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Yaz Attorney Legal Update

Yaz Lawsuit Update 05/17/2012: It has yet to be determined how many more Yaz Lawsuits Bayer will have to face. It is clear that the case is not near an end despite the fact that Bayer is already in settlement talks with a large number of plaintiffs that have already filed a Yaz Lawsuit. Although Bayer has indicated that it plans to start making settlement offers on the 11,000 plus Yaz Lawsuits it currently faces, new Yaz Lawsuits are still being filed. On or about April 04/24/12 Case Number 3:12-cv-20100-DRH-PMH was filed on behalf of 4 adults and one minor child. The Yaz Lawsuits were filed in the United States District of Court of Minnesota.

The Yaz Lawsuit was filed on behalf of all plaintiffs involved as a single lawsuit although each plaintiff’s damages were set forth individually.

This Yaz Lawsuit was filed based on the following cause(s) of action: strict products liability, breach of express and implied warranty, negligence, negligence per se, fraudulent misrepresentation, fraudulent concealment, fraud, negligent misrepresentation, and unjust enrichment brought by Plaintiffs for damages associated with their ingestion of the pharmaceutical drug YAZ/Yasmin, also known generically as Drospirenone and Ethinyl Estradiol .

 

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National Women’s Health Week: The Dangers of Using Tobacco Products

By: Lawrence R. Deyton, M.S.P.H., M.D.

The health of every American is of the utmost importance to the Food and Drug Administration, which regulates the manufacture, marketing, and distribution of tobacco products.  Our Center for Tobacco Products works to improve public health, with the goal of making sure that tobacco-related death and disease is part of America’s past, not its future. Lawrence R. Deyton, M.S.P.H., M.D.National Women’s Health Week, May 13-19, provides an opportunity for us to reach out and remind the women in our lives about the dangers of tobacco use and exposure to second-hand smoke — which claims the lives of nearly 200,000 women every year.

Never starting to use tobacco products and quitting tobacco use – for those who do use tobacco – is proven to lead to longer and healthier lives for everyone.

There is no question that tobacco use is dangerous to women. Just consider a few of the facts:

  • An estimated 173,940 women die every year due to cigarette smoking
  • An estimated 18,000 non-smoking women die every year from exposure to second-hand smoke
  • Smoking causes almost 80% of lung cancer deaths in women
  • Smoking causes cervical cancer and eight other cancers
  • Smoking causes infertility and poor pregnancy outcomes
  • Smoking causes low bone density and hip fractures in women

National Women’s Health Week is the perfect time for you — or one of the important women in your life — to break a dangerous addiction to tobacco, and for those who do not use tobacco, it is a time to be empowered to never start. Need help? Here are some great resources:

When we spend countless hours taking care of our families and friends, it’s far too easy to forget to look after our own health. This coming week, make an investment in yourself and the women who are close to you by committing to a life that’s free of tobacco-related disease and death.

Lawrence R. Deyton, M.S.P.H., M.D., is the Director of FDA’s Center for Tobacco Products

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FDA’s Role in Promoting Women’s Health

By: Marsha Henderson, M.C.R.P.

For one week in May, the nation celebrates women’s health. I often find at these celebrations that no one mentions FDA. This is unfortunate, because throughout its 100-year history FDA has played a leading role in advancing women’s health. 

Marsha Henderson, M.C.R.P.In its early years, the Agency worked to ban harmful, addictive and poisonous tonics that were marketed as cure-alls for women. Later, FDA worked to help women avoid public health tragedies like the serious birth defects seen in many countries where pregnant women used thalidomide – a drug that was not approved in the U.S. thanks to Dr. Francis Kelsey, an FDA medical officer.

When I joined FDA in the 1990’s, the Agency was working hard to remove regulatory barriers that limited our understanding of how medicines and medical devices affect women. We changed the regulations. We partnered with NIH, academia, advocacy groups, and drug companies to support women’s health research. We also developed strategies to increase the number of women included in clinical trials for new medical products. These activities helped all of us learn more about the ways sex differences affect the safety and usefulness of FDA-regulated products.

During this time, I also helped launch the Take Time to Care Outreach Program. Through this program, FDA has been able to use creative partnerships and innovative outreach tools like telenovelas to connect millions of women with reliable information they can use to make better health decisions for themselves and their families.   

All of these efforts have helped to protect and promote the health of women – leading the way to improved policies and greater awareness about vital women’s health issues such as diabetes, mammography, and medication use during pregnancy.  We have made great strides; however, there is still much work to be done. FDA will continue to promote policies, research and educational initiatives that advance women’s health.

During this year’s National Women’s Health Week, I thank FDA employees and our external partners for their continued service to women’s health. I also encourage the nation’s health professionals and the women they serve to look to FDA for women’s health resources.  We are here for you. 

Marsha Henderson, M.C.R.P., is FDA’s Assistant Commissioner for Women’s Health

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Talk With Your Kids About Tobacco

By: Margaret A. Hamburg, M.D.

The next time you’re out with your kids, take a moment to pause and look at the adult smokers you pass on the street.  Research shows that many of them took up the addictive habit when they were kids — and too young to truly understand the very real risks and dangers of tobacco use.

Margaret Hamburg, M.D.By law, a person has to be at least 18 years old to purchase tobacco products, yet more than 80 percent of adult smokers began before they were 18.  Each day in the United States more than 3,800 youth smoke their first cigarette.  It’s estimated that more than 1,000 youth become daily smokers each day.

As a mother and a doctor, I know that this is something that must change.  And, one of the best ways to help our kids grow into healthy, happy adults is to teach them about the dangers of smoking and tobacco use. And, just as you do with your family, you can play an important role in your community when it comes to getting the word out about the dangers of tobacco. FDA is working to ensure retailers are fully aware of regulations that help protect kids from the dangers of tobacco.  Everyone — from moms (and dads!) to retailers and community leaders — can help protect kids from tobacco.

We all know that our nation’s youth hold the key to our future.  This Mother’s Day, let’s make sure it’s a healthy one.

Margaret Hamburg, M.D., is Commissioner of the U.S. Food and Drug Administration

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Paxil Lawsuit Report

Paxil Lawsuit News – 5/11/2012: Did you take Paxil? Please contact us today if you took Paxil and later experienced harmful side effects. We will connect you with a lawyer that is experienced in complex litigation that may be able to help you recover monetary damages.

Paxil Lawsuit: A link has been suggested between Paxil and brain defects. In fact, the topic of Paxil and pregnancy has been popular recently. It is believed that women who take Paxil during pregnancyincrease the risks of their child being born with a brain defect. More specifically, Paxil is a selective serotonin reuptake inhibitor (SSRI), and it is believed that women who take SSRIs during pregnancy significantly increase the risks of their newborns having a brain defect.

Paxil, and other SSRIs, are prescribed to treat depression and other disorders. It may be almost inevitable that there are some women who take Paxil while pregnant. Sometimes women will take Paxil while pregnant because of diagnosed severe depression that has not been successfully treated with a less risky medication. When this is the case, the ratio of benefits versus risks must be considered. Other times, a woman will become pregnant after she has already been taking Paxil for a period of time, but does not yet know about the pregnancy for weeks or even months. Unfortunately, birth defects from Paxil are most likely to develop during the first trimester of pregnancy which involve the earliest stages of the baby’s development. However, it is not impossible to develop Paxil birth defects during the later stages of pregnancy. One of these birth defects includes Anencephaly (no forebrain). This is a terrible Paxil side effect to suffer from. When a baby has Anencephaly, he or she is severely malformed and unable to function normally. A baby with this condition will unfortunately die before or within just a few days of birth. Another side effect of Paxil is called Craniosynostosis. This is a condition that involves the skull of the fetus forming too early, preventing the brain from growing properly. Craniosynostosis is a life-threatening and debilitating brain defect.

If you were pregnant and took Paxil and your child suffers from a side effect of Paxil, contact a Paxil birth defects lawyer. You will then be able to learn more about your legal rights and options. Once your case is evaluated, they may be able to assist you in filing a Paxil lawsuit.

Our use of the term or terms Paxil Lawsuit is for descriptive purposes only. There is no relationship between the owners of this website and the maker of the product discussed in this post. Our use of the words Recall, Class Action Lawsuit and other similar words related to an event do not necessarily mean that this event has occurred. Refer to the website of the United States Food and Drug Administration for information on drug or medical device recalls. If a Class Action Lawsuit is formed in relation to the product discussed in this post we will provide that information at the time the Class Action is formed. A Class Action Lawsuit is not required to exist for you to file a lawsuit if you have been injured by the product discussed in this post.

To keep up to date on Paxil Lawsuit visit our site often.

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FDA’s Modern “Corps of Discovery” in China

By: Christopher Hickey, Ph.D.

I love history.  I especially love the story of Meriwether Lewis and William Clark who, in their famed venture to explore the newly-purchased Louisiana Territory at the direction of U.S. President Thomas Jefferson, fashioned a lean and mean team largely consisting of seasoned, highly qualified frontiersmen. While Lewis and Clark’s “Corps of Discovery” benefitted to some degree from maps that had been developed by previous explorers who had traversed similar terrain, there was a large swath of territory in the middle of their journey that was literally “off the map”—no non-native groups had ever set foot on those pieces of the North American continent.  And while brawny, rough-and-tumble, frontiersmen may have dominated the rolls of the Lewis and Clark expeditionary force, they would have all frozen or starved to death had it not been for the keen and savvy brilliance of Sacagawea, surely one of the unlikeliest heroines in American history.

Christopher Hickey, Ph.D.

The Honorable Margaret Hamburg, Commissioner, FDA and Dr. Christopher Hickey, Country Director, FDA China

I also love my job.  I run FDA’s China Office.  Nearly four years in, I still pinch myself most mornings to make sure I’m actually getting paid to lead this fascinating, unpredictable 21st century expedition to explore new public-health frontiers for my country.

Like Lewis and Clark, we in the FDA China Office have been fortunate enough to benefit from a surfeit of talented “frontiersmen” – and women! – who’ve volunteered for this pioneering venture.  They include inspectors and policy analysts who, in some cases, have served FDA for nearly four decades!  They’ve seen marked similarities between the challenges we face in China in 2012 and the challenges FDA faced in regulating domestic U.S.industry several decades ago.  Our “pioneers” include FDA food scientists and biochemists with deep, rich expertise who are now applying that knowledge to work in collaboration with Chinese authorities as they develop a regulatory system that will keep pace with increasing Chinese economic growth, and ever-expanding exports to U.S.markets. And our “FDA Corps of Discovery” includes legal, policy and health diplomacy professionals.  These professionals apply their knowledge of FDA standards and regulations, as well as their scientific and diplomatic expertise, to enhance the Agency’s knowledge base about China’s regulatory landscape. In addition, they track industry trends to inform U.S. regulatory decisions and actions, and strengthen collaboration on mutual regulatory challenges.     

And we certainly find ourselves, like Lewis and Clark, “off the map,” at times.  How do you navigate a regulatory system that assigns responsibility to government agencies not by product category but by where the product currently sits in the system of production and distribution? How do you engage a regulatory counterpart that has export promotion as a primary mission?  How does FDA engage a regulatory system where the legacy of state-owned enterprises still looms large?  These are all “off-the-map” types of questions we’ve had to face.

And we have our Sacagaweas—unsung, unlikely public-health heroes.  While U.S.civil servants lead the way for our efforts in China, Chinese nationals play a key role to support our work—liaising with the Chinese Government, negotiating cross-cultural communications, and supporting our inspections throughout China.  FDA could not do its work in China—or in any of its overseas offices—without dedicated foreign service nationals.

“Those who cannot remember the past are condemned to repeat it,” Spanish philosopher George Santayana once opined.  In FDA’s China Office, we strive to remember the best of our past so that we can know how best to engage our emphatically globalized future.

Christopher Hickey, Ph.D., is FDA’s China Country Director

 

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Biologic Product Shortages

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Paxil Lawsuit

Paxil Lawsuit News – 5/9/2012: Please contact us today if you took Paxil and suffered unusual side effects or other injuries.

Paxil Lawsuit: Paxil Birth Defect Class Actionlawsuit can be filed on your behalf if you have experienced negative effects from taking the drug Paxil. A Paxil Birth Defect Class Action is a form of lawsuit where a large group of individuals collectively bring a claim to court. The purpose of filing a Paxil Birth Defect Class Action lawsuit is to obtain financial compensation for pain, suffering and medical expenses incurred by you and your family. Complete the form above or call Best Legal Source at 800-611-7080 to get in contact with an experienced an attorney who could file a Paxil Birth Defect Class Action Lawsuit for you.

1-800-611-7080

A Paxil Birth Defect Class Action Lawsuit is a realistic measure if someone in your family has been permanently harmed as a result of the drug Paxil. A Paxil Birth Defect Class Action can help those individuals who are under financial burdens as a result of hospital and doctor related bills due to injuries possibly caused by the drug Paxil. Best Legal Source can help you find the right attorney to file your Paxil Birth Defect Class Action suit. Time is often a matter of extreme importance in cases like these, so call today. Best Legal Source can help you take the first step.

 

1-800-611-7080

 

Our use of the term or terms Paxil Lawsuit is for descriptive purposes only. There is no relationship between the owners of this website and the maker of the product discussed in this post. Our use of the words Recall, Class Action Lawsuit and other similar words related to an event do not necessarily mean that this event has occurred. Refer to the website of the United States Food and Drug Administration for information on drug or medical device recalls. If a Class Action Lawsuit is formed in relation to the product discussed in this post we will provide that information at the time the Class Action is formed. A Class Action Lawsuit is not required to exist for you to file a lawsuit if you have been injured by the product discussed in this post.

To keep up to date on Paxil Lawsuit visit our site often.

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Yaz Lawsuit Process

Yaz Lawsuit News – 5/9/2012: If you were prescribed Yaz and have suffered negative side effects, please contact us today so that we can put you in touch with an attorney to advise you of your legal rights.

Yaz Lawsuit: A Yaz Class Action Lawsuit is a legal process carried out by one or more Yaz Lawyers to represent the interests of a large group of individuals with the same grievance. Yaz, along with other birth control pills that contain the hormone drospirenone, may be linked to blood clots according to the U.S. Food and Drug Administration’s safety review. This has led to the filing of Yaz Class Action lawsuits. If you took Yaz and later developed blood clots, call Best Legal Source at 800-611-7080 or complete the form to the right and we will connect you with a Yaz Lawyer significantly experienced in pharmaceutical litigation like the Yaz Class Action Lawsuit.

A Yaz Class Action is a general term used to describe the legal process and service provided by Yaz Lawyers who pursue a joint case for a group of victims. Using the terms Yaz Class Action, Yaz Class Action Lawsuit, Yaz Lawyer and Yaz Lawyers does not imply any connection between the makers of Yaz and Best Legal Source. Best Legal Source helps women who developed similar injuries find Yaz Lawyers capable of pursuing a Yaz Class Action Lawsuit for them.

Our use of the term or terms Yaz Lawsuit is for descriptive purposes only. There is no relationship between the owners of this website and the maker of the product discussed in this post. Our use of the words Recall, Class Action Lawsuit and other similar words related to an event do not necessarily mean that this event has occurred. Refer to the website of the United States Food and Drug Administration for information on drug or medical device recalls. If a Class Action Lawsuit is formed in relation to the product discussed in this post we will provide that information at the time the Class Action is formed. A Class Action Lawsuit is not required to exist for you to file a lawsuit if you have been injured by the product discussed in this post.

To keep up to date on Yaz Lawsuit visit our site often.

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Complete List of Currently Approved NDA and ANDA Application Submissions

Information updated through April 30, 2012
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