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Raptiva Dear Patient Letter  

April 8, 2009

Dear RAPTIVA Patient,

Re: VOLUNTARY U.S. MARKET WITHDRAWAL OF RAPTIVA® (efalizumab)

Patient safety is a top priority for Genentech. Since September 2008, Genentech has received 3 reports of progressive multifocal leukoencephalopathy (PML), a serious and almost always fatal brain infection caused by a virus, in patients taking RAPTIVA (efalizumab). Because of the following key aspects of PML and our commitment to safety, Genentech has decided to voluntarily stop selling RAPTIVA.

  • Although we believe that there are many psoriasis patients who benefit from RAPTIVA, there is no way to know ahead of time who will get PML.
  • There is no treatment or cure for PML. People who do live with PML are severely disabled.

What You Need to Do

  • Do not stop your RAPTIVA treatment without first talking to your doctor. Stopping RAPTIVA may lead to serious side effects, such as severe worsening of your psoriasis and, in some cases, has led to hospitalization.
  • Call or make an appointment to discuss other psoriasis treatment options with your doctor as soon as possible. Pharmacies will only refill prescriptions until Monday June 8, 2009. It is important that you have enough time to plan a change to another treatment before stopping RAPTIVA.
  • For the limited amount of time that you may still be taking RAPTIVA, it is important that you read the Medication Guide that comes with your medication. Before each injection, read the Medication Guide, which explains serious side effects of RAPTIVA. You should discuss these side effects with your doctor.

A copy of the RAPTIVA US Prescribing Information and Medication Guide are included with this letter. This information does not take the place of talking with your doctor about your condition or treatment. Please speak to your doctor about any questions or concerns you may have. Additional information may be periodically available at www.raptiva.com.

Thank you for your prompt attention to this letter.

Sincerely,

Hal Barron, M.D., FACC Senior Vice President, Development Chief Medical Officer Genentech, Inc.

Source: FDA

See: Raptiva Dear Doctor / Dear Physician Letter

Raptiva Lawsuit Case Review:

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Raptiva / efalizumab recalled by FDA Raptiva Recall News about Get latest Raptiva PML side effects warnings and RaptivaLawsuit Update. Raptiva increases the risk of life-threatening infections, including bacterial sepsis, viral meningitis, invasive fungal disease, and progressive multifocal leukoencephalopathy (PML). PML is a viral disease that causes irreversible brain damage and death. Raptiva was on the market for 5 years before the public was warned about these risks. Talk to a Raptiva Lawyer or Raptiva Attorney to File a Raptiva Lawsuit & Raptiva Class Action Lawsuit. Raptiva or efalizumab has been reported to cause serious rare brain infections, PML and other raptiva side effects, progressive multifocal leukoencephalopathy (pml) Talk to a raptivalawyer about a raptivalawsuit today.

Raptiva Recall Announced by FDA on April 8, 2009

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Raptiva recalled by FDA due to serious Raptiva related injuries. Talk to a Raptiva lawyer about filing a raptiva lawsuit if you took raptiva and have been diagnosed with PML, meningitis, encephalitis, a Lymphoma, Hodgkin's Disease, Rebound or worse Psoriasis, severe psoriasis, death, paralysis, resulting in disability (after cessation of Raptiva usage) or Serious infections (bacterial or viral)resulting in hospitalization.Talk to us about the pros and cons of a raptiva class action lawsuit. Get Raptiva drug information update for any victim of raptiva.

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