept), Remicade (infliximab), Humira (adalimumab), Cimzia (certolizumab pegol), and Simponi (golimumab), has been updated to include the risk of infection from two bacterial pathogens, Legionella and Listeria.

The class of TNFa blockers are used to treat Crohn's disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, plaque psoriasis, and/or juvenile idiopathic arthritis.

The Boxed Warning and Warnings and Precautions sections of the labels for all of the TNFa blockers have also been revised so that they contain consistent information about the risk for serious infections and the associated disease-causing pathogens.

Patients treated with TNFa blockers are at increased risk for developing serious infections involving multiple organ systems and sites that may lead to hospitalization or death due to bacterial, mycobacterial, fungal, viral, parasitic, and other opportunistic pathogens.

Legal Help

If you or a loved one has suffered illness or an adverse health event in this case, please click the link below and your complaint will be sent to a lawyer who may evaluate your claim at no cost or obligation.

Please click here for a free evaluation of your case

Last updated on Sep-7-11

LEGAL HELP NOW!

Please complete this form to request a review of your complaint by an attorney.

First name:

Last name:

Email address:

Phone number(s):

State:

Zip Code:

Defendant:

Describe your complaint:

Subscribe to our free newsletter

There is absolutely no cost to you to submit this form. Doing so places you under no obligations and does not establish an attorney-client relationship.

Legal Help Now!

CLICK HERE

Related Lawsuits

Legal Services: