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Kimberly Beauregard was terrified of losing her memory as she entered her 60s. When she noticed advertisements for Prevagen a number of years ago, they impressed her. "Can a protein initially present in a jellyfish enhance your reminiscence? " asks the voice-over in a single commercial that used to air on prime-time Tv. "Our scientists say sure." The ad cuts from a swarm of the glowing blue sea creatures to scenes of people in white lab coats, smiling senior citizens, and a remaining assurance that Prevagen has been clinically proven to enhance memory. "It was enough to make me say this is sweet, there’s going to be some benefit to it," Beauregard mentioned. She wasn’t alone in that religion. Three million individuals are estimated to have purchased Prevagen because 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-selling branded reminiscence Brain Health Supplement in chain drug stores throughout the United States." A month’s supply of the "extra strength" selection retails for about $60 at Walgreens, CVS, and Walmart.

Beauregard took Prevagen daily for nine months, spending around $500 in all, visit Neuro Surge but stated she hadn’t observed any reminiscence enchancment. Quincy Bioscience has been sued a number of times over allegations of false advertising for Prevagen, including by the federal government. After hearing concerning the lawsuits, Beauregard says she felt like her worst nightmare-of shedding her reminiscences-had been exploited by Quincy. "They almost performed on that concern, actually, to generate income," she stated. She’s not alone there, both. Well over half of American adults take supplements, visit Neuro Surge but there are many misconceptions in regards to the industry and how 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 visit Neuro Surge safety or must approve products earlier than they are bought. Neither is true. Instead, the FDA largely relies on reporting by the companies and shoppers, as well as its personal inspections, to spot potential issues as soon as supplements are on the market.

Commercials for Prevagen have insisted that "it’s secure and efficient," an assurance Quincy echoed to regulators. But an investigation by WIRED now exhibits that for years officials at the FDA questioned the premise for the company’s claims. Multiple FDA inspections, most of which have not been reported before, discovered important issues with Quincy’s manufacturing processes, complaint dealing with, and the standard management testing that was supposed to ensure its products have been protected. And 1000's of Americans have reported experiencing "adverse events" whereas taking Prevagen, including seizures, strokes, heart arrhythmias, chest pain, and dizziness. While the existence of adversarial event reviews alone don’t prove a product is the cause, the nature and pattern of complaints about Prevagen frightened FDA officials, according to agency information. Aside from a warning letter sent to Quincy in 2012, the FDA has not publicly indicated it had any issues about Prevagen. The agency decided in 2018 that Quincy addressed the violations cited within the warning letter.

There isn't any indication in the records obtained by WIRED that the company took further enforcement motion. " a spokesperson for Quincy wrote in an announcement. The corporate stays below scrutiny. Earlier this year, Quincy reached a class-motion settlement to resolve seven lawsuits introduced by prospects over false advertising allegations. Anyone who bought Prevagen in the US earlier than July 21, 2020, is eligible to receive refunds of up to $70

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Pub: 17 Oct 2025 12:41 UTC

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