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10/17/2008 - Accutane Quick Overview

What are the risks? Inflammatory Bowel Disease - A group of serious conditions that cause the intestines to become severely inflammed. Crohn's Disease - A serious inflammatory bowel disease (IBD) that causes ulcers to form in the gastrointestinal (GI) tract. Ulcerative Colitis - A disease of the intestine, specifically the large intestine or colon, that causes ulcers, or open sores, in the colon. Birth Defects - Accutane is classified as FDA Pregnancy Category X and should not be used under any circumstances if pregnant. Accutane is linked with many serious side effects. To discuss your Accutane case with a defective drug lawyer free of charge, please contact us by calling 1-866-50-RIGHTS (1-866-507-4448) or by filling out our Accutane case review form.
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10/16/2008 - You Have Rights Topics Overview

In this current series of podcasts, we are going to be giving our listeners a brief overview of each legal topic on our website. The main areas of interest we will be covering are Dangerous Drugs, Defective Medical Devices, Medical Malpractice, Personal Injury, Corporate Fraud, Toxic Exposure, and Defective Products. Brought to you by Mark & Associates, P.C. please visit our website, youhaverights.com, to download other podcasts, learn more about current legal issues, or fill out form for a free legal consultation. You may also call us toll free at 1-866-50-RIGHTS (866 507 4448).
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08/22/2008 - Antibiotics Cipro & Levaquin linked to Tendon Ruptures and Tendonitis

The safety of a class of antibiotics, known as fluoroquinolones, has recently been called into question after widespread reports of tendon ruptures and severe tendonitis in patients using these powerful medications. After receiving hundreds of reports, they issued a Black Box warning this July that is to be placed on the packing of all fluoroquinolone antibiotics. A black box warning is the most severe warning the FDA can issue for a drug. The warning intends to warn patients of the risk of tendon rupture and tendonitis. These risks should be taken seriously. If you or a loved one or someone you know has taken one of these antibiotics, please call 1-866-50-RIGHTS, 1-866-507-4448 today, or fill out a free case evaluation form on our website: youhaverights.com
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06/19/2008 - Heparin linked to severe allergic reactions and death

U.S. officials announced that Heparin has been linked to 149 deaths in people who had allergic reactions after taking the widely prescribed blood thinner medication. The new tally was posted on June 16, 2008 and can be found the FDA’S website. These new statistics expands the toll of people who took the Heparin and suffered allergic reactions. The agency said in April 2008 it knew of 81 people who died after suffering allergic reactions from the drug, made from pig intestines. Baxter International Inc. recalled its version of Heparin in January 2008 after reports of harmful side effects. Baxter has said it believes the blood thinner was intentionally contaminated during the manufacturing process in China. Members of Congress have called for drug makers to pay higher fees to fund inspection of overseas factories that make drug ingredients.
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06/05/2008 - Pfizer admits to the adverse side effects of Chantix

The Pfizer public relations machine has been running at full speed lately, ever since widespread reports of suicidal thoughts, aggressive behavior and other serious adverse reactions in users of the pharmaceutical giant’s popular Chantix anti-smoking drug intensified. Chantix users have been experiencing angry, irrational behavior, terrifying dreams and a host of other problems, prompting a non-profit pharmaceutical watch dog group to recently publish a report detailing at least 988 “serious adverse events” relating to the drug filed with FDA during the last 3 months of 2007 – more reports than for any other medication received by FDA during the same period
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