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Kimberly Beauregard was terrified of losing her memory as she entered her 60s. When she saw commercials for Prevagen a couple of years ago, they impressed her. "Can a protein originally present in a jellyfish improve your memory? " asks the voice-over in a single business that used to air on prime-time Tv. "Our scientists say yes." The ad 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 memory. "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 individuals are estimated to have purchased Prevagen since it was first launched by Quincy Bioscience, a Wisconsin-based mostly producer, in 2007. Sales reached $165 million by mid-2015, and the corporate claims Prevagen is now a "best-selling 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 on daily basis for nine months, spending round $500 in all, but stated she hadn’t observed any memory improvement. Quincy Bioscience has been sued multiple occasions over allegations of false advertising for natural nootropic brain supplement health supplement Prevagen, including by the federal government. After hearing about the lawsuits, Beauregard says she felt like her worst nightmare-of losing her reminiscences-had been exploited by Quincy. "They nearly performed on that worry, actually, to make money," she stated. She’s not alone there, both. Well over half of American adults take supplements, however there are plenty of misconceptions about the industry and the way it’s regulated. In a 2019 survey by Pew Charitable Trusts, greater than half the respondents believed that the Food and Drug Administration both exams supplements for security or must approve products before 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 spot potential problems once supplements are in the marketplace.