Prescription and over-the-counter medications are used to treat everything from the common cold to a chronic illness. Although these drugs are highly regulated by the Food and Drug Administration (FDA), it can take years to fully understand the drug’s side effects once it’s on the market. By the time a recall notice is issued—many victims have already been affected physically or psychologically by the defective drug. After being injured by a defective drug, it is crucial to consult a St. Louis defective drugs lawyer about filing a personal injury claim. The product liability attorneys at Zevan Murphy, LLC have been fighting negligent drug manufacturing companies for years, and we are ready to advocate on your behalf.
A drug is considered defective if its unintended side effects outweigh its intended benefits. Upon receiving reports of harmful side effects, the FDA will typically launch an investigation into the drug or issue a recall. If the drug’s ill effects are significant enough, the FDA will pull it from the market or require it to have additional information or warnings on the label.
Common defective drugs include:
If you suspect that a drug either harmed you or worsened your condition in St. Louis, reach out to our defective drugs attorneys.
If you have been wrongfully injured as a result of a defective drug, contact a St. Louis defective drugs lawyer right away. Do not wait too long to seek legal representation, as this can affect your right to compensation.