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Kimberly Beauregard was terrified of losing her memory as she entered her 60s. When she saw ads for Prevagen a couple of years in the past, they impressed her. "Can a protein initially present in a jellyfish enhance your memory? " asks the voice-over in one commercial that used to air on prime-time Tv. "Our scientists say yes." The advert cuts from a swarm of the glowing blue sea creatures to scenes of people in white lab coats, smiling senior residents, and a final assurance that Prevagen has been clinically shown to enhance reminiscence. "It was sufficient to make me say this is good, there’s going to be some profit to it," Beauregard stated. She wasn’t alone in that faith. Three million persons are estimated to have bought Prevagen because it was first launched by Quincy Bioscience, a Wisconsin-primarily based manufacturer, in 2007. Sales reached $165 million by mid-2015, and the company claims Prevagen is now a "best-promoting branded memory complement in chain drug stores throughout the United States." A month’s supply of the "extra strength" variety retails for about $60 at Walgreens, CVS, and Walmart.

Beauregard took Prevagen daily for nine months, spending round $500 in all, however stated she hadn’t observed any memory enchancment. Quincy Bioscience has been sued a number of occasions over allegations of false promoting for Prevagen, including by the government. After hearing concerning the lawsuits, Beauregard says she felt like her worst nightmare-of shedding her recollections-had been exploited by Quincy. "They almost performed on that fear, really, to earn cash," she said. She’s not alone there, both. Well over half of American adults take supplements, however there are many misconceptions concerning the trade and the way it’s regulated. In a 2019 survey by Pew Charitable Trusts, more than half the respondents believed that the Food and Drug Administration both assessments supplements for safety or brain supplement ingredients must approve merchandise earlier than they're bought. Neither is true. Instead, the FDA largely relies on reporting by the businesses and consumers, in addition to its personal inspections, to identify potential problems once supplements are available on the market.