Humira (adalimumab)

JANUARY 01, 2006

Abbott Laboratories (Chicago, Ill) recently received FDA approval of Humira for reducing the signs and symptoms of active arthritis in patients with psoriatic arthritis. The product is also indicated for reducing the signs and symptoms, including major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderate-to-severe active rheumatoid arthritis. The recommended dosage regimen for Humira for adult patients with rheumatoid arthritis or psoriatic arthritis is 40 mg administered every other week as a subcutaneous injection. The product is supplied in single- use, 1-mL prefilled glass syringes as a sterile, preservative-free solution for subcutaneous administration. For more information, visit www.humira.com.



SHARE THIS SHARE THIS
0

Conference Coverage

Check back here regularly for live conference coverage from the American Academy of Pain Medicine and the upcoming American Pharmacists Association Meeting and Expo. 


Pharmacy Times Strategic Alliance
 

Pharmacist Education
Clinical features with downloadable PDFs


Next-Generation Pharmacist® Awards


3rd Annual Convenient Healthcare and Pharmacy Collaborative Conference


SIGN UP FOR THE PHARMACY TIMES NEWSLETTER
Personalize the information you receive by selecting targeted content and special offers.