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    To bring you the best content on our sites and applications, Meredith partners with third party advertisers to serve digital ads, including personalized digital ads. Those advertisers use tracking technologies to collect information about your activity on our sites and applications and across the Internet and your other apps and devices. You always have the choice to experience our sites without personalized advertising based on your web browsing activity by visiting the DAA’s Consumer Choice page, the NAI's website, and/or the EU online choices page, from each of your browsers or devices. To avoid personalized advertising based on your mobile app activity, you can install the DAA’s App Choices app here. You can find much more information about your privacy choices in our privacy policy. Even if you choose not to have your activity tracked by third parties for advertising services, you will still see non-personalized ads on our site. Flibanserin, the medicine commonly referred to as the "Viagra for women," may soon be available from your doctor. But there is still a divide among health professionals about whether the little pink pill should receive Federal Drug Administration approval. Here's what you need to know about where things stand: 1. Flibanserin treats hypoactive sexual desire disorder in premenopausal women. Unlike Viagra, which men take immediately before a sexual encounter, flibanserin is taken daily before bedtime. Viagra works by increasing blood flow to the genitals, while flibanserin impacts brain chemicals. HSDD is defined by the Mayo Clinic as "persistent or recurrent lack of interest in sex that causes (women) personal distress." The condition impacts one in 10 women, according to Sprout Pharmaceuticals, the company behind the new drug. "Flibanserin is designed to treat an imbalance in neurotransmitters that are directly related to sexual desire," Sheryl Kingsberg, a clinical psychologist and an advisor to Sprout, told USA TODAY Network. Flibanserin could get approval from the FDA as soon as August 18, the deadline for the federal agency to make a decision. The medicine increases dopamine and norepinephrine and decreases serotonin. The FDA has rejected flibanserin twice before, citing side-effect concerns and doubt over effectiveness. The tipping point this time could be that an FDA advisory panel approved the drug on June 4 with a vote of 18 to 6 in favor of the drug. Critics of flibanserin say the side effects -- such as drowsiness, low blood pressure, fainting, nausea and dizziness -- are too significant to overlook. The FDA often, but not always, follows the recommendations of its advisory committees. One woman reportedly had a concussion when she fainted while taking the medicine and hit her head.

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