We trust our doctors and pharmacists to provide us with safe medications that are meant to help us emotionally, psychologically, and/or physically. Unfortunately, these medications do not always meet this standard and instead can result in harmful side effects that could result in long-term consequences. Victims who suffer injuries from pharmaceutical drug defects can work with a product liability attorney to better understand the risks of consuming such drugs and who should be held responsible.
Causes and Consequences of Defective Drugs
The sale of over-the-counter and prescription medication in the United States is regulated by the Federal Drug Administration (FDA). However, FDA-approved drugs can still end up being defective, as evidenced by the thousands of drugs that have been recalled in recent years.
If consumption of a medication results in negative side effects, including severe side effects that outweigh the potential benefits of the medication, the drug is considered defective. There are multiple manners in which a pharmaceutical drug-related defect can transpire. A drug may result in dangerous and unexpected side effects if it was not adequately tested or if it was manufactured incorrectly. Additionally, drug defects also include drugs that are improperly or insufficiently labeled and fail to include necessary warnings.
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