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Latest Boxed warning Stories

2014-09-28 23:02:43

Wright & Schulte LLC Continues To Investigate Complaints That Janssen Pharmaceuticals Did Not Disclose The Lack of An Effective Means To Treat Uncontrolled Bleeding In Patients Taking Xarelto Columbus, OH (PRWEB) September 28, 2014 Wright & Schulte LLC has learned that a Xarelto bleeding lawsuit complaint was filed on behalf of a California woman who alleges that she suffered life-threatening bleeding as a result of taking the blood thinner medication. According to the Xarelto...

2014-08-05 12:06:50

Boston University Medical Center Study compared warning and withdrawal rates for drugs released before and after the drug industry increased funding to the FDA to expedite drug approvals What's safer: a newly approved drug or one that has been on the market much longer? Newer drugs have a one in three chance of acquiring a black box warning or being withdrawn for safety reasons within 25 years of their approval, according to a new study by researchers from Cambridge Health Alliance...

2014-07-03 23:09:54

On June 26, the FDA informed that prescription oral viscous lidocaine 2% solution should not be used to treat infants and children with teething pain. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. (PRWEB) July 03, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for Lidocaine Viscous. The FDA issued a safety...

2014-05-23 12:24:30

A Group of 50 Adverse Drug Reaction Victims Rally in Washington, DC Before Meeting with Members of Congress; Thousands Connect Via Online Support Groups Emerging Worldwide WASHINGTON, May 23, 2014 /PRNewswire-USNewswire/ -- A group of 50 Americans who call themselves "Floxies" because they each took the prescribed antibiotic medication Fluoroquinolone which they allege has had disastrous health consequences, have appealed to members of Congress for help in warning others. In their...

2014-03-23 23:01:51

An Italian study of 22 clinical trials contains some good news and some bad news for diabetic patients treated with the drug Actos. Raleigh, NC (PRWEB) March 23, 2014 Cancer Monthly is reporting on the results of an Italian Meta-Analysis involving more than 13,197 patients who had taken either the diabetes drug Actos or another thiazolidinedione called rosiglitazone. Researchers at the Careggi Teaching Hospital in Florence, Italy scoured the medical literature for both published and...

2014-02-26 23:35:02

Public Citizen’s Call for Testosterone Heart Attack Warnings Follows Launch of FDA Investigation into Low T Heart Risks, Filing of Several AndroGel Lawsuits. New York, NY (PRWEB) February 26, 2014 Alonso Krangle LLP, an experienced law firm investigating testosterone treatment lawsuits involving AndroGel and other prescription low testosterone, or Low T, therapies, commends the consumer advocacy group, Public Citizen, on its petition calling for new heart attack warnings on this class...

2014-02-26 23:02:53

The Firm is investigating testosterone treatment lawsuits on behalf of men who suffered heart attacks, strokes, deep vein thrombosis, pulmonary embolism, or other serious cardiovascular problems, allegedly due to AndroGel and other low testosterone therapies. New York, NY (PRWEB) February 26, 2014 As testosterone lawsuits (http://www.testosteronelawsuitcenter.com/ ) involving AndroGel continue to mount, Bernstein Liebhard LLP notes that a leading consumer advocacy group is pushing...

2013-11-07 23:32:22

Law firm Zoll, Kranz & Borgess, LLC announces a possible case for patients suffering from negative side-effects from the anti-seizure drug, Potiga (ezogabine). The new label warning update is the most serious boxed warning the FDA gives and individuals taking Potiga may have a potential claim. Toledo, OH (PRWEB) November 07, 2013 Zoll, Kranz & Borgess, LLC has just announced that they are offering free case evaluations for individuals who have taken the Potiga and have...

2013-10-11 23:25:47

The United States Food and Drug Administration (FDA) has recently issued a Drug Safety Announcement and approved a Black Box Warning, one of the harshest warnings, for Pfizer’s antibiotic intravenous (IV) drug Tygacil®. In particular, the FDA warns prescribing doctors and consumers that use of the IV drug Tygacil® is associated with an increased risk of death in comparison to other antibiotic drugs and that the IV antibiotic Tygacil® should only be used in situations where...

2013-09-30 23:02:42

The U.S. Food and Drug Administration reports it has notified health professionals about a new Black Box warning for Pfizer Inc.'s intravenous antibacterial drug Tygacil (tigecycline). The FDA says the warning ramp-up is based on additional analysis the regulator conducted on the drug that reveals it is causing an increased mortality rate among users, Parker Waichman LLP cautions. New York, New York (PRWEB) September 30, 2013 Parker Waichman LLP, a national law firm dedicated to...


Word of the Day
reremouse
  • A bat.
The word 'reremouse' comes from Middle English reremous, from Old English hrēremūs, hrērmūs ("bat"), equivalent to rear (“to move, shake, stir”) +‎ mouse.
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