FDA Drug Rules and Regulations

The FDA regulates advertisements for prescription drugs

Advertising Rules and Regulations for Drugs

The FDA does not control advertising for over the counter drugs. They are only in charge of regulating prescription ones. If the FDA believes that an ad violates the law, then they will send a warning letter directly to the drug company asking that the ads be stopped right away. The amount of warnings issued depends on how serious the matter is. The effects of the violations are not necessarily life threatening, but they certainly can alter the lives of people involved. Companies are not allowed to use reminder ads for drugs with serious health risks. They must submit their ads to the FDA when they first appear in public. The FDA encourages the drug companies to use language that is clear and understandable to the general public. All ads must not make claims that are not supported by adequate evidence, leave out or downplay risk information, and state or imply that the drug can treat a condition when the FDA has not approved the drug for such use. These are just a few of the advertising rules and regulations for drugs. The way information is presented in drug ads can effect whether or not they meet FDA requirements.

The Effect of Drug Rules and Regulations

All of the rules and regulations are highly effective to the individual drug user. They allow the person to know true information about the drug they are taking and its actual side effects. This information is crucial because it allows the individual to know whether or not it is safe to take the product. The FDA makes sure that drug companies do not misrepresent data or gloss over any important information. Without the FDA requirements, drug advertising could get out of control.
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