FREE INITIAL CONSULTATIONTaylor - Martino - KuykendallPharmaceutical Liability Litigation AttorneysWhen the Mobile, Alabama personal injury lawyers of Taylor - Martino - Kuykendall go to court, we mean business. Hundreds of people will be injured every year from dangerous medicines and their side effects: some will die. We take dangerous prescription drug cases to court to get financial compensation for the victims. Taylor - Martino - Kuykendall functions as local counsel on national class action dangerous medicine cases, as well as primary legal counsel on faulty drug cases originating in Alabama and other Gulf Coast states. If you believe you’ve been injured by a dangerous medicine, contact an Alabama pharmaceutical liability attorney at Taylor - Martino - Kuykendall for a free initial consultation to review your case. Pharmaceutical Liability - An Overview“Pharmaceutical liability” is a term used to describe the legal consequences a manufacturer of drugs may face if its products injure people. Cases involving injuries caused by drugs, medical devices and other pharmaceuticals are a subset of products liability cases. Plaintiffs can bring claims against the manufacturer based on theories of strict liability, negligence or for failing to warn about potentially dangerous side effects. In some states, however, a statute creates a single claim for product injuries, which may combine aspects of the two. A lawyer who has experience in pharmaceutical liability law can advise you about your rights and help you decide whether you can pursue a claim. Building a Pharmaceutical Liability CaseDrugs and other medical products may suffer from a variety of defects, including design defects, manufacturing defects, problems with the testing of the drug or device, inadequate warnings or instructions for use, problems with the doctor's prescription or incorrect distribution by the pharmacist. Any of these defects can cause serious injuries. Adverse side effects are one of the most common problems with prescription and over-the-counter medications. Problems can also arise if the manufacturer failed to disclose adverse testing results or adverse reactions to the drug or if contaminates entered the product during manufacturing. If you believe that a medicine, nutritional supplement or medical device has caused you to suffer from serious, adverse side effects or other severe injuries, an experienced pharmaceutical liability attorney can evaluate your situation and explain your options for recovery. Protecting Yourself Against RisksFrom a prescription drug to help control high blood pressure to over-the-counter pain relievers, many people take medications every day. In addition, herbal and nutritional supplements are a part of life for many people. Although these medicines can help you feel better and manage your symptoms, they have risks as well as benefits. Just because a drug is approved by the Food and Drug Administration (FDA) does not mean it is free from risks. The FDA approves a drug and considers it safe when the benefits outweigh the known risks. In fact, many risks are only discovered after a drug has been on the market for an extended period of time and a much larger number of patients than participated in the clinical trials have used the drug. There are steps you can take to minimize your risk of adverse reactions. If you have experienced adverse side effects as a result of taking a drug or herbal supplement, contact a pharmaceutical liability attorney to discuss whether you may be able to recover for your injuries. Dietary Supplements and Herbal RemediesThe production and sale of dietary supplements and herbal remedies is a huge and largely unregulated business in the United States. While dietary supplements and herbal remedies may be safe in most circumstances, they are not risk-free and can cause serious side effects, just as drugs do. The federal Dietary Supplement Health and Education Act of 1994 (DSHEA) governs the regulation of dietary supplements. DSHEA also sets forth rules for making claims about products and information that must appear on labels. A lawyer who is familiar with the statute’s requirements can help you determine whether you have a claim against a manufacturer and whether you can recover damages for your injuries. Medical DevicesClaims for injuries caused by medical devices are also included under the heading of pharmaceutical liability. Under Section 201 of the federal Food, Drug and Cosmetic Act, a medical device is defined as "an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar article that is intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment or prevention of disease." Examples of medical devices include: defibrillators, breast and other cosmetic implants, orthopaedic screws, hip implants, knee implants, heart valves and many other items. If you or a loved one has been injured by a medical device or experienced adverse side effects, you may be able to recover for your injuries. Medical device litigation is complex, and an experienced attorney can evaluate your situation and help you build a case.
This Pharmaceutical Liability Information Center is intended to provide general information only. It is not specific to your case. For answers to your questions about your own situation, contact a dangerous drug lawyer at Taylor ◊ Martino ◊ Kuykendall. |