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Home : Unsafe Drugs : Humira

Humira

Humira (Adalimumab) is an immunosuppresant, approved by the FDA for the treatment of Crohn's Disease, rheumatoid arthritis, and juvenile arthritis. It is administered through a subcutaneous injection.

The most common side effects of Humira are dry cough, fever, weight loss, fever with chills, body aches, flu symptoms. Patients taking Humira are at increased risk for serious adverse effects, including serious infections that can lead to hospitalization or death. Because Humira affects the immune system, it can lower the body's ability to fight infections, such as tuberculosis and other opportunistic infections. Humira is a blocker of TNF (tumor necrosis factor) and may cause lymphomas (a form of cancer) and other malignancies.

Recently, Humira was given a Black Box Label Warning by the FDA. The Black Box Warning is the strongest warning label a drug can have applied to it. Drugs that carry a high risk of serious side effects or potentially deadly adverse reactions are given this warning. This label is given only after medical studies have indicated that there are serious risks associated with the side effects of the medication.

Fast Facts

Name: Humira
Generic: Adalimumab
Manufacturer: Abbott Laboratories
Date approved: 2002
Status: Prescription Only - Black Box Warning Label
Approved uses: Treatment of rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, moderate to severe chronic psoriasis and juvenile idiopathic arthritis.
Off-Label uses: None
Side effects: Feeling short of breath, even with mild exertion; swelling of your ankles or feet; red, purple, or scaly skin rash, hair loss, joint or muscle pain, mouth sores; confusion, seizure (convulsions); pain or burning when you urinate; numbness or tingly feeling, weakness in your legs; or jaundice (yellowing of the skin or eyes). Potentially Deadly Serious Fungal Infection has been reported recently by the FDA.
Related topics: Cimzia, Enbrel, Remicade
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FDA Announces Black Box Label Warning for Humira

In early September, 2008, the FDA announced it would require stronger warnings for four medications commonly used in the treatment of rheumatoid arthritis. The warning label is known as the... read more

View the Humira Main Articles page here

FDA Information Related to Humira

February 2007 Monthly Safety Labeling

FDA Approves New Treatment For Crohn's Disease

View the Humira FDA Information page here

MSN Newsfeeds Related to Humira

Enhanze Technology Clinical Trial Demonstrated Improved Absorption

Halozyme Therapeutics Reports Positive Results For Enhanze Technology ...

View the Humira MSN Newsfeeds page here

News Articles Related to Humira

DIREVO announces validation of bestMab(TM)

News and Press release service TransWorldNews

View the Humira News Articles page here

Wikipedia Entries Related to Humira

Adalimumab

Monoclonal antibodies

View the Humira Wikipedia Entries page here

Books Related to Humira

Famvir, Humira.(NEW & APPROVED)(drug licensing)(drug overview): An article from: Family Practice News

Biologic therapy for psoriasis: an update on the tumor necrosis factor inhibitors infliximab, etanercept, and adalimumab, and the T-Cell-targeted therapies ... from: Journal of Drugs in Dermatology

View the Humira Books page here

Want to contact a Washington, DC Humira attorney? ...Get a free case evaluation from one of our Washington, DC Humira attorneys now.

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