DrugOutlook provides information on
FDA regulated drugs and devices.
Information that guides your decisions.
Drug Outlook provides current information regarding adverse events related to prescription drugs and medical devices. We are dedicated to protecting patients and helping them understand what options are available to them. Through our direct connections with government organizations who provide detailed information about drug and device history, we are able to provide you with free and easy-to-understand information.
Patients who have been injured by a defective medical device or dangerous drug can seek justice and hold negligent companies responsible for their unethical or illegal actions. We have a trusted network of professionals that can help patients evaluate their situation, determine if legal action is the best solution for them, and connect them to the appropriate legal professionals who can help them.
Adverse drug events since 2004
The U.S. Food and Drug Administration (FDA) regulates over-the-counter and prescription drugs in the United States, including biological therapeutics and generic drugs. This work covers more than just medicines. For example, fluoride toothpaste, antiperspirants, dandruff shampoos and sunscreens are all considered drugs.
An adverse event is submitted to the FDA to report any undesirable experience associated with the use of a medical product in a patient. For drugs, this includes serious drug side effects, product use errors, product quality problems, and therapeutic failures for prescription or over-the-counter medicines and medicines administered to hospital patients or at outpatient infusion centers.
When it comes to your health, knowledge is power. We provide patients with the information they need to make informed decisions about dangerous drugs and potentially dangerous medical procedures. Whether you are looking for potential drug side effects, FDA recall information, lawsuit information, or help filing your claim, Drug Outlook is here to help you.
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