Glendale Personal Injury Lawyer articles in category: FDA & Prescription Drugs

The Food and Drug Administration (FDA) informed healthcare professionals and patients alike of their findings regarding the possible links between the use of Singulair and changes in mood and behavior. Their concerns pertain to suicidal thinking, changed behavior and indeed suicide. Merck, the manufacturer of Singulair, is stressing that this warning is based on a small number of studies. (Still...

The Food and Drug Administration (FDA) is working to identify the contaminant that has been found in Heparin, which may be linked to as many as 19 deaths. Although, at this time, the FDA has not established a direct causal link. The drug Heparin is used in dialysis and heart procedures to stave off blood clots. Baxter sells somewhere in the range of 35 million units of heparin sodium injection...

Actavis Inc., announced that its subsidiary Actavis South Atlantic LLC is moving forward with the recall of all of the Fentanyl transdermal system CII patches that were sold in the U. S. The concern pertains to a possible defect that could cause a leakage of the fentanyl gel. Initally, 14 lots of the patches were recalled. However, it is unknown if the defect is present in patches that are still...

Although a defective drug recall has not been issued at this time, the FDA has issued an alert regarding a class of bone-density drugs known as bisphosphonates. It appears the drugs can cause severe bone, joint and/or muscle pain.Severe pain may occur soon after taking the drug, or it may take years to occur. It is currently unknown exactly what the risk of severe musculoskeletal pain is for an...

As a result of the death of their beloved son Michael, due to what is believed to have been medical malpractice, David and Patty Skolnik helped push through House Bill 1331 better known as The Michael Skolnik Medical Transparency Act."The Michael Skolnik Medical Transparency Act will make public, via a Web site, information about doctors' license status and medical malpractice settlements."...

Merck & Co Inc have recalled approximately 1.2 million doses of its popular childrens' vaccines. It is feared that the production equipment was not adequately sterilized. According to the U.S. Centers for Disease Control and Prevention, the recalled vaccine is used to protect against the leading cause of meningitis in children under 5 years old. The potential for contamination of any individual...

It has long been believed by many that the Food and Drug Administration (FDA) is much too close to drug companies, which clearly causes a conflict in terms of regulating those companies. To see the extent of the problem, we only need to take a look at Merck's Vioxx catastrophe, were it was revealed by one scientist that he had actually received vailed threats from the FDA regarding the release...

Merck & Co. have agreed to a $4.85 billion global resolution for claims stemming from claims of heart attacks, strokes and even deaths due to the ingestion of the drug Vioxx. Now these victims can finally be compensated, which will bring an end to the on-going Vioxx litigation. Vioxx was first marketed by Merck & Co. In 1999 to treat arthritis and other types of pain. The drug was made by the...

On October 12, Reno jurors decided that Wyeth, the largest maker of hormone-replacement medicines, must pay $134.1 million, including $99 million in punitive damages. This suit was filed due to the mishandling of menopause drugs that helped cause cancer in three women. The punitive damages were levied on Wyeth for concealing the breast-cancer risks of its Prempro and Premarin drugs. Some six...

In what amounts to a huge legal victory for the manufacturer of Vioxx, Merck & Co, the New Jersey Supreme Court rejected a class-action lawsuit. The company currently has close to 27,000 individual claims from users claiming to have suffered heart attacks and strokes after consuming this defective product. Apparently, the court felt that a class-action suit was not appropriate for this...

As in the United States, the obesity epidemic is growing in the United Kingdom. It is a known fact that obesity greatly increases a person's risk of becoming diabetic. In fact, the use of diabetes drugs, which are given to hundreds of thousands of mostly overweight people in the United Kingdom, are said to be causing another serious problem - heart failure.The drugs in question are Avandia...

It is no secret that an endless parade of defective drugs such as Vioxx, Avandia, Accutane, Ketek and Zyprexa have been approved by the FDA. In fact, the FDA has been accused of being a little too close to the pharmaceutical industry. In an effort to remedy the situation, the House of Representatives recently passed a bill aimed at improving the FDA's current system. The bill, once signed by...

Sales of Avandia, the drug developed to aid diabetes patients, have dropped by approximately 10% since The New England Journal of Medicine posted an Avandia study on May 21, 2007 that was less than favorable. The study showed a huge increase in heart attacks and cardiovascular disease in people taking the drug, which is a product of GlaxoSmithKline.By the drug manufacturer's estimates, the...

Many parents have long thought that there is a direct link between vaccines given to their children and the onset of autism. The case of Michelle Cedillo, of Arizona, is the first to be heard on the subject in the U.S. Court of Federal Claims. Not suprisingly, the case is being closely watched. Most claims contend that thimerosal, which is a mercury-rich preservative, is to blame for the...

Lawmakers are hearing testimony from GlaxoSmithKline, doctors and regulators. The drugs Avandia, Avandaryl and Avandament, all GSK diabetes drugs, will be discussed at length. The discussion will be centered around whether enough was done by the drug maker GlaxoSmithKline to warn the public of the dangers involved with taking these medications, which are considered to be defective drugs by many....