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Rheumatology
Dermatology
06G-64C-Q352-3

The convenience of every-other-week dosing for moderate-to-severe rheumatoid arthritis,psoriatic arthritis, and ankylosing spondylitis 

Now with the ease of the HUMIRA® Pen

Delivery Made Easy - Humira Pen

HUMIRA provides every-other-week, at-home dosing1

  • The recommended dose of HUMIRA is 40 mg eow, administered by subcutaneous injection
    Dosing patients can start with and stay with
  • HUMIRA offers the convenience and independence of at-home, easy-to-administer prefilled syringes
  • myHUMIRA 1-800-4HUMIRA
    For questions about injecting HUMIRA
    To inquire about self-injection training for HUMIRA patients


Humira Pen - 40mg every other week


HUMIRA, Enbrel® (etanercept), and Remicade® (infliximab) dosing regimens for RA, PsA, and AS

HUMIRA1 Enbrel2 Remicade3
Administration Self-injection Self-injection In-office infusion
Dosing frequency Every other week* Once a week At 0, 2, and 6 weeks, then every 8 weeks
Yearly doses 26 52 8

*
Some patients with moderate-to-severe RA not receiving MTX may benefit from increasing the frequency to 40 mg every week.
Doses during the first year.
Enbrel is a registered trademark of Amgen and Wyeth Pharmaceuticals. Remicade is a registered trademark of Centocor, Inc.

This presentation pertains solely to product convenience, and not to safety or efficacy.


06G-64C-Q352-10

HUMIRA is indicated for reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage and improving physical function in adult patients with moderately to severely active rheumatoid arthritis. HUMIRA is indicated for reducing signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis in patients 4 years of age and older. HUMIRA can be used alone or in combination with methotrexate. HUMIRA is indicated for reducing signs and symptoms of active arthritis, inhibiting the progression of structural damage and improving physical function in adult patients with psoriatic arthritis. HUMIRA is indicated for reducing signs and symptoms in adult patients with active ankylosing spondylitis. HUMIRA is indicated for reducing signs and symptoms and inducing and maintaining clinical remission in adult patients with moderately to severely active Crohn's disease who have had an inadequate response to conventional therapy, and reducing signs and symptoms and inducing clinical remission in these patients if they have also lost response to or are intolerant to infliximab. HUMIRA is indicated for the treatment of adult patients with moderate to severe chronic plaque psoriasis who are candidates for systemic therapy or phototherapy, and when other systemic therapies are medically less appropriate. HUMIRA should only be administered to patients who will be closely monitored and have regular follow-up visits with a physician.

Please see Important Safety Information. Serious and sometimes fatal side effects have been reported with HUMIRA, including tuberculosis and other serious infections.

Please see full prescribing information.

References: 1. HUMIRA full prescribing information. 2. Enbrel full prescribing information. 3. Remicade full prescribing information.

Legal Notices/Privacy Policy. Copyright 2007, Abbott Laboratories, Abbott Park, Illinois, U.S.A. If you have any questions about Abbott's HUMIRA.com Web site that have not been answered click here. This Web site and the information contained herein is intended for use by US residents only, is provided for informational purposes only and is not intended to replace a discussion with a healthcare provider. All decisions regarding patient care must be made with a healthcare provider and consider the unique characteristics of each patient.

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