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Patients who suffer from a serious medical condition must take a blood thinner or anticlotting agent to prevent the formation of blood clots that can be deadly.  Patients who suffer from deep vein thrombosis (DVT) and various other conditions need to take these medications to prevent potentially deadly medical conditions from occurring.

whitepillsBlood clotting is an important bodily function.  It is a reaction in the body to stop bleeding.  This can be from internal bleeding or external bleeding, such as when a person gets a cut on his or finger.  People who suffer hemophilia do not clot normally, and this is why even a small cut can lead to serious blood loss.  Continue reading

There is no question that Xarelto has been linked to a lot of serious bleeding disorders, many of which resulted in death.  There are many reasons the drug has proven so dangerous to users, but a lot of the problems are result of the reportedly negligent manner in which Bayer and Janssen Pharmaceuticals performed the safety testing and informed the U.S. Food and Drug Administration (FDA) of the Results.

Pills pouring from a medication bottle

According to a recent news feature from Forbes, one plaintiff’s lawyer that handles Xarelto injury lawsuits states that these experiments were conducted in the same manner that young students would do in an elementary school science fair when making their projects.  Continue reading

We have heard a lot recently about how stem cells can be used to help patients who would typically require the implantation of an artificial joint such as a hip or knee. Using one of these methods, doctors are able to remove bone marrow from the patient and use the stem cells in the bone marrow to attempt to regrow bone tissue and joint material inside the patient.  While this method may work, it is only one method doctors are using with stem cells, but there are others.

surgeryIn a recent news feature form HNGN, doctors are now using stem cells to regrow cartilage in a laboratory and then implant that it into the patient.  Since the cartilage was grown using the patient’s own stem cells, the new cartilage will have the same DNA as the patient.  This should mean that the body will not see the new cartilage as a foreign substance, so there should be no risk of rejection, which is always a major risk in an organ transplant or event the implanting of an artificial joint like a knee or hip. Continue reading

Testosterone replacement therapy (TRT) has become increasingly common over the past decade.  In the past, there had been little interest in giving patients testosterone hormones unless they had a relatively rare medical condition known as hypogonadism.  This condition involves a patient with an extremely low testosterone count caused by a defective hormone gland and is causing developmental disorders in younger patients.  In fact, this was the only medical condition for testosterone hormone was approved by the United States Food and Drug Administration (FDA), and still remains the only approved use.

untitled-1238929-mWhile the vast majority of the millions of men taking testosterone replacement therapy on a regular basis do not suffer from hypogonadism, the reason they can get the drug involves a gray area in FDA regulations that allows a doctor to prescribe a drug for what is known as off-label use.  While this is technically allowed, we have seen recent cases where doctors are being fined and subject to discipline for allowed these so-called Low T clinics to prescribe patients testosterone hormone using their respective DEA numbers without them having actually examined the patients. Continue reading

In total hip replacement surgery, the deteriorated natural hip joint is cut out and site is prepared to receive the artificial hip joint.  The site must be prepared very precisely so as not to allow for any unnecessary movement of the artificial hip joint.

surgery1If the hip joint is not placed exactly as required, it can move from side to side or otherwise rock in place and this can result in device failure.  While the vast majority of surgeons are good at what they do and would never incorrectly implant an artificial hip device, it does happen.  Continue reading

In the past couple months, many people have heard about stem cell treatments being used to try to avoid major joint surgery. Much of these news came from the baseball world, where the Los Angeles Angels of Anaheim (LAA) allowed doctors to perform a stem cell treatment instead of “Tommy John” surgery on two pitchers.

untitled-1238929-mIn the case of these baseball players, Tommy John surgery (named after the first pitcher to get the procedure, more formally known as an ulna collateral ligament or UCL procedure) can save a career, but it takes over a year for the pitcher to return to the game in most cases. The new procedure uses stem cells from bone marrow (not embryonic stem cells), and they may be able to regrow the damaged tissue instead of needing a replacement.  Unfortunately, for one of the two pitchers, it did not work, so they had to do the Tommy John procedure after all. Continue reading

For the second time in a week, the U.S. Court of Appeals for the Sixth Circuit has dismissed a product liability claim, citing forum non conviens. This is a discretionary power a court has to dismiss a case when another court (or forum) is better suited to hear the case. doctor9

The dismissal isn’t going to prevent a plaintiff from re-filing the case, but depending on the facts, he or she may run up against a statute of limitations issue. It’s always better to thoroughly research such issues ahead of time so that it doesn’t become time and money wasted.

There are many considerations that go into determining the proper forum in a product liability lawsuit, including:

  • Where plaintiff lives;
  • Where defendant is headquartered/ operates/ distributes;
  • Where the injury occurred.

Continue reading

Johnson & Johnson lost a $500 million federal case in Texas earlier this year involving its Pinnacle hip replacement devices. However, the company won an important victory recently when the U.S. District judge overseeing the case slashed that damage award to $151 million, finding the punitive damage award excessive. gavel1

The verdict had been in favor of five plaintiffs and three spouses, who after a two month trial were collectively were supposed to receive $360 million in punitive damages and $140 million in compensatory damages.

Although the judge denied the company’s request to set aside the verdict or grant a new trial, the medical product behemoth is now seeking an expedited review of the verdict. The company has argued that jurors were improperly biased after hearing evidence that was both irrelevant and unfair during the trial. Attorneys for plaintiffs, however, say the bid for a new trial is nothing more than a flimsy attempt to snag a “do-over” after the strategy they employed during trial went awry.  Continue reading

A man’s $8 million damage award for a defective hip has survived an appeal before the 4th District Court of Appeal. The trial was the first of thousands of product liability claims filed over the ASR hip device. surgery

Plaintiff alleged that the device failed just 5 years after the surgery, despite promises that it was supposed to last most if not all the rest of his lifetime.

The case was Kransky v. DePuy, and expert witnesses, including a biomedical engineer, testified in the case that internal data from the company showed these hips started to deform and change shape in just one year’s worth of walking in the human body. This high rate of deformity was known to those in the company, who ignored this reported “red flag.”  Continue reading

According to a recent news feature from Food Safety News, over 22 tons of frozen appetizers (marketed as Kabob’s Hors d’oeuvres) have been recalled to due a recent outbreak of E. coli bacterial illness.  There are many different products this company manufactures that are sold to restaurants and big box retailers and discount warehouses. There are dozens of different varieties of recalled products, including mini pizzas, spring rolls, pot stickers, and many other similar frozen appetizers that are not shipped ready to eat, as they do require cooking.

surgery1The problem did not come from the factory where the frozen food products were manufactured, but rather it was from the flour manufactured by General Mills, Inc. and shipped to this company for use in their food products.  As soon as the flour company notified them of the potential for E. coli contamination, the company voluntarily recalled any product that used that flour to avoid any injury. Continue reading

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