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Dangerous and defective drugs, including prescription and over-the-counter medications, are a severe public health and safety risk globally. When the federal government approves a substance to enter the market, the consequences of flaws in the manufacturing, production, or labeling processes can have catastrophic effects on the injured party and their family.
You have the right to pursue damages when a negligent manufacturer caused you harm. Speak to a seasoned Westlake Village dangerous drugs lawyer to discuss your case and schedule a consultation. Our dedicated personal injury attorneys could help file your claim for compensation.
Physicians and other certified medical professionals must closely monitor patients when prescribing newly approved drugs. Those taking recently developed medications should research the potential risks and side effects. Similarly, they should remain educated about all the prescriptions, over-the-counter drugs, and vitamins they take daily to prevent suffering harm from negative substance interactions.
Drug manufacturers have a legal obligation and responsibility to the public. When people suffer harm because of negligence, they have the right to pursue financial damages for their losses.
There are three primary causes of defective drugs. The first is design issues, which lead to the entire line of medicine from that blueprint being harmful. The second is manufacturing errors, which occur during the production phase. The last is failure to warn, which results from the drug manufacturer not providing adequate caution and instructions for using the medication.
When someone unknowingly takes a defective substance, this can have catastrophic effects on their body. Some examples of injuries people sustain from flawed medication include:
Individuals using medical devices, such as implants, may also suffer harm when inherently hazardous and defective products reach the market for consumer use. An experienced dangerous substances attorney in Westlake Village could analyze the case evidence, determine the at-fault parties, and help prove liability in civil court.
The Federal Food and Drug Administration (FDA) must approve all new medications before pharmaceutical companies or manufacturers can make them available to the public. The agency also provinces the Center for Drug Evaluation and Research (CDER) for pharmaceutical industry oversight, and created a search and watchdog tool for doctors and consumers to access the essential information they need about new medications.
The FDA reviews and analyzes data and endorses new drugs when their findings show the benefits outweigh the potential risks. The approval process is a formal structure that includes the following:
Anyone who is harmed due to a defective product, even if it occurred at the FDA level, deserves legal justice. A hazardous drugs lawyer in Westlake Village could collect and carefully review evidence to determine the cause of the harm and the liable party.
On average, the FDA approves one new drug every single week. Despite systems and policies they put in place, substances that pose a significant risk of harm still end up on shelves and in the homes of countless consumers. Defective medications place the public at significant risk of suffering severe or fatal injuries.
Therefore, it is crucial to hold negligent pharmaceutical companies and producers accountable for their carelessness. Contact a compassionate Westlake Village dangerous drugs lawyer to review your case and options today.
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