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Tysabri

Did You Know?

If you have taken Tysabri and you have suffered from brain damage you may be entitled to compensation.

On February 28, 2005, the multiple sclerosis drug Tysabri (previously known as Antegren; generic name: natalizumab) joined the list of more than a dozen high-profile dangerous prescription drugs that have been withdrawn from the market since 1997. Biogen IDEC and Elan, the makers of Tysabri, suspended commercial distribution and advised physicians to stop prescribing the drug. Amazingly, Tysabri was just approved for marketing by the Food and Drug Administration (FDA) in November of 2004. Then, less than four months after approval, Tysabri has been recalled due to the risk of serious side-effects such as brain damage and even death.

While it seems that the dangers of pharmaceutical products have more recently come to light, Brown & Crouppen has been successfully representing the victims injured by unsafe drugs and medical devices for many years. Brown & Crouppen attorneys remain committed to holding big drug companies accountable for the irreparable harm their products cause to the lives of the injured and their families. With the support of some of the nation’s premier drug litigation specialists, our firm is able to offer clients unparalleled support and legal expertise. In addition to Tysabri, we have handled a number of other unsafe prescription drugs including; Vioxx, and Celebrex, Resulin, Fen-Phen, Lotronex, OxyContin, Prempro, Baycol, PPA, and Zyprexa.

Tysabri is the first humanized monoclonal antibody approved for the treatment of MS. The drug works by preventing the cells that cause inflammation and damage to nerve fibers and their insulation (myelin) from migrating from the bloodstream into the brain. Based on partial results from a two-year study, Tysabri won FDA approval. Tysabri, which Biogen had marketed in conjunction with Ireland's Elan Pharmaceuticals, had been heralded as a new hope for multiple sclerosis patients. About 5,000 patients have received intravenous infusions of Tysabri since the drug's approval in November. Subsequent to the drugs’ approval, it has been reported that patients who had been treated with Tysabri in trials had developed a rare and frequently fatal brain disorder called progressive multifocal leukoencephalopathy (PML). More information from the FDA on the Tysabri suspension can be found at: public health advisory and questions and answers: www.fda.gov/cder/drug/infopage/natalizumab.

Biogen-IDEC enjoyed $3 million in Tysabri sales for in the final weeks of 2004 and had excitedly projected annual sales to reach $1.5 billion by 2007. Unfortunately, the prospects of even more profitability for the pharmaceutical giants were dampened when reports of serious events associated with the drug surfaced.

Annually, an estimated 1.5 million (or more than 4,000 people per day) people are admitted to hospitals as a result of adverse drug reactions. These disturbing numbers have led one former FDA expert to advise “...don’t try a drug until it’s been on the market at least 2 to 5 years - whoever takes a newly approved drug is a non-consenting guinea pig...”.

Please consult your physician before discontinuing any medication.

If this advice comes too late for you or someone you love, and you are already suffering the ill-effects of Tysabri such as brain damage, you may be entitled to receive compensation for your injuries. Please call Brown & Crouppen at Toll Free: 866-991-4700 for your free legal consultation, or save time with our online Contact Form. Remember – when you choose our firm to handle your lawsuit, Ron Brown, Terry Crouppen and our legal team of over 70 professionals throughout Missouri become committed to your case. We have helped our clients receive over 200 million dollars in settlements and awards for damages in personal injury cases. We would like to be able to help you.


Call Brown & Crouppen at Toll-Free: 866-991-4700 for your free legal
consultation or save time with our online Contact Form.

Toll-Free: 866-991-4700

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