Florida Surgeon General Joseph Ladapo notes 'DNA fragments detected in mRNA COVID shots'



Florida Surgeon General Joseph Ladapo, who notes that DNA fragments have been detected in mRNA COVID-19 vaccines, has issued a letter asking questions related to the issue.

"On today's episode of: What the FDA... I asked @DrCaliff_FDA to address the DNA fragments detected in mRNA COVID shots & how they are hitchhiking into human cells. DNA integration into the human genome & oncogenesis are known risks, even acknowledged by @US_FDA in '07," Ladapo tweeted when sharing his letter to FDA Commisoner Robert Califf. CDC Director Mandy Cohen is also included on the letter.

— (@)

In a letter earlier this year, Ladapo accused Califf and then-CDC Director Rochelle Walensky of ignoring many of the risks related to mRNA COVID-19 vaccines. In his new letter dated December 6, 2023, he noted that "no response has been received."

"In addition to my previous letter, I am writing to you to address the recent discovery of host cell DNA fragments within the Pfizer and Moderna COVID-19 mRNA vaccines," Ladapo noted in his new letter.

"This raises concerns regarding the presence of nucleic acid contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines, particularly in the presence of lipid nanoparticle complexes, and Simian Virus 40 (SV40) promoter/enhancer DNA. Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells, and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into host cells," he noted.

Ladapo pressed for answers to several questions, including one which reads, "Considering the potentially wide biodistribution of mRNA COVID-19 vaccines and DNA contaminants beyond the local injection site, have you evaluated the risk of DNA integration in reproductive cells with respect to the lipid nanoparticle delivery system?"

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Florida Surgeon General accuses CDC and FDA heads of ignoring 'many of the risks associated with mRNA COVID-19 vaccines'



Florida Surgeon General Joseph Ladapo has written a letter to Centers for Disease Control and Prevention Director Rochelle Walensky and U.S. Food and Drug Administration Commissioner Robert Califf, accusing the public health officials of ignoring many risks related to mRNA COVID-19 vaccines.

"Your ongoing decision to ignore many of the risks associated with mRNA COVID-19 vaccines, alongside your efforts to manipulate the public into thinking they are harmless, have resulted in deep distrust in the American health care system," Ladapo declared in the May 10 letter.

He asserted that their "collective decisions to deny that natural immunity confers comparable or superior protection to COVID-19 vaccination, push mRNA COVID-19 boosters for the young and healthy, and delay acknowledging the risks of vaccine-induced myocarditis have only sowed doubt between the American people and the public health community."

The Sunshine State public health official listed a number of requests — among them, he pressed for the officials to "report why randomized clinical trials were not required prior to the approval of mRNA COVID-19 boosters, including the new bivalent booser." He called for them to "Report the number of adolescents that have died within days of receiving a second dose or booster of the mRNA COVID-19 vaccine," and to "Explain why you have not required Pfizer to report results of its randomized trial in pregnant women ... which was completed in July of 2022." He also made various other requests.

\u201cWhen I asked the feds for more honesty and transparency around COVID-19 vaccine data, they replied with a word salad of pandering and gaslighting. \ud83d\ude44 Here\u2019s my response. Let\u2019s try again, @CDCgov @US_FDA.\u201d
— Joseph A. Ladapo, MD, PhD (@Joseph A. Ladapo, MD, PhD) 1683763252

In a March response to an earlier letter from Ladapo, Walensky and Califf had promoted COVID-19 vaccination.

"We stand firmly behind the safety and effectiveness of the mRNA COVID-19 vaccines, which are fully supported by the available scientific data. Staying up to date on vaccination is the best way to reduce the risks of death and serious illness or hospitalization from COVID-19. Misleading people by overstating the risks, or emphasizing the risks without acknowledging the overwhelming benefits, unnecessarily causes vaccine hesitation and puts people at risk of death or serious illness that could have been prevented by timely vaccination," they wrote.

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SCOTUS acts to keep abortion pill available for now



The Supreme Court acted Friday to keep the abortion pill mifepristone widely available as a pivotal case works its way through the courts, Fox News Digital reported.

Justices Clarence Thomas and Samuel A. Alito Jr. dissented. No justices appointed by former President Donald Trump publicly followed suit, the New York Times reported.

"As is common practice, the Supreme Court has decided to maintain the status quo that existed prior to our lawsuit while our challenge to the FDA’s illegal approval of chemical abortion drugs and its removal of critical safeguards for those drugs moves forward," said Alliance Defending Freedom Senior Counsel Erik Baptist in a statement.

Baptist went on to explain that the case will continue on an expedited basis through the lower courts.

"The FDA must answer for the damage it has caused to the health of countless women and girls and the rule of law by failing to study how dangerous the chemical abortion drug regimen is and unlawfully removing every meaningful safeguard, even allowing for mail-order abortions."

ADF represents the plaintiff in Alliance for Hippocratic Medicine v. U.S. Food and Drug Administration. ADF says the United States Food & Drug Administration's failure to study the safety of the abortion pill regimen "eliminated necessary safeguards for pregnant girls and women." Further, ADF says the FDA disregarded evidence that chemical abortions lead to more complications than their surgical counterparts.

The case quickly made its way to the emergency docket after dueling rulings earlier this month lead to considerable confusion, as Politico reported. The first ruling, in Texas, invalidated the FDA's approval of the drug. A second decision in the state of Washington, on the same day, directed the FDA to keep it available.

The same progressives who were pleased with the court's Friday decision viciously derided that same court when Roe v. Wade was overturned in June 2022. The historic Dobbs v. Jackson Women's Health Organization decision largely left abortion-related lawmaking to the states, as the Wall Street Journal's Editorial Board noted.

"Today’s decision shows how dangerously misguided and abhorrent the ruling by Texas District Court was. While this is a temporary victory, this is hardly the end of the fight to protect women’s health choices," said Senate Majority Leader Chuck Schumer (D-N.Y.) in a statement.

"Democrats won't stop fighting and we will prevail," he added.

"While I’m disappointed in the Court’s decision, we will continue the fight as the case continues to hold the @US_FDA accountable for endangering moms & babies through chemical abortion drugs," Senate Pro-Life Caucus chair Sen. Cindy Hyde-Smith (R-Miss.) tweeted.

The case will now move back to the conservative 5th Circuit where a three-judge panel will hold a hearing May 17, CNN reported.

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FDA and Florida clash over federal restriction of monoclonal antibody treatments



On Monday, the Food and Drug Administration removed two monoclonal antibody therapies from the list of approved COVID-19 treatments, subsequently forcing treatment sites to close despite these locations being pivotol to Florida's COVID-19 response.

The FDA made this announcement Monday in a press release stating that the bamlanivimab-etesevimab cocktail and the REGEN-COV treatments were to be removed from the list of emergency use authorizations.

It continued by saying that these treatments should only be used “when the patient is likely to have been infected with or exposed to a variant that is susceptible to these treatments” because “data show these treatments are highly unlikely to be active against the omicron variant.” The FDA did not elaborate or provide the data.

The FDA argued against the preventive treatments, stating that “treatments are not a substitute for vaccination in individuals for whom COVID-19 vaccination and a booster dose are recommended.”

The Washington Post reported that Patrizia Cavazzoni, the director of the FDA’s Center for Drug Evaluation and Research and author of Monday’s press release, said that these monoclonal antibody treatments are “highly unlikely to be active against the omicron variant” and that “these treatments are not authorized to be used at this time.”

The FDA press release states that “these [monoclonal antibody] treatments are not authorized for use in any U.S. states, territories, and jurisdictions at this time.”

However, the press release did not mention that the Omicron variant can circumvent COVID immunity gained through vaccination.

In an interview with the French outlet Le Monde, Ugur Sahin, the CEO of BioNTech, the co-developer of the Pfizer vaccine, confirmed this by saying, “We must be aware that even triple-vaccinated are likely to transmit the disease. ... It is obvious we are far from 95% effectiveness that we obtained against the initial virus.”

The FDA’s decision will force monoclonal antibody treatment facilities around the country to close their doors to those seeking treatment for COVID-19 other than the mRNA vaccine.

In Florida, monoclonal antibodies proved to be a vital lifeline in the state’s approach to combatting COVID-19. Officials from the state of Florida condemned the FDA’s decision, claiming it was made without any warning and determined through analyzing clinical data not made available to the public.

After @HHSGov avoided communication with @HealthyFla regarding statewide allocations, without any warning, @US_FDA suspended the use of multiple MABs treatments. Such decisions should be made based on clinical data - which the FDA has not provided.pic.twitter.com/zpWl7ZGODQ
— Joseph A. Ladapo, MD, PhD (@Joseph A. Ladapo, MD, PhD) 1643065270

The Florida Department of Health issued a statement countering the FDA. In it, the state’s Department of Health lamented being forced to shut down state-run monoclonal antibody treatment sites, stating, “Florida disagrees with the decision that blocks access to any available treatments in the absence of clinical data.”

As a result of the @US_FDA's abrupt decision to remove the EUAs for two monoclonal antibodies, monoclonal antibody treatment sites will be closed until further notice. Full press release is below.pic.twitter.com/RGeWTPwxCs
— Florida Dept. of Health (@Florida Dept. of Health) 1643080563

Rapper Nicki Minaj blasts 'dumb a**' Joy Reid for chastising her COVID vaccine hesitancy on MSNBC, rips Reid as hypocritical and 'homophobic'



After rapper Nicki Minaj went viral Monday for stating her COVID-19 vaccine hesitancy on Twitter, MSNBC host Joy Reid chastised Minaj on TV for using her "platform" of 22 million followers to "put people in the position of dying from a disease they don't have to die from."

Well, Minaj wasn't about to take Reid's tongue lashing without a fight — and fired back at the far-left host, calling Reid a "dumb ass" and "homophobic" and "thirsty to down another black woman (by the request of the white man)."

What are the details?

Minaj indicated on Twitter that she wouldn't be attending the Met Gala because it required attendees to be vaccinated.

"They want you to get vaccinated for the Met. If I get vaccinated it won't for the Met. It'll be once I feel I've done enough research. I'm working on that now," Minaj tweeted Monday. "In the meantime my loves, be safe. Wear the mask with 2 strings that grips your head & face. Not that loose one."

They want you to get vaccinated for the Met. if I get vaccinated it won’t for the Met. It’ll be once I feel I’ve do… https://t.co/aL4ucdg78a

— Nicki Minaj (@NICKIMINAJ) 1631568090.0

Shortly afterward Minaj tweeted that her "cousin in Trinidad won't get the vaccine cuz his friend got it & became impotent. His testicles became swollen. His friend was weeks away from getting married, now the girl called off the wedding. So just pray on it & make sure you're comfortable with ur decision, not bullied."

My cousin in Trinidad won’t get the vaccine cuz his friend got it & became impotent. His testicles became swollen.… https://t.co/xQJa2xi9TX

— Nicki Minaj (@NICKIMINAJ) 1631569446.0

How did Reid respond?

Reid was in full finger-wagging mode against Minaj during the host's "ReidOut" program.

"You have a platform, sister, that is 22 million followers, OK? I have 2 million followers. You have 22 million followers on Twitter," an animated Reid said. "For you to use your platform to encourage our community to not protect themselves and save their lives — my God, sister, you could do better than that! You got that platform ... it's a blessing that you got that! That people listen to you. And they listen to you more than they listen to me!"

Reid added: "For you to use your platform to put people in the position of dying from a disease they don't have to die from, oh my God. As a fan, as a hip-hop fan, as somebody who is your fan, I'm so sad that you did that, so sad that you did that, sister. Oh, my God!"

.@JoyAnnReid responds to @NICKIMINAJ's tweets on the #COVID19 vaccine: "For you to use your platform to encourage o… https://t.co/jn4adsbyDm

— The ReidOut (@thereidout) 1631575349.0

Minaj fires back

Minaj wasted no time hitting back at Reid: "This is what happens when you're so thirsty to down another black woman (by the request of the white man), that you didn't bother to read all my tweets. 'My God SISTER do better' imagine getting ur dumb ass on TV a min after a tweet to spread a false narrative about a black woman."

The rapper used a racial slur in another tweet, calling Reid a "lying homophobic c**n." The "homophobic" remark presumably refers to Reid getting called out a couple of years ago over anti-LBGTQ blog posts attributed to her — for which she apologized although she couldn't fathom that she wrote them. So Reid figured hackers were out to get her.

Minaj also referred to Reid as "Uncle Tomiana" and pointed out that while she sat on a high horse calling out Minaj's vaccine hesitancy, Reid last September tweeted plenty of vaccine hesitancy herself: "I mean, will anyone ... anyone at all ... ever fully trust the @CDCgov again? And who on God's earth would trust a vaccine approved by the @US_FDA?? How do we get a vaccine distributed after this broken, Trumpist nonsense has infected everything? Even if Biden wins?"

As of Tuesday morning, Reid on her Twitter page has not answered Minaj's pushback.

Horowitz: FDA disseminates dangerous and libelous misinformation against lifesaving COVID treatment



Does our government believe Africans are not human beings?

On Sunday, Surgeon General Vivek Murthy declared, "We've been seeing health misinformation as a problem for years, but the speed, scale and sophistication with which it is spreading and impacting our health is really unprecedented."

Perhaps the surgeon general should look in the mirror and lecture the FDA for dissuading people from taking lifesaving ivermectin. Over the weekend, the FDA tweeted out a message warning that ivermectin is for horses and cows, not people, implying that it is dangerous to consume and is not approved for humans.

You are not a horse. You are not a cow. Seriously, y'all. Stop it. https://t.co/TWb75xYEY4

— U.S. FDA (@US_FDA) 1629547061.0

Evidently, officials believe that millions of human beings in Africa (not to mention thousands in the Western world) are no better than animals.

Ivermectin has been dispensed 3.7 billion times in African countries since 1987 and is regarded as one of the greatest cures of all time for a disease ailing human beings. Here are the facts.

Throughout the 1970s and 1980s, after pesticides were sidelined from use in Africa following the publication of Rachel Carson's "Silent Spring," onchocerciasis, or river blindness, was devastating many central African countries. An estimated 50% of males 40 years and older had been blinded by the disease in some countries. After ivermectin was discovered as a wonder drug for treating river blindness by William C. Campbell, a scientist for Merck, and Satoshi Omura, a scientist at the Kitasato Institute in Tokyo, Merck started the MECTIZAN® Donation Program (MDP). In 1987, when the company was actually dedicated to saving lives as much as to making money, Merck began donating hundreds of millions of doses of MECTIZAN (ivermectin) and essentially eradicated the disease. Over time, 2.8 billion doses were donated.

In 2017, Merck published a press release commemorating the 20th anniversary of this mass rescue from a parasitic pandemic by ivermectin, which saved "more than 250 million people in 32 countries." In other words, this drug was dispensed en masse, exactly what we need to do in this pandemic, and with no known major serious side effects. As one study published in the Lancet notes, "To ensure distribution of the drug is sustained in the long term, the African Programme for Onchocerciasis Control implemented community-directed treatment with ivermectin." Ultimately, this program "had an impressive impact," ensuring that "onchocerciasis is no longer a public health problem." The study observes, "Ivermectin has been widely used for 30 years to combat onchocerciasis and is rightly considered a wonder drug."

This is why the WHO itself lists ivermectin among its Model List of Essential Medicines for 2019, given its efficacy against parasitic infections and its track record of safety.

William C. Campbell and Satoshi Omura were awarded the Nobel Prize for physiology in 2015 for discovering the drug as a cure for river blindness. Here is an excerpt from the press release of the Nobel Assembly:

Today the Avermectin-derivative Ivermectin is used in all parts of the world that are plagued by parasitic diseases. Ivermectin is highly effective against a range of parasites, has limited side effects and is freely available across the globe. The importance of Ivermectin for improving the health and wellbeing of millions of individuals with River Blindness and Lymphatic Filariasis, primarily in the poorest regions of the world, is immeasurable. Treatment is so successful that these diseases are on the verge of eradication, which would be a major feat in the medical history of humankind.

Thus, we have a drug that is regarded as having a wide range of efficacy against infections and achieving a major feat in medical history for "MANKIND," not "horsekind."

The FDA is trashing ivermectin and lying about a drug that fits the safety profile of the quintessential drug you would want to dispense en masse. What front-line COVID doctors seek to do with ivermectin has already been done before, unless of course they don't consider people in Africa to be humans.

Yes, it was originally used for animals, but like many other successful medicines, it was tested for humans decades ago. As Johns Hopkins posted in an article in 2004: "Ivermectin, the compound from which Mectizan is derived, was originally found to be effective against parasites in farm animals. Realizing its potential as a human medicine, Merck and WHO conducted seven years of clinical trials which demonstrated that Mectizan is safe for humans and effectively kills the juvenile form of Onchocerca volvulus" (emphasis added).

Full stop! The science on ivermectin being safe for humans was settled ages ago, and we are all better off for it. The fact that it was used for a parasitic infection rather than a viral infection does not alter its safety profile. For the FDA to suggest that this is animal medicine and is unsafe is a scandalous lie. To suggest that it is a human medicine only currently approved by the agency for parasitic infections is one thing, but that would raise the question as to why the agency has not looked at the dozens of studies showing its efficacy against viral infections as well.

Since 2012, long before this drug became politicized, numerous in-vitro studies began to report highly potent antiviral effects of ivermectin against a diverse array of viruses. Which is not surprising, because the main problem with COVID is the inflammatory response of the body in the lungs. Ivermectin worked wonders on the inflammatory reaction in the eyes.

To the extent that there might be some people messing around with the paste version of ivermectin for animals, that is the fault of the FDA for making it so hard for doctors to prescribe and people to access the version made for people. It's not like the organization is offering any other solutions. If anything, this is an argument for making human ivermectin available over the counter, as it essentially was in Africa.

Imagine if back in the 1970s, people had scoffed at ivermectin as nothing but an animal medicine. Now imagine if we'd actually looked at the success of this drug so far for this pandemic. We need not reinvent the wheel. There are numerous doctors who have successfully treated patients for months with numerous therapeutics now being censored by the medical establishment, including ivermectin.

Dr. Brian Tyson, co-owner of All Valley Urgent Care in El Centro, California, along with Dr. George Fareed, has treated over 6,200 COVID patients and has made ivermectin a part of his standard regimen since October. "Dr Fareed and I have treated over 6,200 patients for COVID and have not lost a single patient who was treated before day seven," Tyson said in an interview with TheBlaze. "I think it's a shame that patients are seeking out veterinary ivermectin because pharmacies are unwilling to fill the human forms because the diagnosis code doesn't coincide with their political beliefs."

Dr. Molly James, an ICU doctor from St. Louis who has also worked and volunteered in New York City ICUs during he peak of the crisis, told me that she even sees miraculous results from ivermectin during late stages of the virus. "It's rare I can prescribe it in the ICU, but I have been able to and seen it miraculously work. I had a patient 10 days into standard treatment and at risk for intubation when I changed his treatment to the MATH+ protocol, and within 48 hours he was almost off oxygen. In the hundreds of ICU and vented patients I've seen, not one has improved that quickly without ivermectin in the protocol."

Dr. James feels that if it works so well in the ICU, why not give it to people from day one and avoid hospitalization? This is why she now offers telehealth consults on her website to prescribe ivermectin and other effective treatments as early as possible.

Sadly, anything that might possibly work against the virus is opposed by those in power. We are now seeing the media bash the Florida governor for even promoting the monoclonal antibodies, which are indeed approved by the FDA and created by the cool kids at Big Pharma. Thus, this is not about ivermectin, just like it wasn't a fight over hydroxychloroquine last year. The medical establishment, including Merck itself, is now opposed to any form of early treatment.

They have gotten Amazon to stop selling NAC (N-acetyl-L-cysteine), a terrific over-the-counter supplement with great qualities against pulmonary inflammation. Proxalutamide, an androgen blocker which has scored higher in studies than nearly anything ever tried against COVID, has still not been made available in the U.S. even for critically ill patients with no other options. Calcifediol or 25-hydroxyvitamin D, the active form of vitamin D that can instantly quell the pulmonary inflammation, is banned by the FDA and cannot be accessed by doctors. Heck, it's only a matter of time before they start removing the inactive D3 from the shelves.

Opponents of every early (or even late) treatment will suggest that there is not enough data behind their use. Yet these are the same people who made remdesivir the standard of care at $3,000 a dose, despite negative efficacy and concerns about side effects to the kidneys! Thus, the imbroglio over ivermectin is not about animal medicine, but about treating humans worse than animals and denying them every ability to treat themselves when all of the solutions from the system have failed.

At a news conference in 1987, when Merck announced the giveaway of ivermectin: Ted Kennedy said, "Merck's gift to the World Health Organization is more than a medical breakthrough–it is truly a triumph of the human spirit." Today, we have a triumph of greed and control that is leading to genocide.