April 2006

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Guidant Defibrillators

In 2005, the Guidant Corporation recalled several models of cardiac defibrillators and cardiac pacemakers because of the risk of potentially fatal malfunctions of these devices.

There are approximately 38,000 patients in the United States with Guidant brand defibrillators. Reports indicate these devices have failed at least 45 times and have been responsible for at least two deaths. Several Guidant defibrillator models are on the recall list.

Contact our office for more information regarding the Guidant defibrillator recall.

Free Legal Advice?

Yes, at Kraft & Associates we are glad to provide our clients and friends with free information on a variety of subjects. If you want details about how to lower your automobile insurance rates, Texas Workers' Compensation law or Social Security Disability claims, please contact us and we will send you any of these brochures without charge or obligation.
 



  Suite 1300
  2777 Stemmons Freeway
  Dallas, TX 75207
  (214) 999-9999
  (817) 999-9999
  (800) 989-9999
 

 FOR THE RECORD


Fosamax Health Warning

There is a potentially very dangerous side effect from taking a drug that supposedly strengthens bones. This drug is frequently taken by older women who suffer from osteoporosis.

Fosamax® (generic name - Alendronate) is a type of drug known as bisphosphonates. Recently a link has been found between bisphosphonates and a serious bone disease called osteonecrosis of the jaw (ONJ, or "Dead Jaw"). This important discovery clearly shows that Fosamax side effects may include "dead jaw."

A report published in the Journal of Oral and Maxillofacial Surgeons prompted the United States Food and Drug Administration and Novartis, the manufacturer of bisphosphonates used in cancer chemotherapy, to issue a warning to health care professionals. The warning letter contained information about bisphosphonates and the risks of osteonecrosis in the jaw.

Bisphosphonates such as Fosamax (Alendronate Sodium), Zometa (Zoledronate), Didronel (Etidronate), Aredia (Pamidronate), Actonel (Risedronate), and Boniva (Ibandronate) are commonly used to treat, prevent, and even to reverse bone loss associated with osteoporosis, chemotherapy, and other bone loss disorders. The strongest forms of bisphosphonates are commonly used in the management of advanced cancers that have metastasized to the bone -- where the disease often causes bone pain and possibly even causes fractures. Several cancers can involve or metastasize to the bone, including lung cancer, breast cancer, prostate cancer, multiple myeloma, and others. When bisphosphonates are given in cancer chemotherapy, the drugs are given intravenously, and usually for longer periods of time.

Osteonecrosis of the Jaw
Osteonecrosis of the jaw is a condition in which the bone tissue in the jaw fails to heal after minor trauma such as a tooth extraction, causing the bone to be exposed. The exposure can eventually lead to infection and fracture, and may require long-term antibiotic therapy or surgery to remove the dying bone tissue. Experts say that prevention and early treatment of individuals using bisphosphonates such as Fosamax is extremely important in preserving the jaw bone. Individuals using Fosamax or other bisphosphonates should attempt to avoid tooth extractions and other major dental work while on the drugs.

Although most cases of osteonecrosis of the jaw related to Fosamax side effects have occurred after dental work, several cases have been reported without any prior dental work. If you are currently taking Fosamax you may be at risk of developing osteonecrosis. If you have been injured by Fosamax side effects you may be entitled to compensation.

The symptoms of osteonecrosis of the jaw include:

• Severe infections
• Loosening of teeth
• Swelling around the jaw

If you or a loved one have taken Fosamax and have been injured as a result of Fosamax side effects such as osteonecrosis of the jaw, please contact our law firm immediately. You should never discontinue the use of any prescription drug without discussing your concerns with your doctor.
 

 FOR YOUR INFORMATION

Cautions About Zyprexa

Zyprexa® is an anti-psychotic medication that was approved in 1996 by the United States Food and Drug Administration for the treatment of schizophrenia. It is a member of a class of drugs referred to as "second generation anti-psychotics" ("SGAs") or "atypical anti-psychotics." When Zyprexa® was approved, there were two other such SGA medications already available on the market. Consequently, Zyprexa is considered a "me-too" drug, joining a class of existing medications prescribed for the treatment of common disorders.

The SGAs were developed as an alternative to the so-called "first generation anti-psychotics" ("FGAs"). The SGAs were designed to be more effective in the treatment of anti-psychotic disorders, with fewer of the side effects generally associated with the use of FGAs. Of the six SGA's currently available, Zyprexa is the most commonly prescribed. The generic name of Zyprexa is olanzapine.

In September 2003, the Food and Drug Administration ordered the manufacturer to revise the label of Zyprexa by adding a warning that "hyperglycemia, in some cases extreme and associated with ketoacidosis or hyperosmolar coma or death, has been reported in patients treated with atypical anti-psychotics." Among the more serious outcomes resulting from hyperglycemic abnormalities are:

• Diabetes
• Diabetic Ketoacidosis
• Diabetic Coma
• Hyperosmolar Coma
• Hyperglycemia

If you are currently taking Zyprexa and have concerns about its safety, you should consult with your doctor regarding your treatment options. Under no circumstances should you discontinue taking any medication, including Zyprexa, without first consulting with your doctor.

If you or a loved one have taken Zyprexa and have experienced severe Zyprexa side effects, or have questions about a possible Zyprexa claim, please contact our firm.

 FEATURED EMPLOYEE

Jo-Ann Martinez
Social Security Secretary

E-mail: jmartinez@kraftlaw.com

Ms. Martinez joined our firm in 1995 as a receptionist. Ms. Martinez has filled several positions with our firm over the years and currently works as a legal secretary in our Social Security department. She also serves as one of that department's Spanish-English translators. Ms. Martinez has more than 20 years' experience as a receptionist and legal secretary.

 

 FEATURED CASE
Latest Developments In Vioxx Litigation

Our law firm is currently accepting claims on behalf of consumers who took the arthritis drug Vioxx, and then suffered a heart attack or stroke. For that reason, we have been keeping a close watch on the Vioxx trials taking place around the country.

A jury this month awarded $9 million in punitive damages to a New Jersey man who blamed Merck & Company's Vioxx for his heart attack.

The punitive damages came on top of $4.5 million in compensatory damages the jury awarded 77-year-old John McDarby after they found that Vioxx was a significant contributing factor to his heart attack, and that Merck failed to adequately warn of the drug's risks. Merck, which pulled the $2.5 billion-a-year drug off the market in September 2004, said it would appeal the verdicts.

In awarding the punitive damages, the jury determined that Merck withheld material information on Vioxx from the U.S. Food and Drug Administration and the company's actions were deliberately meant to harm.

As part of its deliberations, the jury considered whether Merck intentionally withheld from regulators an analysis of several clinical trials done by a company statistician in 2000 that showed a higher incidence of heart attacks among patients taking Vioxx than those taking other drugs.

Merck expressed disappointment over the jury's decision but gave no indication that it was willing to consider settling any of the thousands of lawsuits it is facing. So this result is good news for anyone with a potential claim against Vioxx, but it does not mean that Merck is going to offer to settle any Vioxx cases in the near future.
 HOW CAN WE HELP YOU?
Our law firm has helped thousands of clients over the years. Sometimes clients who use our firm for one type of case may not realize that there are other legal problems we could help them solve.

We handle most types of injury claims — including automobile collisions, "slip and fall" cases, injuries suffered as a result of defective products, injuries resulting from inadequate security, medical malpractice claims, nursing home negligence claims, prescription drug injuries and many others. We invite you to call us about any serious injury to see how we can help you.

Kraft & Associates also represents people who have been denied their Social Security Disability benefits. We can help at the Initial stage, the Reconsideration stage or the Hearing stage.

Our firm represents people who have been injured on the job and are making a claim for workers' compensation. We help people who have problems regarding family issues, such as divorce, child support, adoption, modifications, enforcements, attorney general disputes, paternity and other similar matters. We also represent clients who have been arrested or charged with committing a crime.

Please feel free to call us with any legal questions you may have. If we cannot represent you, we will attempt to refer you to another attorney or to a government agency that can help you. There is never any charge or obligation for our initial consultation.

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Automobile Accident, Wrongful Death, Nursing Home Negligence, Social Security Disability.

DISCLAIMER: This newsletter is presented by Kraft & Associates for informational purposes only, and not as legal advice.