Feds Coming After Doctors & Pharmacies that Market Ivermectin as Effective & Safe for COVID-19

The U.S. Food and Drug Administration (FDA) is coming for any physician or pharmacy that promotes ivermectin as a drug that can “prevent Coronavirus Disease 2019,” or COVID-19. Recently, America’s drug regulatory agency claims they received complaints that the antiparasitic drug off-label can treat the novel coronavirus at the same dose used for authorized treatments, writes FDA Acting Branch Chief Branch Shannon Glueck, PharmD. This letter was sent to Humayun J. Chaudhry, DO, MS, FACP, FACOI, President and Chief Executive Officer Federation of State Medical Boards. 

As a signal that the FDA will start enforcing actions against individuals and groups positioning or making claims that ivermectin is an effective treatment for COVID-19, the letter calls out that “the FDA has neither authorized nor approved any ivermectin drug product for use in preventing or treating COVID-19. Although clinical trials assessing ivermectin tablets for the prevention or treatment of COVID-19 in people are ongoing, currently available data do not show that ivermectin is safe or effective for the prevention or treatment of COVID-19.”

Referring to some of its previous announcements, declaring the drug a risk for side effects, the FDA cautions the board involved with representing the 71 state medical and osteopathic boards in America and its territories, as well as co-sponsors of the United States Medical Licensing Examination. 

Declaring that the drug is not authorized or approved or proven as “safe or effective” for COVID-19, the federal regulator also sent this warning letter to the National Association of Boards of Pharmacy to help “Facilitate communications among associations with shared goals regarding these matters.”

Subscribe to the Trialsitenews "Ivermectin" Channel

No spam - we promise

This effort suggests an escalated effort by the regulatory agency to identify, investigate, and potentially punish groups, whether they be physicians or pharmacies, involved with making any marketing claims associated with ivermectin and COVID-19.

TrialSite’s Sonia Elijah reported how the FDA appeared directly involved in a proactive social marketing smear campaign of the drug, seeking to ensure that the human antiparasitic version of the drug would be conflated with the animal variety as well as a general overall blanket warning of possible harm.

Ivermectin traditionally has a stellar safety record when it is applied at the authorized dose and indication. Although a total of 71 studies involving ivermectin have demonstrated for the most part positive data points, a handful of studies that the U.S. federal government focused on failed to show efficacy results. Many of the studies demonstrating success have been completely ignored for a variety of reasons. Generally, the study data from low-and middle-income countries (LMICs) is trusted less than larger randomized controlled studies in America, the UK, or Europe, for example. 

Physicians and pharmacies should never directly market that the drug is an approved or effective treatment for COVID-19. Do so at your own risk as the FDA has now put licensing boards on notice.

Harvard scientist Dr. Charles Lieber, nanowires, DoD, CCP, Wuhan, covid, 5G, carbon nanotubes (CNT), military vaccines, SpFN Spike Ferritin Nanoparticles and more

File all this under "true conspiracies." See the two podcasts below for even more details on this breaking story. I went on the Alex Jones Show today for 5 segments to discuss this in more detail. Those segments will be posted below as they are available via Brighteon. You need to listen to at least the Part 1 Situation Update podcast below to get up to speed (about 45 min) in order to get the full background on this story. The quick summary summary of the story is that Harvard scientist Dr. Charles Lieber was convicted yesterday on all six counts after lying to authorities about receiving millions of dollars from communist China as he shared his groundbreaking technology with a Wuhan technology institute. (See RT.com) Also arrested were two Chinese nationals, one was a female "academic" who was also a lieutenant in the People's Liberation Army, and another person caught trying to smuggle biological weapons out of Boston's Logan airport (MERS and SARS strains). Dr. Lieber is a genius-level scientist who specializes in exotic nanowire technology and how it interfaces with human neurology and biology. Some of his actual patent titles and numbers: 9,029,836 Controlled synthesis of monolithically-integrated graphene structure 10,369,255 Scaffolds comprising nanoelectronic components for cells, tissues, and other applications 9,595,685 Nanoscale wires, nanoscale wire FET devices, and nanotube-electronic hybrid devices for sensing and other applications 9,457,128 Scaffolds comprising nanoelectronic components for cells, tissues, and other applications 9,252,214 Apparatus, method and computer program product providing radial addressing of nanowires From Townhall.com citing the US DOJ: Dr. Charles Lieber, 60, Chair of the Department of Chemistry and Chemical Biology at Harvard University, was arrested this morning and charged by criminal complaint with one count of making a materially false, fictitious and fraudulent statement. Yanqing Ye, 29, a Chinese national, was charged in an indictment today with one count each of visa fraud, making false statements, acting as an agent of a foreign government and conspiracy. Ye is currently in China. Zaosong Zheng, 30, a Chinese national, was arrested on Dec. 10, 2019, at Boston’s Logan International Airport and charged by criminal complaint with attempting to smuggle 21 vials of biological research to China. On Jan. 21, 2020, Zheng was indicted on one count of smuggling goods from the United States and one count of making false, fictitious or fraudulent statements. He has been detained since Dec. 30, 2019. "According to court documents, since 2008, Dr. Lieber who has served as the Principal Investigator of the Lieber Research Group at Harvard University, which specialized in the area of nanoscience, has received more than $15,000,000 in grant funding from the National Institutes of Health (NIH) and Department of Defense (DOD). These grants require the disclosure of significant foreign financial conflicts of interest, including financial support from foreign governments or foreign entities," DOJ reveals. "Unbeknownst to Harvard University beginning in 2011, Lieber became a “Strategic Scientist” at Wuhan University of Technology (WUT) in China and was a contractual participant in China’s Thousand Talents Plan from in or about 2012 to 2017. China’s Thousand Talents Plan is one of the most prominent Chinese Talent recruit plans that are designed to attract, recruit, and cultivate high-level scientific talent in furtherance of China’s scientific development, economic prosperity and national security."

Nanomesh, neurology interface control systems, "radial addressing" of nanowires

Another patent from Dr. Lieber: 9,252,214 Apparatus, method and computer program product providing radial addressing of nanowires This allows for embedded AI systems to control nano-mesh lattices that interface with human neurology to both monitor and control human beings. This technology was being transferred to China. Speculation is that nano-mesh lattices could be inserted into vaccines and once injected, they would self-assemble into neuralink-like computational interface systems that read and control human neurology. This technology would essentially allow Mark Zuckerberg to project his "Meta" universe into your brain without using goggles. It's a full-matrix scenario, where these nanowire / embedded computational systems could eventually read your own private thoughts (inner dialog) and surveil the most private thing you have -- your mind. This tech represents transhumanism and the "borgification" of humanity. It is the end game of total enslavement and mind control at the neurological level. It can be inserted into your body using hypodermic needles that are falsely labeled "vaccines." (This does not mean that all vaccine injections are nanowire payloads, just that nanowire payloads can be inserted into such needles due to their nano-scale size.)

Carbon nanotube "payload" release systems activated by 5G

Read up on carbon nanotubes (CNTs) and how they can be used to deliver "payloads" to the cells. These CNTs can be activated by external signals including 5G broadcasts that target specific individuals. From FBcoverup.com and mirrored on NN servers: Study title: Molecular origin of drug release by water boiling inside carbon nanotubes from reactive molecular dynamics simulation and DFT perspectives From the study: Since the discovery of carbon nanotubes (CNTs) in 1991 and earlier in 1952, CNTs have come to the focus of attention, and their benefits can be currently found. The idea of using a hollow cylindrical structure as a transporter or container has been proposed for many years. Most recently, special properties of these novel materials were found in the medical communities with the hope to develop a new drug delivery system for small treatment agents such as proteins, nucleic acids, and other biologically active molecules. CNTs are used due to their unique properties in drug delivery, sensors as drug delivery agents, destruction of tumors with increasing temperature, cholesterol and blood sugar measurements, identification of antigens and DNA bonding with no toxic effects. Given the potential abilities of CNTs inside the cells, the potential application of CNTs is used for transport and delivery of drugs and antibodies without toxic effects. As previously mentioned, it was proposed that thermal energy delivered to the CNT by a laser light can be used to accelerate the motion of the molecule inside the tube and hence its release from the nanotubes. It can also be used to weaken and disrupt the CNT-molecule interaction. The local temperature around the nanotubes is controlled by adjusting the laser radiation intensity that results in preventing the death of target biological cell. This technology, combined with Dr. Lieber's nanowire "mesh" systems, once advanced to a sufficient level of complexity, would allow external electromagnetic control of "payload" release into human cells, effectively creating a binary weapon system. Vaccine needles can carry the CNTs. 5G towers can activate them. The only question is: What is the payload?

US military rolls out Spike Ferritin Nanoparticle "universal" vaccines - the final kill switch?

Now, using what we believe to be Dr. Lieber's technology developed over the last two decades using DoD money and NIH grant money totaling millions of dollars, the United States military -- which is already trying to mass murder active duty soldiers with covid vaccines -- has unveiled a nanotech "universal vaccine" that we believe to be based on Dr. Charles Lieber's research. From Army.mil, Dec. 16th, 2021: A series of recently published preclinical study results show that the Spike Ferritin Nanoparticle (SpFN) COVID-19 vaccine developed by researchers at the Walter Reed Army Institute of Research (WRAIR) not only elicits a potent immune response but may also provide broad protection against SARS-CoV-2 variants of concern as well as other coronaviruses. Scientists in WRAIR’s Emerging Infectious Diseases Branch (EIDB) developed the SpFN nanoparticle vaccine, based on a ferritin platform, as part of a forward-thinking “pan-SARS” strategy that aims to address the current pandemic and acts as a first line of defense against variants of concern and similar viruses that could emerge in the future. Thus, the military is using synthetic nanoparticles -- Spike Ferritin Nanoparticles -- to invade the body's cells and deliver a payload. This is of course described as lifesaving technology, but the military has been carrying out mass murder of soldiers for over a century. Just examine the history of medical experimentation on Black soldiers to see the shocking truth. Don't forget that Trump launched Operation Warp Speed and bragged about using the US military to distribute and deploy covid vaccines at record speed. Trump even recently bragged about reducing the usual "5 to 12 years" of vaccine research time down to just "9 months," which he thinks is an amazing thing. To achieve this, he simply ordered drug companies and the FDA to skip all the safety studies and produce a true medical experiment that would be mass injected into billions of people. See full coverage of Trump tripling down on the vaccines here.

The US military ran a "plandemic" in 1918 and labeled it "Spanish Flu" but it was actually caused by vaccines

The 1918 so-called "Spanish Flu" had nothing to do with Spain. It was actually a covid-like "plandemic" that was caused by the vaccines given to US military soldiers at Fort Riley, Kansas. The people who died from the "virus" were actually those who were vaccinated, and just like today, soldiers started dropping dead within minutes after being jabbed. This was all run under the blanket pharma domination of the Rockefeller Institute for Medical Research. From the book, "Swine Flu Expose" by Eleanora I. McBean, PhD, N.D.: The first World War was of a short duration, so the vaccine makers were unable to use up all their vaccines. As they were (and still are) in business for profit, they decided to sell it to the rest of the population. So they drummed up the largest vaccination campaign in U.S. history. There were no epidemics to justify it so they used other tricks. Their propaganda claimed the soldiers were coming home from foreign countries with all kinds of diseases and that everyone must have all the shots on the market. The people believed them because, first of all, they wanted to believe their doctors, and second, the returning soldiers certainly had been sick. They didn’t know it was from doctor-made vaccine diseases, as the army doctors don’t tell them things like that. Many of the returned soldiers were disabled for life by these drug-induced diseases. Many were insane from postvaccinal encephalitis, but the doctors called it shell shock, even though many had never left American soil. The conglomerate disease brought on by the many poison vaccines baffled the doctors, as they never had a vaccination spree before which used so many different vaccines. The new disease they had created had symptoms of all the diseases they had injected into the man. There was the high fever, extreme weakness, abdominal rash and intestinal disturbance characteristic of typhoid. The diphtheria vaccine caused lung congestion, chills and fever, swollen, sore throat clogged with the false membrane, and the choking suffocation because of difficulty in breathing followed by gasping and death, after which the body turned black from stagnant blood that had been deprived of oxygen in the suffocation stages. In early days they called it Black Death. The other vaccines cause their own reactions — paralysis, brain damage, lockjaw, etc. When doctors had tried to suppress the symptoms of the typhoid with a stronger vaccine, it caused a worse form of typhoid which they named paratyphoid. But when they concocted a stronger and more dangerous vaccine to suppress that one, they created an even worse disease which they didn’t have a name for. What should they call it? They didn’t want to tell the people what it really was — their own Frankenstein monster which they had created with their vaccines and suppressive medicines. They wanted to direct the blame away from themselves, so they called it Spanish Influenza. It was certainly not of Spanish origin, and the Spanish people resented the implication that the world-wide scourge of that day should be blamed on them. But the name stuck and American medical doctors and vaccine makers were not suspected of the crime of this widespread devastation — the 1918 Flu Epidemic. It is only in recent years that researchers have been digging up the facts and laying the blame where it belongs.

Also worth reading: This blog entry by Dr. Sal Martingano, FICPA

In the book, Vaccination Condemned, by Eleanor McBean, PhD, N.D., the author describes, in detail, personal and family experiences during the 1918 “Spanish Flu” pandemic. McBean’s coverage of the 1918 “Spanish Flu”, as a reporter and an unvaccinated survivor, requires that the historical basis of the event needs to be revisited, not as a “conspiracy theory” but with evidence that will “set your hair on fire”. A few years ago, I came across another book by Eleanor McBean: “Vaccination…The Silent Killer”. McBean provides evidence that not only were the historical events of the 1918 “Spanish Flu” compromised, but also those of the Polio and Swine Flu epidemics. See the full blog entry here. This chart shows deaths from all vaccines tracked by VAERS in the USA. Notice that covid vaccines now compromise more than half of all deaths from all vaccines combined:

Mother of Maddie de Garay, speaks out about her 13 year old daughter’s life altering injuries from Pfizer’s Covid vaccine.

In late July 2020, the US-based Pfizer-BioNTech phase 3 trial of adolescents aged 12-15 years began, 1131 were administered two-doses of the vaccine and 1129 were given a placebo. Maddie de Garay, aged 12 at the time, was one of the 1131. Stephanie, her mother, shares Maddie’s heart-breaking story of how her daughter can barely see, suffers from tinnitus, mobility issues, vomiting, blood in her urine, numbness in her body, and has at least 10-20 seizures a day. 

Within 24 hours of receiving the second dose in early January, Maddie experienced “zapping pain up and down her spine with severe abdominal pain..her toes and fingers turned white and were ice cold..” Maddie later cried out “Mum, it feels like my heart is being ripped out of my chest!”

After receiving a call back from Pfizer’s trial hotline, they were told to send Maddie to the same hospital where the trial was run, Cincinnati Children’s Hospital. Even though it was obvious to Maddie’s parents that she was suffering from adverse effects to the vaccine, the hospital ran tests for a suspected appendicitis and sent her home after having confirmation that there were no signs of a ruptured appendix. None of the tests that they should have done early on were carried out, Stephanie went on to explain.

Between January-April 2021, Maddie went to the ER nine times. “It got to the point where we were not welcome anymore.”

Subscribe to the Trialsitenews "Vaccine" Channel

No spam - we promise

The major failure of the Trial Max App, set up for those enrolled in the trial to report adverse events by simply “ticking boxes,” was that it only listed the usual Covid symptoms along with typical expected reactions to vaccines like fever, dizziness, and nausea.

The de Garays asked Dr Frenke, the principal investigator of Pfizer’s children’s trial and an infectious disease doctor at Cincinnati hospital, whether he reported Maddie’s case to VAERS. He said, “no, we report directly to Pfizer and they report to the FDA.”

When pressed on what symptoms were reported to Pfizer, he responded “all of them,” but avoided answering any further when the de Garays asked him for a specific list. From looking at the submitted EUA, the only symptoms listed, Stephanie stated, “were neuralgia and functional abdominal pain- which is not even touching everything that’s happened to her.” In May, Dr Frenke, later told her that the hospital doctors had informed him that nothing that Maddie was experiencing was because of the vaccine.

On discussing the reporting process of VAERS, she complained, “It took me almost three days to fill out a report, it kept losing my data..it was a nightmare.”

Stephanie emotionally described how many parents have reached out to her since attending Sen. Ron Jonhson’s June 28 press conference where he provided a platform for victims suffering from severe adverse reactions from the vaccines.

She described it’s been mostly girls that have suffered, and like Maddie, “it starts out as vomiting, with numbness going up the body..then passing out and having seizures, 10-20 a day…their mobility completely goes and then it might come back.”

Stephanie explained that “coincidentally” Maddie’s MRI, which was scheduled for later, was moved up to the very day before the data cut-off for the Pfizer trial for 12–15-year-olds, when she was discharged with the diagnosis of “functional abdominal pain- basically a stomachache and neuralgia. It never mentioned that she couldn’t walk.” Nowhere in Maddie’s hospital report was there any mention of the vaccine being the trigger of any of her symptoms.

On the topic of censorship, shockingly, two of Maddie’s TikTok accounts have been shut down, even though nothing controversial was ever posted. Stephanie explained how she’s had to be very selective with her words when using Facebook. If she uses links, they got blocked. Many of the support groups for victims have been shut down and the ones that are out there have strict rules where you can’t use certain words.

When asked what she thought on the FDA authorizing the booster dose of the Pfizer vaccine for 16 and 17 year olds on December 9, she responded, “I’m afraid..I hear of people who are ok with the first and second dose but then the booster puts them over the edge.”

She explained that many parents of vaccine injured children are afraid of speaking out, “nobody talks.”

On discussing informed consent, “none of the symptoms that Maddie experience were listed, they made it out it was going to be like the flu shot” she explained. “Of course, they said we don’t know what could happen, but they knew what could happen because it was happening with the adults before.” Shockingly, she went on to share how other girls who were pre-diagnosed with anxiety, all their vaccine-induced symptoms were then blamed on that.

“When I posted on my Facebook page for the first time about Maddie, it was for prayers from friends and family..when I was asked to make it public- it literally within hours went all over- I was inundated with all kinds of messages and friend requests.”

Pfizer has not offered to pay any of the hospital bills, the family have been relying on their own insurance, and from April onwards MEDICAID has as well, but that does not cover all of Maddie’s medicine. There is no possibility of them filing a lawsuit against Pfizer because of the PREP Act, where Covid vaccine manufacturers are protected by full immunity.

“There are adults committing suicide because it’s so horrible. I am seeing these other kids who are suffering and their parents don’t know what to do and no one is helping them and they’re saying it’s nothing to do with the vaccine. There was nothing wrong with these kids before though. It’s not just Maddie- it’s so many other kids and there are ones who have died and ones who are dying–Maddie is alive, I’m lucky.”

Outrageous Lack of Transparency—Pfizer Now Asks Court for 75 Years to Hide Details of COVID-19 Vaccine Trial Results

TrialSite has tracked attorney Aaron Siri and his client’s Freedom of Information Act (FOIA) case against Pfizer for full disclosure of clinical trials documentation. Siri shared in a previous post that the Food and Drug Administration (FDA) asked a federal judge to delay the full disclosure of all relevant documentation till 2076—55 years from now! Siri, who is a partner with the law firm Siri Glimstad representing the Public Health and Medical Professionals for Transparency (PHMPT) countered to the court that Pfizer should disclose the entire batch of documentation within 108 days which just happens to be the amount of time it took for the Gold Standard regulatory agency to review and approve Pfizer’s vaccine. After the court-ordered both parties to submit updated briefs, now in what can only be considered an insult to injury, Pfizer “doubles down.” Meaning the pharmaceutical company now wants to hide the extent of all of the material information till 2096.

As attorney Siri writes “this is “Not a typo.” They are demanding 75 years of data secrecy. Yes, the FDA is agreeing to share about 12,000 pages in the first couple of months but thereafter they would release, at a snail’s pace, 500 pages per month till that 2096 date.

Why do these developments matter?

An unprecedented situation, with national mandates and even globalized pressure from the World Health Organization (WHO) on member countries, people in the United States deserve to better understand what actually occurred during this trial. Also, TrialSite has shared that under the PREP Act the pharmaceutical company has no liability in the United States. TrialSite was formed to help bring transparency and accessibility to clinical research—this actually serves to raise the trust levels and confidence in research.

Siri notes in his blog that the U.S. government awarded Pfizer $.195 billion in taxpayer’s money to promote the development of this vaccine via a forward procurement agreement. Thereafter, the government outlaid $15.7 billion to purchase the vaccine product—thus far a total of $18.75 billion in taxpayer money has been given to the company, not to mention hundreds of millions in support for the company’s clinical trials.

Ralph Norman, a congressman went on the record:

The FDA’s only priority should be the health and safety of consumers. The agency has compromised its integrity by delaying information that belongs to the public. Since the Biden administration is hell-bent on forcing these vaccine mandates on us, the public has every right to know how this vaccine was approved, especially in such a short amount of time.  After all, the FDA managed to consider all 329,000 pages of data and grant emergency approval of the Pfizer vaccine within just 108 days.  So, it’s hard to rationalize why it now needs 55 years to fully release that information to the public.

While Senator Ted Cruz called the FDA’s position “Completely outrageous.” 

What’s next?

According to Siri’s blog, Each side gets to file response briefs on December 13, 2021, followed by oral arguments on December 14, 2021, in front of the judge. Siri and partners list the FDA documents for your review.

Call to Action: Check out Siri’s blog to reach the entire statement. 

PFIZER-BIONTECH VACCINES WITHHELD FROM VIETNAMESE CHILDREN AFTER SPATE OF DEATHS & AEs

The program to administer COVID-19 vaccinations to children has been paused in Thanh Hoa and Hanoi due to safety concerns. As reported by TrialSite, health regulators in Vietnam’s south-eastern provinces have stopped the use of the Pfizer-BioNTech COVID-19 vaccine after more than 120 children were hospitalised following a school-wide vaccination. TrialSite also recently reported that a 15-year-old boy from Vietnam’s northern province died, the fourth paediatric death linked to the COVID-19 vaccine.  TrialSite’s Southeast Asia correspondents investigate further.

Pfizer and Moderna vaccines are approved for use on children by the Vietnamese government. Children are divided into three age groups for vaccination: 3-11, 12-15, and 16-17 years old. The Ministry of Health predicted that by the fourth quarter of 2021, 95% of the 8.1 million youngsters aged 12 to 17 would have had two COVID-19 vaccine doses.

Vaccination Halted in Hanoi

A girl in Hanoi’s Thuong Tin District died only one day after vaccination in November. The cause of death was Grade IV anaphylaxis, according to the Post-Vaccination Events Expert Panel. Anaphylaxis is a set of symptoms caused by an allergic reaction to a foreign substance. The most severe form of anaphylaxis is Grade IV, which includes respiratory and cardiac collapse. However, it was concluded the case had nothing to do with the quality of the vaccine or vaccination methods.

The Hanoi Department of Health consequently spoke with the Ministry of Health regarding two batches of Pfizer vaccines, no. 124001 and 123002, which had been used to vaccinate students. These two batches were initially printed with an expiry date of November 30, 2021, but had their expiry extended to February 28, 2022.

Subscribe to the Trialsitenews "COVID-19" Channel

No spam - we promise

“After receiving feedback from parents, Hanoi stopped injecting the two vaccines and consulted the Ministry of Health, the other batches were injected normally,” said Director of the Hanoi Department of Health, Tran Thi Nhi Ha. The Hanoi Department of Health published a press release on December 1 verifying that the Covid-19 vaccine is still being administered to students in Hanoi.  TrialSite reports that news media in North America and Europe kept far away from this story.

Thanh Hoa Follows Suit

Mobile injection sites are set up at schools in Thanh Hoa, south of Hanoi in the far northern reaches of this Southeast Asian nation. They primarily provide the COVID-19 vaccination to children in high schools, as well as students in vocational and continuing education institutes. However, more than 120 youngsters were hospitalised in the province for post-injection treatment. The provincial health department has taken steps to prevent injection of the suspect batches of vaccines, according to the international version of the VN Express, a popular online news media owned by FPT Group, the largest information technology service company in Vietnam.

Luong Ngoc Truong, head of the Thanh Hoa CDC, stated that use of the batch associated with the side effects was stopped, but vaccination of children with other batches, also Pfizer vaccines, would continue. He added that the suspended batch would be put into storage and could be used later for other groups like adults.  

In the Vietnamese language version of the article, Truong refers to the symptoms as a form of “hysteria,” multiplying when children see other vaccinated children faint. Vu Van Chinh, director of the Ha Trung District General Hospital, agreed, suggesting that children who react or faint should be separated to avoid a chain reaction. He also reported that two children referred to his hospital were transferred to the provincial general hospital with convulsive symptoms. Undoubtedly these transfers represented more than simple “hysteria.”

TrialSite interviewed a Thanh Hoa resident. Speaking on the condition of anonymity, she said that the vaccination of children has been paused, but there have been no formal comments from the government indicating that the vaccination programme for children will be terminated altogether.  

A Reluctant Public

Parents or guardians need to sign a consent form for students to participate in the vaccination program. Nguyen Huu Hung, Deputy Director of the Department of Health of Ho Chi Minh City highlighted, “The health sector only injects when the family agrees to give the children the vaccine”.

However as of December 8, more than 1,000 parents in Nam Dinh province, also in the north, have not agreed to get their children vaccinated against COVID-19. This is mostly due to concern about the large number of vaccines in use in Nam Dinh province whose expiry dates have been extended. However, this figure represents less than 2% of the parents and guardians in the province.

An online survey of 6,000 young people in Ho Chi Minh City in March 2021 reported that the top three reasons for their reluctance or refusal to get vaccinated are the perceived necessity of the vaccination, concerns about the vaccine’s side effects, and a lack of access to information.

The Thanh Hoa resident said, “Parents are getting concerned. They want the government to at least slow down the rate of vaccines, to get more confirmation or investigation into the quality of the vaccine, and making sure that the children who are going to get vaccinated will be safe.”

An Incomplete Picture

Previously, TrialSite reported the fatality has been connected to the vaccine in the Vietnamese press. The National Health Ministry stated it was an “overreaction to the vaccine,” clarifying that the reaction was “not linked to the quality of the vaccine or the vaccination process.”

Other governments that have similar cases of vaccine reactions in young people have followed the same steps, assuring citizens that the deaths are unrelated to the COVID-19 vaccine. Government authorities appear to be repeating a consistent message that vaccines are safe and effective.

The Vietnamese Socialist Republic has a tight grip on the media, with the government controlling all print and television channels. Journalists and bloggers are known to be subjected to harsh laws. Those who cover or comment on contentious matters run the danger of being intimidated or worse.

Pfizer and BioNTech released a statement on December 8 saying their preliminary laboratory investigations show that three doses of the Pfizer-BioNTech COVID-19 vaccine are required to neutralize the Omicron variant.

The pharmaceutical companies press on with the development of a variant-specific vaccine for Omicron, which they hope to have accessible by March 2022. TrialSite will keep monitoring if there are further updates on the situation in Vietnam.

SHOCKING! Australian ER Doctor Blows The Whistle: “We Are Seeing Myocarditis And Pericarditis In These Children”

An Australian emergency department doctor has blown the whistle to speak out against the vaccination of children for COVID-19. The doctor, who obscured his identity for fears of repercussion by the government and medical authorities, says he’s “increasingly perplexed at the continued government backing of a medical intervention marked by serious complications in children.”

The doctor goes on to say that the sharp rise in myocarditis and pericarditis in this group after the rollout of the vaccines is a clear indication that there are severe consequences to vaccinating children against COVID-19.

He further states that the Phase 3 trial for 5-11-year-olds had a mere 600 participants of which there were no “serious adverse” side effects reported. However, the trial study goes on to say that there are always serious unknown complications that can arise “after the fact”.

Given the track record of the pharmaceutical companies involved it must be asked whether these trials can be trusted at all.

The doctor continued:

“With these vaccines that don’t prevent infection nor transmission of COVID-19, they carry an inherent risk of permanent heart damage while providing absolutely no benefit to the child nor anyone else. Why should we subject our children to these shots?

Parents, you might think that the vaccine offers your child freedoms even if you know it provides no health benefits to your son or daughter. But what good would that school excursion be if they suffer from a reduction in their heart function for the rest of their lives and will almost certainly shorten their lives?”

CDC ‘Massively’ Inflated Number Of Vaccinated Americans

CDC Director Rochelle Walensky has been wildly inflating the number of “vaccinated” Americans by counting potentially tens of millions of “boosters” and second doses as first-time shots, according to a report from Bloomberg News.

Pennsylvania’s acting health secretary Alison Beam said their review showed that some first doses were actually second doses – meaning that fully inoculated people were counted twice as half-vaccinated. Beam revealed the ‘error’ just after she announced that she will be resigning from her post at the end of 2021.

The CDC over-reported the number of vaccinations of the elderly in the state “by about 850,000”, which is approximately 36% of Pennsylvania’s 2,27 million elderly population.

“CDC data show 240 million people with at least one shot or about 72.5% of the population. But the agency says only 203 million are fully vaccinated, or 61.3%, an 11-percentage-point difference that is far larger than in other developed countries.”

A spokesperson for the Philadelphia Department of Health commented:

“We don’t have any faith in the numbers on the CDC website, and we never refer to them.”

This is not the first time the CDC has been caught fudging data, in July and August, CDC Director Rochelle Walensky was caught lying to the public for grossly underreporting the number of vaccinated Americans who were dying with COVID in hospitals.

Now that the CDC vaccination numbers have been revealed to be fake, the question is how reliable the vaccination numbers from other countries are.