top of page

Covid-19 Vaccine Ingredient Spotlight: Polyethylene Glycol, VAERS Injury Reports Near 600,000

Updated: Aug 20, 2021

Up to 72% of population have medical contraindication for receipt of Moderna & Pfizer Covid-19 Vaccination with antibody presence for chemical ingredient in vaccinations, PEG

In this Post

Headlines, VAERS data review, & spotlight on PEG, ingredient in Pfizer and Moderna mRNA Covid-19 inoculations.


FDA Seeking to Give Pfizer Covid-19 Vaccine Full Approval By Monday.

FDA approval without proper trials and duration are act to bypass emergency use restrictions, and do not indicate actual safety or efficacy of product.

Moderna, Higher Risk for Myocarditis Than Previously Thought:

"There might be a 2.5 times higher incidence of myocarditis in those who get the Moderna vaccine compared with Pfizer's vaccine, the Post quoted a source as saying".

Israel comprehensive study found risk of of development of heart inflammation for men under 30 up to 1 in 3,000 with mRAN vaccines (Pfizer & Moderna are both mRNA based therapy inoculations approved for symptom suppression of Covid-19 attributed viruses).

Young populations are at virtually risk from Covid-19 attributed infection as documented in source links HERE.

This is another example of why statement of safety based on lack of evidence are not valid parameter for ascertaining safety risk. New side effects and warning have been identified monthly on all vaccinations. Any FDA approval without mid or long term safety data has no scientific validity in advising on true risks, without adequate duration study, risks can not be known.

Another FDA Recall Warning of Potential Serious Injury and Death with Use of Certain Breathing Devices - 2 million recalled (responsible for ventilator equipment shortage being misattributed in the media to Covid-19)

"The polyester-based polyurethane (PE-PUR) sound abatement foam, which is used to reduce sound and vibration in these affected devices, may break down and potentially enter the device’s air pathway. If this occurs, black debris from the foam or certain chemicals released into the device’s air pathway may be inhaled or swallowed by the person using the device".

Faulty and contaminated medical devices, drugs, and tests have been ongoing issue with tens of millions of Covid-19 tests and devices recalled due to contamination and severe design flaws. Over 270 different Covid-19 devices and kits have been recalled, 8 million in May alone:

Contaminated Covid-19 Tests, Millions Removed from Market, Implicated in India Black Fungal Outbreak

New Video UPDATE: More Vaccine Cases & Verified Injury Stories included in blog here including Ireland national football player dead three days post Pfizer after immediate reaction with severe brain bleed (according to family sources who have spoken publicly on the death). Media continues to cover up stories of injured who have formed groups of tens of thousand to tell censored stories:

Health Minister of Brazil Admits Covid-19 Vaccines Do Not Prevent Severe Outcomes, Reinfection, or Death:

"However, vaccination does not prevent reinfection or progression to more serious conditions, including death. Therefore, the secretary stressed the relevance of maintaining preventive measures against the new coronavirus"

What is the purpose of a vaccine that does not prevent transmission or reduce severe outcomes? Why must the world be mass vaccinated to prevent a Covid-19 attributed mild cold?

Up to 86% of individuals with a positive PCR test for Sars CoV2 present with no core symptoms of Covid 19, & 98% which do present symptomatically, symptoms are mild. Full documentation and source links HERE. 99.96 mortality survival rate.

Headline: Texas considers medical discrimination policy against law and licensing standards to make ICU status contingent upon Covid-19 vaccination status

Media is currently hyping ICU bed shortages which do not exist or driven by existing bed & staff shortages to create illusion of mass Covid-19 crisis. Full documentation and evidence on media ICU false reporting may be viewed HERE. Texas currently retains over 7,000 available beds with over 20,000 full bed capacity. There are currently a little over 15,000 probable or confirmed Covid-19 attributed cases in Texas out of a population of over 29 million people.

Vaccine mandate policy will decrease access to medical care as staff leave or fired from their employment


Nurse Speaks Out Against Vaccine Mandate Threat to US Health Care System


Over 710,000 total injuries and near 600,000 individual injuries, 13,000 deaths reported to VAERS in association with Covid-19 vaccinations with over 17,000 associated permanent disabilities:

***Note: 83% of VAERS Reports are generated from medical providers, state reporting agencies, and pharmaceutical companies. European reporting systems are documenting exponentially higher rates than VAERS data, as the 30 year old monitoring system captures only 1% of post vaccination injuries per Harvard research report. Low capture rate is central issue not credibility. FDA has admitted the mass vaccination program began without adequate safety monitoring system. A recent study from Mass General, Bingham documented anaphylactic reactions post Covid-19 vaccine occurring up to 120x the rate reported to the CDC. This highly suggests the system is continuing to vastly under capture post vaccination adverse events. See here for why VAERS data matters

-There is no mid or long term safety or efficacy data whatsoever on any Covid-19 vaccination, any health professional or public health officials making safety claims on lack of data is in breach of basic medical and scientific ethic, purporting non-evidence based claims as statements of fact.

All initial Covid-19 vaccine research and trial data has been fatally compromised through use of testing methods unsuitable for detection of Sars CoV2, the virus attributed to cause symptoms of Covid-19. Any FDA approval based on flawed trial design and lack of mid and long term study bears no scientific credibility for ascertainment of safety and efficacy of these drugs. Covid-19 vaccination trials measured for mild and NOT severe outcomes (hospitalizations and deaths.

Vaers Data for Week Ending 8/13/2021:

VAERS Adverse Injury and Death Reports for Age Groups 0 to 18:

VAERS Data Pfizer Adverse Events for Week Ending 8/13/2022:

VAERS Data Moderna Adverse Events for Week Ending 8/13/2021:

VAERS Adverse Events Johnson & Johnson (Janssen) Covid-19 vaccination -*note - Janssen severe distribution restriction due to mass contamination issue & government safety pause)

SPOTLIGHT: Polyethylene Glycol, Moderna/Pfizer Covid-19 vaccine ingredient:

Ingredient list (published):

  • Pfizer Vaccine: The full list of ingredients for the Pfizer vaccine is: mRNA, lipids ((4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate), 2 [(polyethylene glycol)-2000]-N,N-ditetradecylacetamide, 1,2-Distearoyl-sn-glycero-3-phosphocholine, and cholesterol), potassium chloride, monobasic potassium phosphate, sodium chloride, dibasic sodium phosphate dihydrate, and sucrose. The Pfizer vaccine does not contain eggs, preservatives, or latex.

  • Moderna Vaccine: The full list of ingredients for the Moderna vaccine is: Messenger ribonucleic acid (mRNA), lipids (SM-102, polyethylene glycol [PEG] 2000 dimyristoyl glycerol [DMG], cholesterol, and 1,2-distearoyl-sn-glycero-3-phosphocholine [DSPC]), tromethamine,tromethamine hydrochloride, acetic acid, sodium acetate trihydrate, and sucrose. The Moderna vaccine does not contain eggs, preservatives, or latex.

No Safe Screening Process in Place to Screen for Potential PEG Anaphylactic Reaction:

Up to 72% of population has antibodies to PEG (i.e. predisposed sensitivity to PEG) due to the presence of PEG in many common personal care products. An estimated 7%have PEG antibody levels which may induce a severe and life threatening anaphylactic reaction, if exposed to PEG.

"PEGs were long thought to be biologically inert, but a growing body of evidence suggests they are not. As much as 72% of people have at least some antibodies against PEGs, according to a 2016 study led by Samuel Lai, a pharmaco-engineer at the University of North Carolina, Chapel Hill, presumably as a result of exposure to cosmetics and pharmaceuticals. About 7% have a level that may be high enough to predispose them to anaphylactic reactions, he found".

Sensitivity to PEG is a CDC contraindication to receiving Pfizer and Moderna vaccinations,

If You Are Allergic to Polyethylene Glycol (PEG) or Polysorbate

PEG and polysorbate are closely related to each other. PEG is an ingredient in the mRNA vaccines, and polysorbate is an ingredient in the J&J/Janssen vaccine.

If you are allergic to PEG, you should not get an mRNA COVID-19 vaccine. Ask your doctor if you can get the J&J/Janssen vaccine.

However, the vast majority of people are not aware they have any antibodies to PEG, and unless they have been specifically tested for allergies, will associate a sensitivity to PEG as due to products containing the chemical. Many common personal care products such as soaps, tooth paste, cosmetics contain PEG.

The CDC has no screening in place for the 72% of individuals with PEG antibodies who should not receive Pfzer & Moderna inoculations containing the chemical. The CDC ONLY screen for those who are aware of the allergy:

CDC Covid-19 Vaccination Screening Form: (CDC question does not ask about allergies to cosmetics, soaps, toothpastes or other personal care products containing PEG)

Additionally, Not only is PEG a “stealth” medicinal additive, delaying blood clearance due to its properties, but it is a stealth allergen, the vast majority of the population never having heard of it and many in the healthcare industry being unaware of its antigenic properties

A physician survey found:

“Although 91% of respondents were aware of antidrug antibodies in general, only 22% were aware of APA (Anti-PEG Antibody) responses. Further, there was limited awareness (35%) of PEG’s inclusion in prescribed PEGylated therapeutics.”

In sum, the FDA approved Moderna & Pfizer vaccinations with a ingredient the MAJORITY of the population has antibody sensitivity and a significant percentage are predisposed to life threatening anaphylactic reactions and the CDC has NO safe screening mechanism in place to filter out the majority of individuals who are unaware of antibody presence which is a contraindication to the vaccines.

Warning labels were placed on Pfizer vaccination months ago in the UK due to this issue:

“Any person with a history of anaphylaxis to a vaccine, medicine or food should not receive the Pfizer BioNTech vaccine,” MHRA Chief Executive June Raine said in a statement.

Anaphylaxis is occurring at rates up to 120x greater than reported to CDC according to a study from Mass General Bingham:

ICAN sent a letter to CDC director

"According to the CDC, “Anaphylaxis after COVID-19 vaccination is rare and occurred in approximately 2 to 5 people per million vaccinated in the United States based on events reported to VAERS.” This is in stark contrast to a recent study at Mass General Brigham that assessed anaphylaxis in a clinical setting after the administration of COVID-19 vaccines and found “severe reactions consistent with anaphylaxis occurred at a rate of 2.47 per 10,000 vaccinations.” This is equivalent to 50 times to 120 times more cases than what VAERS and the CDC are reporting.

The underreporting of anaphylaxis by the CDC and VAERS is particularly troubling because it is mandatory for medical providers to report anaphylaxis after any COVID-19 vaccine to VAERS. See, e.g., In addition, the CDC reports that most of these reactions occur within 30 minutes of vaccination.

Vaccine administrators, then, should be aware of a majority, if not all, of these cases as recipients are being observed for 15 to 30-minute periods at vaccination sites. Additionally, with regard to COVID19 vaccines, there has actually been a push by health authorities to inform medical providers that they need to report anaphylaxis to VAERS. Nonetheless, the rate of reporting still appears to be only around 0.8 to 2 percent of all cases of anaphylaxis. This raises serious concerns regarding (i) under-reporting.

The study from Massachusetts General Hospital may be viewed HERE: (original link dead)

Acute Allergic Reactions to mRNA COVID-19 Vaccines

Additionally, the CDC is allowing the administration of Moderna & Pfizer vaccinations at clinics and pharmacies without recommended intubation equipment required to intervene in event of a severe vaccine reaction, this goes against their own recommendation's for managing anaphylactic events:

"*COVID-19 vaccination locations should have at least 3 doses of epinephrine available at all times, and the ability to quickly obtain additional doses to replace supplies after epinephrine is administered to a patient. People with a history of anaphylaxis who carry an epinephrine autoinjector could be reminded to bring it to their vaccination appointment. Detailed information on storage, handling, administration, and dosage considerations is available in the package inserts for epinephrineexternal icon (e.g., EpiPenexternal icon®). Expired epinephrine or epinephrine that appears to be in unacceptable condition (per the manufacturer’s package inserts) should be replaced."

Health professionals have every right (and duty) to refuse administration of drugs with severe potential for life threatening anaphylactic reaction with no proper safety screening mechanism in place to prevent expected severe reactions.

The Covid-19 vaccinations should never have been approved without a screening process to account for vaccine contradiction INHERENT in 72% of population.

And, why would a drug developer include ingredient with such widespread inherent risk for serious medical complication from the start?

Note on Graphene Oxide in PEG:

A recent controversy has erupted over whether Covid-19 vaccinations contain graphene oxide (a poisonous substance not approved for human use) . Many have written to ask questions about GO in the vaccinations, and this article documents the patents and evidence for concern. This topic is being extensively covered by outside researchers, and this blog fully support efforts to undergo objective review of evidence. Given the extensive research and patents around GO for use in coronavirus vaccination applications which predate 2020, this research is fully warranted. Given the manufacturer's (PEG supplier for Covid-19 vaccinations) involvement in PEG drug delivery applications utilizing Graphene Oxide, a simple company denial is not sufficient reassurance to warrant complete trust in answer. Pharmaceutical companies with a long history of criminal convictions should not just be allowed to wholesale deny claims with reporters acting as stenographers instead of overseers of government and corporate entities. And, media 'fact checkers' who generate majority advertisement dollars from pharmaceutical companies can not be considered non biased sources.

A 2016 study touted the benefit of injecting graphene oxide into humans to stimulate ''robust immunity', use of Graphene Oxide is being actively studied (click individual study authors for more studies utilizing PEG in vaccine components)

Functionalized graphene oxide serves as a novel vaccine nano-adjuvant for robust stimulation of cellular immunity

For reader's interest in learning more, this article provides source links to documents and patents for review, a full independent analysis of all Covid-19 vaccinations should be undergone to allay public fears:

Graphene Oxide: Patents, Research Studies

Covid-19 Vaccines Under Investigation for Known PEG Kidney Complications:

Covid-19 vaccines are now under investigation for inducing kidney problems, a known serious side of effect of injecting Polyethylene Glycol in medications besides Covid-19. Officials stating safety with drugs containing ingredients with known serious side effects are misrepresenting what is already KNOWN about components of the vaccine.

Pfizer, Moderna COVID vaccines face new safety probe in Europe over possible link to skin condition, 2 kidney disorders

Side Effects: (for other products utilizing polyethylene glycol as injection):


Chronic kidney disease patients:

Using methoxy polyethylene glycol-epoetin beta injection may increase the risk that blood clots will form in or move to the legs and lungs. Tell your doctor if you have or have ever had heart disease, a stroke, a deep venous thrombosis (DVT; blood clot in your leg), a pulmonary embolus (PE; blood clot in your lungs), or if you are going to have surgery. Before having any surgery, even dental surgery, tell your doctor or dentist that you are being treated with methoxy polyethylene glycol-epoetin beta injection, especially if you are having coronary artery bypass graft (CABG) surgery or surgery to treat a bone problem. Your doctor may prescribe an anticoagulant ('blood thinner') to prevent clots from forming during surgery. If you are being treated with hemodialysis (treatment to remove waste from the blood when the kidneys are not working), a blood clot may form in your vascular access (place where the hemodialysis tubing connects to your body). Tell your doctor if your vascular access stops working as usual. If you experience any of the following symptoms, call your doctor immediately or get medical help right away: chest pain; difficulty breathing or shortness of breath; pain in your legs with or without swelling; a cool or pale arm or leg; confusion; trouble speaking; sudden weakness or numbness of an arm or leg (especially on one side of the body) or of the face; vision problems; difficulty walking; dizziness; loss of balance or coordination; or fainting. Do NOT Leave Discouraged: Big Update of Videos of Protests and Individuals Standing Up Globally HERE:

Plus checkout the homepage for new video postings (scroll about halfway down for latest Reiner Fuellmich interview).

2,726 views0 comments
bottom of page