Product Liability Attorney and Ohio Defective Drug Lawyer reviews drug-related injuries and represents plaintiffs nationwide
Defective drugs and unregulated nutritional supplements fill the U.S. market each year, endangering consumers and American patients. The U.S. Food and Drug Administration (FDA) initiates weekly recalls for defective drugs, often after injuries have occurred and lawsuits are filed against negligent drug makers and pharmaceutical companies.
The FDA recalls defective drugs for a myriad of safety issues, including a lack of pre-market testing, drug contamination, and drug injuries reported by patients. Sometimes only after hundreds or thousands of adverse event reports are filed by doctors and patients are drugs taken off the market, discontinued or voluntarily recalled by manufacturers.
Warning labels and “black box” warnings may be applied, and consumers are left wondering if the drug they have been taking for years may be dangerous or the root cause of an existing injury or illness.
Pharmaceutical companies tend to understate the risks of a drug and hype the benefits of a drug, in order to sell more and build profits. Even as the FDA works to regulate the giant drug market, their efforts often lag and injury cases must be filed by plaintiffs and an Ohio defective drug lawyer and product liability attorney.
Joe Lyon is a Product Liability Attorney and Ohio Defective Drug Lawyer representing plaintiffs nationwide in drug injury lawsuits and pharmaceutical defect claims.
Pharmaceutical Negligence & Drug Litigation
When patients and consumers are injured by defective drugs brought to market by negligent pharmaceutical companies, those responsible may be held liable for damages. Drug companies have a lawful and ethical duty to protect American consumers.
If the drug you have been prescribed caused an injury or has been recalled, contact a healthcare professional and a defective drug lawyer to help you weigh your medical and legal options.
Following major mass tort events and high-profile lawsuits, the Institute of Medicine, National Institute of Health, and Veterans Administration proposed several new steps to balance the safety monitoring following the release of new drugs. A few of the recommendations include funding and staffing increases, improved adverse event reporting system, and greater authority for the FDA on post-marketing safety measures.
In response to increasing public concern over a lack of post-approval authority, the Institute of Medicine, National Institute of Health, and Veterans Administration have proposed several new steps to balance the safety monitoring following the release of drug.
Currently, the FDA has little funding or ability to adequately monitor adverse events, off-label uses, compliance with post market studies. When a drug is approved, there is significant uncertainty about the long term safety. Manufacturers are only required to submit data on safety and efficacy from small controlled studies.
The pre-approval studies do not provide a clear picture on how the drug is truly interacting in the market place. A few of the recommendations include funding and staffing increases, improved adverse event reporting system, greater authority for the FDA on post-marketing safety measures.
FDA Warnings & Defective Drugs
- Dietary supplements
Pharmaceutical Lawsuits & FDA Oversight
When drugs are defective or ineffective in their intended uses, injuries may result, includingPrescription Errors, birth defects, cardiac risks, amputation, internal bleeding, toxicity, and other injuries. Dangerous side effects can lead to serious complications and death.
It is prudent to contact your doctor after an injury and call an Ohio defective drug lawyer for a free consultation. The Lyon Firm has the legal resources and works with product liability experts to build the strongest case possible.
Drug companies ought to be held accountable for injuries linked to defective medications, and victims of drug injury should contact an attorney to weigh their legal options. Product liability lawsuits and class action claims can bring in sizable settlements, and plaintiffs can benefit and seek compensation for medical expenses, pain and suffering, long-term disability, and other damages.
Every drug injury case is unique and Joe Lyon takes the time to review viable personal injury cases for plaintiffs nationwide. The Lyon Firm is dedicated to both plaintiffs well-being and the future of consumer safety.
According to New England Journal of Medicine’s Journal Watch, the company, Johnson & Johnson (J&J) “will make all its clinical trial data available to outside researchers.” Utilizing the Yale University Open Data Access (YODA) Project, the company will allow independent parties “to review requests from investigators and physicians seeking access to anonymized clinical trials data.”
According to Johnson & Johnson, this “is the first time any company has collaborated with a completely independent third party to review and make decisions regarding every request for clinical data.” This transparency could have a broad positive influence on science and patient safety.
Johnson & Johnson is one of the largest pharmaceutical companies in the world. The company manufacturers numerous drugs and health-related products. A positive step in the direction of patient safety is a breath of fresh air an industry that often is more profit-oriented than concerned with consumer safety. Patient safety should be first and foremost in any healthcare directive.
Ohio Defective Drug Lawyer
When drugs and nutritional supplements on the U.S. market pose dangers to the health of patients and consumers, the U.S. Food and Drug Administration (FDA) may initiate a recall for the product or ask the drug’s manufacturer to voluntarily issue a recall. When injuries are involved, Johnson Johnson lawsuits quickly follow recalls.
Recalled defective drugs may result from improper testing, lab contamination, or production mishaps, and result in Johnson Johnson Lawsuits. Warnings may be issued by the nation’s safety agencies, typically after a series of complaints about health issues linked to the drug. A drug company may list several side effects on a drug label, but may understate the dangers or overhype the benefits of a particular drug.
If you or a loved one has suffered a drug-related injury, and have questions about the legal remedies available to improve quality of life and medical care, contact The Lyon Firm at (800) 513-2403. You will speak directly with Mr. Lyon, an Ohio defective drug lawyer, and he will help you answer critical questions regarding pharmaceutical injury lawsuits.