FDA Conflicted with Children's Medicines

When the FDA set the standards for over-the-counter (OTC) cough and cold medicines about 30 years ago, no studies were done on children. Now, the FDA is concerned that OTC medicines are having a negative impact on young children. Research shows that about 7,000 children are sent to the emergency room every year due to overdoses.

According to the story in  USA Today, "a government health official rejected pediatricians' calls for an immediate ban on the over-the-counter cough and cold medicines for young children." But, at a public hearing FDA officials said they felt uncomfortable having it on shelves because there is no scientific evidence that supports continued use of OTC in young children.

In my opinion, the FDA cannot sway in their opinion of this matter because it is a nationwide health issue. Instability in an issue will send the wrong message to parents of young children by confusing them or losing trust in the FDA. Also, if there is no solid evidence that supports the OTC medicines then, it should be taken off the shelves.

Another problem that the FDA was concerned with was the possibility of the parents' inadequate usage of the medicine. The main point being that maybe parents, doctors, and teachers should be educated more. Like a campaign, raising awareness in the proper way in using medicine with children.

I believe that medicine, especially in children, should be a collaborative effort between parents, doctors, and the FDA in following the proper and safety precautions. I cannot wait to see what the FDA plans to do.