Home Practice Areas Verdicts & Settlements Anapol TV Our Attorneys About Us Contact Us
LET US REVIEW YOUR CASE
   Name:
   Phone:
   E-mail:
  Comments:
 

Raptiva Recall Attorneys

Raptiva F.A.Q.

What is Raptiva?

A drug developed by the Genentech Inc. company (a division of the pharmaceutical giant Roche). It is administered subcutaneously (under the skin) to treat difficult cases of psoriasis. It is intended as an adult only treatment – for patients 18 years and up.

What does the active ingredient in Raptiva (Efalizumab) do?

Efalizumab works to inhibit the activity of a kind of cell called T-cells. In psoriasis sufferers, T-cells develop at out of control rates.

Are there Efalizumab side effects?

Yes. In fact, that's the reason Genentech Inc. decided to initiate an Efalizumab and Raptiva recall on April 8, 2009. Raptiva side effects include meningitis, fungal and bacterial infections, infections and soreness around the site of injections, and a brain disorder called Progressive multifocal leukoencephalopathy.

What is Progressive multifocal leukoencephalopathy?

Also referred to as PML, Progressive multifocal leukoencephalopathy is a rare, not well understood brain disease associated with the deterioration of the nervous system. Essentially, nerve cells are demyelinated, and this leads to problems walking, talking, seeing, balancing, and thinking clearly. So far, no one has developed a cure for PML.

How many people are currently on Raptiva?

In the U.S., approximately 2000. In Europe and other parts of the world, nearly 46,000 people have received Raptiva treatments.

Should patients currently on Raptiva stop taking the recalled drug immediately?

Patients should consult their doctors regarding how and when to stop Raptiva treatment. The recalled drug will be stocked through June 8th, 2009. Rapid withdrawal from Efalizumab can lead to an aggravation of psoriasis and other potential Raptiva side effects.

Are all Raptiva patients equally at risk for developing side effects?

Apparently no. Out of the four confirmed cases of the Raptiva PML side effect among patients, all have involved people who have taken the drug for several years.

As a Efalizumab patient, should you take legal action against Genentech Inc.?

If you've suffered an illness or side effects, the drug maker may be liable. Consult with the Raptiva recall lawyers of Anapol Schwartz. We can help you understand your rights as a potential plaintiff, and we provide contingency representation for clients.

CALL TODAY 866.735.2792

Home| Practice Areas| Verdicts & Settlements| Anapol TV| Our Attorneys| About Us| Contact Us

Copyright © 2004-2012 All rights reserved. Anapol Schwartz - Raptiva Recall Attorneys - Pennsylvania Raptiva Recall Lawyers - Personal Injury and Pharmaceutical Liability Law Firm.

Locations: 1710 Spruce Street, Philadelphia , PA 19103  |  1040 N. Kings Highway, Cherry Hill, NJ 08034  |  146 N. 6th Street, Reading, PA 1906  |  252 Boas Street, Harrisburg, PA 17101  |  (of Counsel) Clark Perdue & List & Co. LPA 471 E. Broad Street, Suite 1550, Columbus, OH 43215  |  8700 E. Vista Bonita Drive, Scottsdale, AZ 85255

Raptiva Brain Infection Lawyers Disclaimer: This website is dedicated to providing public information regarding Raptiva side effects, Raptiva meningitis, Raptiva brain infection, and other Raptiva drug recall legal information. None of the information on this site is intended to be formal legal advice, nor the formation of a lawyer or attorney client relationship. Please contact a Unsafe Drug Recall Lawyer or Raptiva Side Effects Attorney at our law firm for information regarding your particular case. This website is not intended to solicit clients outside the states of Pennsylvania, New Jersey, Ohio, West Virginia and Arizona.

Website, SEO and Legal Internet Marketing by: SLS Consulting | Sitemap |