Showing posts with label Safety. Show all posts
Showing posts with label Safety. Show all posts

Tuesday, July 10, 2012

FDA unveils safety measures for opioid painkillers

Drugmakers that market powerful painkiller medications will be required to fund training programs to help U.S. doctors and other health professionals safely prescribe the drugs, which are blamed for thousands of fatal overdoses each year.

The safety plan released by the Food and Drug Administration on Monday is designed to reduce misuse and abuse of long-acting opioid pain relievers, which include forms of morphine, methadone and oxycodone. The agency's plan mainly involves educating doctors and patients about appropriate use of the drugs.

The FDA has issued a number of warnings on prescription pain relievers in recent years but with little effect. Inappropriate use of the drugs caused nearly 425,000 emergency department visits in 2009, according to government figures. The drugs were blamed for 15,600 deaths that year, up from 14,800 in 2008.

The FDA said companies that sell the drugs must offer two to three hours of training to prescribers, either for free or for a small fee. The courses will be designed by companies that provide continuing medical education for health professionals, not by the drugmakers themselves.

The agency wants companies to provide training to least 60 percent of the 320,000 U.S. prescribers of the drugs within three years of launching the programs. The programs, which will be vetted by FDA regulators, must be available by March 2013.

"Responsible physicians will welcome the education benefits provided by this program," said Dr. Lynn Webster of the American Academy of Pain Medicine.

In addition to training, drugmakers will be required to distribute safety brochures to patients explaining the risks of the drugs and instructions to seek emergency care in event of an overdose.

The FDA spent more than three years developing the so-called risk management plans for the drugs, with input from industry and health care professionals.

Some health care experts stressed that training should be required for all prescribers. But FDA officials said the programs will be optional for now because making them mandatory would require a new law by Congress.

The new FDA plan covers about 30 opioid drugs, including Purdue Pharma's OxyContin, Johnson & Johnson's Duragesic patch and Pfizer's Embeda. Opioids are drugs that simulate the effects of natural narcotics, such as the opium poppy. They are typically prescribed for people already taking pain medications, including cancer patients, to treat severe pain flare-ups.

The products targeted by the FDA feature extended-release formulations designed to give long-lasting effects. But that potency carries serious risks when doctors prescribe them inappropriately, and when patients abuse them as stimulants.

The FDA reports that many physicians prescribe the painkillers for patients with migraine headaches, an unapproved use. Patients will also sometimes chew extended-release pills that are designed to be swallowed, causing an overdose.



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Thursday, June 28, 2012

FDA Probing Safety of Metal-on-Metal Hip Implants

HealthDay – 31 mins ago TUESDAY, June 26 (HealthDay News) -- While thousands of Americans have benefited from hip replacements over the years, problems with metal-on-metal implants can lead to troubles requiring surgery to replace defective devices, experts say.

Specifically, experts say, tiny fragments of metal can shear off from these joints, causing chronic pain or infection and raising levels of metals in the bloodstream. Experts estimate that more than 500,000 Americans have received a metal-on-metal hip joint, mostly between 2003 and 2010.

Worry over the failure rate of the implants, and the speed at which they were initially approved for the U.S. market, has led to a special two-day session, beginning Wednesday, by experts at the U.S. Food and Drug Administration.

"Data from recent studies and from FDA's own review show some patients experiencing complications, including the need for additional surgeries, which could be attributed to metal-on-metal hip implant devices," said FDA spokeswoman Michelle Bolek.

Since 1999, almost 17,000 problems with these devices have been reported to the FDA. Of these, more than 12,000 were reported last year alone.

According to the agency, the problems with metal-on-metal implants are about the same as those seen with polyethylene and ceramic implants, except for the specific risks caused by the metal itself.

But others say that when it comes to complications, metal-on-metal implants are in a class of their own. Writing earlier this month in the New England Journal of Medicine, Dr. Joshua Rising of the Pew Charitable Trusts, and colleagues said that "there is now compelling evidence that these implants fail at a higher rate than hip prostheses made of other materials; indeed, one type of metal-on-metal hip has a failure rate of nearly 50 percent at 6 years."

Responding to these concerns, the FDA panel is considering the risks and benefits of metal-on-metal implants and what might be needed to monitor the health of patients who have them.

Of the estimated 400,000 hip replacements done in the United States each year, 27 percent involve metal-on-metal devices, according to the FDA.

Critics, including an independent panel of experts at the Institute of Medicine, have noted that metal-on-metal implants may have been approved too quickly under the FDA's "fast-track" program for medical devices.

Responding to concerns, in May 2011 the FDA ordered manufacturers to carry out "post-market" studies, tracking the safety of metal-on-metal hip implants in recipients. But in the NEJM article, Rising and colleagues noted that most of these studies have yet to begin and their first results will take years to arrive.

The FDA's Bolek made it clear that the advisory panel meeting is not a regulatory meeting and is not intended to look at the process that brought the devices to the market, or to deal with any planned or current post-marketing studies.

Metal-on-metal devices have already been recalled twice. In 2008, a device from manufacturer Zimmer, the Durom Acetabular Component, was recalled because instructions were not clear.

And in 2010 a device from DePuy Orthopaedics Inc. was recalled because more patients than expected had to have new surgeries, according to the FDA.

Earlier this month, a device called the R3 Acetabular System from Smith & Nephew was taken off the market because the company said it was "not satisfied with the clinical results of this component."

In Europe these concerns have led to calls to ban metal-on-metal hip replacement devices. Writing in March in the journal The Lancet, British researchers concluded that "metal-on-metal stemmed articulations give poor implant survival compared with other options and should not be implanted." Metal-on-metal implants had a five-year failure rate of more than 6 percent, three times higher that seen with ceramic or plastic joints.

Banning metal-on-metal joints isn't an option being considered by the FDA panel at this time.

"During the panel meeting, FDA will discuss failure rates and modes for these devices, as well as any local and systemic complications that could result from metal debris and metal ion levels in the bloodstream from the device," Bolek said.

The panel will also discuss metal ion testing and soft tissue imaging, tools that can potentially be used in the clinical management of patients who have these devices, Bolek said.

"We will also review specific risk factors for specific patient populations and considerations for post-implant follow-up," she added.

Mindy Tinsley is a spokeswoman for metal implant maker DePuy Orthopaedics Inc., which is owned by Johnson & Johnson. She said that "DePuy believes that no single bearing surface meets the needs of all patients, and metal-on-metal implants provide the potential benefit of greater function and a lower risk of dislocation for some patients."

Tinsley also said that all metal-on-metal implants are not alike and they should not be grouped together if problems arise.

One orthopedic expert agreed. Dr. Joshua Jacobs, first vice president of the American Academy of Orthopaedic Surgeons, said that "metal-on-metal devices are not all the same. You have to go down to the individual product to fully understand the result. When you lump metal-on-metal together you miss a lot of important differences."

According to Jacobs, who is chairman of the department of orthopaedic surgery at Rush University Medical Center in Chicago, the advantages of metal-on-metal implants are that there is typically less wear on the joint, leading to less loosening and less bone loss over time.

In addition, he said, metal allows for a thinner, larger socket and head, which makes it less likely the hip will dislocate after surgery, which is a common failure of other types of hip replacement.

Still, given the problems with these devices, Jacobs agrees that patients need to be monitored.

"We are trying to learn the optimal way of monitoring patients with metal-on-metal implants, so we can understand when it is appropriate to intervene," he said. "Right now we are amassing clinical data to understand that better."

More information

For more on hip replacement, visit the American Academy of Orthopaedic Surgeons.



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Thursday, June 21, 2012

Samsonite pulls bags from HK amid safety scare

Samsonite International SA says it has pulled a line of luggage from Hong Kong stores after a local consumer group reported finding high levels of a chemical linked to cancer in the handles.

The suitcase company said Monday that it commissioned independent tests that showed its bags were safe to use. But it was taking the bags off the shelves to allay customer fears following the report by the Hong Kong Consumer Council.

The council said last week it found that the side handles on three Samsonite suitcases had levels of polycyclic aromatic hydrocarbons that were higher than recommended.

Levels were particularly high in a suitcase sold under the Tokyo Chic line. Samsonite said it has withdrawn all luggage from that line from Hong Kong shelves.



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Thursday, June 14, 2012

FDA reviews safety of innovative heart valve

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Monday, May 28, 2012

Keep Food Safety in Mind This Memorial Day Weekend

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Sunday, May 27, 2012

Tide to change Pods lid over child safety concerns

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Sunday, May 13, 2012

FDA report on Gilead's Quad focuses on kidney safety

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Tuesday, April 24, 2012

HeartWare shares up as FDA safety review minimized

Reuters – 3 hrs ago WASHINGTON (Reuters) - U.S. medical device reviewers said HeartWare International Inc's blood pump seemed to help people with severe heart failure but raised concerns about device-associated clotting rates and stroke.

However, analysts said the review by Food and Drug Administration staff raised few new issues and bet the device would be approved, sending HeartWare shares up 4.3 percent to $70.01 in morning trading on Nasdaq.

FDA staff also said clinical trial results for the mechanical heart-assist device, or the HeartWare ventricular assist device (HVAD), may have missing data and are difficult to compare with a registry of patients.

In clinical trials, HeartWare compared patients who got its device to a registry, or database, of patients with mechanically assisted circulatory support. It was the first blood pump trial to use a registry as a control arm.

FDA staff said the registry may have had more people who were critically ill, skewing results in favor of HeartWare's pump.

The staff also said 16 of the 250 people implanted with HeartWare's device had blood clot-related pump failure, and 15 of them needed to replace their pumps. HeartWare said people who needed to a new device should not be considered as failures.

"(But) FDA continues to believe that the need for device exchange is a relevant consideration when assessing the device's safety and effectiveness and seeks panel input on this issue," the FDA staff said in documents posted online on Monday.

The FDA staff review comes ahead of a meeting of outside experts who were due to vote on the device on Wednesday. The FDA will make a final decision later.

Heart failure is a chronic and incurable condition, in which the heart is too weak to pump enough blood to meet the body's needs. In the most severe cases, people may need a heart transplant.

HeartWare's device helps people with failing hearts pump blood while awaiting a heart transplant. The device is already approved in Europe.

It is estimated that some 50,000 people around the world are candidates for heart transplant, but only some 5,000 patients per year get them.

If approved, the device will compete with Thoratec Corp's HeartMate II, which has been sold in the United States since 2008. It is currently the only blood pump available to people with heart failure who are waiting for a transplant.

Larry Biegelsen, analyst at Wells Fargo, said the FDA review did not contain any major surprises.

"We believe the overall success of the pivotal trial and FDA's desire to have an alternative pump on the market to Thoratec's HeartMate II will result in approval of the HVAD later this year," he said in a research note.

Many investors have been betting HeartWare's device will eventually eclipse the HeartMate II since it is smaller and takes less time to implant. However, concerns about pump-associated thrombosis, or the formation of blood clots, as well as stroke issues, could hurt market share.

Biegelsen said the higher stroke rate with HeartWare's device, especially compared to the Thoratec device, will be the greatest challenge during the panel on Wednesday.

The FDA said 8 percent of patients who got HeartWare's blood pump during clinical trials had an ischemic stroke, compared to a rate of 5 to 6 percent in trials of other devices. In an ischemic stroke, a blood vessel that supplies blood to the brain is blocked by a clot.

HeartWare is also testing its device as a long-term treatment for patients who are not eligible for a heart transplant or may not be able to get one.

(Reporting by Anna Yukhananov; Editing by Gerald E. McCormick, Maureen Bavdek, Dave Zimmerman)



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Monday, April 2, 2012

A New Research-Based Sun Safety Program at 40 Hotels and Resorts in the United States to Include Sun Protection Clothing

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2012The Go Sun Smart program is planned for 40 selected resorts in the United States over the next three years and Sun Threadz, a sun protection clothing company, has been invited to be part of this program. Sun Threadz are designed and produced in the USA.


Philadelphia, PA-NJ (1888PressRelease) April 02, 2012 - Go Sun Smart is a research study sponsored by San Diego State University. The purpose of the project is to educate vacationing Americans about comprehensive sun safety techniques and skin cancer prevention. The study is funded by the National Cancer Institute, and has the potential to reach a significant portion of the US population when they are most vulnerable to skin damage from the sun.

Sun Threadz will join the Go Sun Smart project in the fight against skin cancer. Employees of the project will be outfitted in sun safe attire and will visit the resorts and interface with vacationers from a nationwide market. Damage from the sun can be prevented by applying sunscreen, wearing sun protective clothing, wide brim hats, seeking shade when necessary and recognizing when UV is highest and most dangerous.

This program will start the beginning of spring 2012 at twenty resorts and the other twenty resorts will receive the program one year later.

Over one million cases of non-melanoma skin cancers occur annually, and melanoma increased 4% each year for decades, significantly burdening the nation's health system.

The program will use positive, upbeat messages and stories that stress gains from being sun safe consistent with guests' positive vacation experiences to encourage advanced sun safety behaviors. Vacationers will receive important and accessible information that can shift their understanding about over-exposure to the sun while vacationing. Sun safety behaviors are easy to implement but reminders are required to convince vacationers to be sun safe.

Sun Threadz was founded by a melanoma survivor who is an advocate for a sun safe lifestyle.

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