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Talk to a Raptiva Injury Lawyer 

Raptiva was recalled on April 8. 2009 Genentech and FDA notified healthcare professionals of the voluntary, phased withdrawal of Raptiva, a medication for treatment of psoriasis, from the U.S. market due to a potential risk to patients of developing progressive multifocal leukoencephalopathy (PML). Other Raptiva patients have suffered from rare viral miningitis and rare brain infections.

If you have been diagnosed with progressive multifocal leukoencephalopathy (PML), viral miningitis or other rare brain infections, please fill out the Raptiva Lawsuit Evaluation form below or call and talk to a Board Certified Trial Lawyer with more than 25+ years of product liability and trial experience. Currently we are representing a number of Raptiva clients throughout the nation and understand the nature of the problem and the liability issues that Genetech faces in these Raptiva injury lawsuits.

Raptiva Lawsuit Evaluation

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Full Name:
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Name of Raptiva User
Age of Raptiva patient:
How long have you suffered from psoriasis:
Date of Diagnosis of a Raptiva Injury:
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What have you been diagnosed with:
Progressive multifocal leukoencephalopathy (PML)
Viral Meningitis
Sepsis
Brain Infection (unknown type)
Invasive Fungal Disease
Other injuries or infections
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Please describe in detail the facts surrounding the injury or any questions you may have:
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NOTE: Submitting this form does not create an attorney client relationship.

 

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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