Pharmaceutical Injuries
Our attorneys have more than 50 years of combined experience helping people like you get what they deserve. We can work with clients on an individual basis or assist in filing a class action lawsuit if the problem is believed to affect many more people.
Millions of Americans rely on medications and medical devices to treat serious health conditions. Unfortunately, in some cases, severe adverse side effects can lead to a host of new problems for the patient. While it is impossible to guarantee absolute safety when it comes to drug effects and medical devices, in some cases the drug or device maker may have known about certain adverse side effects but failed to disclose the risk to medical professionals or the public.
If you suffered adverse side effects from a drug or medical device, you may be eligible to file a drug injury lawsuit to seek payment for your injuries. At Bradley/Grombacher, we can help people like you seek fair and just compensation when a drug you are taking or medical device you are using has caused injury.
In some cases, the manufacturer or other affiliated company provides consumers with inadequate warnings or inadequate instructions about how to use the product. Some manufacturers fail to warn consumers and medical professionals about the foreseeable risks of using a product.
A design defect is a product liability claim that refers to cases in which it is foreseeable that a drug or medical device will cause injury because of its design. If the drug maker is aware that the drug could be dangerous, it has a responsibility to conduct extra studies or reconfigure the product to avoid or reduce the risk of injury.
In these cases, the manufacturer or another negligent party could be held liable if a person suffers a foreseeable side effect.
Sometimes mistakes occur during the manufacturing process that can cause a product to be defective and potentially cause harm to a consumer. Once the manufacturer becomes aware that a manufacturing defect has occurred, it has a responsibility to notify consumers and may decide to recall the product over safety concerns.
If you or a loved one has experienced an adverse reaction from a drug or medical device, you may have a legal claim. The pharmaceutical injury lawyers in Agoura Hills and Westlake Village at Bradley/Grombacher LLP can help you evaluate your claim and move forward with it to seek fair and just compensation.
Plaintiffs who have been injured by a medical device defect or a dangerous drug may be eligible to file a product liability or personal injury lawsuit. There are three types of product liability cases: design defects, marketing defects, and manufacturing defects.
Below is a list of drugs and medical devices facing allegations for defects that have seriously injured patients:
Drugs are designed to treat a wide variety of health conditions. Therefore, drug side effects widely vary based on the type of drug and an individual’s reaction to it. Some common side effects of drugs include nausea, gastrointestinal issues, skin reactions, drowsiness, and antibiotic rash.
The manufacturers of drugs and medical devices are required to list the common medication side effects associated with the product on the product’s label. This information allows a consumer to know if the drug side effects they are experiencing are normal or if medical attention is necessary. Failure to seek medical attention for dangerous prescription side effects may lead a person to suffer a catastrophic drug injury, which may have lifelong effects and diminish a person’s quality of life.
If you or a loved one has suffered a medical device injury or dangerous drug side effect, you may qualify to file a drug injury lawsuit. You may be entitled to compensation for your medical bills, pain and suffering, lost wages, and other damages you experienced as a result of the drug or medical device problems.
Contact the pharmaceutical injury attorneys in Agoura Hills and Westlake Village at Bradley/Grombacher LLP to discuss your legal options. If you have a potential case, your defective drug lawyer will work tirelessly on your behalf to put together a compelling case and help you get the compensation you deserve.
Galvan v. Doe
$6,750,000
The U.S. Food and Drug Administration (FDA) regulates drugs and medical devices. This federal agency is responsible for evaluating medications and medical devices for their safety and efficacy. The FDA also may choose to approve a drug or medical device only to treat specific conditions. The approved conditions and safety risks are listed in the safety information that accompanies the drug or medical device.
Physicians who opt to use the drug to treat any unspecified condition are prescribing the drug for “off-label” use. While physicians are permitted to prescribe drugs for an off-label use, drug makers are not allowed to promote the drug for an off-label use. Drug manufacturers are only allowed to promote their drugs to treat illnesses for which the FDA approved them.
Drug and medical device manufacturers have a duty to ensure that their products are safe and that they comply with FDA regulations before they put the products on the market. Medical devices and drugs must be thoroughly and reliably tested to ensure their safety and efficacy before they can be approved to enter the market, and they must disclose all test results with the FDA.
If they fail to do so, drug and medical device makers may be subject to legal liability.
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