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Blog Posts in March, 2012

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Public Calls for Additional Oversight of Implanted Medical Devices

While Congress attempts to speed up the approval process for medical devices, a recent survey shows that the general public wants the opposite to happen. Results from a new Consumer Reports poll ...
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New Bill to Speed Up Drug Approval Process

At a time when drug and medical device recalls are prevalent, due in part to an overly streamlined Food and Drug Administration (FDA) approval process, a group of biotech firms and patient advocates ...
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What Bayer Doesn't Want You to know About Yaz and Yasmine

Yaz and Yasmin are two combined hormonal oral contraceptive pills marketed by Bayer. The major active ingredient in both pills is Drospirenone (DSRP), a type of progestin that prevents pregnancy and ...
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Generic Drug Makers Won't Be Held Accountable

When the Hatch-Waxman Act of 1984 allowed pharmaceutical companies to produce generic drugs, it required that all generic drugs use the same labels as their name brand equivalents, including all the ...
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Merck's New Drug Gives Disappointing Results

Merck & Co., the manufacturer of products like Claritin and Lotrimin, has seen disappointing results from the testing of their new blood thinner Vorapaxar. This was the drug's second large ...
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Chantix and Increased Risk of Suicide

Among the many negative side effects you can suffer from after your use of Chantix, there is one that is extremely serious. The FDA warned in 2007 that there is a possible link between Chantix use and ...
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Hidden Dangers of Medi-Spas

You've probably heard the advertisements on radio and TV—so called "med-spas" offering services from waxing and massage to Botox, lipo and more. It sounds appealing if you are in ...
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Elderly Patients More Likely to Die from Misreading Drug Labels

This blog issued a previous report discussing the fact that patients don't understand the information that comes with their medications, but now a disturbing new study reveals that older ...
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Wright Medical Technology Joins the Multidistrict Litigation Club

Wright Medical Technology is being brought to multidistrict litigation (MDL) by federal lawsuits because of their defective hip replacements. The injuries are similar to those who have suffered from ...
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Accutane Settlement Upheld in Court

In 2008, Karnie Kendall was awarded $10.5 million dollars by a jury, after her attorneys proved that Accutane, a medication she took to treat acne, had caused her to develop ulcerative colitis. ...
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Pradaxa Causing Severe Side Effects

This is important information if you were prescribed and were or are currently taking the drug Pradaxa (dabigatran). Pradaxa is typically prescribed to those at risk for stroke and blood clots because ...
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Current Transvaginal Mesh Lawsuits

Transvaginal mesh is a medical device used to treat pelvic organ prolapse in women and also some cases of stress urinary incontinence. There have recently been many cases of injury popping up as a ...
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U.S. Government to Push for Higher Settlement with Johnson & Johnson

The U.S. Justice Department is demanding that Johnson & Johnson pay $1.8 Billion to resolve complaints that they illegally marketed the atypical antipsychotic drug Risperdal for unapproved ...
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Safety Issues Uncovered at Major Dallas Hospital

Parkland Public Hospital in Dallas is being monitored by federal regulators after an October incident when a suicidal patient was able to escape from her room and light her shirt on fire. Fortunately, ...
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CVS Drug Mix Up Exposes Children to Risk

New Jersey's Attorney General is investigating a CVS pharmacy that mistakenly gave children a breast cancer drug instead of fluoride pills. The attorney general's consumer affairs department ...
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Final Word on Metal-on-Metal Hip Implants: Don't Use Them

A new report issued in the UK has unequivocally warned against implanting metal-on-metal hip devices due to their extremely high failure rate. Patients particularly at risk include women, younger ...
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New Bill Seeks to Identify Safe Online Pharmacies

Illegal online pharmacies are on the rise, and now the government is trying to do something about it. Bipartisan bills were introduced in both the House and the Senate this week, proposing to create a ...
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Still Not Enough Information Available to Determine Safety of Pediatric Drug Treatments

A recent report by the Institute of Medicine (IOM) has revealed that the federal laws which require drug companies to conduct pediatric drug studies have not resulted in sufficient data on the safety ...
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Will New Legislation Permit Over-the-Counter PPIs?

Health care systems are overburdened, according to some lawmakers. That is why the FDA is considering waiving the need for prescription for many diabetes and cholesterol medications. By eliminating ...
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Can Chantix Curb Drinking Problems?

New studies show that the stop-smoking drug Chantix may also help those struggling with a drinking problem. It is not yet known how the drug helps those with a drinking problem, but it may just be a ...
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Reports Say Johnson & Johnson Knew of DePuy Failure Long Before Recall

According to reports, Johnson and Johnson knew that their DePuy hip implants were defective a year before they were recalled. The New York Times published a story including the contents of an email ...
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Mixup at GlaxoSmithKline Plants Leads to Recalls

GlaxoSmithKline, the manufacturer of Avandia, recently issued a recall of near 400k bottles of their high blood pressure medication for fear of a possible mix-up at one of their manufacturing plants. ...
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Patients Don't Understand Instructions About Their Prescription Drugs

Patients don't understand the drug safety information provided with their prescription medications, a new study presented at the American Academy of Pain Medicine's 28th annual meeting has ...
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FDA Gets Pressure to Provide Guidance on Safety of Propecia

The team of drug injury attorneys at Arnold & Itkin is well aware of the dangers surrounding the hair loss drug Propecia, but it appears that the Food and Drug Administration (FDA) still ...
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Penalty for Medical Device Manufacturer that Sold Unapproved Devices

The manufacturer of a spinal implant will pay the U.S. Food and Drug Administration (FDA) a $1 million penalty for marketing an unapproved medical product. The penalty was agreed upon in a settlement ...
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30 results found. Viewing page 1 of 2. Go to page 1 2   Next
FDA Gets Pressure to Provide Guidance on Safety of Propecia
The team of drug injury attorneys at Arnold & Itkin is well aware of the dangers surrounding the hair loss drug Propecia, but it appears that the ... Read More [+]
You May Be At Risk For Suicide If...
While suicidal thoughts don't just occur in people who are taking prescription drugs, a large amount of people who were not at risk for suicide be... Read More [+]
Amgen Fined $762 Million for Illegally Marketing Anemia Drugs
Amgen Inc. has agreed to pay $762 million to resolve allegations that the drug maker illegally marketed its anemia treatment Aranesp for unapproved us... Read More [+]