What types of defective drug injury cases are there?

There are several types of defective drug injury cases that may arise in North Carolina. These cases typically involve a claim that a person has been harmed by a medication manufactured by a drug company, or by a doctor’s prescription of that medication. One type of defective drug injury case is a claim of “defective design.” In these cases, a plaintiff alleges that the drug was designed in a way that was dangerous or defective and that the manufacturer should have foreseen that harm could result from its use. A second type of defective drug injury case is a claim of “defective manufacture.” In these cases, the plaintiff alleges that the drug was manufactured in a way that was dangerous or defective and that the manufacturer should have foreseen that harm could result from its use. A third type of defective drug injury case is a claim of “failure to warn.” In these cases, the plaintiff alleges that the manufacturer failed to provide adequate warnings about the potentially harmful effects of the drug. Finally, a fourth type of defective drug injury claim is based upon improper marketing. In these cases, the plaintiff alleges that the drug company marketed the drug to an inappropriate population or in a deceptive manner, which caused the plaintiff to be injured. Regardless of the type of defective drug injury case, North Carolina law allows those injured by defective drugs to seek monetary compensation for their losses. However, proper legal counsel and representation are needed to prove a claim and to receive a favorable outcome.

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What types of defective drug injury cases are there?

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