Health Friday 2.20.2026 Open Thread: Pfizer-BioNTech COVID-19 modRNA “Vaccine” Negative Effects Proven Ongoing Over Three Years Post-Injection: Part Three

The header image of 1955 vintage Pfizer penicillin bottles is courtesy of Pond5 and Google Images.

Health Friday is a series devoted to information on Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the negative effects and outcomes of the modRNA COVID-19 BIOWEAPON “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have suffered, and/or continue to suffer, injuries, illnesses, or disabilities induced by these “vaccines” that they took; and, to those who have passed away from the negative effects and outcomes induced by these “vaccines” that they took.

There are Important Notifications by our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: If there is AI-generated content in today’s offering, it will be labeled as such. If readers wish to post AI-generated content in today’s discussion thread, they must cite their source. Thank you.

Today’s offering is Part Three of three. The previous two parts of this series are here: https://www.theqtree.com/2026/02/06/health-friday-2-6-2026-open-thread-pfizer-biontech-covid-19-modrna-vaccine-negative-effects-proven-ongoing-over-three-years-post-injection-part-one/; and, https://www.theqtree.com/2026/02/13/health-friday-2-13-2026-open-thread-pfizer-biontech-covid-19-modrna-vaccine-negative-effects-proven-ongoing-over-three-years-post-injection-part-two/.

The Hulscher, McCullough, et al., paper that is the basis for this series is here: https://zenodo.org/records/18460099. “Unprecedented Persistence of Vaccine mRNA, Plasmid DNA, Spike Protein, and Genomic Dysregulation Over 3.5 Years Post-COVID-19 mRNA Vaccination.” Nicolas Hulscher, MPH, Peter A. McCullough, MD, MPH, et al. 2 February 2026.

Today’s offering will discuss the findings of ongoing heart / cardiovascular damage induced by the Pfizer-BioNTech COVID-19 modRNA “vaccine”, BNT162b2, in the patient described in the above-cited paper. Below, from the paper, are screenshots of sections that discuss the heart and cardiovascular damage that was found in the patient well after he took this “vaccine”:

The results of the patient’s home-administered cardiac readout tests:

As can be seen, the evidence of irregular heart rhythm are unmistakable. However, refer to the text above — the symptoms were apparently dismissed as “unlikely” for myocarditis / pericarditis, even though Emergency Room visit records when the patient presented there appear to show otherwise.

Continuing, from the paper:

Finally, a cardiac MRI was performed, which confirmed symptoms “consistent with COVID-19 vaccine-induced myocarditis…”; see below, a reduced image from the paper:

The following are several scientific papers and articles. The first one is the 1992 paper by Dr. Ralph Baric, PhD, of the results of his experiments to induce myocarditis and Congestive Heart Failure (CHF) in rabbits that he injected with a rabbit coronavirus (https://academic.oup.com/jid/article/165/1/134/986090. “An Experimental Model for Myocarditis and Congestive Heart Failure after Rabbit Coronavirus Infection.” Ralph S. Baric, et al. January 1992.) Please see the screenshots from this paper, below. First, the general summary:

Followed by two portions from the Discussion section. “RbCV” = rabbit coronavirus.

Following is a look at Reference paper number 17, cited several times in the Baric, et al., paper above. Reference paper number 17 is found here: https://pmc.ncbi.nlm.nih.gov/articles/PMC2042305/. “Rabbit cardiomyopathy associated with a virus antigenetically related to human coronavirus strain 229E.” Small, JD, Aurelian, L., Squire, R.A., et al. June 1979. The following screenshots are from this paper. First, the general summary:

Then, from the Discussion section:

Note the mention of human coronavirus 229E and its potential for “cross-reactivity” with other coronaviruses, including gastroenteritis in swine. Recall that Dr. Ralph Baric, PhD, invented the “No See-m’s” method for “seamless assembly” of chimeric (lab-created) virus code pieces using the TGEV virus (swine transmissible gastroenteritis virus) model back in 2000 (https://journals.asm.org/doi/10.1128/jvi.74.22.10600-10611.2000. “A strategy for the assembly of large RNA and DNA genomes: the transmissible gastroenteritis virus model.” Ralph Baric, et al. 2000.)

Dr. Joseph Sansone, PhD, a psychotherapist in Florida, speaks to the COVID-19 modRNA “vaccines” causing heart disease, immune system conditions, and more, here: https://usawatchdog.com/world-ignoring-disaster-of-cv19-bioweapon-vax-dr-joe-sansone/, 8 February 2026. Dr. Sansone links to the Hulscher, McCullough, et al., article cited above in today’s offering. Please see the screenshot below, from this article:

There is an earlier article discussing heart damage — at the mitochondrial level — that is induced by the COVID-19 “vaccines”, at The Focal Points, here: https://www.thefocalpoints.com/p/spike-protein-exhausts-cardiomyocyte, “Spike Protein Exhausts Cardiomyocyte Mitochondria”, 8 September 2024. The paper referred to in this article is here: https://doi.org/10.3390/cells12060877. “Spike Protein Impairs Mitochondrial Function in Human Cardiomyocytes: Mechanisms Underlying Cardiac Injury in COVID-19.” Tin Van Huynh, et al. 11 March 2023.

Yours Truly believes that the Hulscher, McCullough, et al., February 2026 paper cited in today’s offering is of incalculable importance. This paper proves that these negative effects and outcomes in “vaccinated” persons can be found more than three years post-“vaccine” injection. This paper proves that an individual “vaccinated” person can present with numerous negative effects and outcomes induced by these “vaccines.” Yours Truly expresses deep appreciation of Dr. McCullough and his colleagues in working with this patient in the long and laborious testing that had to be performed in order to come to the correct diagnoses for the patient; and, from there, coming up with a treatment plan.

The Hulscher, McCullough, et al., February 2026 paper proves that there is risk of multiple types of negative effects and outcomes from having this “vaccine” in the body — damage that can be found years after the “vaccine” is injected into the body, and that can extend to the brain. This risk pool includes those who take the “latest version COMIRNATY COVID-19 vaccine”.

Yours Truly will make it clear that the patient in the Hulscher, McCullough, et al., February 2026 paper took three injections of BNT162b2: two in March 2021 (3 March and 24 March); and, the “booster” injection on 20 February 2022 — then did not take any further injections. The damage to his body and the accompanying associated emotional/psychological effects on him were traced back to these three injections over 3.5 years later. What about the millions upon millions of persons who took the BNT162b2 “primary series” of two injections back in 2021, then the original BNT162b2 “booster” injection in 2022, and then have taken injections of the BNT162b2 “descendant clone COVID-19 vaccines” (under the brand name, COMIRNATY), since the year 2022? What about the persons who have taken six injections so far of this Pfizer-BioNTech injectable — the “primary series” of two injections in 2021 + the “original booster injection” in 2022 + the 2023 “COMIRNATY booster” + the 2024 “COMIRNATY booster” + the 2025 “COMIRNATY booster”? If one person who took only three of the Pfizer-BioNTech COVID-19 “vaccine” injectables (the patient in the Hulscher, McCullough, et al., paper) and presents with multiple negative effects and outcomes over 3.5 years after stopping taking the injections — what about the millions of persons who have a total of at least six Pfizer-BioNTech (COMIRNATY) injections in their bodies as of now? If the potential for multiple negative effects and outcomes from the Pfizer-BioNTech COVID-19 injectables can be found in a “vaccinated” person over three years post-final injection, what is the potential for “rolling accumulated negative effects and outcomes” from these injectables in a person who has taken these injections every year since early 2021?

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The following is not medical advice. They are opinions:

Any person who has ever taken a COVID-19 “vaccine” injection — even if only one injection — of any type (modRNA, DNA viral vector, “protein subunit”, etc.) may be at risk for developing negative effects and/or outcomes induced by these “vaccines.” COVID-19 “vaccinated” persons may wish to consider having the following tests performed:

A lung scan, to investigate whether or not there are issues that can have been induced from these “vaccines”; such as, compromised alveoli or lung tissue inflammation.

A heart / cardiac scan, to investigate whether or not there are issues that can have been induced by these “vaccines”; such as, scarring of heart tissue or symptoms of preclinical myocarditis.

A D-dimer test performed, to investigate whether or not there are elevated levels of microclots in the blood, which can have been induced by these “vaccines.”

An IgG3 panel test and an IgG4 panel test performed, to investigate whether or not there are reduced levels of IgG3 cells (the “fight the enemy cells off” immune system cells), and/or elevated levels of IgG4 cells (the “tolerate but don’t fight off” immune system cells), both of which can have been induced by these “vaccines.”

Note: The above tests usually need to be ordered by a physician; or, by another licensed healthcare professional who is approved to order these types of tests.

Interested persons may wish to consider following a post-“vaccination” recovery treatment protocol, such as the one outlined here, from the Independent Medical Alliance: https://imahealth.org/protocol/i-recover-post-vaccine-treatment.

For those who are not COVID-19 “vaccinated”, there is the now-proven phenomenon of “vaccine shedding” from “vaccinated” persons onto other persons, including onto non-“vaccinated” persons. Please see: https://pierrekorymedicalmusings.com/p/newly-published-study-shows-shedding, “Newly Published Study Shows Shedding Of Covid mRNA Vaccine Products”, 9 December 2024.

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THE COVID-19 “VACCINES” — ALL OF THEM — MUST BE REMOVED FROM THE MARKET AND FROM USE IN THE UNITED STATES. NOW.

THERE MUST BE ACCOUNTABILITY, JUSTICE, AND TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Disclaimer and Notice: The ideas and opinions in today’s offering are by PAVACA. Credit must be given to PAVACA if ideas or opinions in today’s offering are used by other blog writers, by podcasters, or in social or print media.)

Health Friday 11.7.2025 Open Thread: What’s Going on at Pfizer-BioNTech?: Part One

The free image of vintage Pfizer vaccine vials for the header in today’s offering is courtesy of Dreamstime and Google Images.

Health Friday is a series devoted to Big Pharma, vaccines, general health, and associated topics. As today’s offering speaks to the COVID-19 “vaccines”, Yours Truly dedicates it to all persons, of whatever age or location, who have passed away from the negative effects of the COVID-19 “vaccines” that they had in their body. May they rest in eternal Peace.

There are Important Notifications from our host, Wolf Moon; the Rules of our late, good Wheatie; and, certain caveats from Yours Truly, of which readers should be aware. They are linked here. Note: Yours Truly has checked today’s offering for AI-generated content. To the best of her knowledge and belief, there is none, except perhaps for AI-generated images within linked URLS. If readers wish to post AI-generated content to the discussion thread for today’s offering, they must cite their source. Thank you.

This Part One trail begins here, with two news reports regarding the September 2025 agreement reached between the United States government and Pfizer (PfizerUSA, the United States co-partner of Pfizer-BioNTech; BioNTech, the other co-partner, is headquartered in Mainz, Germany.). First, from Virginia Business (https://virginiabusiness.com/pfizer-agrees-to-lower-drug-costs-70b-us-investment/), “Pfizer agrees to lower drug costs, $70B US investment”, 30 September 2025. A screenshot from this article is below:

And, second, the announcement from PfizerUSA (https://www.pfizer.com/news/press-release/press-release-detail/pfizer-reaches-landmark-agreement-us-government-lower-drug, “Pfizer Reaches Landmark Agreement with U.S. Government to Lower Drug Costs for American Patients”, 30 September 2025. A screenshot from this article is below:

Note that the specific details of this agreement, which will affect millions of Americans, “remain confidential.”

The company called Pfizer-BioNTech is a formal co-partnership between Pfizer, also known as PfizerUSA (CEO, Dr. Albert Bourla, DVM); and, BIoNTech of Mainz, Germany (CEO, Dr. Ugur Sahin, MD.) Both PfizerUSA and BioNTech were involved / still are involved, in the development and manufacture of the modRNA COVID-19 “vaccine” line, COMIRNATY (this “vaccine” was previously known as BNT162b2, or “Pfizer-BioNTech COVID-19 Vaccine.“) Both PfizerUSA and BioNTech have agreements regarding their sharing royalty payments for COMIRNATY “vaccines” purchased and used throughout the world. PfizerUSA and BioNTech are also involved in the development and manufacture of other drugs and vaccines, either separately or in coordination with each other.

The most recent (as of 5 August 2025) PfizerUSA (and Pfizer-BioNTech) product “pipeline” website is here: https://www.pfizer.com/science/drug-product-pipeline. Click on “Downloadable PDF” to view the entire pipeline. Screenshots of two pipeline areas, Internal Medicine and Vaccines, follow. The first screenshot, Internal Medicine, with discussion by Yours Truly, is below:

**** WHY is Paxlovid, a combo drug of nirmatrelvir (an antiviral) + ritonavir (an HIV/AIDS treatment drug that targets the immune system) going to be used on CHILDREN who become infected with COVID-19?

**** Ibuzatrelvir (PF-07817883), now in Phase 3 clinical trials, is an oral / enhanced “nirmatrelvir on steroids” treatment for COVID-19 infection that was granted “Fast Track” approval by the FDA The intended use of this drug appears to be as a “replacement” for Paxlovid.. Please see: https://pubs.acs.org/doi/10.1021/jacsau.4c00508, 30 July 2024. Pfizer has already patented this drug. Let’s take a look at the Overview of this Phase 3 clinical trial, as described here: https://clinicaltrials.gov/study/NCT06679140:

Does “Fast Track” approval by the FDA mean that the “Study Completion (Estimated)” of 6 May 2027 will be “bypassed”, and only the data from the “Primary Completion (Estimated)” of 12 December 2026 will be used to push this drug onto the market faster? In addition, WHY is the study subject pool so small (2330 persons) for a drug that would potentially be used on hundreds of thousands of persons?

And, from the Researcher View of this clinical trial, part of the Secondary Outcomes descriptions:

Note that the “viral load” measurement will be performed via EITHER a nasal sample, OR via a nasopharyngeal sample. If a nasopharyngeal sample swab is used, this is the extremely long swab that reaches all the way to the VERY BACK of the nasal cavity and can touch the COVERING OF THE BRAIN. By the way, the correct administration of the nasopharyngeal swab is also to ROTATE the swab a couple of times after insertion.

In addition, in the information about NCT06679140, the “placebo tablet” that will be used is NOT described at all. Is the “placebo tablet” going to be Paxlovid? Is the “placebo tablet” going to be a completely drug-free “empty” tablet?

And now, the second screenshot from the “pipeline” PDF, Vaccines, is below. Yours Truly will discuss an interesting new “vaccine” from this list, under development by PfizerUSA (in conjunction with BioNTech) — PF-07926307, a combination modRNA-based COVID-19 plus influenza “vaccine“:

The available-to-the-public information regarding PF-07926307 is both confusing and concerning. Pfizer-BioNTech insists that this “combo vaccine” is only for “prophylactic” use against COVID-19 plus influenza: https://investors.biontech.de/news-releases/news-release-details/pfizer-and-biontech-provide-update-mrna-based-combination, “Pfizer and BioNTech Provide Update on mRNA-based Combination Vaccine Program Against Influenza and COVID-19 in Individuals 18-64 Years of Age”, 16 August 2024. Only ONE of of the two outcomes measurements of the Phase 3 clinical trial for this “vaccine” were met (NCT06178991.) A screenshot from the company’s press release is below:

Note that this press release emanates from Germany, not the United States;, and that the “combination candidate” is not identified as PF-07926307.

**** In addition, it appears that PF-07926307 is actually a combination of TWO separate Pfizer-BioNTech modRNA “vaccines” formulations: BNT162b2 and BNT 161: https://investors.biontech.de/news-releases/news-release-details/biontech-outlines-2024-strategic-priorities-42nd-annual-jp, “BioNTech Outlines 2024 Strategic Priorities at the 42nd Annual J.P. Morgan Healthcare Conference”, 9 January 2024. Please see the screenshot from this article, below:

**** Note the clinical trial mentioned in the above screenshot: NCT05596734. The modRNA “combo vaccine” used in this clinical trial is none other than BNT162b2 (tozinameran, now marketed as COMIRNATY, but which was the ORIGINAL Pfizer-BioBNTech modRNA COVID-19 “vaccine” against the ORIGINAL Wuhan Hu1 SARS-CoV-2 [COVID-19] virus), plus BNT161 (famtozinameran, the ORIGINAL modRNA COVID-19 “vaccine” against the OMICRON variant BA.4/BA.5) Please see: https://covid-vaccine.canada.ca/comirnaty-original-omicron-ba4ba5/product-details, which also states, “Cancelled by sponsor May 3rd, 2024.”

**** However, at the same time, it appears that this Pfizer-BioNTech modRNA COVID-19 “combo vaccine” of BNT162b2 plus BNT161 — also known as PF-07926307 — IS being used — in Singapore: https://labeling.pfizer.com/ShowLabeling.aspx?id=20959, “Date of last revision: July 2024.” Please see the screenshot from the package information for this product administered in Singapore, below:

And, screenshots from Page 65 (of 65), from the package information for the above injectable:

BNT161, one of the component modRNA “vaccines” in PF-07926307, is an influenza “vaccine”, meaning that it can be used against EITHER influenza OR COVID-19 (Omicron BA.4/BA.5.) The German partner of PfizerUSA — BioNTech — has been working on this injectable since at least 2022: https://biontechse.gcs-web.com/news-releases/press-release-details/biontech-announces-third-quarter-2022-financial-results-and, “BioNTech Announces Third Quarter 2022 Financial Results and Corporate Update”, 7 November 2022. A screenshot from this article is below:

Note that the press release is from BioNTech Sweden.

A screenshot from the Adisinsight Drug Profile for BNT161 is below. Note that this modRNA “vaccine” is a quadrivalent influenza injectable (https://adisinsight.springer.com/drugs/800052769):

**** On the other hand, here is the article on PF-07926307 (BNT162b2 + BNT161) by the tech / AI / data collection and analysis platform, Patsnap: https://synapse.patsnap.com/article/what-is-pf-07926307-used-for?, 28 June 2024. A screenshot of the entire article is below; Yours Truly includes the entire article because it has a wealth of information and clues as to the possible real “agenda” behind this injectable:

**** Note that, per the article above, the “primary indication” for the use of PF-07926307 is for the treatment of cancers caused by overactive kinases responses, such as are found in lymphomas; with what may be called a “secondary indication” for treatment of chronic inflammatory diseases. Lymphomas or chronic inflammatory diseases induced by, say, modRNA COVID-19 “vaccine” injections, such as BNT162b2 (COMIRNATY?) Is it remotely possible that PF-07926307 (BNT162b2 + BNT161) is being redesigned as a “backdoor oncology and/or chronic inflammatory diseases treatment” injectable? How does this square with what Pfizer-BioNTech claims that this “vaccine” is to be used for — against COVID-19 + influenza infection? What is the truth here?

**** In any case, WHY is Pfizer-BioNTech apparently using BNT162b2, the company’s original modRNA COVID-19 “vaccine”, as a foundational component in the development of a “New Molecular Entity” called PF-07926307, which is to used as a “prophylactic” against COVID-19 plus influenza? What happened regarding all those other modRNA COVID-19 “vaccines” made by this company, to be used against the LATEST MUTATIONS of the SARS-CoV-2 virus, such as the “2025-2026 version” of COMIRNATY? Why is Pfizer-BioNTech going all the way back to the ORIGINAL Wuhan Hu1 SARS-CoV-2 virus contained in BNT162b2 (COMIRNATY) to formulate PF-07926307?

What is going on at Pfizer-BioNTech? Does the United States government know about PF-07926307 (BNT162b2 + BNT161)? Did the “Specific terms of the agreement remain confidential” regarding the deal between the United States government and PfizerUSA reached in September 2025 include provisions that our government “looks the other way” about the activities of PfizerUSA’s co-partner, BioNTech? Does the HHS / FDA / CDC / BARDA have the complete details of the “Specific terms of the agreement remain confidential” provisions? Are the “specific details” being shared with only the “top brass” of the FDA / CDC / BARDA — and that HHS Sec. Kennedy, Jr., is being kept in the dark?

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All current COVID-19 “vaccines” — ALL of them — MUST be pulled off the market and from use. Now.

All research and development of “new” COVID-19 “vaccines” that are in ANY form — injectable; oral; nasal; micro-needle — MUST be stopped. Now.

There MUST be complete analysis of the ingredients and mechanisms of the current COVID-19 “vaccines”, performed by impartial testing entities, and with complete results made public. Now.

THERE. MUST. BE. ACCOUNTABILITY.

THERE. MUST. BE. JUSTICE.

THERE. MUST. BE. TRUTH.

Peace, Good Energy, Respect: PAVACA

(Intellectual Property Notice: With the exception of links to published media reports and links to published scientific papers, the ideas and conclusions of today’s post are by PAVACA. Proper credit must be given to PAVACA if other blog writers, or persons on podcasts, social media, or print media, use the ideas and/or conclusions of today’s post. Thank you.)