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  • Digitek: "This Pill is Too Thick"
    Sep-23-08 Tucson, AZ Sue took Digitek for about 10 years to control her irregular heart beat and palpitations and she was doing OK until last fall, when Sue believes she was given pills that were on the Digitek recall ." I got my prescription by mail from Medco and right away, I felt that the pills were too thick," says Sue. "I learn to feel everything because...
  • St. Jude Medical Heart Device Legal News & Lawsuit Information
    Attorneys are investigating possible ICD and CRT-D defibrillator lawsuits resulting from the devices possibly short-circuiting and causing harm to patients. St. Jude Medical Inc., issued a recall of some of its Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) implanted in about 400,000 people...
  • Defective Knee Implant Legal News and Lawsuit Information
    Allegedly defective knee implants have been a cause of concern for medical professionals and patients alike, with some knee implant devices being the subject of recalls due to a high rate of complications, ranging from infection and trauma to loosening or poor implant positioning, along with a defective medical device. Among issues allegedly associated with...
  • FDA Halts Importation of Drugs Manufactured Offshore By Ranbaxy
    Drugs From 2 Plants Affected The FDA has issued an alert for generic drugs produced by Ranbaxy's Dewas and Paonta Sahib plants in India. The problems at these two Ranbaxy plants relate to deficiencies in the company's drug manufacturing process. The Import Alert issued by the FDA on Sept 16, allows for US officials to detain at any US border, any a...
  • Avandia's Safety Questioned
    Mar-14-10 New York, NY It's the stuff movies are made of: company executives arrange a secret meeting with a scientific expert who is trying to discredit the company. The expert secretly tapes the meeting and releases the tape to the media. Yet this is no movie script—according to the New York Times, this is exactly what happened when GlaxoSmithKline, maker of...
  • Diabetes Drug Byetta Causes Hemorrhagic or Necrotizing Pancreatitis
    FDA Issues Alert After Two People Die FDA has received reports of 6 cases of hemorrhagic or necrotizing pancreatitis in patients taking Byetta. Byetta is a medicine given by subcutaneous injection to help treat adults with type 2 diabetes. Of the 6 cases of hemorrhagic or necrotizing pancreatitis, all patients required hospitalization, two patients died...
  • Unum Claims Denials Cited as Defying Medical Science: Court
    Jul-8-12 Chattanooga, TN When the American Association for Justice (AAJ) put out its Top 10 List of worst insurance companies in the US, critics of Unum insurance were not surprised to find Unum named as the second-worst insurance company in America behind Allstate. And blogger Linda Nee writes that it's operational undertakings like systematic requests of poli...
  • FDA Issues Warning for Injectable Silicone for Body Contouring and Enhancement
    Washington, DC The US Food and Drug Administration (FDA) has issued an alert to the public and healthcare providers alike, stating that the agency has not approved injectable silicone for use to enhance or augment the body. Such use can lead to ongoing pain, infections, and serious injuries, such as scarring and permanent disfigurement, embolism (bloc...
  • Medtronic Insulin Pump Lawsuit News and Legal Information
    Medtronic has so far faced at least two lawsuits alleging the Medtronic MiniMed Paradigm insulin pumps are defective and have caused the death of patients relying on the pumps to monitor blood glucose levels. There have been at least two Medtronic recalls of the devices, linked to problems with the pumps providing too much or too little insulin. Attor...
  • FDA Issues Warning for Transvascular Autonomic Modulation (TVAM)
    The Food and Drug Administration (FDA) has issued a safety alert regarding an experimental procedure called Transvascular Autonomic Modulation (TVAM). This procedure may put patients at risk because it is being promoted as treatment for a variety of conditions even though it has not been formally studied in clinical trials. Reported risks include TVAM...
  • Risperdal Lawsuit News and Legal Information
    Risperda l (generic name Risperidone) is an atypical antipsychotic that works by changing the activity of certain natural substances in the brain. Developed by Janssen Pharmaceuticals, a subsidiary of Johnson & Johnson, Risperdal was approved by the FDA in 1993 for the treatment of schizophrenia in adults. Risperdal Lawsuits have shown a link between...
  • Byetta Pancreatic Cancer Lawsuit News & Legal Information
    The use of Byetta has been linked to impaired kidney dysfunction and renal kidney failure as well as serious Byetta side effects including acute pancreatitis. Additionally, a recent UCLA study showed a possible increase in Byetta pancreatic cancer and Byetta thyroid cancer . Byetta attorneys are investigating lawsuits for users diagnosed with Impair...
  • Legal News and Information on Johnson & Johnson Gynecare Mesh
    Johnson & Johnson has about 33,000 Gynecare lawsuits filed against its Ethicon division alleging Gynecare transvaginal mesh is defective. Rather than relieve women with Pelvic Organ Prolapse and Urinary Stress Incontinence, Gynecare Mesh side effects include severe pain, bleeding and infection. Some of the first transvaginal mesh or bladder...
  • Undeclared Milk in Mislabeled Kroger Chicken Noodle Soup
    FDA Annouces Recall Bay Valley Foods is recalling five cases (24 cans per case) of mislabeled Kroger Chicken Noodle Soup because it may contain undeclared milk. The cans actually contain Cream of Celery soup. People who have an allergy or severe sensitivity to milk are at risk if they consume these products. No illnesses have been reported to date in co...
  • Listeria Monocytogenes Alert for Cheese and Milk Products
    Washington,DC: The Massachusetts (MA) Department of Public Health (MDPH) is issuing a warning to consumers to avoid consumption of certain cheese and milk products because the products may be contaminated with Listeria monocytogenes (L. monocytogenes). The presence of L. monocytogenes in foods such as cheese and milk products represents a significa...
  • CardioGen-82 - Bracco Diagnostics, CardioGen-82 Recall, CardioGen Lawsuit
    CardioGen-82 , which uses the radioactive drug rubidium 82 chloride injection for cardiac PET scan or cardiac PET imaging has been recalled by the manufacturer, Bracco imaging . The CardioGen-82 recall occurred after the FDA received two reports of patients who received more radiation than expected. Washington, DC: The U.S. Food and Dru...
  • The Fix is In for St. Jude Defective Batteries, But Is it Enough?
    Nov-9-17 Washington, DC: The announcement last month of a new software tool capable of alerting patients with defective St. Jude cardiac defibrillators when a battery is in danger of failing prematurely may be too little, too late for patients who have suffered adverse events when defective defibrillator batteries failed too soon. Many have filed St. Jude ICD a...
  • "Losing Weight wasn't worth taking Fen-Phen: PPH was the Outcome"
    Jul-22-08 Atlanta, GA Margaret was given a script for Fen-phen and took it every day for two years, right up until it was pulled from the market. "It worked, I lost 100lbs," she says, "but in retrospect, this drug is so dangerous that I wouldn't have taken it had I known that PPH (Primary Pulmonary Hypertension) would ultimately be the outcome." "This drug ma...
  • Wells Fargo Fake Account Scandal Grinds On
    Apr-23-20 Oakland, CA The Northern District of California has approved attorneys’ fees in the settlement of the latest lawsuit arising from the massive Wells Fargo fake account fraud. The scandal came to light in 2016 after account holders raised questions about mysterious bank overdraft fees that they were charged. The bank’s misconduct, however, ma...
  • Liquimax Multivitamin Recalled
    Food and Supplement Recalls Leiner Health Products Inc. announced that it is recalling its 32 ounce plastic bottles of Liquimax Complete Nutrition Multivitamin Formula, labeled with UPC Code 7497052290, 7497023607, or 7497023696 because the product may contain undeclared fish (not shellfish), tree nuts (almonds, pecans and/or walnuts), and wheat. The re...
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