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Raptiva® warnings are quite extensive. As a treatment for moderate-to-severe plaque psoriasis, this drug (generic name, efalizumab) is not a first-line choice for psoriasis; rather, it is to be prescribed only for individuals with the kind of psoriasis that can't be treated with topical medications.
Genentech USA, Inc., the manufacturer of Raptiva®, states on their Raptiva® website that the company has decided to voluntarily stop selling the Raptiva® drug, and they warn patients that:
“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.”
The reason for the withdrawal of Raptiva® from the U.S. market is a potential side effect of this drug — a debilitating, usually fatal brain infection called progressive multifocal leukoencephalopathy (PML). In October 2008, the FDA required that a new, "black box" warning about the Raptiva®–PML risk be added to the packaging and prescription information for Raptiva®. The withdrawal of Raptiva® is the latest development.
Genentech's Raptiva® website also warns patients and physicians that stopping Raptiva® treatment suddenly can lead to serious side effects. The company advises Raptiva® patients to:
As the Warning text that accompanies Raptiva® notes, there is no medical intervention that can treat PML, the following symptoms of which progress over days to weeks:
PML is nearly always fatal, and individuals who don't die from PML are left severely disabled.
Have you or a loved one been injured after taking Raptiva®? If so, contact us to speak with an experienced Raptiva® attorney who specializes in drug recall litigation & lawsuits. Let us help you win the compensation you need and deserve.