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Raptiva Brain Infection Legal News Articles & Interviews

Raptiva Lawsuits Cause of Controversy

Raptiva Lawsuits Cause of Controversy January 10, 2013. By Heidi Turner.
Oakland, CARaptiva lawsuits, alleging patients suffered serious harm and life-threatening Raptiva side effects, caused some controversy in 2012, when a plaintiff's lawyer erroneously announced a Raptiva lawsuit had been settled. The lawsuit, alleging one patient developed so-called Raptiva PML (progressive multifocal leukoencephalopathy), was initially scheduled for court in January but was later pushed back to June.
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Raptiva Pulled from Market Due to Concerns About Side Effects

Raptiva Pulled from Market Due to Concerns About Side Effects December 17, 2012. By Heidi Turner.
San Antonio, TX It has been more than three years since Raptiva was voluntarily withdrawn from the market due to concerns about serious Raptiva side effects. Specifically, the drug was pulled after reports surfaced of a reported increased risk of Raptiva PML (progressive multifocal leukoencephalopathy), a rare progressive neurologic disease that is often fatal. Even though Raptiva was pulled from the market three years ago, lawsuits were scheduled to go to court in 2012.
Read [ Raptiva Pulled from Market Due to Concerns About Side Effects ]

Why Raptiva was Withdrawn

Why Raptiva was Withdrawn June 8, 2009. By Jane Mundy.
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 In April, Genentech's immunosuppressant for psoriasis was withdrawn from the market after it was associated with progressive multifocal leukoencephalitis (PML)—a rare brain disease.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 And given the amount of patients prescribed Raptiva, the drug may be withdrawn but we likely haven't heard the last of it…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 May 28, 2009. By Gordon Gibb.
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 [ Raptiva PML: Brains Appear Eaten Away ]

Raptiva Cause for Concern

Raptiva Cause for Concern May 18, 2009. By Jane Mundy.
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 [ Raptiva Cause for Concern ]

Concerns after Raptiva Withdrawal

Concerns after Raptiva Withdrawal May 6, 2009. By Jane Mundy.
McComb Township, MI Withdrawing Raptiva from the market due to the possible risk of developing progressive multifocal leukoencephalopathy (PML) has left many psoriasis sufferers anxious and concerned. Some users of this psoriasis drug have been taking it for several years and are just now finding out that they might be at risk. Scott F. has unexplainable symptoms and he wonders if they are Raptiva side effects. "When I read about this brain disease it really scared me," says Scott.
Read [ Concerns after Raptiva Withdrawal ]

The Real Impact of FDA Raptiva Removal

The Real Impact of FDA Raptiva Removal April 27, 2009. By Gordon Gibb.
Washington, DC The recent decision to suspend Raptiva by its manufacturer due to concerns over Raptiva and PML (progressive multifocal leukoencephalopathy) represents a bit of good news for critics who had reservations that Raptiva's risks outweighed the benefits. The US Food and Drug Administration (FDA) has been closely monitoring Raptiva for a while now. However the precursor to Raptiva FDA removal from the US market is Health Canada, which ordered the suspension of Raptiva in that country in February.
Read [ The Real Impact of FDA Raptiva Removal ]

Raptiva Risks Outweighed Benefits

Raptiva Risks Outweighed Benefits April 14, 2009. By Jane Mundy.
Washington, DC On April 8, 2009 Genentech Inc., the manufacturer of Raptiva (efalizumab) announced it has voluntarily withdrawn its psoriasis drug from the US market. The decision is based on the association of Raptiva and PML or progressive multifocal leukoencephalopathy, a rare and usually fatal disease of the central nervous system. Sadly, the withdrawal was not soon enough for three patients who have died from PML after taking Raptiva for more than three years. Another patient treated with Raptiva developed progressive neurologic symptoms and died of unknown cause.
Read [ Raptiva Risks Outweighed Benefits ]

Raptiva Joins List of Drugs with Deadly Side Effects

Raptiva Joins List of Drugs with Deadly Side Effects April 2, 2009. By Heidi Turner.
Baton Rouge, LA If you have been taking Raptiva for psoriasis, you can be forgiven if you are a bit hesitant the next time you have your injection. After all, the link between Raptiva and PML, Progressive Multifocal Leukoencephalopathy, is a scary one. Most people would probably think twice before using a medication that can cause brain infections. Although the FDA has taken some action against Raptiva, it has allowed the drug to stay on the market, leaving some critics wondering why, especially when there are other treatments available for psoriasis.
Read [ Raptiva Joins List of Drugs with Deadly Side Effects ]

Psoriasis Drug Raptiva Suspended in Other Countries. Not in US.

Psoriasis Drug Raptiva Suspended in Other Countries. Not in US. March 26, 2009. By Gordon Gibb.
Washington, DC Canada is the latest country to bring the hammer down on the use of Raptiva after the psoriasis drug had been linked to 3 confirmed and one suspected case of progressive multifocal leukoencephalopathy (PML), a neurological condition that can result in reduced brain function and ultimately, death.
Read [ Psoriasis Drug Raptiva Suspended in Other Countries. Not in US. ]


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