Europe’s much-criticized vaccination rollout has just hit another snag, as Danish health authorities are increasingly concerned about harmful side-effects believed to be associated with the AstraZeneca-Oxford jab, the cheap COVID remedy that was supposed to help Europe catch up with the US, UK, and Israel.
Danish authorities on Thursday temporarily suspended AstraZeneca’s COVID-19 shot following reports of cases of dangerous blood clots forming inside patients, including one such incident that took place in Denmark. Authorities didn’t specify exactly how many reports of blood clots there had been, but Reuters reports that Austria has also stopped using a batch of AstraZeneca shots while investigating a death attributed to coagulation disorders, along with an illness attributed to a pulmonary embolism, a condition where one or more of the lung’s arteries becomes blocked by a blood clot. Six other European countries have also reportedly halted the distribution of the COVID jab.
“Both we and the Danish Medicines Agency have to respond to reports of possible serious side-effects, both from Denmark and other European countries,” the director of the Danish Health Authority, Soren Brostrom, said in a statement.
The Danish Medicines Agency said the suspension would last for 14 days as authorities launch an investigation into the blood clots, with assistance from other EU member states.
NEW: Danish Health Authority says use of #AstraZeneca COVID19 #vaccine has been halted due to serious cases of blood clots. This follows similar suspension in Austria.
They did not say how many reports of blood clots there had been, but Austria has stopped using a batch of AstraZeneca shots while investigating a death from coagulation disorders and an illness from a pulmonary embolism.
AstraZeneca claims its vaccine is subject to strict and rigorous quality controls and that there have been “no confirmed serious adverse events associated with the vaccine.” It said it was in contact with Austrian authorities and would fully support their investigation.
“Both we and the Danish Medicines Agency have to respond to reports of possible serious side-effects, both from Denmark and other European countries,” the director of the Danish Health Authority, Soren Brostrom, said. “It is important to emphasize that we have not opted out of using the AstraZeneca vaccine, but that we are putting it on hold.”
The European Medicines Agency said Wednesday there is no evidence linking AstraZeneca to the two cases of blood clots in Austria. The company said the number of (thromboembolic events” (blood clots forming) in people who have received the AstraZeneca vaccine is no higher than that seen in the general population, with 22 cases of such events being reported among the 3MM people who have received it as of March 9.
And at least one investor claimed Denmark’s suspension of AstraZeneca’s COVID vaccine on blood clot concerns shows “the detection systems that look for potential safety issues are working,” and that most of these “safety events” would ultimately be linked to natural processes, not the jab.
“It’s good to see the safety signal detection systems working and it’s important that any safety signal is followed-up using the correct protocols,” Shore analyst Adam Barker told Bloomberg. Data from the vaccine’s phase three trials suggests that “you would expect that most safety signals won’t ultimately be linked to the vaccine,” he said.
However, “it’s hard to make judgments on the impact on shareholder value,” he added, given there are “a lot of moving parts.” But ultimately, a risk-reward trade-off with any therapy; “you can only confidently make judgments on that decision when all the data is finalized and clear”
Nevertheless, shares of AZ tumbled on Thursday on signs that the European vaccine rollout is facing fresh skepticism and obstacles. Shares were down more than 2% in London’s mid-morning trade.
Whether Austria and other EU states will follow suit remains to be seen, though at least one other national health authority is reportedly considering a halt: the Norwegian Institute of Public Health and the Medicines Agency are meeting to discuss Denmark’s decision to halt vaccinations using doses of the vaccine, according to reports from state broadcaster NRK.
Since vaccine distribution began in the United States on December 14, more than 95.7 million doses of mRNA gene therapy have been administered. That means (if we can trust the CDC’s numbers) 18.8% of the total U.S. population, according to federal data collected by the Centers for Disease Control and Prevention have willingly taken this experimental shot.
The U.S. is currently administering over 2.1 million shots a day, according to NPR. And then they admit the truth: most people don’t actually want this garbage injected into their bodies.
The speed of vaccination has improved since December, but there are still millions of more doses distributed to states than have been administered to people. –NPR
Joe Biden wants you all “vaccinated” even though legally speaking, what they are injecting is not a vaccine, but a gene therapy.
If their numbers aren’t being overstated (which is highly likely considering all the false statistics and lies they put out to panic people into getting this shot in the first place) almost 20% of people have taken the vaccine willingly. But 80% have firmly said “no” even as they open up the availability of the gene therapy shots to more and more.
Mainstream media propaganda is also saying they are going to need you to get the vaccine before this virus mutates out of control and the vaccines don’t work. Yet the ruling class and big pharma have already admitted they may need to change the “vaccines” that they also admitted don’t work to make them not work against new mutations of the virus. You can’t make this up. They really want you to believe in this garbage they are selling.
Fauci has a new line of the official narrative and wants the entire world panicked over new variants. Since most people have figured out what a scam this COVID-19 hoax has been (there is no cold or the flu anymore, only COVID) the ruling class has to try to find another scare tactic to keep people panicked and in a constant state of fear using mind control and propaganda to get us to all comply.
Fauci wants everyone to continue to wear masks, and practice social distancing, and get the vaccine. Until he can frighten enough into giving up all of their rights and just complying.
He also said the U.S. is now assessing the impact of “homegrown” variants, including the one that is believed to have originated in New York. The strain, which researchers are calling B.1.526, is rapidly spreading in New York City and carries a mutation that could weaken the effectiveness of vaccines, according to The New York Times.
Last week, Fauci said the Biden administration was taking the emergence of the New York strain “very seriously.” He said U.S. officials would need to “keep an eye” on the strain, including the possibility that it could evade the protection of antibody treatments and vaccines. -CNBC
The good news is that the public isn’t falling for this anymore. Many who were dipped are figuring out the ruling class lied to them to get them to voluntarily and willingly enslave themselves. The bad news is that people in power will never go down without a fight. They will most likely try to pull off something else to maintain control. Because of that, exercise caution, use discernment, practice critical thinking, and most of all, be as prepared as you can for anything.
In a recent comment by CNN‘s parent firm’s CEO, Jason Kilar, it is made clear that the mainstream media doesn’t care one small bit about the propaganda they are pushing on the public. That’s because the fear over COVID-19 has been “really good” for CNN‘s ratings, said Kilar.
The chief executive at CNN’s parent firm is looking on the bright side, telling a virtual audience the scamdemic has been “really good” for the outlet’s ratings, reported RT. A lot of people by now know this whole “pandemic” was a scam from the getgo. It’s being used to force gene therapies in the public by calling it a “vaccine.”
Kilar, the CEO of WarnerMedia, which owns the cable network, appeared at Morgan Stanley’sTechnology, Media, and Telecom’ virtual conference on Thursday, where he was asked about CNN and whether it could keep up its current momentum. He immediately took to gloating over the fear the network has been pushing.
“I’d say that it turns out that pandemic is a pretty big part of the news cycle, and that’s not going away anytime soon,” he replied, adding “if you take a look at the ratings and the performance, it’s going well. And I think it’s going well because, A, the team at CNN is doing a fantastic job. And B, it turns out that the pandemic and the way that we can help inform and contextualize the pandemic, it turns out it’s really good for ratings.”
The CEO also noted that“from a political drama perspective,” the virus has been “good for our society” in “many ways,” though did not offer any examples or elaborate further. He is most likely referring to the slavery forced on all of us while he gets his kickbacks from the ruling class to brainwash the masses into willingly accepting tyranny.
His remarks did receive some backlash online, however. That backlash came after a tweet from the Wall Street Journal’s Joe Flint criticized Kilar’s apparent glee over pushing the fear narrative on the slaves.
"It turns out the pandemic is a pretty big part of the news cycle and that’s not going away any time soon…It turns out it's really good for ratings." Jason Kilar on post-Trump CNN. Careful. That's awful close to Moonves line that Trump may be bad for U.S. but he's good for CBS.
Kilar voiced regret over the candid admission, telling Flint “I wish I could go back and be more thoughtful about my communication” and that he would “like nothing more than for this pandemic to be well behind us.”
“I am sorry for the sentence and for uttering it. My apologies. Thx for highlighting it and holding me accountable,” he added in a second reply.
I agree Joe. I would like nothing more than for this pandemic to be well behind us. I mean that with every fiber in my body. I wish I could go back and be more thoughtful about my communication.
Except, we all already know what he meant. Cnn will continue to keep people in a state of fear to force them into accepting and demanding the chains of their own oppression. And they’ll make them pay for it. Just wait until they can no longer cover up what these “vaccines” are doing to people…
Did you know that mRNA COVID-19 vaccines aren’t vaccines in the medical and legal definition of a vaccine? They do not prevent you from getting the infection, nor do they prevent its spread. They’re really experimental gene therapies.
I discussed this troubling fact in a recent interview with molecular biologist Judy Mikovits, Ph.D. While the Moderna and Pfizer mRNA shots are labeled as “vaccines,” and news agencies and health policy leaders call them that, the actual patents for Pfizer’s and Moderna’s injections more truthfully describe them as “gene therapy,” not vaccines.
Definition of ‘Vaccine’
Neither Moderna nor Pfizer claims this to be the case for their COVID-19 “vaccines.” In fact, in their clinical trials, they specify that they will not even test for immunity.
Unlike real vaccines, which use an antigen of the disease you’re trying to prevent, the COVID-19 injections contain synthetic RNA fragments encapsulated in a nano lipid carrier compound, the sole purpose of which is to lessen clinical symptoms associated with the S-1 spike protein, not the actual virus.
They do not actually impart immunity or inhibit the transmissibility of the disease. In other words, they are not designed to keep you from getting sick with SARS-CoV-2; they only are supposed to lessen your infection symptoms if or when you do get infected.
As such, these products do not meet the legal or medical definition of a vaccine, and as noted by David Martin, Ph.D., in the video above, “The legal ramifications of this deception are immense.”
15 U.S. Code Section 41
As explained by Martin, 15 U.S. Code Section 41 of the Federal Trade Commission Act2 is the law that governs advertising of medical practices. This law, which dictates what you may and may not do in terms of promotion, has for many years been routinely used to shut down alternative health practitioners and companies.
“If this law can be used to shut down people of good will, who are trying to help others,” Martin says, “it certainly should be equally applied when we know deceptive medical practices are being done in the name of public health.”
Per this law, it is unlawful to advertise:
“… that a product or service can prevent, treat, or cure human disease unless you possess competent and reliable scientific evidence, including, when appropriate, well-controlled human clinical studies, substantiating that the claims are true at the time they are made.”3
What Constitutes ‘The Greater Good’?
Martin points to the 1905 Supreme Court ruling in Jacobson vs. Massachusetts,4 which essentially established that collective benefit supersedes individual benefit. To put it bluntly, it argued that it’s acceptable for individuals to be harmed by public health directives provided it benefits the collective.
Now, if vaccination is a public health measure that is supposed to protect and benefit the collective, then it would need to a) ensure that the individual who is vaccinated is rendered immune from the disease in question; and b) that the vaccine inhibits transmission of the disease.
Only if these two outcomes can be scientifically proven can you say that vaccination protects and benefits the collective — the population as a whole. This is where we run into problems with the mRNA “vaccines.”
Moderna’s SEC filings, which Martin claims to have carefully reviewed, specifies and stresses that its technology is a “gene therapy technology.” Originally, its technology was set up to be a cancer treatment, so more specifically, it’s a chemotherapy gene therapy technology.
As noted by Martin, who would raise their hand to receive prophylactic chemotherapy gene therapy for cancer you do not have and may never be at risk for? In all likelihood, few would jump at such an offer, and for good reason.
Moreover, states and employers would not be able to mandate individuals to receive chemotherapy gene therapy for cancer they do not have. It simply would not be legal. Yet, they’re proposing that all of humanity be forced to get gene therapy for COVID-19.
COVID-19 Vaccines — A Case of False Advertising
Now, if the COVID-19 vaccine really isn’t a vaccine, why are they calling it that? While the CDC provides a definition of “vaccine,” the CDC is not the actual law. It’s an agency empowered by the law, but it does not create law itself. Interestingly enough, it’s more difficult to find a legal definition of “vaccine,” but there have been a few cases. Martin provides the following examples:
•Iowa code — “Vaccine means a specially prepared antigen administered to a person for the purpose of providing immunity.” Again, the COVID-19 vaccines make no claim of providing immunity. They are only designed to lessen symptoms if and when you get infected.
•Washington state code — “Vaccine means a preparation of a killed or attenuated living microorganism, or fraction thereof …” Since Moderna and Pfizer are using synthetic RNA, they clearly do not meet this definition.
Being a manmade synthetic, the RNA used is not derived from anything that has at one point been alive, be it a whole microorganism or a fraction thereof. The statute continues to specify that a vaccine “upon immunization stimulates immunity that protects us against disease …”
So, in summary, “vaccine” and “immunity” are well-defined terms that do not match the endpoints specified in COVID-19 vaccine trials. The primary endpoint in these trials is: “Prevention of symptomatic COVID-19 disease.” Is that the same as “immunity”? No, it is not.
There Are More Problems Than One
But there’s another problem. Martin points out that “COVID-19 disease” has been defined as a series of clinical symptoms. Moreover, there’s no causal link between SARS-CoV-2, the virus, and the set of symptoms known as COVID-19.
How is that, you might ask? It’s simple, really. Since a vast majority of people who test positive for SARS-CoV-2 have no symptoms at all, they’ve not been able to establish a causal link between the virus and the clinical disease.
Here’s yet another problem: The primary endpoint in the COVID-19 vaccine trials is not an actual vaccine trial endpoint because, again, vaccine trial endpoints have to do with immunity and transmission reduction. Neither of those was measured.
What’s more, key secondary endpoints in Moderna’s trial include “Prevention of severe COVID-19 disease and prevention of infection by SARS-CoV-2.” However, by its own admission, Moderna did not actually measure infection, stating that it was too “impractical” to do so.
That means there’s no evidence of this gene therapy having an impact on infection, for better or worse. And, if you have no evidence, you cannot fulfill the U.S. Code requirement that states you must have “competent and reliable scientific evidence … substantiating that the claims are true.”
Why Are They Calling Them Vaccines?
As noted by Martin, you cannot have a vaccine that does not meet a single definition of a vaccine. So, again, what would motivate these companies, U.S. health agencies, and public health officials like Dr. Anthony Fauci to lie and claim that these gene therapies are in fact vaccines when, clearly, they are not?
If they actually called it what it is, namely “gene therapy chemotherapy,” most people would — wisely — refuse to take it. Perhaps that’s one reason for their false categorization as vaccines. But there may be other reasons as well.
Here, Martin strays into conjecture, as we have no proof of their intentions. He speculates that the reason they’re calling this experimental gene therapy technology a “vaccine” is because by doing so, they can circumvent liability for damages.
As long as the U.S. is under a state of emergency, things like PCR tests and COVID-19 “vaccines” are allowed under emergency use authorization. And as long as the emergency use authorization is in effect, the makers of these experimental gene therapies are not financially liable for any harm that comes from their use.
That is, provided they’re “vaccines.” If these injections are NOT vaccines, then the liability shield falls away, because there is no liability shield for a medical emergency countermeasure that is gene therapy.
So, by maintaining the illusion that COVID-19 is a state of emergency when in reality it is not, government leaders are providing cover for these gene therapy companies so that they can get immunity from liability.
Under the Cover of ‘Emergency’
As noted by Martin, if state governors were to lift the state of emergency, all of a sudden the use of RT PCR testing would be in violation of 15 U.S. Code FTC Act, as PCR tests are not an approved diagnostic test.
“You cannot diagnose a thing [with something] that cannot diagnose a thing,” Martin says. “That a misrepresentation. That is a deceptive practice under the Federal Trade Commission Act. And they’re liable for deceptive practices.”
Importantly, there’s no waiver of liability under deceptive practices — even under a state of emergency. This would also apply to experimental gene therapies. The only way for these gene therapies to enjoy liability shielding is if they are vaccines developed in response to a public health emergency. There is no such thing as immunity from liability for gene therapies.
Propaganda and Vaccine Rollout Run by Same Company
Martin brings up yet another curious point. The middleman in Operation Warp Speed is a North Carolina defense contractor called ATI. It controls the rollout of the vaccine. But ATI also has another type of contract with the Department of Defense, namely managing propaganda and combating misinformation.
So, the same company in charge of manipulating the media to propagate government propaganda and censor counterviews is the same company in charge of the rollout of “vaccines” that are being unlawfully promoted.
“Listen,” Martin says. “This is a pretty straight-forward situation. You’re being lied to. Your own government is violating its own laws … They have thrown this book [15 U.S. Code Section 41] on more people than we can count.
They have shut down practitioners around the country, time and time again, for violating what are called ‘deceptive practices in medical claims’ … Guess what? They’re doing exactly that thing.”
Martin urges listeners to forward his video to your state attorney, governor, representatives and anyone else that might be in a position to take affirmative action to address and correct this fraud.
Defense contractors are violating FTC law, and gene therapy companies — not vaccine manufacturers — are conducting experimental trials under deceptive medical practices. They’re making claims of being “vaccines” without clinical proof, and must be held accountable for their deceptive marketing and medical practices.
CDC Owns Coronavirus Patents
On a side note, the CDC appears to be neck-deep in this scam pandemic, and is therefore wholly unsuitable to investigate the side effects of these experimental COVID-19 therapies. As noted by Martin, it’s like having a bank robber investigate its own crime.
Details about this came out in the documentary “Plandemic,” in which Martin explained how the CDC has broken the law — in one way or another — related to its patenting of the 2003 SARS virus.
Martin is a national intelligence analyst and founder of IQ100 Index, which developed linguistic genomics, a platform capable of determining the intent of communications. In 1999, IBM digitized 1 million U.S. patents, which allowed Martin’s company to conduct a review of all these patents, sending him down a proverbial “rabbit trail” of corruption.
In 2003, Asia experienced an outbreak of SARS. Almost immediately, scientists began racing to patent the virus. Ultimately, the CDC nabbed ownership of SARS-CoV (the virus responsible for SARS) isolated from humans.
So, the CDC actually owns the entire genetic content of that SARS virus. It’s patented under U.S. patent 7776521. They also own patents for detection methods, and for a kit to measure the virus.
U.S. patent 7279327,5 filed by the University of North Carolina at Chapel Hill, describes methods for producing recombinant coronaviruses. Ralph Baric, Ph.D., a professor of microbiology and immunology who is famous for his chimeric coronavirus research, is listed as one of the three inventors, along with Kristopher Curtis and Boyd Yount.
According to Martin, Fauci, Baric and the CDC “are at the hub” of the whole COVID-19 story. “In 2002, coronaviruses were recognized as an exploitable mechanism for both good and ill,” Martin says, and “Between 2003 and 2017, they [Fauci, Baric and CDC] controlled 100% of the cash flow to build the empire around the industrial complex of coronavirus.”
How the CDC Broke the Law
The key take-home message Martin delivers in “Plandemic” is that there’s a distinct problem with the CDC’s patent on SARS-CoV isolated from humans, because, by law, naturally occurring DNA segments are prohibited from being patented.
The law clearly states that such segments are “not patent eligible merely because it has been isolated.” So, either SARS-CoV was manmade, which would render the patent legal, or it’s natural, thus rendering the patent on it illegal.
However, if the virus was manufactured, then it was created in violation of biological weapons treaties and laws. This includes the Biological Weapons Anti-Terrorism Act of 1989, passed unanimously by both houses of Congress and signed into law by George Bush Sr., which states:6
“Whoever knowingly develops, produces, stockpiles, transfers, acquires, retains, or possesses any biological agent, toxin, or delivery system for use as a weapon, or knowingly assists a foreign state or any organization to do so, shall be fined under this title or imprisoned for life or any term of years, or both. There is extraterritorial Federal jurisdiction over an offense under this section committed by or against a national of the United States.”
So, as noted by Martin in the documentary, regardless of which scenario turns out to be true, the CDC has broken the law one way or another, either by violating biological weapons laws or by filing an illegal patent. Even more egregious, on May 14, 2007, the CDC filed a petition with the patent office to keep their coronavirus patent confidential.
Now, because the CDC owns the patent on SARS-CoV, it has control over who has the ability to make inquiries into the coronavirus. Unless authorized, you cannot look at the virus, you cannot measure it or make tests for it, since they own the entire genome and all the rest.
“By obtaining the patents that restrained anyone from using it, they had the means, the motive, and most of all, they had the monetary gain from turning coronavirus from a pathogen to a profit,” Martin says.
In the lecture above, Dr. Simone Gold — founder of America’s Frontline Doctors, which has been trying to counter the false narrative surrounding hydroxychloroquine — reviews the dangers discovered during previous coronavirus vaccine trials, and the hazards of current mRNA gene therapies, including antibody-dependent immune enhancement.
Antibody-dependent immune enhancement results in more severe disease when you’re exposed to the wild virus and increases your risk of death. The synthetic RNA and the nano lipid it is encased in may also have other, more direct side effects. As explained by Mikovits in our recent interview:
“Normally, messenger RNA is not free in your body because it’s a danger signal. The central dogma of molecular biology is that our genetic code, DNA, is transcribed, written, into the messenger RNA. That messenger RNA is translated into protein, or used in a regulatory capacity … to regulate gene expression in cells.
So, taking a synthetic messenger RNA and making it thermostable — making it not break down — [is problematic]. We have lots of enzymes (RNAses and DNAses) that degrade free RNA and DNA because, again, those are danger signals to your immune system. They literally drive inflammatory diseases.
Now you’ve got PEG, PEGylated and polyethylene glycol, and a lipid nanoparticle that will allow it to enter every cell of the body and change the regulation of our own genes with this synthetic RNA, part of which actually is the message for the gene syncytin …
Syncytin is the endogenous gammaretrovirus envelope that’s encoded in the human genome … We know that if syncytin … is expressed aberrantly in the body, for instance in the brain, which these lipid nanoparticles will go into, then you’ve got multiple sclerosis.
The expression of that gene alone enrages microglia — literally inflames and dysregulates the communication between the brain microglia — which are critical for clearing toxins and pathogens in the brain and the communication with astrocytes.
It dysregulates not only the immune system, but also the endocannabinoid system, which is the dimmer switch on inflammation. We’ve already seen multiple sclerosis as an adverse event in the clinical trials … We also see myalgic encephalomyelitis. Inflammation of the brain and the spinal cord …”
Making matters worse, the synthetic mRNA also has an HIV envelope expressed in it, which can cause immune dysregulation. As we discussed in previous interviews, SARS-CoV-2 has been engineered in the lab with gain-of-function research that included introducing the HIV envelope into the spike protein.
Are You in a High-Risk Group for Side Effects?
Mikovits’ hypothesis is that those who are most susceptible to severe neurological side effects and death from the COVID-19 vaccines are those who have previously been injected with XMRVs, borrelia, babesia, or mycoplasma through contaminated vaccines, resulting in chronic disease, as well as anyone with an inflammatory disease like rheumatoid arthritis, Parkinson’s disease or chronic Lyme disease, for example, and anyone with an acquired immune deficiency from any pathogens and environmental toxins.
The chart below lists 35 diseases that are likely to render you more susceptible to severe side effects or death from COVID-19 gene therapy injections.
Many of the symptoms now being reported are suggestive of neurological damage. They have severe dyskinesia (impairment of voluntary movement), ataxia (lack of muscle control), and intermittent or chronic seizures. Many cases detailed in personal videos on social media are quite shocking. According to Mikovits, these side effects are due to neuroinflammation, a dysregulated innate immune response, and/or a disrupted endocannabinoid system.
Another common side effect from the vaccine we’re seeing is allergic reactions, including anaphylactic shock. A likely culprit in this is PEG (polyethylene glycol), which an estimated 70% of Americans are allergic to.
Experimental Gene Therapy Is a Bad Idea
Circling back to where we began, COVID-19 vaccines are not vaccines. They are experimental gene therapies that are falsely marketed as vaccines, likely to circumvent liability. World governments and global and national health organizations are all complicit in this illegal deception and must be held accountable.
Ask yourself the question Martin asked in his video: Would you agree to take an experimental chemotherapy gene therapy for cancer you do not have? If the answer is no, then why would you even consider lining up for an experimental gene therapy for COVID-19 — a set of clinical symptoms that haven’t even been causally linked to SARS-CoV-2?
These injections are not vaccines. They do not prevent infection, they do not render you immune, and they do not prevent transmission of the disease. Instead, they alter your genetic coding, turning you into a viral protein factory that has no off-switch. What’s happening here is a medical fraud of unprecedented magnitude, and it really needs to be stopped before it’s too late for a majority of people.
Government and big money media continue trumpeting the message that everyone should take experimental coronavirus vaccines. They also continue downplaying or not mentioning even the risks the government and drug companies admit come with taking the experimental vaccines that are not even vaccines under the normal meaning of the term.
People need to look elsewhere for information about the many people who suffer health problems or die after taking the shots.
The number of deaths and injuries among people who took the experimental coronavirus vaccines keeps rising. But, those numbers remain largely unknown while reports of the numbers for cases and deaths attributed to coronavirus are spread far and wide. Children’s Health Defense provides the latest update on the less well-known deaths and injuries in a Monday report that begins with the following:
The latest data made public by the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) on deaths and injuries reported after COVID vaccines are in line with trends that have been emerging since the first data were released in December.
Between Dec. 14, 2020 and Feb. 18, 2021, 19,907 reports of adverse events have been reported to VAERS, including 1,095 deaths and 3,767 serious injuries.
About a third of the deaths reported occurred within 48 hours of vaccination, and 48% of the people who died became ill within 48 hours of being vaccinated.
Continue reading the Children’s Health Defense report here.
EDITOR’S NOTE: Here’s a question to ponder: if these “vaccines” aren’t legally or definitively “vaccines” and they are “gene therapy,” why are they being labeled as vaccines? Is this to avoid liability? Is it because the ruling class knows people won’t take an experimental gene therapy if they called it that, but will willingly line up for a vaccine like sheep?