CDC Says Vaccinated May be as Likely to Spread COVID as Unvaxxed, as Reports of Serious Injuries after Vaccines Surge

“The bottom line was that, in contrast to the other variants, vaccinated people, even if they didn’t get sick, got infected and shed virus at similar levels as unvaccinated people who got infected”

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VAERS data released today by the CDC showed a total of 518,770 reports of adverse events from all age groups following COVID vaccines, including 11,940 deaths and 63,102 serious injuries between Dec. 14, 2020 and July 23, 2021.

Data released today by the Centers for Disease Control and Prevention (CDC) showed total reports of serious injuries following COVID vaccination, across all age groups, spiked by 14,717 — to 63,000 — compared with the previous week.

The data comes directly from reports submitted to the Vaccine Adverse Event Reporting System (VAERS), the primary government-funded system for reporting adverse vaccine reactions in the U.S.

Every Friday, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Data released today show that between Dec. 14, 2020 and July 23, 2021, a total of 518,770 total adverse events were reported to VAERS, including 11,940 deaths — an increase of 535 over the previous week. There were 63,102 serious injuries reported during the same time period — up 14,717 compared with the previous week.

From the 7/23/21 Release of VAERS data

Excluding “foreign reports” filed in VAERS, 435,007 adverse events, including 5,612 deaths and 34,890 serious injuries, were reported in the U.S.

In the U.S., 340.4 million COVID vaccine doses had been administered as of July 23. This includes: 137 million doses of Moderna’s vaccine, 189 million doses of Pfizer and 13 million doses of the Johnson & Johnson (J&J) COVID vaccine.

Of the 5,612 U.S. deaths reported as of July 23, 14% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 34% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

This week’s U.S. data for 12- to 17-year-olds show:

  • 15,086 total adverse events, including 909 rated as serious and 16 reported deathsone less than what VAERS showed last week. Two of the nine deaths were suicides.
  • The most recent reported deaths include a 13-year-old boy (VAERS I.D. 1463061) who died after receiving a Moderna vaccine, a 16-year-old boy (VAERS I.D. 1466009) who died after receiving his second dose of Pfizer and a 16-year-old boy (VAERS I.D. 1475434) who died with an enlarged heart six days after receiving his first Pfizer dose.

Other reports include two 13-year-old boys (VAERS I.D. 1406840  and 1431289) who died two days after receiving a Pfizer vaccine, three 15-year-olds (VAERS I.D. 1187918, 1382906 and 1242573), three 16-year-olds (VAERS I.D. 1420630, 1225942 and 1386841) and three 17-year-olds (VAERS I.D. 1199455, 1388042 and 1420762).

This week’s total U.S. VAERS data, from Dec. 14, 2020 to July 23, 2021, for all age groups combined, show:

Internal CDC document reveals vaccinated, even if not sick, can spread virus

 

The CDC now says even those people fully vaccinated for COVID are able to get, and spread, the virus.

According to internal documents obtained by The Washington Post, the CDC said it’s time to “Acknowledge the war has changed.”

The document outlined unpublished data showing fully vaccinated people might spread the Delta variant at the same rate as unvaccinated people, CNN reported.

It concludes the delta variant is “highly contagious, likely to be more severe” and that “breakthrough infections may be as transmissible as unvaccinated cases.”

The Washington Post reported:

“‘I think the central issue is that vaccinated people are probably involved to a substantial extent in the transmission of delta,’ Jeffrey Shaman, a Columbia University epidemiologist, wrote in an email after reviewing the CDC slides.

“‘In some sense, vaccination is now about personal protection — protecting oneself against severe disease. Herd immunity is not relevant as we are seeing plenty of evidence of repeat and breakthrough infections.’”

Since January, people who got infected after vaccination make up an increasing portion of hospitalizations and in-hospital deaths among COVID patients, according to the CDC documents. That trend coincides with the spread of the Delta variant.

The Post also reported today on a CDC study revealing three-fourths of people infected in a Massachusetts COVID outbreak were vaccinated. The report bolsters the hypothesis that vaccinated people can spread the more transmissible variant, and may be a factor in the summer surge of infections.

The data, detailed in the CDC’s Morbidity and Mortality Weekly Report, provided key evidence that convinced agency scientists to reverse recommendations on mask-wearing and advise that vaccinated individuals wear masks in indoor public settings in some circumstances, The Post reported.

Thus far, researchers have focused on viral load — a term for how much of the virus is present in infected peoples’ bodies — which can affect transmissibility and severity. Infections with the Delta variant lead to higher levels of virus in the body, even in breakthrough cases in fully vaccinated individuals, the document said.

If vaccinated people get infected anyway, they have as much virus in their bodies as unvaccinated people — that means they’re as likely to infect someone else as unvaccinated people who get infected, CNN reported.

“The bottom line was that, in contrast to the other variants, vaccinated people, even if they didn’t get sick, got infected and shed virus at similar levels as unvaccinated people who got infected,” Dr. Walter Orenstein, who heads the Emory Vaccine Center and who viewed the documents, told CNN.

The CDC is scheduled to publish more data today.

Biden says federal workers must get vaccinated or submit to regular testing — postal union, others push back

President Biden on Thursday announced all civilian federal employees will be required to show proof of vaccination against COVID or be forced to submit to regular COVID testing, wear masks and socially distance.

Biden also called on state and local governments to use COVID relief funds to give $100 to residents who get vaccinated. In a statement released by the White House, the administration said the new rules were issued because of the Delta COVID variant, and because unvaccinated people present a problem to themselves, their families and co-workers.

“Every federal government employee will be asked to attest to their vaccination status.  Anyone who does not attest or is not vaccinated will be required to mask no matter where they work; test one or two times a week to see if they have a — they have acquired COVID, socially distance and generally will not be allowed to travel for work,” Biden said.

Biden directed his administration to apply similar standards to all federal contractors. “If you want to do business with the federal government, get your workers vaccinated,” he said.

In one early sign the policy may not go as smoothly as planned, the American Postal Workers Union (APWU) said it opposes the Biden administration’s vaccine mandate as a condition for employment, arguing it isn’t the role of the federal government to mandate vaccines or other testing measures.

“Maintaining the health and safety of our members is of paramount importance,” the APWU said in a statement issued Wednesday. “While the APWU leadership continues to encourage postal workers to voluntarily get vaccinated, it is not the role of the federal government to mandate vaccinations for the employees we represent.”

In advance of Biden’s official announcement, Children’s Health Defense on Thursday issued a statement disagreeing with the new policy.

The statement quoted CHD Chairman Robert F. Kennedy, Jr:

“Coerced medical interventions have been abhorrent to advocates of liberty and human dignity in every age. The fact that these vaccines are shoddily tested, experimental, unapproved and so risky their manufacturers can neither obtain insurance coverage nor indemnify users against grave injuries or death should magnify our ethical revulsion.”

FDA urges Moderna, Pfizer to include thousands more children in clinical trials

Pfizer and Moderna will expand their COVID vaccine clinical trial to include thousands more children prior to seeking EUA, after the U.S. Food and Drug Administration (FDA) told the vaccine makers the size and scope of their pediatric studies, as initially envisioned, were inadequate to detect rare side effects.

The rare side effects cited by the FDA included myocarditis, an inflammation of the heart muscle, and pericarditis, inflammation of the lining around the heart, multiple people familiar with the trials told The New York Times.

Expanding the pediatric trials means thousands more children as young as 6 months old may soon be recruited and enrolled in COVID vaccine trials. According to the Times, the FDA asked the companies to include 3,000 children in the 5- to 11-year-old group, the group for whom results were expected first.

Moderna’s shot is authorized for emergency use in people 18 and up, and Pfizer’s vaccine is authorized for children as young as 12. No COVID vaccines have yet received EUA approval for children younger than 12.

America’s Frontline Doctors sue UC over vaccine mandates

With supporting declarations from top medical experts and students, America’s Frontline Doctors(AFLDS) filed a civil rights lawsuit in Federal Court against the University of California (UC), targeting the university system’s plan to mandate COVID vaccination for all students regardless of natural immunity.

As The Defender reported July 28, AFLDS, students and even the UC’s own top doctors, are criticizing the rushed mandate as arbitrary, unscientific and medically unnecessary.

Attorneys for the plaintiffs in this civil rights case cite the 14th Amendment to the U.S. Constitution’s protection of bodily integrity, as well as two California civil rights statutes (Cal. Civ. Code sec. 51, Cal. Gov. Code sec. 11135) that prohibit discrimination on the basis of medical or genetic status.

Accordingly, AFLDS is requesting an injunction to restrain the UC from utilizing coercion and segregation of naturally-immune and unvaccinated people in violation of Federal and State law.

The primary target of the lawsuit is the UC’s unscientific one-size-fits-all vaccine mandate where the UC rejects scientifically accepted prescreening for natural immunity.

The CDC, NIH pull in millions from licensing deals, including COVID-related technologies

Aggregated data for fiscal year 2020 show the National Institutes of Health (NIH) and CDC collected a combined $63.4 million in royalty revenues under a business model that allows the NIH to grant technology licenses to the private sector.

As The Defender reported earlier this week, with 27 different institutes and centers housed under the NIH umbrella — including the National Institute of Allergy and Infectious Diseases (NIAID) — NIH is the largest biomedical research agency in the world with an annual budget of nearly $42 billion.

Within NIH, the Office of Technology Transfer plays a “strategic role” in supporting patenting and licensing for inventions that emerge from laboratories at the NIH and CDC. In a win-win business model, the NIH routinely grants technology licenses to the private sector for use or commercialization of its inventions, with those licenses then driving billions of dollars in royalties back to the NIH.

In fiscal year 2020 alone — October 2019 through September 2020 — aggregated data for NIH and CDC show the agencies collected $63.4 million in royalty revenues.

Where public health agencies are concerned, COVID appears to be very good for business, with a flurry of unprecedented funding — conveniently mobilized by the pandemic — ushering in profound and likely permanent changes in a public health infrastructure once lamented as weak and fragmented.

As The Defender reported this week, Pfizer now projects $33 billion in COVID vaccine revenues, a sharp increase over earlier projections. The vaccine maker anticipates booster shots, a vaccine designed for the Delta variant and pending authorization of COVID vaccines for children will drive sales even higher next year.

144 days and counting, CDC ignores The Defender’s inquiries

According to the CDC website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”

On March 8, The Defender contacted the CDC with a written list of questions about reported deaths and injuries related to COVID vaccines. We have made repeated attempts, by phone and email, to obtain a response to our questions.

Despite multiple phone and email communications with several people at the CDC, and despite being told that our request was in the system and that someone would respond, we have not yet received answers to any of the questions we submitted. It has been 144 days since we sent our first email to the CDC requesting information.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

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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.

Featured image is from CHD

NOTE FROM Expanding Awareness Relations:

NECESSARY QUESTIONS TO REFLECT ON:

“If vaccinated people get infected anyway, they have as much virus in their bodies as unvaccinated people — that means they’re as likely to infect someone else as unvaccinated people who get infected”

– So why the incessant continual push to get people vaccinated who are willing to risk the virus symptoms? Instead of just dealing with potential symptoms of COVID, the vaccinated individuals are under the risk of NOT ONLY COVID, but ALSO the possibility of DANGEROUS SIDE EFFECTS from the vaccine. Why can’t individuals make the decision to only risk the COVID infection? Especially since there are BENEFICIAL TREATMENTS to help cure COVID (that is, unironically, being attacked on mainstream media/big tech platforms)? Not to mention that the CDC studies are showing that the vaccine MAY only reduce symptoms in the individual vaccinated – without any benefit to not spreading the virus?

And even if the report from the CDC turns out to be incorrect, do we still want to leave our health in the hands of corporations/organizations who have proven to be not only inept at every single guideline they have initiated during this “pandemic”, but also the numerous times they have flip-flopped, backtracked, retracted, reversed, changed their mind, etc. on their incorrect assessment of the situation, but who is also implementing growing endorsement for an experimental vaccine that has not yet been tested for genuine safety and efficacy? (And on that matter, according to the alarmingly increasing numbers of adverse events reported to VAERS, these vaccines are proving undoubtedly that they are NOT SAFE AND EFFECTIVE.)

Science does not change. And with their (the government health agencies) ever-pervasive push on others to “trust the science”, yet show incredible incompetence as the “experts”, while at the same time denouncing thousands of doctors who HAVE BEEN CORRECT in their conclusions of this COVID/vaccine narrative, I’d say their roles in offering their “expertise” needs to be revoked and more attention needs to be focused on the TRUTHFUL doctors who are giving us more accurate statements than the NIH, CDC, NIAID, WHO, UN, etc.

Of course, in an honest world, this would happen. As it is, the world is seeing a corruption/collusion of unprecedented proportion, that is slowly but surely jolting multiple people awake, yet unfortunately not nearly enough. But the more of us that recognize this deception and who are spreading this awareness will eventually reach those who have remained in the dark, even if it may seem like a fruitless endeavor, and we can continue to make informed decisions while helping others break out of this manipulative system.

CDC, FDA Prepare Mass Distribution of a Merck/Sanofi Six-in-One Vaccine for Kids, Turning Blind Eye to Safety Signals

Egregious oversteps endangering children’s lives.

All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version).

Visit and follow us on Instagram at @crg_globalresearch.

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The FDA approved Vaxelis in late 2018, but only now is the shot being readied for widespread distribution — in Europe, where infants have been given six-in-one vaccines for years (including Vaxelis since 2016), the vaccines have been associated with reports of sudden infant death.

Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled. When parents express reluctance about turning their little ones into perpetual pin cushions, drug makers and doctors have a ready answer — combination vaccines that “simplify” the schedule by decreasing the number of injections administered.

This month marks the U.S. launch of the Merck/Sanofi joint-venture vaccine, Vaxelis, a six-in-one (hexavalent) combination vaccine that contains diphtheria, tetanus and acellular pertussis (DTaP) components as well as components said to protect against polio, Haemophilus influenzae type b (Hib) and hepatitis B.

Public health officials optimistically believe that bundling all of these components into one shot will help close noncompliance loopholes and increase the likelihood that children will complete “all recommended vaccinations.”

Though Vaxelis is the nation’s first hexavalent injection, it joins other four- or five-in-one vaccines already on the CDC schedule. The U.S. Food and Drug Administration (FDA) approved Vaxelis in late 2018 — as a three-dose series for 2-, 4- and 6-month-old infants — but it is only now, two-and-a-half years later, that the shot is being readied for widespread distribution.

Warning signs were ignored

There are numerous warning signs that potent all-in-one vaccines are too much for immature immune systems to handle. Concerning safety signals have emerged not just for hexavalent but also pentavalent (five-in-one) vaccines.

In Europe, where infants have been given hexavalent vaccines for some years (including Vaxelis since 2016), the formulations have produced many troubling reports of sudden infant death.

Absurdly, none of the clinical studies assessing Vaxelis safety and efficacy conducted fair comparisons against an inert placebo. Instead, in the two U.S. clinical trials for Vaxelis, not only did investigators compare infants receiving Vaxelis to babies who received Sanofi’s five-in-one Pentacel — but babies in both groups also received rotavirus and pneumococcal vaccines at the same time!

In this context, the CDC’s sales pitch to the public — and its claims that side effects are “usually mild” — cannot be considered credible.

Here are some of the other facts missing from the CDC’s communications:

  • In the two U.S. trials six infants died (slide #27) in the Vaxelis group (some after receiving just one dose); one infant also died in the “control” group that received five-in-one vaccines.
  • All six Vaxelis recipients died within six weeks of vaccination. This timing matches other published accounts of infant deaths “clustering” following hexavalent vaccination.
  • The reported causes of death for the infants who received Vaxelis included asphyxia, sepsis, fluid in the brain and sudden infant death syndrome (SIDS). These outcomes correspond to the types of adverse events reported following hexavalent vaccination in Europe.
  • Package inserts for other vaccines on the CDC schedule list similar causes of death, suggesting these fatal Vaxelis outcomes are plausibly associated with vaccination.
  • In the clinical trials, the rate of fever was notably higher in Vaxelis recipients even when compared to children receiving five-in-one vaccines (47% vs. 34%).

Juicing vaccine sales

In the no-liability context enjoyed by vaccine makers in the U.S., combination vaccines are already quite popular. In fact, market watchers and health economists praise the jumbo shots as being a catalyst for positive industry trends and a “key to commercial success.”

 

Thus, financial analysts expect Vaxelis to “garner significant patient share following its [U.S.] launch” — predicting that it will account for almost a third of U.S. DTaP vaccinations by 2028 — or $841 million in annual sales.

These predictions represent good news for Merck and Sanofi, two of the “big four” pharma giants that dominate the childhood vaccine market in the United States. Merck is already doing a booming vaccine business, recently reporting annual sales growth of 14.8% for its pneumococcal vaccine (Pneumovax 23) and 5.4% for its human papillomavirus (HPV) vaccine Gardasil-9.

However, Merck also faces proliferating Gardasil-related lawsuits — including legal actions alleging that the company knew about and ignored life-changing adverse events from the get-go, many of which (when not fatal) have involved autoimmunity and chronic pain. In fact, before the advent of emergency use COVID vaccines (responsible for an alarming escalation of vaccine-related adverse events), Gardasil had had “more side effects reported than all other vaccines combined.”

Sanofi, too, is embroiled in thousands of lawsuits worldwide — notably for its disastrous and sometimes fatal dengue vaccine. As with Merck, this has not dampened overall vaccine sales growth, which continues its strong upward trajectory, likely to be further strengthened by the U.S. Vaxelis rollout.

Although Sanofi has not been a front-runner in the COVID vaccine race, the company is currently running clinical trials for messenger RNA (mRNA) vaccines for both COVID and seasonal influenza.

Aluminum secrecy and grandfathered ingredients

Merck’s proprietary, “super-powered” aluminum adjuvant — amorphous aluminum hydroxyphosphate sulfate (AAHS) — which is believed to play a significant role in Gardasil’s risk profile, is also present in Vaxelis.

After Merck developed AAHS, it began to “preferentially” feature AAHS in its vaccines even though, as Danish scientists outlined last year, the company appears to have disregarded procedures ordinarily required for approval of new adjuvants.

According to the Danes, at the time AAHS appeared, it represented a “new type of aluminium adjuvant with excipients that [had] not been used earlier in [European Medicines Agency] authorised vaccines.” It should have been — but apparently was not — tested against an inert placebo. For this and other reasons, the Danish scientists question the ethical underpinnings of the Gardasil clinical trials.

In noting that Merck also “seems to have prevented independent studies of AAHS,” the Danes repeated a critique aired by world-famous aluminum expert Christopher Exley in 2018. In an extensive discussion of different aluminum-based adjuvants and their immunological mechanisms of action, Exley and co-authors emphasized the importance of studying aluminum adjuvants one by one, as each is “chemically and biologically dissimilar with concomitantly potentially distinct roles in vaccine-related adverse events.”

Concerningly, the Vaxelis liquid suspension is adjuvanted onto not just AAHS, but also another aluminum adjuvant — aluminum phosphate). The package insert disingenuously shorthands the combination of adjuvants as “aluminum salts.”

How this double whammy of aluminum (319 micrograms per vaccine dose) interacts with the vaccine’s six antigens, or Vaxelis’s numerous other ingredients, or the heavy aluminum load in other childhood vaccines is largely unknown.

According to the Vaxelis package insert, the vaccine also includes: polysorbate 80 (an ingredient flagged for its propensity to induce hypersensitivity reactions); glutaraldehyde and formaldehyde (problematic chemicals deemed necessary to inactivate pertussis toxin); bovine serum albumin (often harvested from bovine fetuses when female cows are found to be pregnant at slaughter); three different antibiotics (neomycin, streptomycin and polymyxin B); ammonium thiocyanate (also a rust inhibitor, weedkiller and defoliant); and yeast protein (associated, notably in hepatitis B vaccines, with autoimmune reactions).

Regulatory loopholes allow manufacturers to “grandfather” ingredients into new vaccines if the components are already present in other licensed vaccines — regardless of how inadequate the original safety testing may have been.

Thus, Merck and Sanofi perceived no need to test Vaxelis for DNA-damaging or cancer-causing effects, and conducted no studies of the ingredients’ pharmokinetics (i.e., how the substances move “into, through, and out of the body”).

The main cautionary note sounded in the meager Vaxelis patient information sheet is to not give Vaxelis to children if they are “allergic to any of the ingredients.”

For thee and thee … but not for me?

The CDC seems to be particularly interested in ensuring that poor and non-white children get Vaxelis. The agency began laying the groundwork to offer Vaxelis through the Vaccines for Children (VFC) Program — the agency’s vaccine program for the poor — over two years ago, in March 2019.

In September of that year, the CDC followed up with an affirmative vote. Public health departments have been promoting Vaxelis to participating VFC providers since early June 2021.

At its September 2019 meeting, CDC outlined another topic deemed important for discussion in the near future — raising the issue of whether Vaxelis should be “preferentially recommended” for the American Indian/Alaskan Native (AI/AN) pediatric population.

The tenuous rationale, according to the meeting notes, was because, “in the pre-vaccine era” (more than 35 years ago), “Hib disease occurred at a younger age among the AI/AN population compared to the general population.”

Wave of the future?

Judging from its website, the CDC perceives combination vaccines to be the wave of the future, and has signaled its strong endorsement of Vaxelis by incorporating the new vaccine into its 2021 vaccine schedule.

As if exposure to six antigens were not enough, FDA and CDC also say it is okay for healthcare providers to administer the six-in-one shot at the same time as other vaccines.

These agencies’ characterization of the Vaxelis safety profile as “acceptable” indicates they have either not done their due diligence, or are willing to accept a high level of collateral damage in exchange for the “convenience” of six-in-one shots.

However, as the “overwhelmed by guilt” parents of COVID-vaccine-injured teens are increasingly finding out, convenience is poor consolation for life-changing or life-threatening adverse outcomes.

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