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COVID-19 VACCINES
Research Compiled by Cecile Petra,
concerned citizen, Salt Spring Island, BC
December 2020

The United Kingdom recently began rolling out the Pfizer Covid-19 vaccine after less than a year of study. Several other countries will be doing the same, and on December 9^th Canada also approved the Pfizer vaccine. Other vaccine manufacturers such as Moderna and Astra Zeneca are waiting in the wings for approval as well.

Doctors, scientists, and lawyers are speaking out about these rushed vaccines for many reasons:

•  In the 70 years that coronaviruses have been around, there has been no coronavirus vaccine successfully brought to market
•  There has never been a licensed mRNA vaccine
•  It usually takes several years to bring a vaccine to market re: safety testing
  
•  The Covid-19 vaccine trials have not been completed and full disclosure of findings/protocols/ingredients has not been freely given except recently, under legal duress, to one citizen action group (ICAN)
•  There is obviously no data on the long term effects
•  There are serious concerns with some of the known ingredients
•  The rt-PCR test upon which the efficacy data is based seriously flaws the results/interpretations of the studies

 

The UK government is expecting so many adverse responses that they tendered this urgent notice for AI software development support to track the “expected high volume of adverse reactions”: https://ted.europa.eu/udl?uri=TED%3ANOTICE%3A506291-2020%3ATEXT%3AEN%3AHTML&src=0

Two healthcare workers in the UK who received the vaccine this in early December had suffered anaphylactic shock after the vaccine. The next day the UK National Health Service (NHS) issued a warning that all vaccination centers needed to have resuscitation equipment on hand and that no one with a history of allergies should get the vaccine.

https://www.theguardian.com/world/2020/dec/09/pfizer-covid-vaccine-nhs-extreme-allergy-sufferers-regulators-reaction

On December 8^th, the US Food and Drug Administration (FDA) revealed that 6 people in the Pfizer vaccine trials died and 4 suffered Guillain-Barre Syndrome (a type of paralysis). https://www.fda.gov/media/144245/download

The NHS website page, “Information for Healthcare Professionals”, makes these preliminary warnings regarding the Pfizer vaccine, none of which have been reported by the mainstream media:

“4.6 Fertility, pregnancy and lactation Pregnancy: There are no or limited amount of data from the use of COVID-19 mRNA Vaccine BNT162b2. Animal reproductive toxicity studies have not been completed. COVID-19 mRNA Vaccine BNT162b2 is not recommended during pregnancy. For women of childbearing age, pregnancy should be excluded before vaccination. In addition, women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose. 6 Breast-feeding: It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk. A risk to the newborns/infants cannot be excluded. COVID-19 mRNA Vaccine BNT162b2 should not be used during breast-feeding. Fertility: It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility"

https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/941452/Information_for_healthcare_professionals.pdf

Apart of 30 mg of mRNA per dose, two of the ingredients are:

•  ALC-0315 = (4-hydroxybutyl) azanediyl)bis (hexane-6,1-diyl)bis(2-hexyldecanoate)
•  ALC-0159 = 2-[(polyethylene glycol)-2000]-N,N-ditetradecylacetamide
  

ALC-0315 is a hexane containing compound and these are known to be potentially neurotoxic. https://pubmed.ncbi.nlm.nih.gov/7251182/ Further, 4-hydroxybutyl, which is a component of ALC-0315, contains hydroquinone which is known to have chromosomal impacts when injected https://pubmed.ncbi.nlm.nih.gov/10379810

ALC-0159 contains polyethylene glycol (PEG) that is associated with hypersensitivity and allergenic reactions, including anaphylaxis. https://aacijournal.biomedcentral.com/articles/10.1186/s13223-016-0172-7

https://childrenshealthdefense.org/news/a-dangerous-inactive-ingredient/

The mRNA delivery system itself cannot be determined because neither have the concentrations been declared, nor has the nanoparticle delivery system, surface charges and other physiochemical characteristics been declared – these may dramatically increase the toxicological profile https://www.intechopen.com/books/recent-advances-in-novel-drug-carrier-systems/nanoparticles-toxicity-and-their-routes-of-exposures

A major concern for mRNA vaccines (Moderna and Pfizer) is the risk of ADE: “This is called Antibody Dependent Enhancement (ADE), and is a common problem with Dengue Virus, Ebola Virus, HIV, RSV, and the family of coronaviruses. In fact, this problem of ADE is a major reason why many previous vaccine trials for other coronaviruses failed. Major safety concerns were observed in animal models. If ADE occurs in an individual, their response to the virus can be worse than their response if they had never developed an antibody in the first place. This can cause a hyperinflammatory response, a cytokine storm, and a generally dysregulation of the immune system that allows the virus to cause more damage to our lungs and other organs of our body.”

(All of the previous coronavirus vaccine studies on animals (monkeys, mice, ferrets) showed that when they were exposed to the wild virus after vaccination, they developed ADE and died.)

Further, “Several vaccine candidates are expected to induce the formation of humoral antibodies against spike proteins of SARS-CoV-2. Syncytin-1 (see Gallaher, B., “Response to nCoV2019 Against Backdrop of Endogenous Retroviruses” - http://virological.org/t/response-to-ncov2019- against-backdrop-of-endogenous-retroviruses/396), which is derived from human endogenous retroviruses (HERV) and is responsible for the development of a placenta in mammals and humans and is therefore an essential prerequisite for a successful pregnancy, is also found in homologous form in the spike proteins of SARS viruses. There is no indication whether antibodies against spike proteins of SARS viruses would also act like anti-Syncytin-1 antibodies. However, if this were to be the case this would then also prevent the formation of a placenta which would result in vaccinated women essentially becoming infertile. To my knowledge, Pfizer/BioNTech has yet to release any samples of written materials provided to patients, so it is unclear what, if any, information regarding (potential) fertility-specific risks caused by antibodies is included.”[1]

A little more digging shows that Synctin-1 is also present in male sperm, so what does the mean for male fertility? https://www.researchgate.net/publication/261257414_Syncytin-1_and_its_receptor_is_present_in_human_gametes

The US FDA Safety Surveillance of Covid-19 vaccines lists the possible adverse event outcomes: https://www.fda.gov/media/143557/download

•  Guillain-Barre Syndrome
•  Acute disseminated encephalomyelitis (brain inflammation)
• Transverse myelitis (essentially a type of polio: https://pubmed.ncbi.nlm.nih.gov/16630313/)
•  Encephalitis/myelitis/encophalomyelitis/meningoencephalitis/meningitis
  
•  Convulsions/seizures
•  Stroke
•  Narcolepsy and cataplexy
  
•  Anaphylaxis
  
•  Acute myocardial infarction (heart attack)
•  Myocarditis/pericarditis (inflammation of the heart and membranes)
•  Autoimmune disease (this may not be seen until months/years down the road)
•  Deaths
  
•  Pregnancy and birth “outcomes” (guess what outcomes means)
•  Other acute demyelinating diseases
•  Non-anaphylactic allergic reactions
•  Thrombocytopenia
•  Disseminated intravascular coagulation
•  Venous thromboembolism
•  Arthritis and arthralgia/joint pain
•  Kawasaki disease
•  Multisystem Inflammatory Syndrome in Children
  
•  Vaccine Enhanced Disease

It should be noted that vaccine manufacturers, and those that administer them are immune (pun not intended) from liability – i.e. there are laws in most countries that prevent them from being sued for injury.

Regarding the Moderna vaccine there are other serious concerns:

· The experimental design included a non-inert placebo in the control group (AstraZeneca’s “placebo” for the control group was in fact the meningitis vaccine, with at least one death in this control group – the meningitis vaccine having this potential risk already well documented)

·  The stated “efficacy” of the vaccine of “94%” is actually based on a very small portion of the 30,000-person study – 196 people to be exact, in both the control and experimental groups. Think about it: 196 people to base a vaccine efficacy on that will be given to billions of people, and the rt-PCR testing for that group of 196 is highly inaccurate to begin with.[2]

· The study was not designed to determine if the vaccine reduces transmissibility of Covid-19, or serious symptoms or hospitalization rate, only a reduction of “mild symptoms”

· Moderna has never successfully brought a vaccine to market to this point and there has never been a commercial product utilizing mRNA technology approved for use [3]

The concerns with these vaccines are so great that there is currently a petition before the UK government to immediately stop the vaccine trials and upcoming program for dissemination. One of the petitioner writers is Dr. Michael Yeadon, a former head respiratory researcher with Pzifer itself.

https://dryburgh.com/wpcontent/uploads/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_signed_with_Exhibits_geschwarzt.pdf

There is another petition put forth to the US FDA to stay the vaccine trials/dissemination by pathologist Dr.  Sing Hang Lee, director of Milford Molecular Diagnostics Laboratory, for reasons to do with the vaccine trial testing flaws which profoundly put into question the validity of the trial findings. “Until an accurate count of Covid-19 cases in the vaccinated and placebo groups has been determined for vaccine efficacy evaluation, we are asking the FDA to stay its decision regarding the emergency use authorization for this vaccine,” said Dr. Lee.

https://vaccineimpact.com/wp-content/uploads/sites/5/2020/11/Stay-Pfizer-vaccine-phase-3-trial.pdf

And yet another Stay of Action put forth to the FDA by the Informed Consent Action Network: https://www.icandecide.org/wp-content/uploads/2020/11/Stay-of-Efficacy-Petition_FINAL.pdf

As an additional note, pharmaceutical companies have been fined BILLIONS of dollars for fraud and corruption. Stats on Pfizer alone since 2000: $4.7 billion for false claims acts, off-label or unapproved promotion, foreign corrupt practices, with $103 million for drug/medical equipment safety violations, and $34 million for kickbacks and bribery.

If a producer of herbal or homeopathic health products had ANY of the above safety issues or corruption history, would you consume their products? Why are governments promoting these scandalous products and foisting them upon their citizens, including mobilization of the military to help with deployment?

I am profoundly concerned for my fellow Canadians, and the citizens of the world, who now have to contend with a poorly tested vaccine being mass distributed, at enormous cost, with potentially severe/life-altering consequences, possibly mandatory/forced, and no legal recourse in the case of harm.

I URGE PEOPLE TO DO THEIR HOMEWORK (beyond the mainstream narrative)

Stay informed, take action:

https://vaccinechoicecanada.com/

https://www.nvic.org

https://www.icandecide.org

https://childrenshealthdefense.org/defender_category/covid/

FOOTNOTES:

[1] https://dryburgh.com/wpcontent/uploads/2020/12/Wodarg_Yeadon_EMA_Petition_Pfizer_Trial_FINAL_01DEC2020_signed_with_Exhibits_geschwarzt.pdf [2] https://vaccineimpact.com/wp-content/uploads/sites/5/2020/11/Stay-Pfizer-vaccine-phase-3-trial.pdf 
[3] https://investors.modernatx.com/news-releases/news-release-details/moderna-provides-updates-clinical-development-and-production-its    

Compiled by Cecile Petra, concerned citizen, Salt Spring Island, BC, cecile.petra@protonmail.com]

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