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Moderna Plunges After Pfizer Sees Just 24% Of Americans Seeking Covid Boosters
Moderna Plunges After Pfizer Sees Just 24% Of Americans Seeking Covid Boosters | ZeroHedge

Shares of mRNA maker Moderna - better known as one of the main sponsors of the US open tournament which was won by the vocally unvaccinated Novak Djokovic who was barred from participating previously due to his unwillingness to succumb to Moderna's only product and Democrat brainwashing - tumbled as much as 9%, the biggest intraday drop since Aug. 7 and making it the worst performer in the S&P500 and Nasda q 100, after rival drugmaker Pfizer laid out a forecast of how many Americans are likely to get newly approved Covid-19 vaccinations. And yes, Pfizer and BioNTech shares also slipped.



Speaking at a JPMorgan conference, Pfizer CFO David Denton said his company projected that just 24% of the US population recommended to take the shots will decide to roll up their sleeves, representing a slight increase in takeup from the previous round of boosters. As a reference, 70.5% of the world population has (forcibly) received at least one dose of a COVID-19 vaccine.
 
Myocarditis & COVID-19 Vaccines: How The CDC Missed A Safety Signal And Hid A Warning
Myocarditis & COVID-19 Vaccines: How The CDC Missed A Safety Signal And Hid A Warning | ZeroHedge

COVID-19 vaccines cause heart inflammation, U.S. authorities now acknowledge. But after being warned in early 2021 about a "large number" of cases among healthy, young people in Israel after COVID-19 vaccination, authorities did not immediately alert the public while also failing to detect a safety signal that was present in the United States, an Epoch Times investigation has found.



Even after deaths from myocarditis - inflammation of the heart - were reported and myocarditis was designated as a likely side effect of the shots, U.S. officials kept recommending vaccination for virtually the entire populace.

That led to millions of young people receiving a vaccine.

Many of those people suffered.

Aiden Ekanayake, 14, was one of them. He received a dose of the Pfizer-BioNTech vaccine in May 2021, and a second dose in June 2021.

Two days after the second dose, Aiden was woken in the middle of the night with pain that was comparable to when he tore his anterior cruciate ligament. His mother, Emily, rushed him to the hospital, where he spent days receiving care. Even after he was discharged, his exercise was limited for more than four months.

Ms. Ekanayake trusted the U.S. Centers for Disease Control and Prevention (CDC) before the experience. Now, she does not.

"I hate them. I think they're evil," Ms. Ekanayake told The Epoch Times.

No Transparency
The CDC, America's public health agency, was warned by Israel on Feb. 28, 2021, about a "large number" of myocarditis cases after Pfizer COVID-19 vaccination, documents obtained by The Epoch Times show.

Internally, the warning was designated as "high" importance and set off a review of U.S. data. The review found 27 reported cases in the United States, according to a U.S. government memorandum dated March 9, 2021. The incidence rate was low, but "missing and incomplete data make it challenging to assess causation," the memo stated. The U.S. Food and Drug Administration (FDA), it said, "has not made a final determination regarding the causality."



People receive a dose of the COVID-19 vaccine at Tel Aviv Sourasky Medical Center in Tel Aviv, Israel, on Dec. 20, 2020. (Amir Levy/Getty Images)

Weeks later, neither the CDC nor the FDA had alerted the public to the issue, even after the death of a previously healthy 22-year-old Israeli woman and briefings from Israeli officials and U.S. Department of Defense (DOD) researchers.

Like Israel, the DOD was recording a higher-than-expected number of myocarditis cases. Patients were mostly young, healthy males.

The CDC met with military officials twice behind closed doors in April 2021. Military officials presented data during at least one of the meetings to the CDC. That presentation, which has never been released to the public, "included our preliminary patient data and analysis that suggested to us that myocarditis was indeed a possible side effect to the messenger RNA COVID-19 vaccines (within the US military)," Dr. Jay Montgomery, one of the presenters, told The Epoch Times via email.

The Pfizer and Moderna vaccines use messenger RNA (mRNA).

On April 27, 2021, after the meetings, then-CDC Director Dr. Rochelle Walensky finally spoke about the matter in public, during a White House briefing.

Dr. Walensky said "we have not seen any reports" of myocarditis after vaccination. That's false, according to CDC data—the agency received 141 reports of myocarditis in the Vaccine Adverse Event Reporting System (VAERS) by the end of March 2021. Another 24 cases were recorded in the Vaccine Safety Datalink, a second system run by the CDC.

Additionally, before the briefing, Dr. Walensky was copied on multiple threads discussing myocarditis and a related condition, pericarditis, including a thread about doctors in California seeing the cases, internal emails obtained by The Epoch Times show. She responded to one of the threads, saying the information was "super helpful."

"We have not seen a [safety] signal," Dr. Walensky also told reporters during the briefing, "and we’ve actually looked intentionally for the signal in the over 200 million doses we’ve given."

Signal Found
The FDA authorized the Moderna and Pfizer vaccines in late 2020.

The CDC and FDA are supposed to monitor data from VAERS, which officials have described as the country's "early warning system" for possible vaccine problems. But they failed to detect a safety signal for myocarditis after COVID-19 vaccination that triggered on Feb. 18, 2021, when using a statistical analysis method called Proportional Reporting Ratio (PRR), according to archived VAERS data from the National Vaccine Information Center, The Epoch Times confirmed.

The CDC initially said it started running PRRs in February 2021, but later acknowledged that was false. The agency now says it did not start PRRs until 2022. The first time the CDC ran complete PRRs, officials detected a signal for myocarditis, according to files obtained by The Epoch Times.

"It's unimaginable that they wouldn't have seen the signal," Brian Hooker, senior director of science and research at Children's Health Defense, who detected an early signal for myocarditis in VAERS using a different method, told The Epoch Times. "They were alerted by the DOD. They were alerted by the Israeli Ministry of Health. And so, if they just didn't know then, they have absolutely no excuse because they were warned."

Children's Health Defense, a nonprofit that says its mission is to end childhood health epidemics, first obtained the emails between Israel and the CDC.

Dr. Walensky, who has since departed the CDC, has not responded to a request for comment about her myocarditis claims.

A CDC spokesperson told The Epoch Times via email: "CDC has been continuously monitoring the safety of COVID-19 vaccines since they began to be administered in the United States. At the time of the director’s press conference, CDC did not have sufficient evidence to conclude there was a safety signal for myocarditis following mRNA COVID-19 vaccination."

The CDC has said it did not run PRRs in 2021 because officials were relying on a different analytic method, called Empirical Bayesian data mining. It's unclear when that method, utilized by the FDA, first detected a signal for myocarditis. The FDA has declined to answer questions on the matter. The CDC has told The Epoch Times that its 2022 detection of a signal for myocarditis using PRRs was "consistent with" the data mining results.

Both the CDC and FDA use contractors to process VAERS data.

"Even FDA doesn't really know the mechanics of how its contractor does the data mining," one CDC official said in an email obtained by The Epoch Times. The official and the FDA did not respond to requests for comment on the email.

A safety signal is a sign that an adverse event may be caused by a vaccine. Authorities say signals can only be substantiated with further research.

"Once the safety signal comes up, why not start warning the public about the fact that' hey, you can take it if you want, but understand that there is this risk that we have discovered and we are looking into it," Dr. Anish Koka, an American cardiologist, told The Epoch Times.

One possible motivation for not fully examining the issue was that it could have led to a halt in vaccination. The CDC and FDA essentially imposed a pause on Johnson & Johnson's shot on April 13, 2021, after a small number of blood clotting cases.

"A pause of the Pfizer/Moderna administration (much like the J&J blood clot pause) will have an adverse impact on US/CA vaccination rates," one military official said in a message obtained by The Epoch Times that was flagged for top CDC officials.

Between February 2021 and May 2021, the percentage of the U.S. population that had received a COVID-19 vaccine soared from 14.2 percent to 50.5 percent.

"It was most likely a strategic move in order to make sure that they didn't curtail vaccination rates," Mr. Hooker said.
 
just 24% of the US population recommended to take the shots will decide to roll up their sleeves,
That population is probably the 30% that think Biden is great according to the polls.
 
Just to be balanced and fair, here's a meta analysis (not a clinical study) from late 2022 supposedly showing the rate of Myocarditis was greater in "previously infected" people than in jabbed people... Though there could be crossover, IE previously infected but also jabbed...as there are millions who have been infected but never went to a hospital or other care unit and had the PCR test... IF you assume the PCR test to to be valid to begin with... so lots of IF's = uncertainty.

Myocarditis in SARS-CoV-2 infection vs. COVID-19 vaccination: A systematic review and meta-analysis
Myocarditis in SARS-CoV-2 infection vs. COVID-19 vaccination: A systematic review and meta-analysis
 
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Funny how those COVID causes of death have dropped off..
Funny how those COVID causes of death have dropped off...


As if there were not enough scandals with COVID and its horrendous mismanagement by the government, Steven Hayward of Power Line has found yet another one: a causal link between whether "COVID" was listed as a cause of death or a contributing factor and federal funding dollars.

He has a chart on Power Line, showing the steep drop in deaths due to COVID, or with COVID as an underlying factor, which spanned from March 2020 to February 2022, the first part of the COVID pandemic. Then the line on the chart continues, steeply dropping as from a cliff as of March 2022 to May 2023.

See the chart here.

And why did people suddenly stop dying of COVID?

Well, because hospitals were suddenly not getting federal funding dollars for claiming COVID as a cause of death.

........ The money came from the CARES Act, passed by the Democrat-led Congress, which included the $178-billion "Provider Relief Fund."
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The money was doled out to hospitals for increased expenses due to treating COVID cases, but also from lost revenue as patients put off elective surgery and even necessary medical care.

According to STAT, a website about the medical field, it was quite the money spigot. (According to these government charts, California was the most ravenous user of these funds by far.)

The federal government allocated more than $170 billion in subsidies to hospitals across the country. These subsidies not only defrayed their operational losses but also substantially improved their financial standing, particularly helping the most vulnerable hospitals. For those with January-December fiscal years, from January 2019 to December 2020, the average annual profit margin stayed stable around 7%, but increased from 4% to 7% for government and small hospitals, and from 2% to 8% for rural ones.

Payouts dropped off sharply around January 2022 as Phase Four distributions came to a close, as this government chart shows...and suddenly people weren't dying of COVID. Amazing how these medical miracles happen when government money is cut off.
 
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FDA Has 'Gone Rogue' In Its Approval Of New COVID-19 Boosters: Dr. Robert Malone
FDA Has 'Gone Rogue' In Its Approval Of New COVID-19 Boosters: Dr. Robert Malone | ZeroHedge

The Food and Drug Administration (FDA) has "gone rogue," according to virologist Dr. Robert Malone, who accused the federal agency of sacrificing its own rules and regulations with its decision to recommend the latest batch of COVID-19 boosters, which only have limited clinical trial data attesting to their efficacy and safety.


Dr. Robert Malone, inventor of mRNA vaccines, speaks at the Conservative Political Action Conference in Dallas at the Hilton Anatole on Aug. 5, 2022. (Bobby Sanchez for The Epoch Times)


Dr. Malone made the remarks in an interview with EpochTV's "Crossroads" program on Sept. 11, the day that the FDA cleared new COVID-19 vaccines in a bid to counter the waning effectiveness of the currently available shots.

"It's difficult to conclude anything other than the FDA is no longer feeling bound by their own rules and regulations," Dr. Malone said. "The term is—they've gone rogue."

Dr. Malone said the lack of human clinical trial data demonstrating effectiveness and safety of the updated vaccines should have precluded their approval by the FDA.

He said that, essentially, the FDA authorized the new vaccines on the premise that “neutralizing antibodies as detected in mice and their cross-reactivity are correlative protection,” which he said “is a lie, there are no established correlates of protection for SARS-CoV-2."

FDA officials didn't respond by press time to a request by The Epoch Times for comment.

The agency cleared Moderna's and Pfizer's newest mRNA vaccines on Sept. 11 without analyzing data from any human trials.

............ The new vaccines target XBB.1.5, a sub-type of the Omicron variant of the SARS-CoV-2 virus, which causes the disease COVID-19. However, the XBB.1.5. subvariant has already largely been displaced by newer strains of the quickly evolving virus, including EG.5, according to the CDC.

............
'Lot of Red Flags'
"There's essentially no data," Florida Surgeon General Dr. Joseph Ladapo said at a recent news conference, where he suggested that people might be better off passing on the new round of shots.
"Not only that, but there are a lot of red flags," Dr. Ladapo added, while pointing to studies finding that the effectiveness of the vaccines turns negative over time.

“There's been no clinical trial done in human beings showing that it benefits people, there's been no clinical trial showing that it is a safe product for people."

He also noted that studies have linked previous versions of the COVID-19 vaccine to cardiac problems such as heart inflammation.

"It's truly irresponsible for FDA, CDC, and others to be championing something ... when we don't know the implications of it," Dr. Ladapo said.
 
New Study Detects Spike Protein 6 Months After COVID-19 Vaccination
New Study Detects Spike Protein 6 Months After COVID-19 Vaccination | ZeroHedge

According to the Centers for Disease Control and Prevention (CDC), mRNA from COVID-19 vaccines is “broken down within a few days after vaccination and doesn’t last long in the body”—a position it has adhered to since the pandemic's beginning, despite research suggesting otherwise (pdf). The CDC refers to mRNA as “messenger RNA,” whereas regulatory documents and Pfizer refer to the mRNA in COVID-19 vaccines as “modified RNA.”

Yet a new study published on Aug. 31 in Proteomics Clinical Applications found spike protein in the biological fluids of people who received an mRNA COVID-19 vaccine six months after vaccination, suggesting mRNA may be integrated or retranscribed in some cells.

.............CDC Says Vaccines Do Not Affect DNA, Despite Conflicting Evidence
The CDC, in addition to claiming mRNA from COVID-19 vaccines quickly break down within the body, also states on its website that these vaccines “do not affect or interact with our DNA”—the genetic material contained within the nucleus of cells—because these vaccines do not “enter the nucleus of the cell.”
The agency says “messenger RNA” COVID-19 vaccines work by “delivering instructions (genetical material) to our cells to start building protection” against SARS-CoV-2, and that the body discards all vaccine ingredients after producing an immune response just as it discards “any information cells no longer need.” According to the CDC, this process is a “part of normal body functioning.”

The current analysis and previous studies challenge this position. A February 2022 study published in Current Issues in Molecular Biology shows reverse transcription of vaccine mRNA into DNA using human liver cell lines. Additional studies have shown RNA from SARS-CoV-2 can be reverse-transcribed and integrated into the genome of cultured human cells—and expressed in patient-derived tissues or by virus-infected cells.
 
Red State Pharmacists Use 'Religious' Loophole To Deny Patients Ivermectin: Doctor
Red State Pharmacists Use 'Religious' Loophole To Deny Patients Ivermectin: Doctor | ZeroHedge

Doctors claim a law created to protect pro-life workers from going against their religious beliefs is being employed by pharmacists to deny patients access to ivermectin.



“Right to refuse” laws initially enacted in many states to shield pro-life pharmacists from being forced to violate religious convictions are used by pharmacists as legal cover for denying patients COVID-19 treatments that they find objectionable, according to a medical expert.

In Texas, Dr. Mary Talley Bowden, a practitioner and founder of Coalition of Health Freedom, told The Epoch Times that the law, along with greater discretion granted to pharmacists during the pandemic, has become a roadblock in ensuring her patients receive the care needed, especially when it comes to prescribing ivermectin off-label to treat COVID-19.

“I can’t imagine how anyone can claim a religious or moral belief in denying my patients access to ivermectin, but that appears to be exactly how they are able to legally do this,” said Dr. Bowden. “It makes no sense and creates significant delays in getting patients access to the medications they need.”