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Heparin Side Effects and Recall: 2008 Heparin Lawsuit Update

The blood thinner drug Heparin made by Baxter International Inc. has caused severe side effects including a profound drop in blood pressure, difficulty breathing and sometimes vomiting. This adverse reaction happens within a few seconds of the injection of the drug and can be fatal.
On April 21, 2008, the FDA updated its report of deaths associated with Heparin use to include 81 deaths in the United States. In addition, hundreds of patients worldwide have suffered severe reactions linked to contaminated Heparin.
Earlier, the FDA announced that the active ingredient in heparin sold by Baxter was contaminated at Chinese manufacturing facilities with a chemically altered form of chondroitin sulfate. It is still unknown if the contaminant was deliberately added to the crude Heparin or if it was the result of sloppy production. The FDA has identified 12 Chinese companies that have produced contaminated Heparin.
In addition to the Heparin-related deaths, hundreds of severe allergic reactions have also been linked to contaminated Heparin. In statistics on Heparin-related fatalities released in early April, the FDA's month-by-month adverse Heparin event reports show that 47 of 62 deaths (known at the time of the report) occcured between November and February.
Concern had previously arisen over irregularities in samples of heparin that were processed by Baxter’s supplier in China, Changzhou SPL. According to press reports, despite the fact that Changzhou SPL began shipping Heparin to Baxter International in 2004, the Changzhou factory was never inspected by the FDA nor by its Chinese regulatory counterpart until late February 2008.
The FDA sent a warning letter on Monday, April 21, 2008 to Changzhou SPL, identifying production problems including use of unclean tanks to make Heparin, raw materials received from an unacceptable vendor and no adequate way to remove impurities. Heparin is derived from the mucous membranes of the intestines of slaughtered pigs that are often cooked in unregulated family workshops in China.
 
Lieff Cabraser represents persons across America injured by contaminated and defective prescription drugs, including Heparin. Click here to submit your case.
Our lawyers have years of experience successfully representing clients in personal injury cases.
There is no charge or obligation for our review of your case.
In death and serious injury cases, we are pleased to visit you where you live, at no cost, to discuss your legal rights and answer your questions.
We have retained product safety and medical experts nationwide to assist our Heparin clients with their claims.
For our personal injury cases, we bring a team of experienced lawyers. In addition, we have on staff multiple nurses, legal assistants, scientific analysts and case clerks to assist our attorneys. Learn more about advantages we offer our clients.
Authorities are urging doctors to use non-Baxter vials of heparin. Baxter sells roughly half the heparin sold in the U.S. and has agreed to halt making heparin products associated with the reported adverse effects.
Legal Rights of Patients
The law in most states provides several personal injury claims for persons who have been seriously injured due to defective prescription drugs and treatments. These claims include strict liability for a defective product, failure to warn, and negligence. Damages sought against drug manufacturers can include compensation for:
  • Physical pain and suffering, mental anguish and physical impairment;
  • Past and future medical expenses;
  • Loss of earnings and/or earning capacity; and
  • Punitive damages for extreme wrongful conduct.
Why Baxter is Liable
In Heparin lawsuits against Baxter, Lieff Cabraser clients have charged that Baxter sold Heparin that was defective due to contamination and inadequate inspection of its product. Baxter allegedly failed to undertake adequate testing that would have shown that its Heparin posed a life-threatening risk to patients.
"Prescription drug manufacturers have a duty to produce products that are safe and free of dangerous ingredients," stated attorney Wendy R. Fleishman of Lieff Cabraser. "Only through a lawsuit or otherwise making a claim against Baxter can patients obtain compensation for their injuries. The American public needs the drug companies, like Baxter, to take responsibility for the safety of their products -- especially those like Heparin, which are manufactured in part in China."
Submit Your Case
If you have suffered a serious adverse reaction from Heparin or are a relative of patient that died after receiving Heparin, please click here to contact Lieff Cabraser. Our firm is representing injured Heparin patients nationwide and will review your claim without charge or obligation on your part.
Alternatively, you may call Lieff Cabraser personal injury attorney Heather Foster in our San Francisco office at 1-800-541-7358 (the call is toll-free).
About Lieff Cabraser
Founded in 1972, Lieff Cabraser Heimann & Bernstein, LLP is an over fifty attorney law firm with offices in San Francisco, New York and Nashville. For the last five years, the National Law Journal has recognized Lieff Cabraser as one of the top 20 plaintiffs’ law firms in America.
For our personal injury cases, we bring a team of experienced lawyers. Each client is assigned an individual lawyer. In addition, we have on staff multiple nurses, legal assistants, scientific analysts and case clerks to assist the attorneys. To learn more about our firm, click here.
     Trademark Notice: Personal Injury Lawyer America is an electronic newsletter from Lieff Cabraser Heimann & Bernstein, LLP. Lieff Cabraser represents clients in a wide range of cases, including personal injury and wrongful death lawsuits. Our personal injury attorneys | lawyers are committed to providing the very best representation and support possible for our clients. This website provides information on the legal rights of the injured and the latest news on product defects and related lawsuits.
     Lieff Cabraser is not affiliated in any way with any trademark owner. The use of any trademarks on this site is for product identification and information purposes only.
     About Lieff Cabraser: We have offices in San Francisco, New York and Nashville. Our lawyers have represented clients in personal injury, wrongful death and rollover crashes and product defect lawsuits across America, including residents of Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming.
     Among the cases our personal injury attorneys are prosecuting are the Medtronic heart lead recall, the AMO contact lens solution recall, the Peter Pan peanut butter recall, Guidant pacemaker defects, SUV rollover accidents, popcorn workers lung injuries, and Ford switch fires.
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