FDA and health experts warn against use of e-cigarettes

23 de julho de 20095min3

art.e.cigarette.cnnCNN health.com

WASHINGTON (CNN) — The U.S. Food and Drug Administration announced Wednesday that laboratory tests on popular smoking devices known as electronic cigarettes have found they contain carcinogens and other toxic chemicals dangerous to humans.

E-cigarettes are battery-operated and contain cartridges filled with nicotine and other chemicals.

E-cigarettes are battery-operated and contain cartridges filled with nicotine and other chemicals.

Known as “e-cigarettes,” the devices are battery-operated and contain cartridges filled with nicotine and other chemicals, spiced with flavors such as chocolate, cola or bubble gum.

While manufacturers tout e-cigarettes as a “healthy way” to smoke, federal health officials say the devices turn nicotine, which is highly addictive, and other chemicals into a vapor that is inhaled by the user.

“The FDA is concerned about the safety of these products and how they are marketed to the public,” said Dr. Margaret A. Hamburg, commissioner of the FDA.

CNN contacted Florida-based Smoking Everywhere, one of the largest manufacturers of e-cigarettes, after the FDA announcement, and a spokeswoman said the company had no comment.

Because e-cigarettes have not been submitted to the FDA for evaluation or approval, the agency had no way of knowing the levels of nicotine or the amounts or kinds of other chemicals that the various brands of these products deliver to the user. That is why the FDA began to test them.

The FDA’s Division of Pharmaceutical Analysis analyzed the ingredients in a small sample of cartridges from two leading brands of e-cigarettes. In releasing its information, the FDA did not identify the two companies, but said in one sample, diethylene glycol — a chemical used in antifreeze that is toxic to humans — was detected. Other samples detected carcinogens that are dangerous to those who smoke them, the FDA said.

The FDA has been examining and seizing shipments of non-U.S.-made e-cigarettes at the U.S. border since summer 2008. To date, 50 shipments have been stopped. The products examined thus far meet the definition of a combination drug-device product under the Federal Food, Drug, and Cosmetic Act.

“We know very little about these devices, said Dr. Jonathan Samet, director of the Institute for Global Health at the University of Southern California, “but to say they are healthy — that’s highly doubtful.”

Samet and other health experts attended the FDA announcement on its findings.

Dr. Jonathan Winickoff, chairman of the American Academy of Pediatrics Tobacco Consortium, said parents need to be aware of e-cigarettes. “It is very important that parents let their children know these are not safe and to make recommendations, or even enforce rules that they not be used,” he said.

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“Children who use these products may also be using other tobacco products,” said Dr. Matthew McKenna, director of the Office of Smoking and Health, Centers for Disease Control and Prevention. “It’s a good idea to make sure the child is aware of the dangers of tobacco in products in general.”

The FDA has been challenged regarding its jurisdiction over certain e-cigarettes in a case pending in federal court. The FDA suggested health care professionals and consumers report serious side effects or product quality problems with the use of e-cigarettes to the FDA’s MedWatch Adverse Event Reporting Program either online, by regular mail, fax or phone.


Sobre a UNIAD

A Unidade de Pesquisa em álcool e Drogas (UNIAD) foi fundada em 1994 pelo Prof. Dr. Ronaldo Laranjeira e John Dunn, recém-chegados da Inglaterra. A criação contou, na época, com o apoio do Departamento de Psiquiatria da UNIFESP. Inicialmente (1994-1996) funcionou dentro do Complexo Hospital São Paulo, com o objetivo de atender funcionários dependentes.


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