InjuryBoard Philadelphia Archives

  • Many Ties Between Physicians and Drug/Device Companies

    Jamie Sheller | April 29, 2007 5:53 PM | 0 Comments
    Category: FDA & Prescription Drugs

    Marketers for pharmaceutical and medical device companies actively pursue high-prescribing physicians. A study recently reported in the New England Journal of Medicine, indicated that most of the physicians questioned had a relationship of some kind with the industry in the previous year. Cardiologists received the most perks, while pediatricians and anesthesiologists received the least. ...

  • Recall of Beef Due to E. Coli Fear

    Jamie Sheller | April 21, 2007 1:01 PM | 0 Comments
    Category: Defective & Dangerous Products

    Almost 400,000 pounds of beef have been recalled by two beef producers, due to concerns about E. Coli contamination. HFX, Inc. and Richwood Meat Co., the two beef producers involved in the recall, are in California and Pennsylvania. The Pennsylvania beef was distributed in Pennsylvania, Virginia and West Virginia. The California beef was distributed in California, Idaho, Washington, Oregon...

  • More Evidence Linking Hormone Use To Cancer Risk

    Jamie Sheller | April 19, 2007 6:21 PM | 0 Comments
    Category: FDA & Prescription Drugs

    The results of research done in the United States and in the United Kingdom, affirms earlier evidence linking the use of hormones to increased cancer risk. The recent research demonstrates that hormone use can raise the risk of breast cancer. Breast cancer is the second leading cause of cancer deaths in American women. Hormone replacement therapy is also linked to a slightly elevated risk of...

  • FDA Committee Says No to Merck's Vioxx Successor

    Jamie Sheller | April 14, 2007 6:47 PM | 0 Comments
    Category: FDA & Prescription Drugs

    Merck is seeking FDA approval for a new Cox-2 inhibitor, etoricoxib (Arcoxia). However, according to the FDA's Arthritis Drugs Advisory Committee, the drug's cardiovascular risk outweighed its benefits. One member of the committee also indicated that it was unclear that there was the need for another product in this class of drugs. Though it is not required to, the FDA usually follows the...

  • More Recalls of Guidant Heart Devices

    Jamie Sheller | April 12, 2007 12:36 PM | 0 Comments
    Category: Medical Malpractice

    Due to a defect causing shortened battery life, Guidant has recalled several models of its implantable cardiac defibrillators (ICD's) and cardiac resynchronization therapy defibrillators (CRT-D's). The recall involves about 73,000 devices, which have faulty capacitors possibly leading to rapid battery depletion. The Guidant ICD's and CRT-D's included in this recall are the Contak Renewal 3 HE...

  • Diagnosis and Potential Cause of Nephrogenic Systemic Fibrosis

    Jamie Sheller | April 07, 2007 8:18 PM | 0 Comments
    Category: FDA & Prescription Drugs

    Nephrogenic Systemic Fibrosis (NSF)/Nephrogenic Fibrosing Dermopathy (NFD) is a disorder characterized most visibly by skin lesions and hardened plaques on the skin. Usually, the extremities are most affected. NSF/NFD can also be found in other parts of the body, such as lungs, myocardium and skeletal muscle. The disorder is found in patients with kidney failure. NSF/NFD can be fatal. ...

  • Halt to Sales of IBS Drug Zelnorm

    Jamie Sheller | April 05, 2007 11:30 PM | 0 Comments
    Category: FDA & Prescription Drugs

    Pharmaceutical company Novartis has halted sales of Zelnorm. The drug is used to treat irritable bowel syndrome and constipation. The FDA requested that the drug be withdrawn from the market after trial results showed an increase in ischemic events, including angina and strokes, in patients taking Zelnorm, compared with a placebo group. Novartis does not believe that the trials demonstrate a...

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