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Kimberly Beauregard was terrified of losing her memory as she entered her 60s. When she saw advertisements for Prevagen a number of years ago, they impressed her. "Can a protein originally present in a jellyfish improve your memory? " asks the voice-over in one industrial 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 last assurance that Prevagen has been clinically shown to improve reminiscence. "It was sufficient to make me say this is sweet, there’s going to be some profit to it," Beauregard stated. She wasn’t alone in that faith. Three million people are estimated to have bought Prevagen since it was first launched by Quincy Bioscience, a Wisconsin-primarily based producer, in 2007. Sales reached $165 million by mid-2015, and the corporate claims Prevagen is now a "best-promoting branded reminiscence complement in chain drug shops across the United States." A month’s supply of the "extra strength" selection retails for about $60 at Walgreens, CVS, Alpha Brain Supplement and Walmart.
Beauregard took Prevagen daily for 9 months, spending round $500 in all, however said she hadn’t noticed any reminiscence enchancment. Quincy Bioscience has been sued a number of instances over allegations of false advertising for Prevagen, together with by the government. After listening to about the lawsuits, Beauregard says she felt like her worst nightmare-of dropping her reminiscences-had been exploited by Quincy. "They virtually played on that worry, really, to make cash," she said. She’s not alone there, both. Well over half of American adults take supplements, but there are many misconceptions about the industry 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 exams supplements for safety or must approve products earlier than they're bought. Neither is true. Instead, the FDA largely relies on reporting by the businesses and customers, in addition to its own inspections, to spot potential issues once supplements are in the marketplace.
Commercials for Prevagen have insisted that "it’s secure and efficient," an assurance Quincy echoed to regulators. But an investigation by WIRED now reveals that for years officials on the FDA questioned the basis for the company’s claims. Multiple FDA inspections, most of which haven't been reported before, found significant issues with Quincy’s manufacturing processes, complaint dealing with, and the standard control testing that was supposed to make sure its merchandise had been secure. And hundreds of Americans have reported experiencing "adverse events" while taking Prevagen, including seizures, strokes, coronary heart arrhythmias, chest pain, and dizziness. While the existence of antagonistic occasion reports alone don’t prove a product is the cause, the character and pattern of complaints about Prevagen anxious FDA officials, according to agency data. Except for a warning letter sent to Quincy in 2012, the FDA has not publicly indicated it had any concerns about Prevagen. The agency determined in 2018 that Quincy addressed the violations cited within the warning letter.