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Raptiva Psoriasis Drug PML Brain Infection Deaths

FDA Issues Public Health Advisory

The U.S. Food and Drug Administration (FDA) has issued a public health advisory concerning 3 confirmed, and 1 possible report of progressive multifocal leukoencephalopathy (PML), a rare brain infection, in patients using the psoriasis drug Raptiva (efalizumab). Three of those patients have died. All 4 patients were treated with the drug for more than 3 years. None of the patients were receiving other treatments that suppress the immune system.

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Raptiva Brain Infection

PsoriasisRaptiva is a once-weekly injection approved for adults with moderate to severe plaque psoriasis who are candidates for systemic (whole body) therapy or phototherapy.

PML is caused by a virus that affects the central nervous system. PML usually occurs in people whose immune systems have been severely weakened. It leads to an irreversible decline in neurologic function and death. Symptoms may include unusual weakness, loss of coordination, changes in vision, difficulty speaking and personality changes. There is no known effective prevention or treatment.

The FDA strongly recommends that health care professionals carefully monitor patients on Raptiva, as well as those who have discontinued the drug, for any signs or symptoms of neurologic disease, and that they periodically reassess the benefits of continued treatment. Patients should be aware of the symptoms of PML and contact their health care professionals immediately if they experience any such symptoms.


Raptiva PML Brain Infection Legal Help

If you or a loved one has suffered or is suffering adverse health effects such as PML from using this drug, please click the link below and your complaint will be sent to a lawyer who may evaluate your claim at no cost or obligation.

Last updated on Jun-17-09

RAPTIVA BRAIN INFECTION ARTICLES AND INTERVIEWS

Why Raptiva was Withdrawn
Why Raptiva was Withdrawn Daly City, CA: After getting FDA approval in 2003, Raptiva was used to treat about 46,000 patients worldwide. In April, Genentech's immunosuppressant for psoriasis was withdrawn from the market after it was associated with progressive multifocal leukoencephalitis (PML)—a rare brain disease. So far only three cases have been associated with the drug, but PML is often undiagnosed or misdiagnosed. And given the amount of patients prescribed Raptiva, the drug may be withdrawn but we likely haven't heard the last of it…

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Raptiva PML: Brains Appear Eaten Away
Raptiva PML: Brains Appear Eaten Away Chicago, IL: In less than two weeks Raptiva will no longer be available in the United States, and doctors for weeks have been instructed not to start new patients on the psoriasis drug due to concern over Raptiva side effects and Raptiva PML [READ MORE]

Raptiva Cause for Concern
Raptiva Cause for Concern Memphis, TN: Gloria was prescribed Raptiva for severe psoriasis and she says it worked "like a charm". She stayed on it for about 4 years, until she developed troubling side effects. Gloria has been a registered nurse for over 30 years—right away she thought these symptoms were associated with Raptiva.
[READ MORE]


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