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FDA & Prescription Drugs
Did Merck & Co. act appropriately back in 1999 when it discovered the dangers of heart attack and stroke associated with its product Vioxx? A new article published in today’s NPR puts that question to the test by questioning three renown scientists who are authorities on heart disease and clinical s
FDA & Prescription Drugs
A jury panel of 5 women and 5 men has been selected in the latest trial asserted against Vioxx in Atlantic City, New Jersey. In this trial, the drug manufacture Merck & Co. is defending its pain mediation against the allegations of Elaine Doherty, a 68-year-old grandmother who suffered a heart attac
FDA & Prescription Drugs
According to a new study published in the British Medical Journal, those who take Ibuprofen in high doses for long periods of time more than double the chances of having a heart attack when compared to those who use the drug less often. The common painkiller, which is available over the counter with
FDA & Prescription Drugs
Wyeth, the manufacture of the notorious diet drug “Fen-Phen”, recently got final judicial approval to set up a legal settlement fund for the remaining consumers who were adversely affected by its use. The drug caused heart valve damage and primary pulmonary hypertension (PPH) from users of the drug
FDA & Prescription Drugs
Canadian researchers recently discovered there is an increased risk of heart attack and other heart related problems when using Merck and Co.’s pain reliever Vioxx during the first two weeks. Previously, other studies emphasized the increased risks of heart related problems stemming from Vioxx after
FDA & Prescription Drugs
The FDA recently updated safety labels on numerous drugs including Daypro, Motrin, Aleve, Carbatrol, and Midol among many others. These safety label changes are reflected in the BOXED WARNING, CONTRAINDICATIONS, WARNINGS, PRECAUTIONS, or ADVERSE REACTIONS sections. The FDA suggests that any consumer
FDA & Prescription Drugs
Everyone knows about the thousands of lawsuits the drug marker Merck is currently facing in regards to its now recalled drug Vioxx that reportedly increased the risk of heart attacks and strokes in it consumers. Now a Tennessee woman, Gwendolyn Wolfe, has filed suit over another Merck drug called Fo
FDA & Prescription Drugs
A jury reached a $9 million verdict today regarding the punitive damages phase of the latest Vioxx Trial involving John McDarby and his wife. This verdict comes just days after the same jury awarded John McDarby and his wife $4.5 million in compensatory damages for his related heart attack while usi
FDA & Prescription Drugs
A new Jersey jury found Vioxx had concealed the dangers of its painkiller Vioxx and awarded one of the two plaintiff’s $4.5 million dollars in compensatory damages. A second trial for the sole purpose of determining if punitive damages should be awarded is scheduled to start today. Generally, puniti
FDA & Prescription Drugs
A state judge in Philadelphia approved a class action settlement against Bayer, the German manufacture of Baycol, that would re-pay unions, employers and various health plans for money spent on the withdrawn drug Baycol. The national class action suit could result in a settlement that exceeds $10 mi
FDA & Prescription Drugs
The FDA recently warned several manufactures and distributors to stop selling unapproved drugs that contain steroids promising increased muscle, strength, and weight loss. The FDA expressed concerns that products such as Anabolic Xtreme Superdrol or Methyl-1-P by Legal Gear may cause long-term healt
FDA & Prescription Drugs
The FDA has announced that the popular asthma medications Advair and Serevent will now contain a new “black box” warning after discovering the medications may cause an increased risk of asthma-related death. Black box warnings are the most severe warnings the FDA can require of prescription drugs. A