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Blog Posts in 2012

113 results found. Viewing page 1 of 5. Go to page 1 2 3 4 5   Next

AstraZeneca CEO Steps Down as Earnings Fall

David Brennan, CEO of AstraZeneca, is leaving his position following a dramatic drop in the company's performance. Investors have recently become discontent with the performance of the company. ...
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New Research Says Pradaxa More Dangerous Than Warfarin

Ongoing studies have been taking place to determine just how dangerous the drug Pradaxa is. Pradaxa is a drug that is prescribed to patients to treat blood clots and prevent strokes. Patients started ...
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Depakote Makers Pay $1.6 Billion over Illegal Drug Marketing Practices

Abbott Laboratories has agreed to pay $1.6 billion in fines to state and federal governments for illegally promoting unapproved uses of its anti-seizure drug Depakote. At specific issue was the ...
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Louisiana Attorney General gets $25.2 Million from Fraudulent Drug Companies

Five pharmaceutical companies—Actavis, Boehringer Ingelheim, Dey, GlaxoSmithKline and Schering-Plough—will pay the state of Louisiana a combined $25.2 million for misreporting drug price ...
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West Virginia Trans-Vaginal MDL Running Smoothly

According to recent reports, the U.S. District Court for the West Virginia transvaginal mesh MDL is underway and running smoothly. This case was consolidated in February of this year and includes four ...
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Debate over FDA "Conditional Approval" of New Drugs

Existing policies by the Food and Drug Administration (FDA) allow "accelerated approval" of some developing drugs. "Accelerated approval" lets the FDA approve drugs in phase II of ...
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FDA has no Monitoring System for Medical Devices

Five years ago, the Food and Drug Administration (FDA) received permission from Congress to set up a unique identifier system to monitor medical devices after they were approved for entry into the ...
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Psychiatrists Want a New Name for PTSD

Thousands of individuals suffer from post-traumatic-stress disorder (PTSD), a condition characterized by a wide variety of intense symptoms experienced in the wake of a traumatic event. As incidents ...
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AARP Sues Nursing Home over Antipsychotic Drug Prescriptions

The American Association of Retired Persons (AARP) has joined a class-action California nursing home neglect suit which claims the Ventura Convalescent Hospital has broken the law by providing ...
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Joining an Actos MDL May Be Easier Than You Think

Federal judge Rebecca Doherty who is overseeing the Actos drug injury multidistrict litigation (MDL) has recently made a decision that will make it easier for patients injured by the drug to join the ...
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Long Term use of Osteoporosis Drugs may be Harmful

A new Food and Drug Administration (FDA) study published this week in the New England Journal of Medicine warns that women who take bone-building drugs to treat osteoporosis are at risk of developing ...
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What Doctors aren't Telling you about Cellulaze

Cellulaze is a new laser treatment for cellulite removal. It was approved by the Food and Drug Administration (FDA) for the improvement of cellulite for up to three months. While doctors and some ...
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Report Reveals Current FDA Drug Safety Tracking System Needs Improvement

A new report published by the Institute of Medicine (IOM) says that the Food and Drug Administration (FDA) needs to create a public database to track a drug's safety record even after it receives ...
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Pain Experts in Unethical Relationship with Makers of Painkillers

Two senators have opened an investigation into financial ties between the producers of prescription painkillers and pain experts in the medical field. The Senate Finance Committee published several ...
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Too Many Medications Don't Provide Children's Dosing Information

A new study published by researchers at the Food and Drug Administration (FDA) reveals that at least half of the drug labels they reviewed did not contain any information related to the safety of the ...
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New Concern Over Severe Side Effect of Blood Pressure Drug

ACE (angiotensin converting enzyme) inhibitors, a class of drug used to lower blood pressure, work by blocking the formation of angiotensin II, a potent chemical that narrows blood vessels, raising ...
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Trial Date Set for First Federal Vaginal Mesh Trial

The first of approximately 600 federal cases related to C.R. Bard Inc's dangerous vaginal mesh implant is set for February 5, 2013. More than 75,000 women have vaginal mesh devices inserted each ...
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How the FDA Intervenes

After any assessed risk with a product, the FDA will then intervene in some way. This may take on a number of different forms. One thing they will do is regulate product labeling. Products such as ...
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Consumer Group Urges Recall of Dangerous Drug

Public Citizen, a consumer safety advocate group, petitioned the Food and Drug Administration (FDA) last week to recall the diabetes drug Victoza because of the dangerous side effects it can cause in ...
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How the FDA Assesses Risk

The Food and Drug Administration has a process by which they assess and manage the possible risk of products. This goes for products that are both on the market and those that have not yet entered the ...
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Exploring the Debate Over FDA User Fees

The Prescription Drug User Fee Act (PDUFA) of 1992 ruled that companies applying for approval of new drugs or medical devices would be required to pay a user fee to the Food and Drug Administration ...
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Pfizer Must Pay Damages for Dangerous Drug

A New Haven jury has ruled that drug maker Pfizer must pay a woman at least $4 million in damages because she developed breast cancer after taking Prempro, the company's menopause drug. The jury ...
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Boston Scientific Defibrillator May Malfunction

Boston Scientific Corporation's Cognis and Teligen defibrillators may be at risk for malfunction. These defibrillators are used to restart a stopped heart. The device has been linked to one known ...
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Paxil Settlement Reaches $64 Million

A $64 million class-action settlement has officially received the OK which means that parents of children who took the antidepressant can start receiving reimbursements. The suit was based upon the ...
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St. Jude Medical to Stop Sales of Faulty Heart Device Wires

St. Jude Medical Inc. has decided to stop selling two different types of heart device wires after they were discovered to come out of insulation and cause problems for patients. The wires were ...
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113 results found. Viewing page 1 of 5. Go to page 1 2 3 4 5   Next
Johnson & Johnson Fined for Hiding Drug Risks
In a suit filed by the state of Arkansas, a jury found Johnson & Johnson guilty of hiding the risks associated with the antipsychotic drug Risperd... Read More [+]
New Study Reveals Unintended Consequences of Hair Loss Drug
For men experiencing male pattern hair loss, Propecia seemed like a miracle drug, stopping hair loss and even causing new hair to grow. Sure, there we... Read More [+]
FDA Issues Voluntary Recall of RegenErect
A voluntary recall is not to be confused with a decision that is optional. A voluntary recall actually means that the product has been deemed unsafe a... Read More [+]