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Phyllis E. Greenberger

Phyllis is senior vice president of science & health policy for HealthyWomen. Previously, Phyllis was the president and CEO of the Society for Women's Health Research (SWHR), a national nonprofit organization widely recognized as the thought leader in women's health research, for 26 years. Phyllis was awarded the Trailblazer Award by the U.S. Department of Health and Human Services Office of Women's Health in 2016 and the Perennial Hero Award by the Alliance for Aging Research in 2021. Most recently, she was the recipient of the Women in Government Relations Lifetime Achievement Award and has published a book, Sex Cells, about the fight to overcome bias and discrimination in women's healthcare.

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FDA Focuses Attention on Flavors Added to Tobacco and Liquid Nicotine
FDA Focuses Attention on Flavors Added to Tobacco and Liquid Nicotine

Nicotine and Women's Health—FDA's Initiative Signals Progress

The FDA recently recommitted to reduce tobacco use, particularly among children, by taking a closer look at flavors that are added to both tobacco.

Women's Health Policy

April 24, 2018

Thank you, Food and Drug Administration (FDA), for recently restating a commitment to reducing tobacco use, particularly among children, by taking a closer look at flavors that are added to both tobacco (for smoking or chewing) and to the liquid nicotine formulas used in vaping devices.

FDA Commissioner Dr. Scott Gottlieb noted that, "The thought of any child starting down a path of a lifelong addiction to tobacco, which could ultimately lead to their death, is unacceptable. We need to take every effort to prevent kids from getting hooked on nicotine."

The FDA will also focus on flavors in tobacco, as well as e-cigarettes—the devices used in "vaping"—since that is the greatest route of first exposure to nicotine for middle and high school students.

Learn more about the FDA's ban on e-cigarette sales to minors.

In a previous blog, I highlighted the important role the FDA has in protecting women's health, particularly through the activities of the FDA's Office of Women's Health. I mentioned the FDA's responsibility for regulating tobacco products—a critical issue for women's health. While smoking is still the number one preventable cause of death and disease in the United States, exposure to nicotine is also a health risk because it so often leads to tobacco addiction.

The FDA's initiative is particularly important for women's health because "almost 90 percent of adult smokers start smoking by the age of 18." Although women use tobacco products at a slightly lower rate than men, consider these facts about how nicotine and smoking affect women's health:

  • Women have different biological responses to nicotine, are more easily addicted to nicotine than men, and become dependent sooner.

  • Women have lower rates of successfully quitting using the nicotine replacement patch but may have better results than men using other delivery methods such as a pill containing varenicline (Chantix).

  • Women are less likely to quit smoking once they start and more likely to relapse after quitting.

  • In 2010, 23 percent of women reported smoking in the first three months of pregnancy, 10 percent in the last 3 months of their pregnancy, and 16 percent after delivery.

  • Smoking also makes it harder for women to become pregnant, and it increases miscarriages, premature births and sudden infant death syndrome in children of women who smoked during or after pregnancy.

  • Smoking rates are much higher for lesbian, gay and bisexual individuals.

  • Smoking rates vary dramatically from state to state in the United States and vary significantly depending on race/ethnicity, income and educational level.

  • Smoking increases women's risks for developing cancer, including lung cancer, but also, colon and cervical cancer.

  • Smoking is the leading cause of cardiovascular diseases (heart attack and stroke) in women—diseases for which women continue to face challenges getting accurately diagnosed and treated.

I would note, however, that the FDA's work on e-cigarettes is not without controversy. It has delayed rules regulating them (and cigars). This delay was reported recently by The Washington Post. A group of health organizations has sued the FDA to encourage faster action by reestablishing the original timeline for companies to submit their products for FDA review by August of this year.

In HealthyWomen's ongoing work with the FDA, other state and federal government organizations and health advocates of all types, we will continue to stress the importance of reducing nicotine addiction and tobacco exposure in all forms. This is the right thing to do for women and families and for the country. We are encouraged that the FDA is generally continuing to pursue this important objective seriously and strenuously.

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