WebMD Medical News
Louise Chang, MD
(Editor's note: On April 8, 2009, Genentech announced it was voluntarily pulling Raptiva from the market.)
Oct. 16, 2008 -- The psoriasis drug Raptiva is getting a "black box" warning, the FDA's sternest warning, about the risk of life-threatening infections including a rare brain infection and meningitis.
The FDA announced that news today. Raptiva's warning will highlight the risk of opportunistic infections including:
Raptiva is given by injection once a week to treat moderate to severe plaque psoriasis in adults who are candidates for systemic (whole body) therapy or phototherapy (light therapy) to control their psoriasis. Raptiva works by suppressing the immune system to reduce psoriasis flare-ups, but suppressing the immune system can raise the risk of serious infections and malignancies.
Raptiva's label will also be updated to include data from studies done on young mice that show a potential risk for permanent suppression of the immune system when given repeatedly in this age group, which the FDA says is equivalent to children up to 14 years old. Raptiva isn't approved for use in children younger than 18.
The FDA ordered Raptiva's "black box" warning and other label changes after receiving reports of serious infections in some patients taking Raptiva, notes Janet Woodcock, MD, director of the FDA's Center for Drug Evaluation and Research, in a news release.
But the FDA acknowledges that those reports, which include one case of PML, don't prove that Raptiva caused any illnesses.
The FDA isn't telling patients to stop taking Raptiva.
"Doctors and other prescribers should carefully evaluate and weigh the risk/benefit profile of Raptiva for patients who would be more susceptible to the risks," Woodcock says.
The FDA also urges patients to get up to date on their vaccinations before starting Raptiva, and not to get vaccinations while taking Raptiva, because they may not develop immunity to the vaccination virus.
Patients taking Raptiva should also watch for signs and symptoms of infection, as well as these problems:
The FDA recommends that patients taking Raptiva seek immediate medical attention for those problems.
Genentech, the drug company that makes Raptiva, says it will issue a letter to doctors and other health care providers detailing the label changes. "We feel it's important that patients and doctors are educated about the signs and symptoms of infections and the other information included in the boxed warning," Genentech spokeswoman Krysta Pellegrino tells WebMD.
SOURCES:News release, FDA.Krysta Pellegrino, spokeswoman, Genentech.
Here are the most recent story comments.View All
The views expressed here do not necessarily represent those of CW Arkansas
The Health News section does not provide medical advice, diagnosis or treatment. See additional information.