As Russian troops entered Ukraine, the government in Kiev ordered the“emergency destruction” of pathogens including plague and anthrax at US-funded laboratories near the Russian border, the Ministry of Defense in Moscow claimed on Sunday. Earlier rumors that the Russian military was targeting US-run biolabs were written off as conspiracy theories, but the ministry has promised to back up its claims with documents.
“We have received documentation from employees of Ukrainian biolaboratories on the emergency destruction on February 24 of especially dangerous pathogens of plague, anthrax, tularemia, cholera and other deadly diseases,” read a statement from the ministry.
The statement accused the “Kiev regime” of conducting an “emergency cleansing” to hide evidence of the supposed biological weapons program, which the ministry claimed was funded by the US, and involved the production of “biological weapons components” at at least two laboratories in the cities of Poltava and Kharkov, both of which have seen intense fighting between Russian and Ukrainian forces in recent days.
The documents published by the ministry purportedly include an order from the Ukrainian Ministry of Health to destroy the pathogens, and lists of the germs in question.
RT can not independently verify the authenticity of these documents. Russia’s Defense Ministry said that they are currently being analyzed by radiation, chemical and biological protection specialists.
“In the near future we will present the results of the analysis,” the ministry said, adding that it believes the documents will prove that Ukraine and the US were violating Article 1 of the UN Biological Weapons Convention. The US, Ukraine and Russia are among more than 180 parties to this treaty, and under Article 1 of the agreement, all parties agree “never under any circumstances to develop, produce, stockpile, acquire, or retain” biological weapons.
As of the moment of this article’s publication, Washington has not commented on the ministry’s claims, and neither has Kiev.
In the initial days of Russia’s military offensive last month, claims circulated online that Russia was targeting western-funded biolabs with missile strikes. These allegations were never verified and were derided by western sources as conspiracy theories, although the Pentagon has publicly stated that it works with the Ukrainian government to “consolidate and secure pathogens and toxins of security concern in Ukrainian government facilities,” for “peaceful research and vaccine development,” according to the US embassy in Kiev.
On December 16, 2021, ICAN, through its attorneys, issued a Freedom of Information Act request to the CDC seeking any documents reflecting why a certain VAERS report was no longer available in the VAERS database. The report described an extremely disturbing incident wherein a two-year-old boy “began bleeding out of the mouth, eyes, nose and ears within six hours” of his first dose of Pfizer’s COVID-19 vaccine on November 18, 2021, and died later that night. On February 14, 2022, the CDC finally responded to ICAN’s request, stating: “A search of our records failed to reveal any documents pertaining to your request.”
Significantly, the CDC has made repeatedassurances that “COVID-19 vaccines are being administered under the most intensive vaccine safety monitoring effort in the United States’ history.” The CDC’s VAERS Standard Operating Procedures for COVID-19 even states that the “CDC will perform clinical reviews” for certain “Adverse Events of Special Interest,” which include death, “especially in children (<18 years of age) and recipients of newly licensed vaccines).”
But despite all of these claims of about the unprecedented level of “intensive” safety monitoring of these vaccines, the CDC claims to have no records that would explain why a VAERS report describing the horrific death of a toddler suddenly disappeared from the primary government-funded system for reporting adverse vaccines reactions in the United States, VAERS—a system of which the CDC is a co-sponsor.
ICAN intends to get to the bottom of the disappearance of this deeply disturbing report and will persist in holding the CDC accountable for its purported claims of intensive vaccine safety monitoring.
President Biden during Tuesday’s State of the Union address falsely claimed the billion-dollar gun manufacturing industry is the only industry in the U.S. that can’t be sued — when in fact, vaccine makers in the U.S. have total liability protection for injuries or deaths caused by COVID vaccines.
“Repeal the liability shield that makes gun manufacturers the only industry in America that can’t be sued,” Biden said. “These laws don’t infringe on the Second Amendment. They save lives.”
CNN fact-checked Biden’s claim and said it was “false.”
“Gun manufacturers are not entirely exempt from being sued, nor are they the only industry with some liability protections,” CNN said. “Under the 2005 Protection of Lawful Commerce in Arms Act, gun manufacturers cannot be held liable for the use of their products in a crime.”
But gun makers can be held liable for “negligence, breach of contract regarding the purchase of a gun or certain damages from defects in the design of a gun.”
According to CNN:
“Other industries also have some exemptions in liability. For example, vaccine manufacturers cannot be held liable in a civil suit for damages from a vaccine-related injury or death. And for the next four years, pharmaceutical companies developing the Covid-19 vaccines will have immunity from liability under the 2005 Public Readiness and Emergency Preparedness Act.
“Those who claim to have been harmed by vaccines may receive money from the government, not the pharmaceutical company, via the Vaccine Injury Compensation Program.”
Although CNN was correct that vaccine manufacturers cannot be held liable for harm caused by vaccines, those injured by COVID vaccines cannot seek compensation under the National Vaccine Injury Compensation Program (NVICP).
Instead, claims must be submitted through an obscure government program called the “Countermeasures Injury Compensation Program (CICP).” The CICP, which almost never awards money, is the only program that accepts claims related to COVID vaccines and other COVID countermeasures.
There are important differences between the two programs that make it more difficult to get compensation through CICP, which is run by the U.S. Department of Health and Human Services (HHS).
Vaccine makers are exempt from liability, the injured have no recourse
The NVICP, a special, no-fault tribunal housed within the U.S. Court of Federal Claims, handles injury claims for 16 common vaccines. To date, it has awarded more than $4 billion to thousands of people for vaccine injuries.
It is difficult to obtain compensation within the NVICP. Payouts, including attorneys’ fees, are funded by a 75-cent tax per vaccine. There is a $250,000 cap on pain and suffering. The proceedings are often turned into drawn-out, contentious expert battles and the backlog of cases is substantial.
The National Childhood Vaccine Injury Act of 1986 established the NVICP, and U.S. Supreme Court Decision, Russell Bruesewitz et al v. Wyeth et al, guaranteed vaccine manufacturers, doctors and other vaccine administrators almost always have no legal accountability or financial liability in civil court when a government-recommended or mandated vaccine(s) causes permanent injury or death.
As for the CICP, only about 8% of the people who have applied for compensation for vaccine injuries have ever received payouts. The statute of limitations for the CICP is one year from the time of injury and the program does not cover attorney fees.
The agency’s website outlines the parameters of the program, which is authorized by the Public Readiness and Emergency Preparedness (or PREP) Act.
In March 2020, HHS issued a PREP Act Declaration covering “COVID tests, drugs and vaccines,” providing liability protections to manufacturers, distributors, states, localities, licensed healthcare professionals and qualified persons who administer COVID countermeasures.
A PREP Act declaration is specifically for the purpose of providing immunity from liability, which is why people who are injured by COVID vaccines can’t seek redress via the NVICP.
To be compensated by the CICP for a COVID vaccine injury, it must be established, based on “compelling, reliable, valid, medical and scientific evidence,” that the injury or death was directly caused by the vaccine.
The program provides compensation only for medical expenses, lost employment income and survivor death benefits as “the payer of last resort,” covering only what remains unpaid or unpayable by other third parties such as health insurance.
A detailed chart of alleged injury claims filed with the CICP includes anaphylactic shock, myocarditis and blood-clotting disorders. Other conditions listed involve claims affecting virtually all major health systems including appendicitis, hearing loss, kidney injury, arthritis and depression.
As of Feb. 1, the CICP had approved only one COVID vaccine-related claim, but that claim has not been paid out.
Since the program’s inception in 2010, 7,033 claims have been filed, but only 29 claims were compensated, with an average payout of around $200,000. The other 452 claims (91.4%) were denied. Ten claims won approval but were deemed ineligible for compensation.
According to the most recent data from the Vaccine Adverse Reporting System, the primary government-funded system for reporting adverse vaccine reactions in the U.S., there have been 24,827 deaths related to COVID vaccines reported as of Feb. 25. Of those deaths, 11,312 cases occurred within the U.S. and 22% occurred within 48 hours of vaccination.
The low number of applicants to the CICP fund for injuries or death from the COVID vaccine suggests people don’t know the program exists.
Families could wait ‘many many years’ for compensation if injury claim approved
According to Sean Greenwood, a vaccine injury attorney in Texas, even if the family does get an approved claim through CICP, they could wait “many many years” to receive compensation.
As The Defender reported Feb. 25, a family whose 21-year-old son developed a life-threatening reaction to Pfizer’s COVID vaccine has been waiting six months to learn if the U.S. government’s CICP will help cover their son’s medical bills.
The family of Kartik Bhakta in August 2021 submitted a claim on behalf of their son. So far, the claim has been ignored. Bhakta’s parents quit their jobs to take care of Bhakta — who is unable to return to medical school — and do not know how they will continue to pay for their son’s medical expenses.
Asked what the family would do if denied assistance, Bhakta’s father replied, “I don’t know. Then why is the government forcing us to take a vaccine if they’re not taking responsibility?”
Kendra Lippy was a healthy 38-year old woman — until she got the Johnson & Johnson (J&J) shot.
Lippy was diagnosed with severe blood clots that subsequently sent most of her organs into failure. She also was left without most of her small intestine and more than $1 million in medical bills that she said the federal government should compensate her for.
Lippy’s case was one of the six that led federal agencies to temporarily pause the J&J shot in mid-April. Her blood clots developed in March. She was hospitalized for 33 days, including 22 days of intensive care.
Lippy wants to see a federal compensation system that is fair to her and others who are harmed by COVID vaccines.
Because the government shielded vaccine makers from liability, she can’t sue J&J. She also doesn’t have a legitimate legal route to sue the government.
Biden extends national emergency to protect COVID vaccine manufacturers
As countries around the world drop COVID restrictions and downgrade the virus to “flu-like status,” Biden on Feb. 18 announced the U.S. national emergency declared in March 2020 for COVID will be extended beyond March 1.
Citing the ongoing risk to “public health and safety” posed by the virus, Biden told House Speaker Nancy Pelosi (D-Calif.) — in a letter released by the White House — there “remains a need to continue this national emergency.”
Biden wrote:
“The COVID-19 pandemic continues to cause significant risk to the public health and safety of the Nation. More than 900,000 people in this Nation have perished from the disease, and it is essential to continue to combat and respond to COVID-19 with the full capacity and capability of the Federal Government. Therefore, in accordance with section 202(d) of the National Emergencies Act (50 U.S.C. 1622(d)), I am continuing the national emergency declared in Proclamation 9994 concerning the COVID-19 pandemic.”
“For this reason, the national emergency declared on March 13, 2020, and beginning March 1, 2020, must continue in effect beyond March 1, 2022,” Biden wrote in a second statement released by the White House for publication in the Federal Register.
The emergency would have been automatically terminated unless, within 90 days prior to the anniversary date of its declaration, Biden notified Congress of his intent to continue it.
Extending the “national emergency” keeps COVID vaccines covered under the PREP act, which allows manufacturers to escape liability for the harms caused by their products.
According to Greenwood, once the government approves the COVID vaccine for children under 5 years old and pregnant women, compensation requests will move over to the NVICP.
It is unknown whether CICP claimants will also be able to file in the NVICP if the COVID vaccine is added to the program.
Megan Redshaw is a freelance reporter for The Defender. She has a background in political science, a law degree and extensive training in natural health.
HOW long until we get reports of people pelting Siberian huskies on the street?
Probably not too long. Already there are videos of Russian food shops being vandalised such as this one in Germany.
A friend who runs a Russian language school in Britain has received threats, including that all Russians should leave the UK. That the school employs mostly Ukrainians and the owner’s wife is from Kiev is neither here nor there when you’re caught up in the latest tide of moral righteousness.
Having forgotten utterly about the preoccupations of yesterday – Covid, Partygate (whatever happened to Sue Gray’s report?) – we are now fully at work with our latest, all-consuming passion. War. Lots of it. Each detonation of a mortar round more titillating than the last. I haven’t seen this much unanimity since the first days of the Covid-19 pandemic.
Do you believe what you read in the media? Plucky Ukrainians, incompetent Russians. After a few days, claims that ‘Russia has lost the war’ abound. Stuck in the mud and stranded without fuel. That wars are rarely decided on the opening day seems lost to a world obsessed with only the present moment. There is plenty more time for Ukraine to fall.
But not without additional, unnecessary bloodshed, all encouraged by our politicians and media. Those wishing to volunteer for Kiev are sent away on a bandwagon of positive vibes and profile pictures with superimposed Ukrainian flags. That they are being sent to a probable death is neither here nor there.
The Russians are evil. The West never puts a foot wrong. Ignore the wars of the past – Iraq, Afghanistan, Libya – we are geopolitically chaste and without sin. That Ukraine is of approximately zero geostrategic interest to us does not matter. The forward march of Western hubris in its institutional form cannot be impeded.
Why would Nato not just say Ukraine will remain a buffer state? That nation’s entry into the alliance was so clearly a red line for the strategists of Moscow, nevertheless we courted its favour, assuming that being on the ‘right side of history’ would be enough. When Russia finally did invade, our ignorance leads us to throw our hands up and scream ‘bully!’ at Putin. I do not care much for Putin, but it is for the birds to assume that the West is entirely without blame.
Having been systematically lied to about every imaginable topic, I cannot simply buy our government’s line. Warrior Truss, whose unfamiliarity with the geography of the area should set alarm bells ringing, solemnly plays her role as a second-rate Thatcher-at-war. Johnson, who until yesterday was on the ropes of various scandals, is recast as a latter-day Churchill.
We’re fighting for democracy and freedom. Fighting for it in a corrupt eastern European state, cleft in two by a linguistic and ethnic fault line, and whose elites have bought the ear of the American President and his family.
We’re fighting it from the high horses of the West, which has just spent two years imprisoning its own citizens and demanding they undergo forced medical procedures. From the same West which would not dare comment on Trudeau’s totalitarian seizure of the bank accounts of those who dared disagree with him, nor on the dictatorial powers used daily in the Antipodes.
Forget all of that. We are the good guys. They are the bad guys. The world is black and white. We are not to blame, not one iota. Cheerlead for war and let the stakes get higher. Assume that Russia’s interests are invalid and to be ignored. We’re back to the gilded age of liberal democracies beating the drum of war.
Whatever you do, don’t look back or think about the recent past. Let your minds be firmly occupied by the indulgent orgy of violence, peddled by the same people who conned you so many times before, and who seek to keep us in a perpetual state of crisis. And certainly, never think about the law of unintended consequences.
“Oh what a tangled web we weave, when first we practice to deceive” – Sir Walter Scott
Throughout the last two years Public Health Scotland (PHS) has punched above its weight by providing reliable data that has quantified the impact of the Scottish government’s COVID-19 response on the health of the Scottish population. In particular, it has documented the unprecedented excess death that occurred in summer and autumn 2021, prompting the establishment of an official enquiry as to the cause, and uncovered a spike in September 2021 in the number of stillbirths in Scotland that is currently under investigation.
However, in its report of 14th February 2022, PHS has declared that it will no longer publish data on COVID-19 outcomes (cases, hospitalisations and deaths) classified by vaccination status, a hitherto valuable component of the COVID-19 vaccination surveillance strategy. The reason given for making this change is that ‘PHS is aware of inappropriate use and misinterpretation of the data when taken in isolation without fully understanding the limitations’.
It is certainly true that claims have been made about the deleterious effects of COVID-19 vaccines that go well beyond what can be supported by the data published by PHS. In this case critical appraisal of these unsubstantiated claims, rather than the blanket withdrawal of valuable information, would seem the better antidote to the spread of misinformation.
However, it is important to note that implicit in the decision made by PHS is that the information they provide is above reproach, both in terms of inappropriate use and misrepresentation of the data to which they alone are privy. To investigate whether PHS analysis is indeed above reproach, we can look in a little detail at the way in which they have presented the information on COVID-19 outcomes by vaccination status in their last report of February 2022. We will concentrate on the analysis of death with COVID-19 by vaccination status, unvaccinated or booster, found in Table 15, using the data for week 29 January – 04 February 2022. The relevant data from that table is reproduced below:
No. of Deaths
Population
Age Standardised Mortality Rate per 100,000 with 95% confidence intervals
Unvaccinated
13
1,524,406
10.95 (3.40 – 18.50)
Booster
73
3,229,938
1.50 (1.15 – 1.85)
A superficial inspection of this table would suggest to the casual reader that the death rate with COVID-19 in those who have received a booster is far lower than that suffered by those who are unvaccinated when the difference in age distributions of the booster and unvaccinated populations are taken into account. Indeed, PHS draw the conclusion that ‘the death rate in individuals that received a booster or 3rd dose of a COVID-19 vaccine was between 4.6 and 9.5 times lower than individuals who are unvaccinated or have only received one or two doses of a COVID-19 vaccine’. Let us look in detail at how the data were treated to arrive at this conclusion, and ask whether this very strong affirmation of the benefits of the booster can be substantiated.
We first look at the way in which the two populations that we are comparing, unvaccinated and booster, are defined. For this we turn to Appendix 6 of the report. Here we learn that the unvaccinated population is not, as we might have assumed, those that have never been vaccinated. Instead, it also includes all those individuals who have received a first vaccine, but for whom the time since vaccination is less than 22 days. Thus, if any deaths occur within the 21 days post first vaccine, these deaths will be attributed to the unvaccinated category. This misattribution may have significant consequences because deaths from adverse vaccination reactions principally occur shortly after vaccination. This idiosyncratic classification of the unvaccinated artificially, and misleadingly, inflates the death rate in the unvaccinated population. Would it not have been better to classify the unvaccinated as those never receiving a vaccine, to preclude the introduction of such bias against the unvaccinated into the analysis?
Turning to the boosted population we find that this is not defined as the number of individuals who have received a booster, but rather the number that have received a booster at least 14 days prior to the reporting period. Therefore, if deaths of boosted individuals occur within the first 14 days of this vaccination, they will not be counted as booster deaths, but as a 2-dose death. The mortality rates given are also dependent on the size of the vaccinated population. If the addition of boostered individuals is a continuous process then, depending on accounting, the last two week cohort added to the boostered population may effectively be excluded from contributing to deaths, while the unvaccinated population during the same time period will not. PHS’s redefinition of the booster population again serves to artificially and misleadingly reduce the reported rate of deaths in the PHS booster population relative to the unvaccinated population. Would it not have been better to classify the booster population simply as those who have received a booster shot, and avoided the inevitable bias in favour of the boosted population that is introduced by the PHS redefinition?
Notwithstanding the biases introduced by PHS’s redefinition of the populations to be compared, we can now concentrate our attention on the methods they have used to correct for the fact that the age distribution of the unvaccinated is likely to be much younger than that of the boosted population. To begin our explanation, it is helpful to use the raw data provided in table 15 for week 29 January – 04 February 2022 to calculate the individual rate of death with COVID-19 per 100,000 per week without making any adjustment for differences in age distribution. This can be compared with the figures PHS calculated from the data to quantify ‘Age Standardised Mortality Rate per 100,000 per week’.
Unvaccinated
Booster
Unadjusted COVID-19 mortality per 100,000 per week
0.85
2.26
Age Standardised Mortality Rate per 100,000 per week
10.95
1.50
The comparison is illuminating and a little worrying. An unadjusted death rate 2.7 times higher in the booster population than in the unvaccinated population has been converted into an age standardised mortality rate that is now 7.3 times higher in the unvaccinated population than in the booster population. To understand what is going on we have to know both how to calculate an Age Standardised Mortality Rate per 100,000 per week, and to understand what this value actually represents.
The Age Standardised Mortality Rate is a measure of the impact, in terms of mortality, on the whole population rather than a particular age group. Rather than calculating a population Age Standardised Mortality Rate based on the age distribution of the Scottish population, Public Health Scotland used the standard WHO age distribution. In this age distribution there is a much lower representation of older people. The consequence is that a very low weight is given to deaths in older age groups and a disproportionately high weighting to deaths in young age groups. In fact, the weighting of a young death can be 10 times higher than for an old death. Through this unjustified weighting a raw mortality rate which was 2.7 times greater in the vaccinated is turned into an age standardised mortality rate which is 7.3 times greater in the unvaccinated.
The age standardised mortality does not relate to individual risk – we may have much higher risk in old age groups individually, but this translates into a very small effect on overall deaths at a population level because the percentage of old people in the population is very low. The point of calculating age standardised mortality is not to compare risks. It is designed to allow comparison of the relative burden of a disease on a population – what proportion of a population will be lost from that population by a particular disease. Its use to somehow correct for differences in age distributions on risk of death is completely inappropriate.
The important thing to note is that what has been calculated is a measure of population impact of COVID-19 in a hypothetical population; what proportion of the population die in this hypothetical population as a consequence of the disease. It is assuredly not a measure of individual mortality risk from COVID-19. As such it is completely inappropriate and misleading to use it to compare the risk of death with COVID 19 between populations of different vaccination status as has been done by PHS. Therefore, their statement that ‘the death rate in individuals that received a booster or 3rd dose of a COVID-19 vaccine was between 4.6 and 9.5 times lower than individuals who are unvaccinated or have only received one or two doses of a COVID-19 vaccine’ is utterly false and misleading and completely unsupported by the data. The simple and transparent way of comparing individual mortality risk would be to use the data in PHS’s possession to estimate individual risk of death for each age category and population, and compare these values within each age category. Rather than compare the whole population, the risk for each age group by vaccination status would provide useful information. UKHSA do provide this data but PHS never have done. The magnitude of the error in using Age Standardised Mortality Rates as a metric calls into question the competence of PHS to analyse and interpret data that are critical to the formulation of Scottish government health policy which directly impacts the wellbeing of literally millions of people.
The final point to make is that in order to receive a booster, an individual must previously have received both a first and a second dose of vaccine. There is a risk of a bias being introduced whereby only survivors, who are by definition less likely to die, are being measured. Therefore, deaths that occurred after first and second vaccinations should be included with deaths after the booster vaccination itself in order to properly assess the overall COVID-19 death rates in the vaccinated population. In other words, the appropriate comparison to make when assessing the effect of booster doses on COVID-19 mortality is between the unvaccinated population and the vaccinated population, where the latter includes anyone who has received any injection.
In conclusion, by announcing that data on COVID-19 outcomes by vaccination status will no longer be provided due to “misrepresentation and misinterpretation of their analyses”, PHS has drawn attention to their own glaring shortcomings in this area. They have been shown to introduce unwarranted bias into their analyses by manipulation of the definitions of vaccination status, and they have used a wholly inappropriate metric to compare the risk of death with COVID-19 among the vaccinated and unvaccinated in the Scottish population.
Washington, DC, — In a 55,000-page set of documents released on Tuesday, the U.S. Food and Drug Administration’s (FDA’s) Center for Biologics Evaluation and Research (CBER) is for the first time allowing the public to access data Pfizer submitted to FDA from its clinical trials in support of a COVID-19 vaccine license. This follows U.S. District Judge Mark T. Pittman’s decision on January 6 to deny the request from the FDA to suppress the data for the next 75 years which the agency claimed was necessary, in part, because of its “limited resources.”
A 38-page report included in the documents features an Appendix, “LIST OF ADVERSE EVENTS OF SPECIAL INTEREST,” that lists 1,291 different adverse events following vaccination. The list includes acute kidney injury, acute flaccid myelitis, anti-sperm antibody positive, brain stem embolism, brain stem thrombosis, cardiac arrest, cardiac failure, cardiac ventricular thrombosis, cardiogenic shock, central nervous system vasculitis, death neonatal, deep vein thrombosis, encephalitis brain stem, encephalitis hemorrhagic, frontal lobe epilepsy, foaming at mouth, epileptic psychosis, facial paralysis, fetal distress syndrome, gastrointestinal amyloidosis, generalized tonic-clonic seizure, Hashimoto’s encephalopathy, hepatic vascular thrombosis, herpes zoster reactivation, immune-mediated hepatitis, interstitial lung disease, jugular vein embolism, juvenile myoclonic epilepsy, liver injury, low birth weight, multisystem inflammatory syndrome in children, myocarditis, neonatal seizure, pancreatitis, pneumonia, stillbirth, tachycardia, temporal lobe epilepsy, testicular autoimmunity, thrombotic cerebral infarction, Type 1 diabetes mellitus, venous thrombosis neonatal, and vertebral artery thrombosis among 1,246 other medical conditions following vaccination.
“This is a bombshell,” said Children’s Health Defense (CHD) president and general counsel Mary Holland. “At least now we know why the FDA and Pfizer wanted to keep this data under wraps for 75 years. These findings should put an immediate end to the Pfizer COVID vaccines. The potential for serious harm is very clear, and those injured by the vaccines are prohibited from suing Pfizer for damages.”
The U.S. government has already purchased 50 million doses of the Pfizer vaccine intended for children under five years of age to be delivered by April 30, 2022 although the FDA has yet to grant an Emergency Use Authorization (EUA) for this age group. The risk of serious injury or death from COVID to healthy children is practically nil and so far, the vaccine is not effective when used in young children.
According to The Guardian, “Pfizer made nearly $37bn (£27bn) in sales from its Covid-19 vaccine last year – making it one of the most lucrative products in history – and has forecast another bumper year in 2022, with a big boost coming from its Covid-19 pill Paxlovid.” President Biden advertised Paxlovid in his State of the Union address on Tuesday, the same day the Pfizer data was released to the public. “We’re launching the ‘Test to Treat’ initiative so people can get tested at a pharmacy, and if they’re positive, receive antiviral pills on the spot at no cost,” Biden said during his speech.
From mid-December, 2020 through February 18, 2022, the U.S. government’s database, the Vaccine Adverse Events Reporting System (VAERS), has received 1,134,984 reports of adverse events, including 24,402 deaths, following COVID vaccination. Additionally, there have been 4,021 cases of myocarditis and pericarditis in the U.S. with 2,475 cases associated with Pfizer, 1,364 cases with Moderna and 171 cases with J&J’s COVID vaccine. These include 643 reports of myocarditis and pericarditis in children aged 12 to 17.
“It would be criminal to expose infants and young children to this extremely risky product,” said Holland. “VAERS data show the catastrophic health impacts the vaccine is having on millions of people, yet Pfizer and other vaccine makers are raking in billions of dollars with no fear of being held accountable for injuries and deaths from their vaccines.”
The FDA’s attempt to suppress these data in support of the pharmaceutical industry’s bottom line isn’t a new phenomenon in this country’s public health system. For more information on pharmaceutical corruption and the tight relationship the industry has with government regulatory agencies, read The Real Anthony Fauci: Bill Gates, Big Pharma and the Global War on Democracy and Public Health by CHD Chair and lead counsel Robert F. Kennedy, Jr.
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Children’s Health Defense is a 501(c)(3) non-profit organization. Its mission is to end childhood health epidemics by working aggressively to eliminate harmful exposures, hold those responsible accountable, and establish safeguards to prevent future harm. For more information, visit ChildrensHealthDefense.org.
The spokesman for the Russian Ministry of Defense, Major General Igor Konashenkov, issued an official statement on Friday morning concerning the shootout and fire that had occurred at Ukraine’s Zaporozhskaya nuclear power plant earlier the same day.
“Last night, an attempt to carry out a horrible provocation was made by Kiev’s nationalist regime on the area surrounding the station,” he announced, claiming the Russian troops patrolling the territory had been attacked by a Ukrainian sabotage group.
According to the spokesman, the Ukrainian forces had attacked Russian soldiers at about 2am local time, opening heavy fire from the training facility next to the power station in order to “provoke a retaliatory strike on the building.”
The Russian patrol had neutralized the group’s firing points, but the saboteurs had then set fire to the training facility as they retreated, Konashenkov said. The blaze was put out by the Ukrainian State Emergency Service’s firefighters. “At the moment of provocation, no staff members were at the facility,” he noted.
In response to the Russian Ministry of Defense’s statement, Ukrainian president Volodymyr Zelensky denied the provocation claims and accused Russian forces of having staged the attack.
The mayor of the nearby town of Energodar had originally reported that the fire had been caused by Russian shelling, and that the blaze had engulfed the power plant itself, but the emergency services dismissed the latter claim.
It was reported on Monday that the facility had been captured by Russian forces, and that staff were keeping operations going and monitoring radiation levels. The International Atomic Energy Agency has offered assurances that there has been no change in those levels in the wake of the incident.
Russia began its military offensive in Ukraine last week, claiming its invasion was aimed at “demilitarizing” and “denazifying” the government in Kiev and stopping what it called the “genocide” in the two breakaway regions of Donetsk and Lugansk. Ukraine has accused Moscow of an unprovoked offensive, with the US and its NATO allies following suit and imposing severe economic sanctions.
In a resolution passed on Thursday by its board of directors, the International Atomic Energy Agency (IAEA) reportedly “deplored” Moscow’s invasion of Ukraine. Russia has denounced the document, calling it politicized and factually incorrect.
The resolution, which is yet to be published, apparently calls on Russia to allow the Ukrainian authorities to resume control of its nuclear sites. Moscow says the assertion that they are not already in control is incorrect.
There were claims that Russian troops had occupied the site of the destroyed Chernobyl nuclear power plant as they moved from Belarus towards Kiev. The Russian Defense Ministry has denied them, stating that Ukrainian guards remained in control of the facility.
On March 1, Reuters gave a preview of the draft of the damning resolution, which was penned by Poland and Canada on behalf of Ukraine.
The news of the resolution’s passage, with just two votes having been cast against it at the session of the 35-member board, was welcomed by Ukraine. Foreign Minister Dmytro Kuleba claimed in a tweet that it showed the world was “united against Russia’s actions, which threaten Ukraine and all of Europe.”
Russia’s representative at the IAEA, Mikhail Ulyanov, blasted the document, claiming it contained “intentional politically motivated lies and mistakes.” In particular, the assertion that the Ukrainian authorities were not in control of the nation’s nuclear sites was wrong, the official said in a series of tweets.
Moscow was satisfied that “countries whose populations taken together exceed a half of the mankind refused to support the resolution,” Ulyanov added.
China has confirmed that it voted against the resolution. Its representative, Wang Qun, said the document “obviously” overstepped the agency’s mandate to monitor nuclear security, and that by adopting the resolution, it had undermined the IAEA’s position as a professional, non-political organization.
The diplomat complained that some nations had “forcibly pushed” the draft and rejected suggestions submitted by other board members about how to improve the document.
Earlier on Thursday, IAEA Director General Rafael Mariano Grossi confirmed to journalists that all safety precautions the agency had taken in Ukraine remained intact.
The Army’s premier biolab changed its mission statement after a 2014 report by high-ranking officials concluded its work has become less useful since its Cold War heyday and no longer delivers medical products for service members.
The report, which had not been previously released, was obtained through a state public records request by U.S. Right to Know.
The challenges at the U.S. Army Medical Research Institute of Infectious Diseases, or USAMRIID, come to light at a time of fierce debate about the degree to which research on novel pathogens contributes tangible benefits. Scientists with different theories about the COVID-19 pandemic’s origins have been tangled in arguments over whether certain work on dangerous pathogens can help predict pandemics or poses unacceptable risks.
Located 50 miles outside of Washington at Fort Detrick, USAMRIID was once charged with responding to the Soviet Union’s biological weapons program, but stopped developing bioweapons in 1969. It now conducts research on biological threats including Ebola, Zika, anthrax and plague, and conducts research for universities and private companies. It employs about 900 military, civilian and contract researchers.
The global biological threat landscape has changed due to gain-of-function technology, the limited capacity of the intelligence community to identify biological threats, and the proliferation of “dual use” research programs that generate pathogens that could be harmful in the wrong hands, the report states.
USAMRIID has in recent years suffered many troubles, including biosafety breaches, a shut down of its high security work, and accusations from Department of Defense leadership of wasting taxpayer funds.
The report by government experts, including former USAMRIID Commander David Franz, describes an agency adrift as America’s first biodefense research facility struggled to deliver on the promises in its mission statement.
The report concludes that the lab’s work may not always generate medical advances, and should not be expected to in the eyes of its funders in Washington.
“The emphasis on products to the warfighter has become less relevant,” the report reads. “Because prophylaxis for ‘biological agents’ (traditional vaccines) requires great specificity and a period of at least weeks before protection is achieved, the era of vaccines for the force, one of USARMIID’s greatest historic strengths, is essentially over.”
The experts behind the report recommended changing the mission of the military lab away from generating vaccines and drugs.
It appears USAMRIID’s leaders listened.
By Jan. 2015 – several months after study’s authors had convened in June 2014 – the vision of the lab had changed on its website from “right product, right time for the Warfighter” to a more general statement about leadership in medical biological defense, according to changes accessed via the WayBack Machine.
“To be the leader in the advancement of medical biological defense with world renowned experts dedicated to protecting our military forces and the nation,” USAMRIID’s vision statement now reads.
In the years since USAMRIID’s 2014 consultants fought to prove its importance to the Pentagon, the lab has faced allegations of “financial mismanagement,” according to a Defense Department letter reported by CQ Roll Call.
Other problems
USAMRIID is one of two facilities at Fort Detrick with laboratories designed to handle the most dangerous pathogens in the world, so-called BSL-4 labs. There are 14 BSL-4 labs in North America.
These labs have come under greater scrutiny amid concerns by Republicans and some independent biosecurity experts that the COVID-19 pandemic may have arisen from a lab accident in China.
USAMRIID has not developed a COVID-19 vaccine candidate, though the lab has tested COVID-19 vaccines in the pre-clinical trial stage, according to Caree Vander Linden, public affairs officer at USAMRIID.
Vander Linden also provided U.S. Right to Know with a spreadsheet of 43 scientific papers produced by the lab about COVID-19. For example, the lab recently announced engineering hamsters to increase their expression of the human ACE2 receptor — a key protein used by SARS-CoV-2 to enter airway cells — to enable the study of more severe disease. Remdesivir, the first therapeutic with approval from the Food and Drug Administration to treat COVID-19, was also developed with the help of USAMRIID.
Vander Linden did not respond to questions about the report and the change of the USAMRIID mission statement. Franz did not respond to requests for comment.
Morale has plummeted since the deadly release of anthrax from the lab in 2001, the 2014 report suggests. That has been worsened by the expansion of work on biorisks at other labs. Now USAMRIID struggles to retain talent. Much of the work at USAMRIID is that of a contract research organization performing tasks for the private sector.
“The concept that USAMRIID is more of an ‘insurance policy’ to deal with the unknown and unexpected than a ‘factory’ to produce medical ‘things’ for the soldier should be understood by all,” it states.
The report criticizes the biosafety regulations at the Fort Detrick lab, saying the routine presence of inspectors is a distraction.
“The heavy regulatory burden … and oversight following the 9-11 attacks and the anthrax letters has diverted both funding and human resources from the research mission,” the report states.
Yet in the years since, serious safety breaches have occurred at USAMRIID. The Centers for Disease Control and Prevention flagged failures to “implement and maintain containment procedures sufficient to contain select agents or toxins” in biosafety level 3 and 4 laboratories, the Frederick News-Post reported, culminating in a shutdown of USAMRIID’s two top security labs and a suspension of its registration with the Federal Select Agent Program.
Though work resumed in November 2019, the lab’s Defense Department funding remained frozen until April 2020.
Both the Biden and Trump administrations have sought cuts to USAMRIID. But members of the Maryland congressional delegation have fought to maintain funding levels.
Congress appropriated $130 million for the expansion of USAMRIID in fiscal 2021.
Unpredictable threats
While USAMRIID once focused on responding to the Soviet Union, new biological threats are more diverse and harder to nail down, according to the report.
“The intelligence community is limited in its ability to identify specific threats,” the report states.
This unpredictability is due in part to so-called “gain-of-function” research, a term used to describe research that can make pathogens more virulent or transmissible.
“Threat agents … might include traditional ones to those that blur the line between chemistry and biology or even those modified through ‘gain of function’ techniques,” the report reads.
Potentially dangerous biological research is now characterized by “small footprint, dual-use offensive capabilities that might be found in a few large and medium nation states,” according to the report.
Two of the 2014 report’s authors – Franz and former director of the National Science Foundation Rita Colwell – have connections to EcoHealth Alliance, a nonprofit under investigation for its gain-of-function work on coronaviruses with the Wuhan Institute of Virology. Colwell is on the board of directors, while Franz was a booster of the organization, according to a 2019 social media post.
Other consultants who coauthored the report include former secretary of the Navy Richard Danzig; former deputy commander-in-chief of United States Strategic Command Robert Hinson; former director of the Biomedical Advanced Research and Development Authority Carol Linden; and former chief of staff of the U.S. Army Dennis J. Reimer; executive director of the Maryland Biotechnology Center Judy Britz; distinguished research fellow at National Defense University Seth Carus; Harvard professor of biologically inspired engineering David Walt; and NIH researcher Richard Whitley.
The official US embassy website recently REMOVED all evidence of bio-labs in Ukraine. These bio-labs are funded and jointly operated by the US Department of Defense (DOD). The laboratory documents were public knowledge up until February 25, 2022. These documents include important construction, financing and permit details for bioweapon laboratories in Ukraine. But now the US government is scrubbing these documents from the internet and becoming less transparent with this critical information. This comes at a time when the world population is waking up to the reality of gain-of-function bioweapons research, lab leaks and predatory vaccine and diagnostics development. These bio-labs generate pathogens of pandemic potential that exploit human immune systems and are the foundation for which medical fraud, malpractice, vaccine-induced death and genocide originates.
Could the existence of these bioweapons’ labs have something to do with Russia’s “special military mission?” For years, Russia has accused the US of developing bioweapons near its borders. Are the Russians currently gathering evidence from these labs? What is the current status of these facilities? What if Russia was not conducting an imperialist invasion and occupation of Ukraine — a reality that has been propagated by Western media outlets? What if Russia was instead targeting international crime syndicates and going after criminal elements in the Ukrainian government that have harmed the Ukrainian people and others around the world?
The U.S. erected a vast network of bio-labs in Ukraine and is scrubbing details from the net
The US DOD funded at least 15 different bio-labs in Ukraine. These are not Chinese or Russian bio-labs. At least eight of these are bioweapons labs are operated exclusively by the US. These laboratories “consolidate and secure pathogens and toxins of security concern” to conduct “enhanced bio-security, bio-safety, and bio-surveillance measures” through “international research partnerships.” Each facility costs the US taxpayers anywhere from $1.8 to over $3 million. The DOD facilitated the permit process to allow Ukrainian scientists to work with pathogens of pandemic potential.
The US DOD works directly with Ukraine’s Ministry of Health, State Service of Ukraine for Food Safety and Consumer Protection, the National Academy of Agrarian Sciences and the Ministry of Defense. This network of bio-labs includes facilities in Odessa, Vinnytsia, Uzhgorod, Lviv, Kiev, Kherson, Ternopil, Crimea, Luhansk and two suspect facilities in Kharkiv and Mykolaiv.
In recent years, many of these labs have reached Bio-safety Level 2 status, allowing scientists to experiment with viruses and bacteria. Over the past two years, these laboratories, in cooperation with the Ukrainian Ministry of Defense, erected four more mobile laboratories to conduct epidemiological surveillance of the Ukrainian people. These laboratories are part of a multi-national working group that creates disease surveillance networks that “strengthen global health security.”
Up until February 25, 2022, the existence and details of these bioweapons labs were public knowledge. The US embassy had previously disclosed the locations and details of these laboratories in a series of PDF files online. On February 26, 2022, the official embassy website shut down the links to all 15 bioweapon laboratories. All the documents associated with these labs have been removed from the internet. If you click on any of the links, the PDF files are no longer available. Thankfully, these files have been archived and can still be accessed. What is the US embassy trying to hide?
Countries all over the world are totally scrubbing their Covid measures, mask mandates and social distancing rules.
The CDC has changed their guidance on vaccine doses, and said people don’t need to wear masks anymore. Boris has done the same, and (some) of the UK’s emergency powers are going to expire soon.
It seems like Covid is over, and the good guys won, right?
Well, not exactly.
The pandemic narrative may be fading away, but certainly not without a trace. Covid might be dying, but vaccine passports are still very much alive.
This week, while the eyes of the world are fixed on Ukraine and the next wave of propaganda, the World Health Organization is launching an initiative to create a “trust network” on vaccination and international travel.
According to a report in Politico published last week:
WHO making moves on international vaccine ‘passport’”
The article quotes Brian Anderson, co-founder of the Vaccination Credential Initiative, which describes itself as:
a voluntary coalition of public and private organizations committed to empowering individuals with access to verifiable clinical information including a trustworthy and verifiable copy of their vaccination records in digital or paper form using open, interoperable standards.
They are, to take the PR agency sheen off this phrase, a corporate/government joint project researching and promoting digital medical identification papers.
In short, vaccine passports.
The VCI has existed since January 2021, and its list of “members” is very revealing, including Google, Amazon, dozens of insurance companies, hospitals, “bio-security firms” and seemingly every major university in the US.
It’s run by a steering committee made up of representatives from Apple, Microsoft, the MAYO Clinic and the MITRE Corporation, a multi-billion-dollar government-funded research organization.
Anderson – who was an employee of MITRE before founding the VCI – tells Politico that the current system of international travel and vaccine records is:
piecemeal, not coordinated and done nation to nation… It can be a real challenge.”
Discussion of an international “Pandemic Treaty” gets underway today in Geneva, and any eventual agreement will doubtless include provisions on the matter of international vaccine certification.
If the VCI is involved – and with their backers, they doubtless will be – any international system will likely be based on their SMART Health Cards system.
SMART CARDS IN THE US – A COVERT FEDERAL VACCINE PASSPORT
VCI’s SMART Health Cards are the dominant tech in the emerging field of biosurveillance and “inoculation certification”. They are already implemented by 25 different US states, plus Puerto Rico and DC, and have become the US’s de-facto national passport
According to this article from Forbes (a puff piece which is little more than an advertisement):
While the United States government has not issued a federal digital vaccine pass, a national standard has nevertheless emerged.
They use the word “emerged” as if it’s a natural, organic process. But it’s not.
The US government, unlike many European countries, has not issued their own official vaccine passport, knowing such a move would rankle with the more Libertarian-leaning US public, not to mention get tangled in the question of state vs federal law.
The SMART cards allow them to sidestep this issue. They are technically only implemented by each state individually via agreements with VCI, which is technically a private entity.
However, since the SMART cards are indirectly funded by the US government, their implementation across every state makes them a national standard in all but name.
The Politico article repeats the claim the US has no national system, adding that the US doesn’t have a federal vaccine database either:
The Biden administration has said it wouldn’t issue digital credentials and hasn’t rolled out standards for vaccine credentials it said it would issue. Complicating the situation is that the U.S. doesn’t have a national inoculation database.
The propaganda message here is underlining what the government doesn’t have and doesn’t know. The suggestion being that the SMART system is totally separate from the government, that it’s a private company that would never share your medical records with the state.
But only the terminally naive would believe that.
SMART Health Cards are run by VCI, which was created by the MITRE Corporation, which is funded by the United States government.
If you give SMART access to your medical records, you’d better believe the US government and its agencies will get their hands on them. They might not have their own database, but they would have access to MITRE’s database when and if they needed or wanted it.
And so would Apple, Amazon, Google and Microsoft.
That’s how private-public partnerships work. Symbiosis.
Corporate giants serve as fronts for government programs and, in return, they get a big cut of the profits, bailouts if they’re needed, and regulatory “reforms” that cripple their smaller competitors.
We’ve seen this social media already.
Quasi-monopolies like Facebook and Twitter harvest data for the government and censor anyone they are told to, then they are rewarded with “regulation” that barely hurts them whilst targeting smaller companies such as Gab, Parler or Telegram.
The Smart Health Cards clearly fall into this model.
Microsoft, Google et al. take government money to help create the tech, they then run the program, harvest and store the data, and make it available to the government when they want it.
This allows the federal government to “truthfully” claim not to be implementing a federal passport system, OR keeping a vaccination database, all the while they are sub-contracting tech giants to do it for them.
This system of backdoor government surveillance via corporate veneer is already spreading across the US, and it looks like it will play some part in any future “pandemic treaty” too.
They may have stopped talking about Covid for now, but they got a good chunk of what they wanted out of it.
And if they don’t get the rest of what they want out of the war in Ukraine, they’ll just bring Covid back.
Two weeks ago, BKK ProVita chairman Andreas Schöfbeck caused a small uproar by writing to Germany’s vaccine regulator, the Paul-Ehrlich-Institut, to inquire about the high rate of vaccine side-effects evident from BKK billing data.
Representatives from the Paul-Ehrlich-Institut, including its president, Klaus Cichutek, had agreed to meet with Schöfbeck and other BKK officials about their concerns this afternoon. Schöfbeck’s termination was obviously timed to prevent his participation at that meeting, which will now go forward without him.
This is the behaviour of people who have deep confidence in the safety and effectiveness of our Corona vaccines.
By Mazin Qumsiyeh | Popular Resistance | August 18, 2013
There is no way to say this truth nicely: Politicians lie. That includes Japanese, American, Egyptian, Israeli, and Palestinian politicians! Is there something more common sense than that? Yet, so many citizens around the world believe their own politicians or wistfully acknowledge lies but think it is part of the job needed to run things. They believe even when politicians contradict themselves blatantly. This phenomenon is rather remarkable. It is a dissonance and disconnect from reality that many seem oblivious to. It is very dangerous because it can lead to accepting rationales for going to war. These can be deadly wars that lead to millions of lives lost as happened in what was called World War 1 and WW2. Even when incredible and declassified evidence abound, politicians continue to lie and old mythologies refuse to die. Here are just a few of the countless lies told to us over the past few decades… continue
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