Health
Kennedy’s Views Mix Mistrust of Business With Unfounded Health Claims
Seven years after Americans celebrated the licensing of Jonas Salk’s polio vaccine, President John F. Kennedy called on Congress to finance a nationwide vaccination program to stamp out what he called the “ancient enemies of our children”: infectious disease.
Now Kennedy’s nephew, Robert F. Kennedy Jr., is the nation’s chief critic of vaccines — a public health intervention that has saved millions of lives — and President-elect Donald J. Trump’s pick to become the next secretary of health and human services. Mr. Kennedy calls himself a vaccine safety activist. The press calls him a vaccine skeptic. His detractors call him an anti-vaxxer and a conspiracy theorist.
Whatever one calls him, Mr. Kennedy is a polarizing choice whose views on certain public health matters beyond vaccination are far outside the mainstream. He opposes fluoride in water. He favors raw milk, which the Food and Drug Administration deems risky. And he has promoted unproven therapies like hydroxychloroquine for Covid-19. His own relatives called his presidential bid “dangerous for our country.”
If there is a through line to Mr. Kennedy’s thinking, it appears to be a deep mistrust of corporate influence on health and medicine. In some cases, that has led him to support positions that are also embraced by public health professionals, including his push to get ultra-processed foods, which have been linked to obesity, off grocery store shelves. His disdain for profit-seeking pharmaceutical manufacturers and food companies drew applause on the campaign trail.
People close to him say his commitment to “make America healthy again” is heartfelt.
“This is his life’s mission,” said Brian Festa, a founder of We the Patriots U.S.A., a “medical freedom” group that has pushed back on vaccine mandates, who said he has known Mr. Kennedy for years.
But like Mr. Trump, Mr. Kennedy also has a tendency to float wild theories based on scanty evidence. And he has hinted at taking actions, like prosecuting leading medical journals, that have unnerved the medical community. On Friday, many leading public health experts reacted to his nomination with alarm.
“This is the first time we’ve ever had someone that walking in the door whose public views, you just can’t trust,” said Dr. Georges Benjamin, the executive director of the American Public Health Association, which represents 25,000 public health professionals.
He called Mr. Kennedy, an environmental lawyer, “totally unprepared, by skill and by training,” for the job of secretary, which involves managing a department with more than 80,000 employees and 13 operating divisions, overseeing everything from Medicare to biomedical research.
Mike Pence, the former vice president under Mr. Trump, publicly opposed Mr. Kennedy’s nomination on Friday, citing his support for abortion rights.
The pharmaceutical industry’s trade group issued a statement neither praising nor criticizing Mr. Kennedy’s nomination. Calling itself “a crown jewel of the American economy,” the group vowed to “work with the Trump administration to further strengthen our innovation ecosystem and improve health care for patients.” Shares of stock in vaccine makers fell after Mr. Trump announced his selection of Mr. Kennedy on Thursday.
Mr. Kennedy did not respond to a request for an interview, and he has not publicly outlined his priorities. But if he is confirmed by the Senate, he would have wide latitude as health secretary, and has forecast his plans to shake things up.
In an interview in January 2024 with Dr. Mark Hyman, before he suspended his own independent presidential campaign and endorsed Mr. Trump, he spoke about what he would do if elected, outlining some of his lesser-known goals.
He said he would steer the nearly $48 billion annual budget of the National Institutes of Health away from drug development and toward studies that would explain high rates of chronic disease. He also said he would seek to prosecute medical journals like The Lancet and The New England Journal of Medicine under the federal anti-corruption statute.
“I’m going to litigate against you under the racketeering laws, under the general tort laws,” he said during the interview. “I’m going to find a way to sue you unless you come up with a plan right now to show how you’re going to start publishing real science and stop retracting the real science and publishing the fake pharmaceutical science by these phony industry mercenaries, scientists.”
More recently, Mr. Kennedy has said Mr. Trump would advise communities to stop fluoridating their water, contradicting the advice of Centers for Disease Control and Prevention, which cites fluoridation to reduce tooth decay as on of the ten great public health achievements of the 20th century. He has said he would slash 600 jobs at the N.I.H. and has instructed Food and Drug Administration officials to “preserve your records” and “pack your bags.”
Mr. Kennedy has argued that the F.D.A. is a victim of “corporate capture.” Under a three-decade-old “user fee” program, drug, device and biotech companies make payments to the agency partly to seek product approvals. The fees now account for nearly half the F.D.A.’s budget.
“The F.D.A. is just a sock puppet to the industries it is supposed to regulate,” Mr. Kennedy said in the interview with Dr. Hyman. “All of this is easily changed. I’m not saying I’m going to be able to accomplish it all on Day 1, but I’m going to accomplish it very quickly.”
Public health experts typically focus on Mr. Kennedy’s views on vaccination. Mr. Kennedy has cast doubt on Covid vaccines and has promoted the long-debunked theory that vaccines cause autism. His detractors say that his critiques of vaccine safety have cost lives, pointing in particular to a visit Mr. Kennedy made to Samoa in 2019.
That year, the island nation put its measles vaccination program on hold after the death of two infants who had received measles shots. Mr. Kennedy visited and, according to news reports, met with a prominent vaccine opponent, giving a boost to the anti-vaccination movement there.
The deaths were subsequently attributed to a mistake by the nurses who administered the vaccine, not to the vaccine itself. But the dip in vaccination rates led to a measles outbreak and 83 deaths.
Dr. Jonathan E. Howard, an associate professor of neurology and psychiatry at New York University who has been tracking the anti-vaccine movement for the past 15 years, said Mr. Kennedy would be “a disaster” as health secretary, adding, “He is an anti-vaccine paranoid crank who has a trail of dead children in Samoa.”
Often, Mr. Kennedy uses a “we don’t know” construction to spin out unproven theories, such as his suggestion that the coronavirus might have been engineered to attack specific races.
“Covid-19 is targeted to attack Caucasians and Black people,” Mr. Kennedy said at a fund-raiser, according to The New York Post. “The people who are most immune are Ashkenazi Jews and Chinese.”
“We don’t know whether it was deliberately targeted or not, but there are papers out there that show the racial or ethnic differential and impact,” he added.
Mr. Kennedy was apparently referring to a 2020 study looking at genetic differences in Covid-19 patients, but numerous studies examining racial disparities attribute them to socioeconomic factors, including poverty and lack of access to health care.
Mr. Kennedy also has repeatedly suggested that chemicals in the water might be responsible for “sexual dysphoria” in children. In a clip aired by CNN, he noted that atrazine, a herbicide sometimes found in well water in agricultural areas, will “concentrate and forcibly feminize” frogs. He went on, “What this does to sexual development in children, nobody knows.”
There is no evidence that the chemical, typically used on farms to kill weeds, causes the same effects in children, although studies show it has been linked to birth defects in babies whose mothers are exposed to it. But according to the Agency for Toxic Substances and Disease Registry, an arm of the C.D.C., “Most people are not exposed to atrazine on a regular basis.”
Mr. Kennedy came to health advocacy through his work as an environmental lawyer. In 1999, he was named a hero of the planet by Time magazine for his work with the Riverkeeper organization, among the groups credited with cleaning up New York’s polluted Hudson River. One of his aims was to get mercury out of waterways.
In a speech last year at Hillsdale College, he said that in 2005, when he was giving speeches around the country, mothers of children with autism approached him to ask him to take a look at vaccines, some of which had in the past contained a mercury-based preservative, thimerosal. The preservative was removed by manufacturers in 2001 at the request of the Centers for Disease Control and Prevention, and subsequent studies showed no link between the preservative and autism.
In the years since, Mr. Kennedy has made millions of dollars railing against vaccines. The windfall has come through books, including one denigrating Dr. Anthony S. Fauci, the former government scientist both celebrated and despised for his work on Covid, and through Children’s Health Defense, the nonprofit he has used as a platform to sow doubts about vaccination.
Allies of Mr. Kennedy say he has earned the right to make policy, given the support he generated while campaigning alongside Mr. Trump. Calley Means, a health care entrepreneur who has been an adviser to Mr. Kennedy and who was instrumental in connecting him to Mr. Trump, said in an interview last week that Mr. Kennedy had “a true mandate to take on broken health care institutions, and to deliver the change.”
Health
Hantavirus exposure risk may be higher than believed in parts of US, study finds
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Researchers found unusually high hantavirus levels in rodents in the Pacific Northwest, suggesting greater exposure risk in the surrounding agricultural communities.
The area with the biggest prevalence is the Palouse region, which includes parts of eastern Washington and north-central Idaho in the Pacific Northwest.
Researchers from Washington State University’s College of Veterinary Medicine found unexpectedly high levels of Sin Nombre virus (SNV), which is the strain most strongly linked to hantavirus pulmonary syndrome (HPS) — among local rodent populations.
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In summer 2023, they collected samples from 189 deer mice, voles and chipmunks at eight farms and two forest sites.
Nearly 30% of sampled rodents showed evidence of prior exposure and about 10% had active infections, according to the study press release. The rodents that tested positive were from both agricultural environments (farms) and natural settings (wilderness).
Researchers found unusually high hantavirus levels in rodents in the Pacific Northwest, suggesting greater exposure risk in the surrounding agricultural communities. (iStock)
While deer mice are the primary carriers of hantavirus pulmonary syndrome, the researchers found infections across multiple rodent species.
This suggests that Sin Nombre virus may be more widespread in the region than previously thought.
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The findings were published in 2026 in Emerging Infectious Diseases, a peer-reviewed journal from the Centers for Disease Control and Prevention.
“We were surprised both by how common the virus was locally and by how little data existed for the Northwest,” said Stephanie Seifert, the study’s corresponding author and principal investigator of the Molecular Ecology of Zoonotic and Animal Pathogens lab in the College of Veterinary Medicine’s Paul G. Allen School for Global Health, in the press release.
“We’re really just beginning to understand how widespread and complex this virus is in rodent populations here.”
The hantavirus detected in this study is different from the Andes virus, the strain linked to the recent outbreak on board the MV Hondius cruise ship. (Getty Images)
The Sin Nombre virus, the most common hantavirus in the U.S., is typically spread to humans through inhalation of aerosolized rodent urine, droppings or saliva and is not known to spread person-to-person.
This is different from the Andes virus, the strain linked to the recent outbreak on board the MV Hondius cruise ship. Andes virus is the only hantavirus that is capable of spreading between people through close, prolonged contact.
“People may be exposed more often than we realize, but severe cases are more likely to be tested for hantavirus.”
Dr. Sonja Bartolome, an expert in pulmonary and critical care at UT Southwestern Medical Center in Dallas, pointed out that since national tracking began in 1993, the illness has remained rare, with 864 cases reported between 1993 and 2022.
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“Most cases have occurred in Colorado, New Mexico and Arizona, and 94% have been reported in states west of the Mississippi River,” Bartolome, who was not involved in the study, told Fox News Digital.
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“It is important to conduct research that expands our understanding of how the virus spreads,” she went on. “Studies like this – which obtain and compare viral genetic sequences across regions and animals – help clarify how the virus moves geographically and between species.”
The researchers recommend efforts to prevent rodent exposure for living and farming in rural areas. (AP Photo/Godofredo A. Vásquez, File)
Although similar findings have been reported in other regions, this is the first study to reveal the pattern in this part of the country, Bartolome noted.
“Because humans most commonly contract hantavirus through exposure to aerosolized rodent urine or droppings, precautions remain essential when cleaning areas with evidence of rodent activity,” she added.
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The study presented some limitations, primarily that it only measured the infection in rodents and did not evaluate human transmission risk.
Additionally, the samples were only taken in the Palouse region and may not be generalized to all the Pacific Northwest.
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The research was also conducted during a single season, which means the conclusions don’t reflect year-round data.
The study suggests the need for expanded hantavirus monitoring in the Pacific Northwest, especially in agricultural areas.
The study presented some limitations, primarily that it only measured the infection in rodents and did not evaluate human transmission risk. (iStock)
The researchers recommend efforts to prevent rodent exposure for living and farming in rural areas. Longer-term studies could help clarify how environmental conditions and seasonal changes affect prevalence of the virus, they added.
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“People may be exposed more often than we realize, but severe cases are more likely to be tested for hantavirus,” said Pilar Fernandez, a co-author on the study and a disease ecologist in the Allen School whose research focuses on the eco-epidemiology of zoonotic diseases, in the release.
“Understanding that gap — how exposure translates into disease — is the next big step.”
Health
Finding the sleep ‘sweet spot’ could help you live longer, study suggests
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How long you sleep could be linked to how long you’ll live.
A new study, published in the journal Nature, found that people who slept too little or too long showed signs of “older biology.”
Researchers from Columbia University in New York used global biobank data from about 500,000 people who disclosed self-reported sleep duration in a 24-hour period, including naps.
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Reported sleep times were compared with 23 biological aging clocks, estimating whether various parts of the body looked biologically older or younger than the individual’s actual age.
Short and long sleep were both linked with signals of a higher biological age. They were also associated with a higher risk of future diseases and all-cause mortality, the researchers found.
According to study results, short sleep and long sleep were both linked with signals of higher biological age. (iStock)
In nine of the aging clocks, the researchers found “statistically significant” links between sleep and aging, including in the brain, heart, immune system and skin.
Those with the “lowest biological age gap” were women who slept for 6.5 to 7.8 hours and men who slept for 6.4 to 7.7 hours, according to the study.
Longer sleep had a stronger link to psychiatric-related outcomes, while short sleep had more physical impacts on cardiovascular, metabolic, musculoskeletal, psychiatric, neurological, pulmonary and gastrointestinal conditions.
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The U-shaped results also showed that shorter sleep led to a 50% higher relative risk for all-cause mortality, while longer sleep had about a 40% higher risk.
The researchers noted that self-reported sleep poses a limitation to the study. As it was observational in design, it does not prove that sleeping exactly six to eight hours will slow aging.
Both women and men who slept roughly six to eight hours showed the lowest signals for biological aging. (iStock)
Saema Tahir, MD, a New York-based board-certified sleep medicine physician, reflected on these findings in an interview with Fox News Digital.
“Sleep is really when the body does its most critical repair work, including cellular restoration, immune regulation, hormonal balance, and even clearing out metabolic waste from the brain through what we call the glymphatic system,” said Tahir, who was not involved in the study.
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“When sleep is consistently too short or too long, those processes get disrupted. Over time, that disruption accumulates at the cellular level.”
This effect is proven in increased inflammatory markers and cellular changes, which are “hallmarks of accelerated aging,” Tahir noted.
“So, the relationship isn’t just correlational; there are real physiological mechanisms connecting poor sleep to the body aging faster than it should.”
“Sleep is really when the body does its most critical repair work,” the doctor noted. (iStock)
Tahir cautions her patients not to treat the six- to eight-hour recommendation as a “rigid prescription,” as sleep is individualized.
For example, a healthy 25-year-old and a 70-year-old with cardiovascular disease have “very different sleep architecture and needs,” according to the expert.
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“What I tell my patients is to use that range as a starting framework, but pay attention to how you feel,” she advised. “Are you waking up refreshed? Can you stay alert throughout the day without caffeine propping you up? Those functional cues matter just as much as the number on the clock.”
For certain people, like pregnant women, athletes and people recovering from illness, these sleep needs can shift “considerably.”
As sleep is individualized, a rigid six- to eight-hour framework may not work for everyone. (iStock)
“Sleep duration is important, but … getting adequate sleep and REM sleep that allows our bodies to heal, clear, process and repair is much more important,” Tahir said.
Regardless of sleep time, those who don’t achieve quality sleep often struggle, she shared.
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“I’ve seen patients who log seven hours but spend most of that time in light sleep, barely touching the deep slow-wave or REM stages that are most restorative,” Tahir said. “They age just as poorly, sometimes worse, than someone getting six hours of genuinely consolidated, high-quality sleep.”
Deep sleep is the phase when growth hormone is released and tissue repair peaks, and REM sleep is “critical” for cognitive health and emotional regulation, according to the expert.
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“So, chasing hours without addressing sleep fragmentation, sleep apnea or poor sleep architecture is missing the bigger picture,” she said.
The takeaway from this study, according to Tahir, is that sleep is not a “lifestyle luxury,” but a “biological necessity with measurable consequences for how we age and how healthy we are.”
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There’s still a cultural tendency to see sleep deprivation as a “badge of productivity,” which she pushes back against. “But I also want people to avoid the other extreme — health anxiety about their sleep can actually make sleep worse.”
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The sleep expert concluded that “consistent, good-quality sleep is one of the most accessible tools we have for healthy aging.”
“It doesn’t require a prescription or expensive intervention — it requires prioritization.”
Health
‘Wild West’ peptide craze surges beyond GLP-1s as FDA faces pressure to ease access
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As GLP-1 weight-loss medications gain traction, the peptide market is experiencing a surge in interest.
A variety of peptides — commonly marketed for weight loss, muscle building, injury recovery and other uses — have emerged as largely unregulated drugs sold through both licensed compounding pharmacies and unverified vendors.
The U.S. Food and Drug Administration is set to evaluate whether to loosen regulations on several peptides during a meeting this summer.
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Peptides are short chains of amino acids — the building blocks of proteins — that play key roles in biological functions, according to the National Institutes of Health. Peptide drugs are lab-made versions of natural molecules in the body that are designed to mimic or influence biological signals to treat disease, experts say.
GLP-1s are “incredibly effective at what they do when it comes to changing body composition, benefiting metabolic health, cardiovascular health [and] neurologic health,” the expert said. (iStock)
Though the peptide market has been described as the “Wild West,” demand remains strong, potentially challenging pharmaceutical giants that dominate the GLP-1 market.
Dr. Alex Tatem, an Indiana-based board-certified urologist with expertise in men’s health and peptides, discussed how “life-changing” GLP-1s kicked off the rise of peptides.
“These were all medications that were designed to help people live well and live as healthy as possible.”
“They are incredibly effective at what they do when it comes to changing body composition, benefiting metabolic health, cardiovascular health [and] neurologic health,” he said. “These are truly miracle compounds, and as a result we’ve seen an explosion of interest – not just on the pharmaceutical side or the doctor’s side, but from the general public.”
According to Tatem, the challenge is that nearly all commercial GLP-1 products are administered in a single-dose weekly pen, which works for the “overwhelmingly majority” of patients, but not for everyone.
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“There are patients I can prescribe tirzepatide to and they can do OK with a once-a-week [dose], but they end up developing nausea with that initial injection – and then by the end of the week, they’re hungry again.”
Because some patients respond better to smaller, more frequent doses — an option not offered by commercial drugs — compounding, or the customization of medications, has grown in popularity, Tatem said.
Several GLP-1 weight loss medications have been approved by the FDA with positive results from consumers. (iStock)
“We’ve had compounding pharmacies that have now developed compounded versions of semaglutide and tirzepatide that allow that sort of dosing flexibility,” he said.
“The reason compounders had to do this was because there was so much demand for GLP-1s that there was actually a national shortage.”
Current legislation allows compounders to step in during widespread national shortages, according to Tatem, prompting the industry to invest millions of dollars into developing and manufacturing these drugs.
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Once commercial pharmaceutical companies could catch back up, compounders continued making these medications in smaller batches for custom doses, allowing for more patient accessibility.
“That creates a huge clash between commercial pharmaceutical companies and compounders, because commercial pharmaceutical companies view that as an infringement of their property,” Tatem noted.
The expert noted a “huge clash” between pharmaceutical companies and compounding pharmacies in peptide production. (iStock)
Tatem raised concerns about the FDA’s regulation of compounding pharmacies, warning that it could limit patients’ access to customized medications.
“That is a real concern for clinicians like me who really care more about patient access, making sure we can get the right medication to the right patients at the right time,” he said.
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Some peptides have been widely administered for more than a decade without major health complications like toxicity or cancer, according to Tatem.
“These are compounds that haven’t gone through the full FDA approval process that you would normally see for a commercial drug, [yet] we didn’t see anything adverse,” he said.
The FDA plans to consider loosening restrictions on several peptides during a summer 2026 meeting. (Issam Ahmed/AFP)
In September 2023, the FDA “quietly” tightened regulation of 19 peptides, making them illegal to manufacture and cutting off patient access.
“They seemed to be working and seemed to be efficacious for patients, and all of a sudden they were banned, which inadvertently ended up contributing to this surge in interest,” Tatem said. “We kind of saw the same thing happen with peptides that we saw with prohibition.”
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While the rising popularity of GLP-1 drugs has fueled growing public and regulatory interest in peptides, most of the so-called “trendy” peptides still are not available by prescription, according to Tatem.
They may help with injury recovery, skin rejuvenation, sleep improvements and boosting of natural growth hormones, he said.
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“These were all medications that were designed to help people live well and live as healthy as possible,” the doctor told Fox News Digital. “And in reality, that was also their downfall in the American healthcare system, because if you are going to get a drug approved and to market, it has to treat a disease state.”
“These were all medications that were designed to help people live well and live as healthy as possible,” Tatem told Fox News Digital. (iStock)
Tatem confirmed that he’s seen a shift in patients confronting more than just baseline ailments, seeking advice on how to feel their best through new modes like testosterone therapy.
“The desire to function at our highest level is something that we all feel,” he said.
While nothing replaces the fundamentals — getting eight hours of sleep, eating a high-protein diet and maintaining a fitness routine that blends resistance training and cardio — Tatem said individualized treatments such as peptides may help support those healthy habits.
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“If you end up pulling a tendon or pulling a hamstring, and you’re just now starting to get some momentum in the gym, that’s really where peptides start to step in,” he added.
Experts advise consumers to avoid gray-market products, to work only with qualified physicians and reputable pharmacies, and to treat peptides as part of a broader health plan — not a shortcut or risk-free supplement.
Semaglutide (GLP-1) weight-loss drug Wegovy, made by pharmaceutical company Novo Nordisk, is designed to treat type 2 diabetes, but is widely known for its effect on weight loss. Picture date: Wednesday, October 16, 2024. (James Manning/PA Images via Getty Images)
In a statement shared with Fox News Digital, a Novo Nordisk spokesperson said the drugmaker is committed to working with regulators, law enforcement and “other key stakeholders” to ensure “affordable access to safe, effective and FDA-approved GLP-1 obesity medication like Wegovy and to protect patients from unapproved and untested knockoff drugs.”
“The desire to function at our highest level is something that we all feel.”
“Novo Nordisk supports FDA’s recent thorough scientific analysis and conclusion that there is no medical basis or clinical need for the continued mass compounding of unapproved semaglutide and liraglutide drugs,” they went on.
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“The agency’s decision reaffirms that compounding is meant to be a rare and limited exception to FDA’s gold-standard drug approval framework that ensures that medicines in the U.S. are safe and effective.”
Fox News Digital reached out to the FDA and Eli Lilly for comment.
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