FDA Considers Lowering Nicotine Levels in Cigarettes

News Picture: FDA Considers Lowering Nicotine Levels in Cigarettes

THURSDAY, March 15, 2018 (HealthDay News) -- In an unprecedented move, the U.S. Food and Drug Administration on Thursday said it plans to cut the amount of addictive nicotine in the nation's cigarettes.

"As part of our comprehensive plan on tobacco and nicotine regulation announced last summer, we're issuing an advance notice of proposed rulemaking to explore a product standard to lower nicotine in cigarettes to minimally or non-addictive levels," FDA Commissioner Dr. Scott Gottlieb said in a statement.

He explained that, "given their combination of toxicity, addictiveness, prevalence and effect on non-users, it's clear that to maximize the possible public health benefits of our regulation, we must focus our efforts on the death and disease caused by addiction to combustible cigarettes."

One lung health expert applauded the move.

"Exploring a product standard to lower nicotine content in cigarettes to minimally or non-addictive levels is an exciting concept," said Andrea Spatarella, from the Center for Tobacco Control at Northwell Health, in Great Neck, N.Y. "Any and all efforts to reduce or eliminate the health burdens and tobacco-related deaths to millions of Americans deserves consideration."

Tobacco use -- mainly cigarette smoking -- kills more than 480,000 Americans a year and costs nearly $300 billion a year in direct health care and lost productivity, the FDA noted.

Reducing nicotine levels and other policy measures could help prevent millions of tobacco-related deaths in the United States, Gottlieb said.

The proposal on reducing nicotine levels includes a review of current science about how nicotine creates and sustains addiction to cigarettes, and asks for public input and review.

Gottlieb said answers will be sought on questions such as "what potential maximum nicotine level would be appropriate for the protection of public health? Should a product standard be implemented all at once or gradually?"

Also, he added, there could be "unintended consequences" to making cigarettes less addictive, for example, the growth of a black market in high-nicotine cigarettes.

Still, Gottlieb said a new analysis, published online Thursday in the New England Journal of Medicine, has suggested that millions could benefit from the proposed move.

"If this scenario were implemented, this analysis suggests that approximately 5 million additional adult smokers could quit smoking within one year of implementation," Gottlieb said.

"And with this scenario, an even greater impact could be felt over time: by the year 2100, the analysis estimates that more than 33 million people -- mostly youth and young adults -- would have avoided becoming regular smokers. And smoking rates could drop from the current 15 percent to as low as 1.4 percent," he added.

"All told, this framework could result in more than 8 million fewer tobacco-caused deaths through the end of the century -- an undeniable public health benefit," Gottlieb said.

Young people would benefit hugely from the proposed move, one lung health expert said.

"The benefits the FDA cites for this proposal are extraordinary," said Matthew Myers, president of the Campaign for Tobacco-Free Kids.

"Given these enormous public health benefits and the millions of lives that would be saved, it is critical that the FDA move as quickly as possible to turn this plan into reality," Myers said. "There is no other single action our country can take that would prevent more young people from smoking or save more lives."

Still, another expert said the move could backfire.

"Lowering the nicotine level in cigarettes may simply lead to more cigarettes smoked by current smokers," said Dr. Len Horovitz, a pulmonary specialist at Lenox Hill Hospital in New York City. He believes that to really put an end to the scourge of smoking, "tobacco and nicotine -- in other words, cigarettes -- must be eliminated as a threat to health."

Spatarella agreed the nicotine-lowering strategy could fail.

"It is feasible that the end user may react to the decrease in the addictive chemical nicotine by smoking more. What they perceive as a lack in quality, or the amount of nicotine needed to satisfy their nicotine craving, they may make up for in quantity, the number of products consumed," she suggested.

"The smoking behaviors may remain unchanged and the smoker may seek other tobacco products to fill that nicotine gap," Spatarella added. "They may seek to purchase traditional cigarettes with higher nicotine content from illegal sources."

In its proposal, the FDA said that it also plans to examine the role that flavors -- including menthol -- play in people starting, continuing and quitting smoking, to assess regulation of premium cigars, and to update how it deals with the development and regulation of nicotine-replacement products, such as nicotine gums, patches and lozenges that help smokers quit.

-- Robert Preidt

MedicalNews
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SOURCES: Len Horovitz, M.D., pulmonary specialist, Lenox Hill Hospital, New York City; Andrea Spatarella, DNP, Center for Tobacco Control, Northwell Health, Great Neck, N.Y.; Matthew Myers, president, Campaign for Tobacco-Free Kids; U.S. Food and Drug Administration, news release, March 15, 2018

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