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COVID booster warning from Florida surgeon general, who advises people not to get new vaccine

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COVID booster warning from Florida surgeon general, who advises people not to get new vaccine

While speaking at a Thursday news conference for Gov. Ron DeSantis in Jacksonville, Florida, Dr. Joseph Ladapo, that state’s surgeon general, advised people to steer clear of the updated booster vaccine for COVID-19.

The U.S. Food and Drug Administration (FDA) has not yet approved the new vaccine — which is reportedly designed to protect against the BA.2.86 omicron subvariant.

“There’s a new vaccine that’s coming around the corner, a new mRNA COVID-19 vaccine, and there’s essentially no evidence for it,” Ladapo said during the news conference, according to local news outlets. 

FAUCI’S MASKING MESSAGE AMID RISING COVID CASES HAS DOCTORS SOUNDING OFF: ‘WILL NOT REDUCE THE SPREAD’

“There’s been no clinical trial done in human beings showing that it benefits people” he said. 

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“There’s been no clinical trial showing that it is a safe product for people — and not only that, but then there are a lot of red flags.”

While speaking at a Thursday news conference for Gov. Ron DeSantis in Jacksonville, Florida, Dr. Joseph Ladapo, surgeon general of Florida, advised people to steer clear of the updated booster vaccine for COVID-19. (Getty Images/iStock)

In terms of specific concerns, Ladapo warned that the updated vaccines “actually cause cardiac injury in many people.”

The state surgeon general urged Floridians to make their own decisions based on their particular “resonance of truth,” rather than on “very educated people telling you what you should think.”

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“When they try to convince you to be comfortable and agree with things that don’t feel comfortable, [that] don’t feel like things you should agree with, that is a sign, right? That’s a gift,” he said.

Instead of relying on the new vaccines, Ladapo urged people to adopt healthy nutrition habits.

DeSantis appointed Ladapo, a doctor who trained at Harvard and was previously a UCLA medical researcher, as surgeon general in 2021.

COVID booster

The U.S. Food and Drug Administration (FDA) has not yet approved the new vaccine, which is reportedly designed to protect against the BA.2.86 omnicron subvariant. (Scott Olson/Getty Images)

COVID vaccines safe in ‘vast majority’ of cases, says New York doctor

Dr. Marc Siegel, a professor of medicine at NYU Langone Medical Center and a Fox News medical contributor, pointed out that vaccines “have been given to trillions around the world and in the vast majority of cases, they are safe.”

He told Fox News Digital, “Physicians with knowledge of vaccines should be involved in deciding the risk/benefit for their patients and offering advice, but it is ultimately up to the individual.”

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“For younger, healthier patients with intact immune systems and a foundation of immune memory against SARS-CoV-2 from prior vaccines and infection, I may choose to not recommend an additional booster at this time, but vilifying it is a dangerous move that undermines patient choice and the vaccine as one of my most important tools,” he went on. 

High-risk groups — including the elderly, along with those who have obesity, diabetes, chronic heart disease, lung disease and cancer — should be prioritized in receiving vaccines, the doctor said.

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“The new version that targets the XBB 1.5 subvariant, which is still about 20% of cases, has also been shown to be effective against the emerging EG.5 and BA.2.86 subvariants,” Siegel said.

Although this is not an entirely new vaccine, it is a slight variation of the previous version, the doctor noted. 

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Woman getting vaccinated

“The new version that targets the XBB 1.5 subvariant, which is still about 20% of cases, has also been shown to be effective against the emerging EG.5 and BA.2.86 subvariants,” Siegel said. (iStock)

“There is no reason for full clinical trials prior to use,” he said. “We will quickly amass new data. It is no longer an experimental vaccine.”

There is a much higher risk of myocarditis from COVID than from the vaccine, according to the doctor, who added that the vaccine also decreases the risk of developing long COVID.

“Additional fearmongering about an effective and safe vaccine is not helpful. It is an individual choice.”

“Additional fearmongering about an effective and safe vaccine is not helpful,” he added. 

“It is an individual choice,” said Dr. Siegel.

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“COVID is still a nasty virus that can affect multiple organ systems, including the brain,” Siegel said. “The vaccine is a useful tool that should not be maligned, attacked or mischaracterized.”

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The doctor added that he will be recommending the booster for many people — but not for all.

“I won’t offer it to those who just had COVID recently,” he said. 

‘Booster not necessary,’ says Florida doctor

Dr. Brett Osborn, a board-certified neurosurgeon and longevity expert in West Palm Beach, Florida, said he agrees with Dr. Ladapo’s recommendation “as it applies to the masses.”

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Osborn told Fox News Digital, “As time goes by, RNA viruses tend to lessen in pathogenicity, meaning that they cause lesser symptoms as the virus mutates further away from its original strain (of SARS-COV-2) that was responsible for the pandemic of 2020.”

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As time goes on, the severity and mortality rate of COVID will continue to decline and soon will be comparable to influenza, the doctor predicted — “therefore, the booster is simply not necessary.”

In his Florida clinic, Osborn said he does not recommend the influenza vaccine to patients, as “the infection itself nearly always assumes a benign course in low-risk individuals, and similarly, I do not believe that our immune systems should be deprived of challenges.”

Older woman vaccine

The “high-risk” population of Americans — namely the elderly, the morbidly obese and/or those with type II diabetes — may want to consider getting boosted, Dr. Osborn of Florida said. (iStock)

Osborn said he himself very seldom gets sick — perhaps every five years, he estimated — “because I take care of my body, not because I am routinely vaccinated (which I am not).”

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That said, Osborn added that the “high-risk” population — namely the elderly, the morbidly obese and/or those with type II diabetes — may want to consider getting boosted.

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“For that population, the risks of a COVID-19 infection, or even one of its less aggressive variants, may be greater than the risk of a booster, even if it has undergone limited testing,” he said.

A young girl receives the coronavirus vaccine

The CDC, for its part, recommends that everyone six months of age and older in the United States receive a COVID-19 vaccination. (Scott Olson/Getty Images)

Osborn also pointed out that vaccines for influenza and other viruses undergo testing for 10-15 years before they are publicly deployed.

“Getting boosted is a personal decision — one that must be made in conjunction with your physician, who can best determine your risk-benefit ratio,” he said. 

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The Centers for Disease Control and Prevention (CDC) recommends that everyone six months and older in the United States receive a COVID-19 vaccination.

“Getting boosted is a personal decision — one that must be made in conjunction with your physician, who can best determine your risk-benefit ratio.”

The CDC website also states that “most people ages six years and older who are not moderately or severely immunocompromised and have received 1 dose of a bivalent mRNA vaccine do not need any further vaccine doses at this time.”

It added, “People ages 65 years and older who received 1 dose of a bivalent vaccine have the option to receive 1 additional dose at least 4 months after the first bivalent dose.”

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Health

FDA bans red food dye due to potential cancer risk

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FDA bans red food dye due to potential cancer risk

The U.S. Food and Drug Administration (FDA) has officially banned red dye — called Red 3, or Erythrosine — from foods, dietary supplements and ingested medicines, as reported by the Associated Press on Wednesday.

Food manufacturers must remove the dye from their products by January 2027, while drug manufacturers will have until January 2028 to do so, AP stated. 

Any foods imported into the U.S. from other countries will also be subject to the new regulation.

RED FOOD DYE COULD SOON BE BANNED AS FDA REVIEWS PETITION

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“The FDA is taking action that will remove the authorization for the use of FD&C Red No. 3 in food and ingested drugs,” said Jim Jones, the FDA’s deputy commissioner for human foods, in a statement. 

The U.S. Food and Drug Administration has officially banned red dye — called Red 3, or Erythrosine — from foods, dietary supplements and ingested medicines (iStock)

“Evidence shows cancer in laboratory male rats exposed to high levels of FD&C Red No.3,” he continued. “Importantly, the way that FD&C Red No. 3 causes cancer in male rats does not occur in humans.”

      

The synthetic dye, which is made from petroleum, is used as a color additive in food and ingested drugs to give them a “bright cherry-red color,” according to an online statement from the FDA.

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Red cough syrup

Food manufacturers must remove the dye from their products by January 2027, while drug manufacturers will have until January 2028 to do so. (iStock)

The petition to ban the dye cited the Delaney Clause, which states that the agency cannot classify a color additive as safe if it has been found to induce cancer in humans or animals.

The dye was removed from cosmetics nearly 35 years ago due to potential cancer risk.

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“This is a welcome, but long overdue, action from the FDA: removing the unsustainable double standard in which Red 3 was banned from lipstick but permitted in candy,” said Dr. Peter Lurie, director of the group Center for Science in the Public Interest, which led the petition effort, as reported by AP.

Red Jello

Nearly 3,000 foods are shown to contain Red No. 3, according to Food Scores, a database of foods compiled by the Environmental Working Group. (iStock)

Dr. Marc Siegel, clinical professor of medicine at NYU Langone Health and Fox News senior medical analyst, applauded the FDA’s ban.

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“It was a long time coming,” he told Fox News Digital. “It’s been more than 30 years since it was banned from cosmetics in the U.S. due to evidence that it is carcinogenic in high doses in lab rats. There needs to be a consistency between what we put on our skin and what we put into our mouths.”

“There needs to be a consistency between what we put on our skin and what we put into our mouths.”

Siegel said he believes the FDA’s decision could be tied to the incoming new head of the Department of Health and Human Services, Robert F. Kennedy Jr.

“They knew it would have happened anyway under RFK Jr.,” he said. “It is already banned or severely restricted in Australia, Japan and the European Union.”

Kid eating sugary cereal

The food additive also “drew kids in” to a diet of empty calories and ultraprocessed foods, one doctor stated. (iStock)

The food additive also “drew kids in” to a diet of empty calories and ultraprocessed foods, Siegel added.

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“It has also been linked to behavioral issues in children, including ADHD.”

Nearly 3,000 foods are shown to contain Red No. 3, according to Food Scores, a database of foods compiled by the Environmental Working Group.

For more Health articles, visit www.foxnews.com/health

The National Confectioners Association provided the below statement to Fox News Digital.

“Food safety is the number one priority for U.S. confectionery companies, and we will continue to follow and comply with FDA’s guidance and safety standards.”

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The petition to remove Red No. 3 from foods, supplements and medications was presented in 2022 by the Center for Science in the Public Interest and 23 other organizations and scientists.

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How Yvette Nicole Brown Lost Weight and Got Her Diabetes Under Control

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How Yvette Nicole Brown Lost Weight and Got Her Diabetes Under Control


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As bird flu spreads, CDC recommends faster 'subtyping' to catch more cases

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As bird flu spreads, CDC recommends faster 'subtyping' to catch more cases

As cases of H5N1, also known as avian flu or bird flu, continue to surface across the U.S., safety precautions are ramping up.

The U.S. Centers for Disease Control and Prevention (CDC) announced on Thursday its recommendation to test hospitalized influenza A patients more quickly and thoroughly to distinguish between seasonal flu and bird flu.

The accelerated “subtyping” of flu A in hospitalized patients is in response to “sporadic human infections” of avian flu, the CDC wrote in a press release.

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“CDC is recommending a shortened timeline for subtyping all influenza A specimens among hospitalized patients and increasing efforts at clinical laboratories to identify non-seasonal influenza,” the agency wrote.

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The CDC now recommends accelerated subtyping of influenza A in response to “sporadic human infections” in the U.S. (iStock)

“Clinicians and laboratorians are reminded to test for influenza in patients with suspected influenza and, going forward, to now expedite the subtyping of influenza A-positive specimens from hospitalized patients, particularly those in an intensive care unit (ICU).”

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The goal is to prevent delays in identifying bird flu infections and promote better patient care, “timely infection control” and case investigation, the agency stated.

These delays are more likely to occur during the flu season due to high patient volumes, according to the CDC.

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For more Health articles, visit www.foxnews.com/health

Health care systems are expected to use tests that identify seasonal influenza A as a subtype – so if a test comes back positive for influenza A but negative for seasonal influenza, that is an indicator that the detected virus might be novel.

Patient on hospital bed

Identifying bird flu infections will support better patient care and infection control, the CDC says. (iStock)

“Subtyping is especially important in people who have a history of relevant exposure to wild or domestic animals [that are] infected or possibly infected with avian influenza A (H5N1) viruses,” the CDC wrote.

In an HHS media briefing on Thursday, the CDC confirmed that the public risk for avian flu is still low, but is being closely monitored.

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The agency spokesperson clarified that this accelerated testing is not due to bird flu cases being missed, as the CDC noted in its press release that those hospitalized with influenza A “probably have seasonal influenza.”

Niels Riedemann, MD, PhD, CEO and founder of InflaRx, a German biotechnology company, said that understanding these subtypes is an “important step” in better preparing for “any potential outbreak of concerning variants.”

Blood collection tubes H5N1 in front of chicken

The CDC recommends avoiding direct contact with wild birds or other animals that may be infected. (iStock)

“It will also be important to foster research and development of therapeutics, including those addressing the patient’s inflammatory immune response to these types of viruses – as this has been shown to cause organ injury and death during the COVID pandemic,” he told Fox News Digital. 

Since 2022, there have been 67 total human cases of bird flu, according to the CDC, with 66 of those occurring in 2024.

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The CDC recommends that people avoid direct contact with wild birds or other animals that are suspected to be infected. Those who work closely with animals should also wear the proper personal protective equipment (PPE).

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