Approximately 73,000 more implantable Guidant defibrillators have been recalled as a result of a faulty capacitor which could cause the batteries to deplete sooner than expected. This recall involves the same defective component which has led to prior Guidant recalls. (more…) Read More
On April 11, 2007, an FDA advisory committee will discuss concerns about Ditropan side effects for children. The committee will review whether the maker of this drug is doing enough to warn about the increased risk of problems with hallucinations, which could result in serious physical… Read More
Zelnorm (generic tegaserod maleate) has been linked to an increased risk of heart attacks, strokes and other potentially life-threatening injuries. Last week the FDA requested that the Novartis Pharmaceutical Corporation halt sales of the drug for treatment of irritable bowel syndrome since the dangers associated with… Read More
The drug recall lawyers at Saiontz & Kirk are investigating potential Permax lawsuits and Dostinex lawsuits for users who suffered serious injury or death after using one of the drugs for management of Parkinson's disease symptoms. >>INFORMATION: Permax side effects (more…) Read More
An FDA public health advisory has been issued regarding three drugs used for anemia treatment, Epogen, Procrit and Aranesp. High doses of the drugs could increase the risk of serious injury or death. Potential lawsuits are being reviewed for individuals who suffered injuries as a result… Read More
The makers of the Actiq lollipop pain medication are one of five pharmaceutical companies who received a letter from U.S. Congress Rep. Henry A. Waxman earlier this month, as part of his investigation into inappropriate marketing and incomplete research regarding drugs and medical devices. In recent… Read More
The FDA announced that new warnings will be added to Ambien, Lunesta and other popular sleeping pills, containing information about an increased risk of sleep driving and other complex behaviors while asleep. Potential sleeping pill side effects will also be outlined by drug makers in information… Read More
Today a New Jersey jury awarded $47.5 million in a Vioxx lawsuit filed after the popular pain killer caused a heart attack for an Idaho postal worker. The jury found that Vioxx caused the Plaintiff's heart attack and that the drug maker acted in a fraudulent… Read More
Fosamax lawsuits are pending in courts across the country for users of the popular osteoporosis drug who have suffered serious jaw side effects. Recently Merck, the maker of Fosamax, announced that they have set aside nearly $50 million dollars to cover the initial defense costs associated… Read More
According to the FDA, warning labels for ADHD drugs will be updated to indicate that medications such as Adderal, Strattera and Ritalin have side effects which could lead to heart problems. There have been reports of serious injuries, including sudden death, for children and adults who took… Read More
