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  • Abbott confirms it will withdraw diet drug Meridia

    Karl Truman | October 11, 2010 4:55 PM | 0 CommentsLouisville, KY Category: FDA & Prescription Drugs

    Abbott confirms it will withdraw diet drug Meridia Abbott Laboratories said Friday that it would withdraw the diet drug Meridia at the request of the U.S. Food and Drug Administration less than a...

  • Drug Safety: Avandia

    Karl Truman | October 10, 2010 2:20 PM | 0 CommentsLouisville, KY Category: FDA & Prescription Drugs

    In a higly unsusual coordinated announcement, U.S. and European drug regulators sharply limited sales of Avandia, a diabetes drug that has been linked to strokes and heart attacks in patients, said...

  • Trasylol Linked to Thousands of Deaths(2)

    Jennifer Moore | February 23, 2008 10:50 AM | 0 CommentsLouisville, KY Category: FDA & Prescription Drugs

    60 Minutes recently reported that the drug, Trasylol, may be linked to the death of thousands of patients. Trasylol had been on the market for 14 years and was made by Bayer. Estimates show that worldwide over four and a half million people have been given the drug -- about a third of them were Americans. Trasylol was given in the operating room to control bleeding. Bayer aggressively...

  • E. coli Sickens 21 People Prompting Burger Recall

    Lee Coleman | September 27, 2007 9:18 AM | 0 CommentsBowling Green, KY Category: FDA & Prescription Drugs

    E. coli strikes again. At least 21 people in eight states may have become ill due to the latest outbreak. CDC has confirmed two in New York and one in Florida directly linked to the ground beef, the others are under investigation. The recall comes from Topps Meat Company out of Elizabeth, NJ. The frozen beef patties, 331,582 pounds, were distributed nationwide.The boxes recalled carry the number...

  • Baby Bliss Gripe Water Recalled

    Lee Coleman | September 21, 2007 1:09 PM | 0 CommentsBowling Green, KY Category: FDA & Prescription Drugs

    The FDA along with MOM Enterprises, Inc. posted a recall of Baby's Bliss Grip Water, apple flavor, code 26952V and expire date of October 2008 due to Cryptosporidium infection. The herbal formula is used ease stomach discomfort in infants associated with colic, hiccups and teething. Cryptosporidium infection causes a watery diarrhea. It can also have symptoms of weight loss, stomach cramps or...

  • E. Coli in Dole Salad Mix Prompts Recall

    Lee Coleman | September 18, 2007 8:32 AM | 0 CommentsBowling Green, KY Category: FDA & Prescription Drugs

    E. coli was found in a package of Dole's Hearts Delight salad mix in Canada and has prompted a recall in at least nine states. Neither the U.S. or Canadian health officials have received reports of illnesses at this point. The recall issued Monday affects all packages of Hearts Delight sold in the United States and Canada. It has a best if used by date of September 19th, 2007. Production codes...

  • Braun Recalls Lot "SFR" Flush Saline Syringes

    Courtney Mills | 2007-09-17T14:53:40 | 0 Comments Category: FDA & Prescription Drugs

    Braun Medical has issued a recall of all normal saline flush syringes with lot numbers ending in "SFR". There have been a heightened number of customer complaints of particulate matter in Braun's saline solution, which has prompted the recall. Patients may not develop any signs of injury until receiving multiple exposures to tainted saline, but multiple exposures pose a risk of severe injury. ...

  • Trasylol Ups Risk of Death and Kidney Failure

    Lee Coleman | 2007-09-11T11:46:39 | 0 Comments Category: FDA & Prescription Drugs

    According to MSNBC yesterday documents released show that Bayer AG's heart surgery drug does indeed increase the risk of kidney failure and death. The FDA will review the safety of the drug Trasylol again Wednesday. German drugmaker Bayer says it mistakenly withheld a study of 67,000 hospital records suggesting the drug could increase the risk of death, serious kidney damage, congestive heart...

  • Nephrogenic Systemic Fibrosis (NSF) Linked to MRI Scans

    Lee Coleman | 2007-08-30T12:09:42 | 0 Comments Category: FDA & Prescription Drugs

    We are representing several individuals who have developed an extremely serious condition called Nephrogenic Systemic Fibrosis. The FDA has issued a warning linking this condition to the injection of a toxic substance, Gadolinium, as part of a contrast agent injected before an MRI scan is performed. Our clients have suffered devastating injuries and we have filed lawsuits on their behalf. We...

  • MRI Contrast Agents Being Questioned

    Lee Coleman | 2007-08-29T11:02:21 | 0 Comments Category: FDA & Prescription Drugs

    Hundreds of individuals have now been diagnosed with NSF (Nephrogenic Systemic Fibrosis) after receiving an injection of a Gadolinium based contrast agent. The people most at risk were those with kidney failure, renal disease, because their kidneys were not functioning well enough to get the Gadolinium out of their system. Once Gadolinium enters the human cells it causes horrible damages. The...

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