Hackensack Dangerous Drugs Lawyer
Modern medication has made medical treatment more efficient and dramatically extended the number of healthy years you can expect to live. Over-the-counter and prescription drugs are integral to keeping people healthy. However, sometimes a manufacturer releases a drug into the marketplace that does more harm than good.
If you experience adverse or potentially life-threatening effects after taking a prescription or over-the-counter medication, contact a compassionate Hackensack dangerous drugs lawyer on our team. Our personal injury attorneys fight tenaciously to win the compensation you deserve.
Who Is Liable for Dangerous Drug Injuries?
The U.S. Food and Drug Administration (FDA) is the government agency that approves debut drugs after they have undergone a rigorous testing period. The FDA continues to monitor drugs as more patients take them. Unfortunately, manufacturers sometimes hide troubling results or curtail testing to expedite the release of a new drug.
Manufacturers may be liable if patients suffer an injury because of substandard protocols. The premise of the lawsuit is negligence, and other parties involved in getting the drug to market could also be liable. The defendants could include:
- Testing labs
- Drug distributors
- Doctors who prescribe a drug for unapproved conditions
- Nursing homes that overmedicate patients
- Pharmacies that do not take care while filling prescriptions
Our Hackensack dangerous drugs attorneys identify possible defendants and hold them accountable. We ardently negotiate with insurance companies and do not accept inadequate settlement agreements. Our attorneys maximize the value of your case because you deserve compensation for your losses.
Drugs Are Dangerous When Formulated, Manufactured, or Labeled Wrong
Under product liability law, a medication is defective if the manufacturer makes a substance incorrectly, stores it improperly, or uses an inaccurate label. In these cases, the harm results from the manufacturing process, not the formula used to make the drug.
Dangerous side effects can also occur when the scientists who formulate the drug make a grievous error. Sometimes, it takes years for patterns in side effects to appear as more users report them to the FDA. For example, the main ingredient in the discontinued over-the-counter heartburn drug Zantac was ranitidine, a chemical proven to cause cancer, which Zantac did in many people. When injured users filed a class action lawsuit, the drugmaker replaced ranitidine with famotidine to develop Zantac 360, which the FDA approved to treat heartburn.
Drug companies disclose side effects in print and televised advertising, which helps consumers weigh the risks and rewards of the product. Drug companies must also include warning labels on the products themselves, often in large print to catch users’ attention. Failure to follow labeling practices can lead to a negligence claim if a consumer uses the product as recommended but experiences harm because the manufacturer did not advise them of the associated risks.
Our Hackensack attorneys meticulously prepare each dangerous drugs case to win at trial if settlement negotiations are not fruitful. We think of our clients as family and will work tirelessly on your behalf.
Ask a Hackensack Harmful Medications Attorney To Seek Justice for You
Prescribed and over-the-counter medication is generally safe because the FDA requires rigorous testing and monitors the drugs after they enter the stream of commerce. Unfortunately, sometimes careless drug companies prioritize profits over health and safety, and their errors cause injury for consumers.
If you believe a medication has harmed you, call us now. Speak to a Hackensack dangerous drugs lawyer who can assess your case and advise you about your options.
