Dutch researchers examined rates of Severe Adverse Events between different BNT162b2 vaccine batches administered in Denmark (population 5.8 million) from December 2020 to January 2022.

Unexpectedly, rates of SAEs per 1000 doses varied considerably between vaccine batches ranging from 0.09–3.59 Events per 1000 doses with 71% of the suspected adverse reactions occurring in 4.2% of the vaccine batches.

Three predominant trendlines were discerned, with noticeable lower SAE rates in larger vaccine batches and additional batch-dependent heterogeneity in the distribution of SAE seriousness between the batches representing the three trendlines.

The results suggest the existence of a batch-dependent safety signal for the BNT162b2 vaccine, and more studies are warranted to explore this preliminary observation and its consequences.

https://onlinelibrary.wiley.com/doi/10.1111/eci.13998

T cell immunity from previous human Coronavirus infection protects certain individuals from symptomatic infection.

"Suggesting that this genetic association is due to pre-existing T cell immunity, we show that T cells from pre-pandemic samples from individuals carrying HLA-B*15:01 were reactive to the immunodominant SARS-CoV-2 S-derived peptide NQKLIANQF."

https://www.nature.com/articles/s41586-023-06331-x

A group of STEM-policy professionals that included 14 members of Biosafety Now's leadership team submitted a letter to the Editor of Nature Medicine asking them to publish an expression of editorial concern for the paper “The proximal origin of SARS-CoV-2,” and to begin a process of withdrawal or retraction of the paper.

"We are seeking to expose a clear case of scientific fraud and misconduct that has had a major impact on public opinion and policy. The removal of 'The proximal origin of SARS-CoV-2' from the scientific literature is the first step in a long process to repair the damage this paper has caused to public trust in science."

https://biosafetynow.org/open-letter-to-nature-medicine/

Seasonal human coronaviruses (HCoV) NL63, 229E, OC43, and HKU1 are globally endemic. An observation over time was carried out in France and serum from children and adults was collected between 2020 and 2021.

The estimated seroconversion rate in children was consistent with 20%–39% of children being infected every year with each HCoV.

The majority of HCoV infections remain undiagnosed and are successfully handled with no medical intervention in the home.

https://academic.oup.com/ofid/article/10/7/ofad340/7218418

Detection of recombinant Spike protein in the blood of individuals vaccinated against SARS-CoV-2

"The specific PP-Spike fragment was found in 50% of the biological samples analyzed, and its presence was independent of the SARS-CoV-2 IgG antibody titer. The minimum and maximum time at which PP-Spike was detected after vaccination was 69 and 187 days, respectively.

Three hypotheses are possible and are shown in the Figure.

1. It is possible that the mRNA may be integrated or re-transcribed in some cells.

2. It is possible that pseudo-uridines at a particular sequence position, as described in the article, induce the formation of a spike protein that is always constitutively active. But it seems very remote as a hypothesis.

3. It is possible that the mRNA-containing nanoparticle will be picked up by bacteria normally present at the basal level in the blood."

https://onlinelibrary.wiley.com/doi/full/10.1002/prca.202300048

New data suggests genetic vaccines are making long COVID worse.

A recent study by Diexer et. al. demonstrated that the risk of developing long-COVID did not differ based on the vaccination status (among those who had been infected). The data suggested that immunological memory in individuals that had a previous infection offered protection against development of long-COVID.

The study determined that participants infected with the Omicron variant had the lowest risk of developing long-COVID, followed by the Delta, Alpha, and Wild-type variants. The lowest risk group was the unvaccinated who had their first infection with Omicron. There was strong evidence that the risk of developing long-COVID was substantially lower among those who had had previous infections and vaccination offered no meaningful protection against developing long-COVID upon subsequent infection.

https://www.ijidonline.com/article/S1201-9712(23)00702-6/fulltext

⚖️ California Bill censoring doctors has been REPEALED!

Signed into law in September 2022, California Assembly Bill (AB) 2098 violated Medical Board of California-certified physicians’ First Amendment rights to free speech and their Fourteenth Amendment rights to due process of law.

With the help of NCLA, Drs. Tracy Hoeg, Ram Duriseti, Aaron Kheriaty, Pete Mazolewski and Azadeh Khatibi, in Høeg, et al. v. Newsom, et al., brought forth a lawsuit challenging the vague and censorious statute. Thank you to NCLA and the brave individuals who stood against medical tyranny.

On October 1, 2023, California Gov. Gavin Newsom signed legislation repealing AB 2098, a major victory for NCLA.

https://aaronkheriaty.substack.com/p/in-ncla-victory-gov-newsom-repeals

https://nclalegal.org/

Vaccines for COVID-19 and influenza may increase the risk of strokes caused by blood clots in the brains of seniors, particularly when the two vaccines are given at the same time.

This is the SECOND study to find an elevated risk of stroke for seniors after Covid-19 and flu vaccinations given together.

"Our study did identify an elevated risk of stroke when the COVID-19 bivalent vaccines were administered with a concomitant high-dose/adjuvanted influenza vaccine."

There have been no clinical trials studying the effects of giving flu mRNA injections at the same time as other vaccines. NONE!! No provider or pharmacist can give informed consent when offering to administer these injections to you at the same time.

Physicians are routinely neglecting their oath to do no harm by recommending concurrent COVID and flu vaccination!

https://www.medrxiv.org/content/10.1101/2023.10.10.23296624v1.full

A new study published by Naomi Wolf's group, Daily Clout, found evidence of an over 3.7-fold increase in number of deaths due to cardiovascular events in subjects vaccinated with Pfizer's mRNA vaccine compared to placebo controls during a clinical trial.

Additionally, there was no significant difference between number of deaths in vaccinated versus placebo arms which was analyzed up to week 20 prior to unblinding.

This is the first study of original data from Pfizer/BioNTech BNT162b2 trial CA4591001 to be carried out by a group unaffiliated with the sponsor.

https://ijvtpr.com/index.php/IJVTPR/article/view/86

Study Finds Paxlovid Treatment Does NOT Reduce Risk of Long COVID

A team of researchers from University of California San Francisco (UCSF) has found Paxlovid did not reduce risk of developing long COVID for vaccinated, non-hospitalized individuals during their first COVID-19 infection.

They also found a higher proportion of individuals than previously reported experience rebounds after taking Paxlovid. Among 666 individuals treated with nirmatrelvir who responded to the rebound survey, 139 of the 650 who experienced symptomatic improvement during nirmatrelvir treatment (21%) reported rebound symptoms.

“We found a higher proportion with clinical rebound than previously reported but did not identify an effect of post-treatment rebound on long COVID symptoms,” said study first author Matthew Durstenfeld, MD, MAS, a cardiologist and UCSF assistant professor of Medicine. “Our finding that Paxlovid treatment during acute infection is not associated with lower odds of long COVID surprised us, but it is consistent with two other rigorously conducted studies finding no difference in post-COVID conditions between 4 and 6 months after infection.”

https://onlinelibrary.wiley.com/doi/full/10.1002/jmv.29333

https://www.ucsf.edu/news/2024/01/426906/study-finds-paxlovid-treatment-does-not-reduce-risk-long-covid

Virologist Simon Wain-Hobson describes why the University of Wisconsin-Madison should not support research that enhances potential pandemic pathogens (ePPP research).

In 2011, University of Wisconsin-Madison virologist Dr. Yoshihiro Kawaoka performed research that created genetically engineered avian influenza viruses that, if they were to escape his lab, could cause a pandemic far more devastating than COVID-19.

Dr. Simon Wain-Hobson, is a world renowned virologist who has published more than 230 papers on virology and cancer. Wain-Hobson and his colleagues were the first to report the genetic blueprint of the AIDS virus. (Nature 1984;312(5996):757-60; Nature 1985;313(6005):743; Cell 1985 Jan;40(1):9-17). Wain-Hobson is a long-time vocal critic of ePPP research--such as that performed in the Kawaoka lab.

On January 10, 2024 the Wisconsin State Assembly Committee on Colleges and Universities will hold a public hearing on Assembly Bill 413 (AB 413). AB 413 would prohibit University of Wisconsin-Madison scientists from conducting "gain-of-function" research that enhances potential pandemic pathogens (ePPP research).

https://m.youtube.com/watch?si=uxNQfGqLKVCXAaJi&fbclid=IwAR3LAZcn4Iks6w6hb7hMIDtOdVDRH9EmY0KygBEQuOTuQ7fBpKKByi-gwgs&v=_sJb8SwcsGs&feature=youtu.be

Learn more about AB 413:
https://biosafetynow.org/protect-the-public-from-high-risk-pathogen-research/

https://biosafetynow.org/gain-of-function-research-legislation-in-wisconsin/

💔 New data reveals long term outcomes of vaccine induced myocarditis. Physicians have a responsibility to uphold their Hippocratic Oath to do no harm and keep patients informed of well documented adverse events following vaccination.

“This is the largest follow up study to date in Australia of patients who experienced myocarditis following COVID-19 vaccination.

Our findings suggest that around half of all patients experiencing myocarditis following COVID-19 vaccination still experience symptoms 6 months after initial diagnosis. This builds on existing work where 50% of some previously studied cohorts reported ongoing symptoms at 90 days following onset of myocarditis after COVID-19 vaccination.

This is particularly important as a significant portion of cases are adolescents or young adults who were otherwise well prior to vaccination, and the potential for lifelong complications adds significantly to the benefit-risk evaluation of COVID-19 vaccination.”

https://www.sciencedirect.com/science/article/abs/pii/S0264410X23015165

💉 mRNA COVID vaccine impairs neural pathways and causes autism-like behavior in rat offspring.

"Pregnant rats received the COVID-19 mRNA BNT162b2 vaccine during gestation. Subsequent evaluations on male and female offspring included autism-like behaviors, neuronal counts, and motor performance.

Our findings reveal that the mRNA BNT162b2 vaccine significantly alters WNT gene expression and BDNF levels in both male and female rats, suggesting a profound impact on key neurodevelopmental pathways. Notably, male rats exhibited pronounced autism-like behaviors, characterized by a marked reduction in social interaction and repetitive patterns of behavior. Furthermore, there was a substantial decrease in neuronal counts in critical brain regions, indicating potential neurodegeneration or altered neurodevelopment. Male rats also demonstrated impaired motor performance, evidenced by reduced coordination and agility."

https://link.springer.com/article/10.1007/s11064-023-04089-2

CDC ordered to release data on vaccine side effects.

"Following a lawsuit brought by Freedom Coalition of Doctors for Choice, U.S. District Court Judge Matthew Kacsmaryk has ordered the CDC to begin releasing the 7.8 million responses documenting negative side effects of Covid vaccines beginning on Feb. 15.

The judge wrote that there is a “substantial public interest in the data,” given that the CDC says 81 percent of Americans have received at least one dose, including nearly 32 million children.

The CDC must now produce all free-text responses with the registrant number (personal identifying information) redacted by Jan. 15, 2025.

Disclosures must be made in 12 separate batches by the 15th of each month, with the first batch of data due out by Feb. 15, 2024."

https://scnr.com/article/federal-judge-orders-cdc-to-release-data-on-7-8-million-covid-vaccine-adverse-event-reports_37707416b15711ee9c930242ac1c0002

We have a problem in public health!!

International health institutions are emphasizing an urgency to prioritize prevention and response to pandemics.

A review of evidence base for pandemic preparedness finds that the data and evidence is poorly supportive of current pandemic risk assumptions, suggesting that the urgency is unwarranted and that more time is required to formulate policy that reflects the true risk of pandemics in the wider healthcare context.

https://essl.leeds.ac.uk/downloads/download/228/rational-policy-over-panic

A global cohort study following the Observed vs. Expected Analyses of COVID-19 Adverse Events of Special Interest Study Protocol with data from 10 sites was conducted across eight countries participating in the unique Global COVID Vaccine Safety (GCoVS) Project of the Global Vaccine Data Network™ (GVDN®). The GCoVS Project, initiated in 2021, is a Centers for Disease Control and Prevention (CDC) funded global collaboration of investigators and data sources from multiple nations for the purpose of COVID-19 vaccine safety monitoring.

This multi-country analysis confirmed pre-established safety signals for myocarditis, pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis. Other potential safety signals that require further investigation were identified.

Most of the risk factors were calculated based on a single dose. When you consider many people took three or MORE, the results of the study become even more alarming.

https://www.sciencedirect.com/science/article/pii/S0264410X24001270

The monitoring and analysis of adverse drug reactions (ADR’s) play a pivotal role in ensuring drug safety.

Nearly 24 million Adverse Events (AEs) were reported through vigiacces.org for the Covid-19 vaccines between December 1, 2020 and January 31, 2023, of which nearly 8 million were serious (SAEs).

Over one million people experienced at least one SAE ranging from a combination of debilitating and life-threatening conditions and death. A total of 58,091 people were reported to have died in the dataset.

Global and national authorities on the COVID-19 pandemic such as the World Health Organization (WHO) need to immediately investigate the COVID-19 vaccine safety signals.

Safe and effective?! The signals were always clear

osf.io/preprints/osf/67njd

CDC panel green lights another COVID mRNA shot.

In just three year’s time, the CDC’s vaccine advisory committee has authorized NINE separate injections of an experimental gene product.

CDC continues to ignore the fact that these injections do not prevent infection nor transmission of the virus. Even worse, well documented adverse events and clear safety signals from mRNA vaccination are largely ignored.

New evidence demonstrates that the vaccines contain extremely high levels of contaminating DNA vector from manufacture. The mRNA also produces unintended proteins, adding further insult.

Only 17% of the US population received an updated booster shot.

https://www.cdc.gov/media/releases/2024/s-0228-covid.html

Court rules FDA take down anti-ivermectin ads

During the pandemic many doctors writing prescriptions for ivermectin had their license revoked or suspended. Pharmacists refused to fill prescriptions and people were ridiculed for taking ivermectin for treating COVID-19.

Three doctors sued the FDA, the Department of Health and Human Services and the agencies’ leaders in Galveston federal court in June 2022. Last week the courts found that the FDA overstepped and interfered with the doctor-patient relationship by posting false information regarding the use of ivermectin.

“The FDA interfered in the practice of medicine with their irresponsible language and posts about ivermectin. We will never know how many lives were affected because patients were denied access to a lifesaving treatment because their doctor was ‘just following the FDA.'" said Paul E. Marik, M.D., FCCM, FCCP, a plaintiff in the case.

https://www.courthousenews.com/wp-content/uploads/2023/08/322cv184-three-doctors-sue-fda-over-ivermectin.pdf