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FDA concerns on E-cigarette
The Food and Drug Administration (FDA) along with the other health experts have come up to a point to warn people of the risks involved in e-Cigarettes. Electronic cigarettes, also known as e-Cigarettes are basically a battery operated device that looks alike traditional cigarettes but are different from them as they provides nicotine directly inside the body without burning tobacco leaves. Generally, in most of the e-Cigarettes the puffing activates the battery-powered heating device which in result vaporizes the liquid present in the container. The vapor generated as a result is generally termed as “Vaping”. This resulting aerosol or vapor is then inhaled by the smoker. They are in many ways look alike of conventional cigarettes and are easily available on e-Stores and shopping malls. This device is generally available with flavored nicotine, chemicals which is converted in vapor that is inhaled by the smoker! The main concern of the FDA is the way they are marketed amongst the public, it should be safe!
The Food and Drug Administration (FDA) is concerned on few points:
There are several actions FDA did to do their responsibility and they were doing it because of some reasons. And below are some of them.
- E-cigarettes can upsurge nicotine obsession among young individuals and may lead teenagers to try other tobacco yields, as well as traditional cigarettes, which are known to cause disease and lead to untimely death.
- E-Cigarettes may comprise ingredients that are known to be toxic to human being.
- Just because clinical studies about the safety and efficacy of such products for their envisioned use have not been succumbed to FDA, consumers presently have no way of knowing whether e-cigarettes are safe for their envisioned use, or What types or concentrations of feasibly harmful chemicals or what quantity of nicotine they are inhaling when they use these kind of products.
Actions taken by The Food and Drug Administration (FDA):
1. FDA has been investigating and hindering shipments of e-cigarettes at the border and has been able to find that the products it has examined thus far meet the definition of a combination drug device product under the Federal Food, Cosmetic Act and Drug.
2. The agency has been confronted about its jurisdiction over certain e-cigarettes in a case currently pending in federal district court.
3. FDA is planning additional activities to address its concerns about electronic cigarettes.
4. Because these products have not been surrender to to the FDA for evaluation or approval, at this time the agency has no way to deliberate, except for the limited testing it has accomplished, the levels of nicotine or the amounts or kinds of other chemicals that the numerous brands of these products provide to the smoker. A good resource to learn further is http://quitsmokingcigarettes.org
5. Meanwhile, health care professionals and consumers may report serious adversative events or product quality problems with the use of e-cigarettes to FDA through the MedWatch program, either online or by phone.
So next time you overhear someone saying that they are concerned about the possible risks of e-cigarettes, prompt them of Voltaire’s saying — “don’t let the best be the enemy of the good.”