Archive for the ‘ NC auto accident lawyers ’ Category

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12
Sep

Strong Cautions on Bone-Building Drugs

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[photo from The New York Times

About 4 million women in the United States—more than 10 percent of women over age 50—take medications called bisphosphonates as a treatment for osteoporosis or osteopenia (pre-osteoporosis). Unfortunately, many of those women may not have been informed about the risks of these so-called bone-building drugs. There are serious risks associated with these medications…risks that aren’t always adequately explained when the drugs are prescribed.

Bones are not static; they are made of living cells, and like all other cells in the body, they are constantly dying and being reformed. With bone, the process is called remodeling. Old cells are resorbed—they leave the bone and are absorbed by the body. One of the earliest bisphosphonate medications was used to treat Paget’s disease, a condition in which bone resorption happens faster than formation of new bone cells. The drug slowed the resorption of bone.

In his book Worried Sick, Dr. Nortin M. Hadler, professor of medicine and microbiology/immunology at the University of North Carolina at Chapel Hill, noted that in high doses or during prolonged treatment bisphosphonate medications can actually cause–rather than thwart–osteopenia. He writes:

In fact, one has to be wary of all bisphosphonates as double-edged swords. For example, there was one agent that was withdrawn from the market because leukemia was a side effect.

Other serious side effects that have been documented are:

  • Osteonecrosis (bone death) of the jaw. This painful side effect is the total destruction of bone tissue in the jaw. This degenerative condition involves soft-tissue swelling in the mouth, infection, loosening of the teeth, drainage, and exposed bone. It is often the result of blood not properly reaching the bone.
  • Fractures of the hip and/or the femur (the long bone of the thigh). These fractures have occurred with no apparent trauma in patients taking bisphosphonates. They can occur after tripping (not falling) over a rug, or from simply walking down stairs. Dr. Kenneth Egol, professor of orthopedic surgery at NYU Langone Medical Center, said these bone fracture patients had X-ray results that looked like those of car accident victims.

FDA Urges Stronger Cautions

In November, the U.S. Food and Drug Administration (FDA) will issue a revised label for bone-building medications, including Fosamax, Actonel, and Boniva. It is expected that there will be stronger cautionary language on the product labels. According to an article in The New York Times, the FDA’s safety review was:

…prompted by concerns over a relatively small number of long-term users who had suffered unusual thigh fractures or a serious jaw disease. The benefits of the drugs have only been proven for three to five years, not longer, F.D.A. staff members said, warning about links to those rare conditions after longer use….

The committee also called for more study of the overall effectiveness of the drugs in their desired goal of preventing fractures. And the advisers recommended that the F.D.A. take a close look at why the drugs are prescribed as preventive medicine for women who do not even have osteoporosis.

There is the possibility that the FDA might recommend a “drug holiday” for some women, with the hope that it might prevent the effects that happen with long-term use.

“In my opinion, after five years in most cases it ought to be stopped,” [Dr. Susan M. Ott, an associate medical professor and bone specialist at the University of Washington] said in an interview. She prescribes the drugs for shorter periods, but said evidence shows growing risks and no proven benefits after five years.

“The longest anybody could have taken this drug is 15 years now,” Dr. Ott said. “It’s an ongoing experiment, and there are a few million women in the country who are participating in it. I keep wanting to say, ‘You’re all guinea pigs after five years because that’s when the studies stopped.’ ”

Right now, Merck, the pharmaceutical company that manufactures Fosamx, is facing more than 1,600 lawsuits over serious bone and jaw injuries. A woman in Florida was awarded $8 million by a jury after Fosamax destroyed her jaw and caused significant pain. The jury concluded that Fosamax was “unreasonably dangerous due to defective design, and that its defective design was a legal cause of Mrs. Boles’ injury.”

WHAT TO DO

Most importantly, do not discontinue taking any medications without first consulting your physician. If you have concerns about the side effects of taking bisphosphonate drugs, talk with your doctor. Seek immediate care if you are taking these drugs and experience pain in your thigh—this symptom has been a precursor to fracture in some women.

If you have experienced fractures, osteonecrosis of the jaw, or other serious side effect after taking Fosamax, Actonel, Boniva, or other bisphosphonate medications, and you want to explore your legal options, feel free to contact one of our experienced drug injury lawyers. Someone is available to take your call 24 hours a day, 7 days a week. Contact us by phone at 1-800-4-LAWMED, or fill out an online request on our website http://www.lawmed.com. The initial consultation is free. We will put our considerable resources behind all cases in which pharmaceutical drugs have harmed innocent victims.

If you have questions, HensonFuerst has answers.

RESOURCES

To read the full article in The New York Times, click there:  Stronger Cautions Backed on Bone Drugs for Women

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6
Sep

Congratulations Again, Terrell Grice!

The 2010 winner of our “My PSA Contest!” was Terrell Grice of Fayetteville. We received the following update from Terrell’s high school video teacher (Patricia Barnard, of Douglas Byrd High School):

Terrell Grice has graduated and is now attending Full Sail University in Florida after receiving a generous scholarship based on his video work. He won first place in the NC SkillsUSA Contest called “TV production skills.” He also competed at the SkillsUSA National Conference in June 2011 in Kansas City, Missouri, representing all of North Carolina. He completed a full length movie, which showcased this summer at Douglas Byrd High School, and was attended by our school board members and our School Superintendent, Dr. Till.

Terrell’s prize of an Apple MacBook computer with Final Cut Pro software allowed him to achieve his dreams by extending classroom learning into the workplace. Thank you, HensonFuerst, for supporting the TV and video programs across the state of North Carolina.

We say: Thank YOU, Patricia. We love to hear that HensonFuerst’s MY PSA CONTEST! has such a profound impact on North Carolina students. While we are delighted to help nurture Terrell’s considerable talent, we also recognize that his success—and the success of all North Carolina youth—is due to the dedication and creativity of teachers like you.

Thanks for the update! We look forward to seeing what artistry comes from the students’ imaginations in 2012.

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19
Aug

Labor Day “Booze It and Lose It” Campaign Begins

Ahh… you know summer is almost over when the Labor Day festivities begin. And today, the “festivity” in question is the annual Booze It & Lose It campaign by the Governor’s Highway Safety Program (GHSP).

From today, Friday, August 19 through Monday, September 5, the state will see checkpoints and stepped-up patrols in an effort to remove impaired drivers from the roads. How much of a force will be rallied? Well, in 2010, the Labor Day Booze It & Lose It campaign conducted more than 11,000 patrols and checkpoints.

“As summer comes to an end, law enforcement officers across the state will be removing impaired drivers from our roads,” North Carolina’s Transportation Secretary Gene Conti said. “Celebrating responsibly is simple; plan ahead and always designate a sober driver.”

According to the GHSP, in 2010, there were 500 alcohol-related crashes in North Carolina during the Labor Day campaign, resulting in 20 fatalities and 395 injuries. In addition, officers charged more than 3,200 North Carolina motorists with driving while impaired.

Enjoy summer, but please don’t drink and drive… you risk the loss of your license, at the very least.

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16
Aug

North Carolina Teen Driver Logs

A new North Carolina law that goes into effect on October 1, 2011, changes the rules for teen drivers and how they can progress from having a learner’s permit to a provisional license. And according to an article in the News & Observer, a quirk in the language of the law could keep about 110,000 teens from getting their provisional licenses when expected. According to the N&O:

The law’s most sweeping change affects teens who want to trade up from a learner’s permit, which requires Mom or Dad in the front seat, to a provisional driver’s license, which carries fewer restrictions. They’ll have to produce logs – signed by parents – to show they drove with front-seat supervision for 60 hours. The logs must be spread over at least six weeks, including some night driving.

The problem is that teens who already have their learner’s permits and hoped to get their provisional licenses after October 1 will have to have driving logs…even though the logs hadn’t been required when their permits were issued. In fact, the blank forms haven’t even been distributed.

Sixty hours of front-seat time is a huge time commitment for teens, and even worse for parents. Can you imagine trying to find an extra 10 hours each week to go driving with your child?

Fortunately, the N&O has offered a solution:  Start keeping your own logs. When the official log forms are distributed, you can simply transfer the information from your own logs to the proper forms required by law.

Today’s N&O offers downloadable copies of a sample driving log you can print out and use until an official form becomes available, the Teen “Driving to Live” Contract, and a Skills Mastery Checklist. We’ve also provided the links to the forms here (click for a pdf link):

Driving Log

Driving To Live Contract

Skills Mastery Checklist

To read the full article describing the new law from the News & Observer, click here: http://www.newsobserver.com/2011/08/16/1415694/obstacle-to-teen-license-under.html#ixzz1VDjU92rZ

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10
Aug

Study to Examine Driving in Triangle Area

An article on WRAL.com reports that a federal project will be studying the driving behavior of about 3,100 people in six states, including our own. The goal is to discover the underlying causes of crashes and traffic congestion, and eventually to reduce driving fatality rates. The project, called the Second Strategic Highway Research Program’s Naturalistic Driving Study, or SHRP2, is the largest coordinated safety program every undertaken in the United States.

Researchers will install cameras in cars to  record drivers’ movements, and radar on the front of the cars to measure the cars’ proximity to other cars and objects.

“We’re actually getting in the car with the driver to see what’s happening prior to the crash,” said Martha Wilaby, Triangle site manager of the Second Strategic Highway Research Program’s Naturalistic Driving Study.

The study is recruiting drivers of all ages, but would like to find more drivers under age 25 and older than age 65. Study participants in North Carolina must live within 50 miles of Morrisville, own or lease a qualifying vehicle, and be willing to complete questionnaires and allow driving data to be collected every 3 to 6 months for the duration of the study, which could last up to about 2 years. (Click here for a link to qualifying vehicles: Eligible Vehicle List)

The study is still recruiting. To be considered for participation, contact Martha Wilaby, at 919-388-3424, or MarthaWilaby@westat.com.

To read the full study on WRAL.com, click here:  Study looks at behavior of Triangle drivers

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8
Aug

Failure of Surgical Mesh a Serious Worry for Women

Surgical mesh is a common medical product used to repair conditions in which body organs need extra support. For example, one of the most common uses has been to repair hernias. In women, surgical mesh is also used to treat pelvic organ prolapse (POP) or stress urinary incontinence (SUI), conditions that occur when the muscles and ligaments supporting internal organs weaken. Treatment can include surgery to shore up the organs, with surgical mesh being used to keep the organs from “sagging” inside the body cavity.

Over the past three years, the U.S. Food and Drug Administration (FDA) received nearly 4,000 reports of severe complications (including 3 fatalities) associated with surgical mesh used to treat POP and SUI. The most frequent complications include:

  • erosion through vaginal epithelium (inner wall of the vagina);
  • mesh contraction, leading to vaginal shortening and pain;
  • infection;
  • abscesses;
  • pain;
  • urinary problems;
  • recurrence of prolapse and/or incontinence.

There were also reports of surgical complications when the insertion of the mesh perforated bowel, bladder, or blood vessels. In some cases, vaginal scarring and mesh erosion led to a significant decrease in patient quality of life due to discomfort and pain, including dyspareunia (painful sexual intercourse).

recent study published in the New England Journal of Medicine revealed troubling results with these procedures. Compared with traditional surgery without mesh, women who had a transvaginal mesh (TVM) inserted to treat pelvic organ prolapse suffered higher rates of serious complications, including bladder perforation and pelvic hemorrhage… and they had an increased number of adverse events after the surgery, including newly acquired urinary incontinence.

On July 13, 2011, the FDA issued an update on TVM, which clarified its recommendations:

The FDA is issuing this update to inform you that serious complications associated with surgical mesh for transvaginal repair of POP are not rare. This is a change from what the FDA previously reported on Oct. 20, 2008. Furthermore, it is not clear that transvaginal POP repair with mesh is more effective than traditional non-mesh repair in all patients with POP and it may expose patients to greater risk. [emphasis added by the FDA]

The FDA recommends that surgeons recognize that most cases of POP can be treated successfully without surgical mesh.

Unfortunately, doctors and the FDA have known about the problems with surgical mesh for at least 3 years, without warning women about the serious risks of the surgery. If you or someone you care about has a transvaginal mesh (TVM) used to correct pelvic organ prolapse or urinary incontinence and suffered any of the above symptoms, our law firm may be able to help. Contact us today to learn how. We are available 24/7 at 1-800-4-LAWMED; or contact us via our website at www.lawmed.com.

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2
Aug

Ford Recalls 1.1 Million Pickup Trucks

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[from MSNBC.com

Some Ford pickup trucks are being recalled due to a problem with the way the fuel tanks are attached. Straps that hold the fuel tanks in place can corrode and break, which can cause the fuel lines to separate from the tank, ore for the tank to actually fall to the ground. The most common cause of the corrosion seems to be road de-icing chemicals.

According to an article on MSNBC.com, Ford reports three vehicle fires and one injury related to the fuel tank strap problem.

The recalled vehicles are:

  • Ford F-150 full-size pickups, model years 1997-2004
  • Ford F-250 pickups of less than 8,500 pounds, model years 1997-1999
  • Lincoln Blackwood trucks, model years 2002-2003

Ford will notify owners in mid-September and recommend that the fuel tank straps be replaced with versions that have a greater resistance to corrosion. In addition, dealers may install a cable support under the strap an an interim repair, or a steel reinforcement over the existing straps as a permanent repair.

For more specific information, visit the recall page from the National Highway Traffic Safety Administration (NHTSA) here:  Ford truck recall information

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27
Jul

Describe Your Pain….

Anyone who has ever been severely injured in an accident, had surgery, or been diagnosed with a chronic illness knows that one of the most difficult parts of a doctor’s visit is trying to explain the quality and severity of your pain. Now, researchers are working to make that process easier for patients and their doctors.

“Pain research is very difficult because nothing allows the physician to see the patient’s pain directly,” says Werner Ceusters, MD, professor of psychiatry in University at Buffalo’s School of Medicine and Biomedical Sciences, and principal investigator on a new National Institutes of Health grant, An Ontology for Pain and Related Disability, Mental Health and Quality of Life. “The patient has to describe what he or she is feeling.”

Anyone who has ever lived with pain knows that describing it is no easy task. Typically, the first step is for the physician to ask about severity: On a scale of 0 to 10, where 0 is no pain, and 10 is pain severe enough to send you to the emergency room, how would you describe your pain. That might be easy to rate the pain at the moment, but if you go 3 months between doctor appointments, it doesn’t suffice. Some pain spikes to level-10, but settles back at a level-5.  And sometimes, living for months or years with level-6 pain can make a person feel helpless and hopeless.

The next step is to describe the pain. Healthcare workers sometimes offer a list of acceptable adjectives:  Burning, stabbing, aching, sharp, dull. That doesn’t begin to cover it. What if the pain is like nothing you’ve ever felt, and the only word that seems to describe it is, simply, pain? What if the pain feels like tiny trucks are driving over your bones–does that description make sense to a doctor?

In an article in ScienceDaily, researcher Ceusters says:

…each patient’s subjective experience of pain is different. Descriptions of pain therefore lack the precision and specificity that is taken for granted with other disorders, where biomarkers or physiological indicators reveal what health-care providers need in order to assess the severity of a particular disorder.

An added complication is that people have different vocabularies, different linguistic capabilities, and different cultural backgrounds, all of which can affect how people evaluate and describe pain. That’s why Ceusters is beginning to find ways to describe pain in uniform, formal ways. His research, funded by a grant from the National Institutes of Health, will study data gathered from thousands of patients with chronic pain in the United States, the United Kingdom, Sweden, Israel, and Germany.

In the end, the goal will be to represent what pain is, and how it relates to body parts, activities, and functions. According to Ceusters:

“Our goal is to create a software program that will allow all pain specialists to express themselves in crystal clear terms,” he says, “We will create a symptom checklist that can be understood by computers. We have to define the terminology of pain.”

For people whose lives are defined by pain, that is a worthy goal that could eventually lead to a greater understanding and treatment of a variety of chronic pain conditions.

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25
Jul

Workplace Accidents Worse After Lunch

Researchers in Spain have verified the existence of the Lunch Effect, that workplace accidents that occur between 1:00 pm and 5:00 pm are more serious and more likely to be fatal than accidents at any other time of day.

According to an article describing the research in ScienceDaily, the hours closest to lunchtime account for only about 18% of accidents, but nearly 30% of all workplace fatalities. The Lunch Effect is true for workers who are young or old…just starting on the job, or with years of experience…in small businesses, or in large corporations…at all times of the year…with all types of machinery…and for all manner of falls.

“The gravity and mortality rate of accidents are higher in the hours around lunchtime, regardless of who, how, when, where or with what the accident happens,” Miguel A. Camino López, lead author of the study, said. The researcher in the Engineering and Responsible Management Group at the University of Burgos focused on the construction sector for this study.

The Lunch Effect remained true, even after researchers took other factors into account, such as the possibility of alcohol consumption at lunch, or whether the workers took naps (remember: this was Spain, where the siesta is still respected). The researchers looked at all accidents suffered by constructions workers in Spain from 1990 to 2002–a total of 10,239,303 accidents.

“Companies can use these figures to help them understand the times of day with especially high levels of accident gravity and mortality,” stresses Camino. “Workers should be informed of these risks, and the Ministry of Employment should make greater efforts to promote preventive measures in the construction sector, such as continuous shifts.”

To read the full ScienceDaily article, click here:  Workplace Accidents Are Worse After Lunch

To read the article abstract from the journal Accident Analysis & Prevention, click here:  The special severity of occupational accidents

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13
Jul

Tainted Wipes Linked To Brain Damage, Deaths

Before every injections…before every catheter insertion…before anytime the skin needs to be punctured, the first step is to wipe the skin with an alcohol prep pad. Those are the little packets of rubbing alcohol-soaked gauze that are ever-present in hospitals and doctors’ offices. The alcohol pads sterilize the skin so that an injection is as safe as can be—last thing anyone wants is for dirt, bacteria, or other organisms to enter the body through the injection site.

So imagine what would happen if the pads were full of bacteria, if instead of sterilizing the skin, the pads themselves were a source of infection.

Unfortunately, we don’t have to imagine it. The worst did, indeed, happen.

In January, the U.S. Food and Drug Administration (FDA) announced the recall of Triad alcohol prep pads, alcohol swabs, and alcohol swab sticks due to potential microbial contamination. (Later, the recall was extended to include sterile lubricating jelly, used during vaginal examinations.)

The specific infecting bacteria were Bacillus cereus, which is rare, but most typically found in food poisoning, not hospital infections.

In April, the FDA took further action and seized more than $6 million in products distributed by Triad Group, including cough and cold products, nasal sprays, suppositories, medicated wipes, antifungal creams, and hemorrhoidal wipes. This action was taken after an FDA inspection found multiple violations of manufacturing safety practices.

NOT SOON ENOUGH

JoNel Aleccia, a reporter with MSNBC, has been tracking this story from the beginning, and is conducting her own investigation into the problems caused by the tainted wipes. (To read all related articles, click here: MSNBC’s investigation.) It’s a lot of information, so we’ll summarize the major points.

  • The FDA claims that the severity of the contamination wasn’t known until a Colorado hospital reported a life-threatening infection in November 2010. [MSNBC-1]
  • Then, on December 1, 2010, a lively 2-year-old boy in Houston died of acute bacterial meningitis caused by Bacillus cereus. [MSNBC-2]
  • By July 1, 2011, the FDA had received reports of a total of 8 deaths, 11 infections, and about 250 other health problems all linked to Triad Group products. Bacillus cereus was specifically cited as the cause of death of a 66-year-old man who was being treated for skin cancer and diabetes. [MSNBC-3]
  • Just this week, there was another heartbreaking story of a child whose life was permanently altered by an infection, possibly caused by a Triad wipe. Twin boys were born on September 1, 2007. One twin has developed normally, while his brother cannot walk or speak and must be fed through a stomach tube. He suffers from cerebral palsy and mental delays. And all his problems have been linked to a bacterial infection with Bacillus cereus, which damaged portions of his brain shortly after birth.

It is possible that Triad wipes were to blame. According to an MSNBC article:

An msnbc.com review of the documents shows that FDA inspectors in 2006 found that an H&P Industries Inc. plant in Mukwonago, Wis., “failed to adequately address potential contamination in raw material” used for drug products. In 2002, the firm was cited for failing to “verify the effectiveness of the sanitation process.” An investgation in 2000 found similar problems, inspectors reported.

According to the article, a top DFA official admitted to members of Congress that the agency should have issued a formal warning letter to the firm in August 2010, instead of allowing voluntary compliance.

It’s almost enough to make a person lose faith in the ability of the FDA to properly protect the public.

AFFECTED PRODUCTS

The contaminated products were made by Triad, but could be marketed under a variety of different names and different packaging kits, including:

  • Triad
  • Cardinal Health
  • PSS Select
  • Boca/Ultilet
  • Moore Medical
  • Walgreens
  • CVS
  • Conzellin
  • Smith & Nephew
  • Arixtra Starter Kit
  • Relistor
  • Betaseron pack
  • Boniva pack
  • Fuzeon pack
  • Nutropin A.Q. Pen pack
  • Pegasys Pak
  • TNKase pack
  • Extavia pack
  • Trelstar pack
  • Forteo starter kit
  • Churchill Medical Systems’ Skin-Prep Wipes

To read the initial FDA recall notice, and to learn how to report adverse effects, click here:  FDA recall notice

If you believe that you or someone you love has been injured as the result of infection caused by one of these products, the lawyers of HensonFuerst Attorneys can help you investigation your legal options. Someone is available 24/7 at 1-800-4-LAWMED. If you have questions, HensonFuerst has answers.

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