Darvocet Side Effects

Darvocet Side Effects of heart rhythm abnormalities and possible heart failure has lead to a Darvocet recall in the United States and lawsuits are being filed by Darvocet attorneys on behalf of injured victims.

Xanodyne Pharmaceuticals, makers of Darvocet, removed their pain medication from the market in 2010 at the request of the FDA, after the agency found that the drug was associated with serious heart-related side effects. The pain reliever propoxyphene was first approved by the FDA in 1957 and has been sold under various brand names, including Darvon and, in combination with acetaminophen, Darvocet. Before the Darvocet recall was instituted, Darvocet was used to treat mild to moderate pain, typically following dental surgery such as the extraction of wisdom teeth. Both Darvocet and Darvon were manufactured by Xanodyne Pharmaceuticals and have been subjected to this nationwide propoxyphene recall. The FDA also informed generic manufacturers of propoxyphene-containing products like Darvocet of Xanodyne's decision to pull Darvocet from the market, requesting that they voluntarily remove their products as well. The side effects associated with Darvocet are serious and may even lead to death. If you or a loved one has suffered from a Darvocet side effect, contact a Darvocet attorney to discuss your legal options.

Darvocet Recall

New information about potential heart-related side effects led to a Darvocet recall effective throughout the United States late last year. Because these Darvocet side effects are so severe, the FDA advised healthcare providers in 2010 to stop prescribing Darvocet to patients and to help their patients find alternative treatments for managing their pain. The Darvocet recall was initiated by the FDA after the agency reviewed Darvocet side effect data from clinical trials and epidemiological studies. These studies sought to examine the adverse effects associated with Darvocet use and indicated that Darvocet puts patients at risk of suffering serious and potentially fatal heart rhythm abnormalities. The most significant data which led to the Darvocet recall was collected during a safety assessment of the drug, in which researchers found that Darvocet can cause severe heart-related side effects including a slowed heartbeat, a decreased ability of the heart to contract properly, and an interruption of the heart's transmission of electrical impulses. In light of this information, the FDA determined that the potential risks linked to Darvocet outweighed the possible benefits of the medication, and requested that Xanodyne remove both pain-relievers Darvocet and Darvon from the U.S. market.

Darvocet Heart Rhythm Side Effects

The FDA previously received two requests to remove Darvocet from the market since 1978, due to the drug's potential to cause serious side effects among patients. Until recently though, the FDA had concluded that the benefits of Darvocet for pain relief at recommended doses outweighed the safety risks of the drug. In response to Darvocet side effect data however, the European Medicines Agency recommended that marketing authorizations of Darvocet be removed across the European Union in 2009, leading to a phased withdrawal of Darvocet. Later that year, the FDA made the decision to permit continued marketing of Darvocet, but added a new boxed warning to Darvocet's label warning patients and healthcare professionals about the risk of a fatal overdose. The FDA also required Xanodyne to conduct a new safety study examining the adverse effects of Darvocet on the heart.

After reviewing the results of this study, the FDA determined that, even at recommended doses, Darvocet causes severe changes to the electrical activity in the heart, which can be seen on an ECG. These changes can increase an individual's risk of suffering serious abnormal heart rhythms, which have been linked to significant adverse effects, including death. According to the study, the risk of adverse events for any particular patient is even subject to change based on small alterations in the patient's health status, such as dehydration, changes in medications, and decreased kidney function. With this new Darvocet side effect information, the FDA was finally equipped with data showing that the standard dose of Darvocet can be harmful to the heart. In fact, FDA officials reported that the new heart data indicated that Darvocet's effectiveness in relieving pain was no longer enough to outweigh the drug's serious potential heart risks.

Darvocet Attorneys for Heart Rhythm Side Effects

Side effects involving the heart are some of the most dangerous complications of certain pharmaceutical drugs, especially those with the potential to cause disturbances in the heart's electrical activity. If you or a loved one has suffered from a Darvocet side effect, contact a Darvocet attorney to discuss the benefits of filing a Darvocet lawsuit against Xanodyne Pharmaceuticals. The goal of Darvocet lawsuits is to seek financial compensation for your injuries and medical expenses, as well as the pain and suffering endured by your family. Pharmaceutical companies like Xanodyne are responsible for the safety of their medications, even after a drug recall, and should be held liable for any serious injuries sustained by consumers of their products. Unfortunately, some drug companies intentionally conceal the more serious side effects of their medications in order to make their product more appealing to the public. This deceptive practice puts millions of consumers unknowingly at risk of suffering severe and even life-threatening side effects. Victims of Darvocet side effects are not at fault and should not be held accountable for the resulting consequences. Contact an experienced Darvocet lawyer today to discuss your best options for seeking the financial compensation you deserve.

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