Dallas Fort Worth Injury Lawyer Blog

Merck & Co. (MRK) is defending a woman’s claim that its osteoporosis drug Fosamax weakened her femur, causing her leg to break when she fell in her driveway. This is the second Fosamax femur fracture injury claim going to trial. The first trial, in state court in Atlantic City, New Jersey, was called off after plaintiff Christina Su suffered a “sudden illness” that was unrelated to her use of Fosamax.

A three-week jury trial has started before U.S. District Judge Joel Pisano in Trenton, New Jersey. The plaintiff, Bernadette Glynn fell and injured herself in April 2009. Merck claimed that Glynn, 58, tripped over a chainsaw in her garage and that the fracture is typical of women with osteoporosis.

Fosamax and Femur Fracture Allegations

The U.S. Judicial Panel on Multidistrict Litigation (JPML) has issued an order to consolidate all Mirena IUD injury perforation injury lawsuits. This order applies to all cases filed throughout the federal court system. All Mirena IUD injury cases will be centralized before one judge as part of an MDL, or multidistrict litigation.

According to the JPML order, all defective Mirena IUD product liability lawsuits will be transferred to U.S. District Judge Cathy Seibel in the Southern District of New York for coordinated handling during pretrial proceedings.

What is Mirena IUD?

Can You Die From Januvia Pancreatic Cancer? The short answer is; it depends. Some 25 to 30 million people in the United States have diabetes, and 80 million folks have medical condition known as pre diabetes.

And the numbers are increasing slowly but surely. And Type 2 or adult onset diabetes is generally considered a man made problem (excluding Type 1 diabetes which occurs in childhood and usually as a result of genetic factors, autoimmune disease and or environmental problems).

Januvia is a drug manufactured by Merck, and it is used to treat adults with type-2 diabetes. In September 25, 2009 the FDA issued a revision to the warning label of the drug Januvia or Janumet, a combination drug comprised of Januvia and Metformin, regarding Januvia side effects, including Januvia pancreatic cancer and Januvia thyroid cancer.

As a Texas medical doctor and Dallas Januvia/Byetta/Victoza dangerous drug Pancreatic Cancer attorney I am providing this latest information and investigation from the FDA.

According to the FDA notice, posted on March 14, the agency is:

“Evaluating unpublished new findings by a group of academic researchers that suggest an increased risk of pancreatitis, or inflammation of the pancreas, and pre-cancerous cellular changes called pancreatic duct metaplasia in patients with type 2 diabetes treated with a class of drugs called incretin mimetics. These findings were based on examination of a small number of pancreatic tissue specimens taken from patients after they died from unspecified causes.”

According to a recent medical study, patients taking the newer diabetes drugs were affected by pancreatic cell growth and damage that may turn cancerous. The study, by UCLA Medical Center, provides evidence of increased pre-cancerous changes in diabetic patients using incretin mimetics drugs such as Januvia, Byetta and Victoza.

FDA Investigates Incretin Mimetics

According to the U.S. Food and Drug Administration, it was reviewing unpublished data by medical researchers which suggest that pre-cancerous cellular changes may be associated with Type 2 diabetes drugs known as incretin mimetics, including Bristol-Myers Squibb’s Byetta and Novo Nordisk’s Victoza.

The jury finally rendered a verdict today, in a hotly contested Johnson & Johnson defective hip lawsuit, being tried in California state court, Los Angeles. Johnson & Johnson (J&J)’s DePuy subsidiary unit was found liable for defectively designed metal-on-metal hip implant, in the first of 10,750 lawsuits over the device to go to trial.

Jury: Clear Message

The California jury sent a clear message today that Johnson & Johnson and DePuy put profit over safety by awarding Loren Kransky, the plaintiff in the California case of Kransky v. DePuy Orthopedics, $ 8.3 million for damages caused by Mr. Kransky’s implantation and revision of the recalled DePuy ASR XL hip implant.

As a Dallas, Texas Defective Metal on Metal Hip attorney, I have written extensively about the problems and the lawsuits filed against the manufacturers of metal on metal hips. It appears that the problems associated with the metal on metal hips is neither unique or limited to one manufacturer.

Johnson and Johnson’s DePuy ASR and Pinnacle models, Biomet’s M2a Magnum, Stryker Rejuvenate and ABG II models, Wright Conserve, Zimmer Durom cup and Smith and Nephew R3, have all been implicated as being defective, prone to early failure and subjected to revision surgeries.

The most recent recall involving Stryker hips took place quietly on July 4, 2012, while most Americans were busy with fireworks and apple pie.

The first Actos bladder cancer trial is currently underway in Los Angeles, California state court and the trial started February 19th. The plaintiff, Jack Cooper, was diagnosed with bladder cancer after using Actos for more than two years. The case was given a fast track trial date because of Cooper’s terminal condition.

According to the plaintiff, Jack Cooper, Takeda Pharmaceutical Co., the manufacturer of its blockbuster diabetic drug Actos, failed to warn doctors of the cancer risk associated with its diabetes treatment. This is the first of more than 3,000 lawsuits over the drug goes to trial. Takeda Pharmaceutical Co., is Asia’s biggest pharmaceutical company.

Takeda sales representatives never warned Jack Cooper’s doctor in more than 195 visits, according to Cooper’s lawyer Michael Miller in state court in Los Angeles.