The U.S. Food and Drug Administration (FDA) oversees the manufacture and production of prescription and over the counter (OTC) medications in the United States. The FDA enforces strict guidelines and must approve any drug before it is released to the public, but despite these precautions, dangerous drugs often make it through to the marketplace.
These drugs carry a high risk of adverse side effects, and often, the risks of taking these drugs is greater than the benefit the drug may offer. Stroke, heart attack, increased risk of suicide, blood clots, and other dangerous side effects are frequently associated with high-risk drugs.
These side effects cause serious medical emergencies, lifelong illnesses and health conditions, and even wrongful death. Anyone harmed by taking dangerous and defective medications can seek financial compensation from the pharmaceutical companies responsible for the dangerous drugs through a pharmaceutical liability lawsuit.
A Louisville personal injury lawyer represents those suffering from illness or injury after taking a defective pharmaceutical. Through a personal injury lawsuit or class action lawsuit, an attorney can help plaintiffs obtain financial compensation for medical expenses, lost wages, pain and suffering, and other consequences of harmful side effects of medication.
How Dangerous Drugs Reach Consumers
Despite years of clinical testing and trials, pharmaceutical companies often release drugs into the marketplace that do more harm than good. These dangerous drugs may be released with FDA approval when the risks identified during testing are considered unlikely side effects or when a drug is rushed through testing and released before the drug’s effects are completely evaluated and understood.
Often, after a drug is released, the use of the drug by a large population unveils that identified risks are widespread and likely to occur with use.
Side effects that were not previously identified during testing may become well-known after patients begin presenting with adverse health conditions after taking the drug. When a drug is considered dangerous or defective, the FDA may encourage or require a recall of the drug.
However, sometimes the drug remains available with the FDA requiring only that the medication’s packaging carries a warning label advising consumers of the risk of severe side effects. If someone has suffered adverse side effects or developed a serious health condition from taking OTC or prescription medication, they should contact a dangerous drugs lawyer in Louisville for an evaluation of their claim.
Work With Chad and Sheila Today
Dangerous Drugs Lawsuits
Over the years, many common medications have been subject to pharmaceutical litigation after these prescriptions and OTC drugs caused significant harm to patients and consumers.
Oral contraceptives, acne medications, anti-anxiety medications and antidepressants, and medications for the treatment of osteoporosis, diabetes, high blood pressure, and low testosterone are just a few of the many drugs which have been subject to lawsuits after causing serious medical conditions in those who relied on the medications for help.
Need An Experienced And Dedicated Team On Your Side?
Contact a Dangerous Drugs Attorney Today
If someone has suffered a stroke, blood clot, seizure, pulmonary embolism, psychological disorder, suicide, heart attack, liver failure, or another serious side effect as a result of taking dangerous or defective drugs, they should contact an attorney for help.
A Louisville dangerous drugs attorney can help you pursue financial compensation from the pharmaceutical companies responsible for your illness or injury. Call today to learn more about pharmaceutical liability and how you can obtain compensation for your suffering.
Let Us Put Our 58 Years Of Trial Experience Towards Your Case.