Supporting Evidence

The FDA, which denied any wrongdoing, said it will remove content warning people not to use ivermectin to treat COVID-19 within 21 days. Plaintiffs called the settlement a big win for patients and the patient-physician relationship.

The time to speak up about it is now, rather than after the event. If there is nothing for the government and the WHO to hide, they should disclose this information.

They want the UK ONS is to produce a detailed time-series cohort analysis like they should have done 3 years ago. The request was validated by UK Professors Norman Fenton and Carl Heneghan.

What is Serialization? Serialization is a mandatory requirement in the pharmaceutical industry. It was introduced in order to protect against counterfeit or other misbranded products entering the legitimate supply chain. This article, Serialization in the Pharmaceutical Industry,

The data that shows the less appreciated forgotten consequences of vaccination.

A group of respected physician-scientists in Australia and in America with specialties in gastroenterology and immunology collaborated to educate their peers on the criticality of multi-drug therapy targeting COVID-19, given the imminent threat of microbial resistance. The recognized experts in gut health and the microbiome affiliated with Australia’s Center for Digestive Diseases, University of Queensland and Progenabiome, California address the escalating threat of microbial resistance and COVID-19. Articulating the need for multi-drug combinations to counter this trend, the physician-scientists introduce the combination of ivermectin, antibiotics and zinc as a regimen to consider. While it’s important to note that the medical and health establishment in the United States has rejected ivermectin as an off-label repurposed option for COVID-19, recent court battles slapped the Food and Drug Administration (FDA) for its information war against the anti-parasite drug used by hundreds of millions annually for various parasite-borne diseases such as Merck’s Mectizan program.

Mika Vauhkala has sued the Finnish government and Fazer for the violation of basic human rights by demanding CovidPass.

The World Health Organization’s Dr. Hanna Nohynek testified in court that she advised her government that vaccine passports were not needed but was ignored

Government throws safeguards out of the window in rush for new gene drugs

Examining international data shows there is a real problem

United Kingdom-based AstraZeneca has admitted in court that the company’s Covid shots developed with the University of Oxford caused blood clots. And the news traveled fast to Australia. An ex-Minister from Australia asks if didn’t top government representatives and institutions--from the former Chief Medical Officer and the vaccine regulator (Therapeutic Goods Administration) to the Australian Technical Advisory Group on Immunization (ATAGI) and the World Health Organization (WHO) at one point or another all gave assurances there was no link between AstraZeneca and blood clots? What is there to do about the real-world scenario where people died from the AstraZeneca countermeasures, after relying on this advice from the Chief Medical Officer? Back in the UK, 51 legal cases were filed in the High Court, as both vaccine injured victims along with grieving relatives pursue countermeasure damages in a sum that could reach £100 million (US$125.35m). But how many injuries are just bypassed, accepted, never to be litigated? These are questions that will likely never be known, and a majority of the vaccine injured will be ignored by the history books as the overwhelming medical literature points to a COVID-19 vaccine countermeasure success story, with millions of lives saved as the vaccines, especially in the earlier period of the pandemic, induced antibodies and immunity to reduce morbidity and mortality. 

When an antigen stimulates the immune system, specific T regulatory (Treg) and T effector (Teff) subpopulations develop from naïve T cells. The Treg cell population will produce the memory Treg (mTreg) cells against that specific antigen. An inappropr

Pharmaceutical company says newer shots led to decline in demand for AstraZeneca vaccine, which is no longer being manufactured or supplied

To summarize, while it’s sensible to prepare for outbreaks and pandemics, it’s even more sensible to improve health. This involves directing resources to where the problems are and using them in a way that does more good than harm.

How the Spike Protein invades intestinal epithelium and BBB allowing microbial/lipopolysaccharide translocation.

In a series of Phase 1 trials, 7-18% of participants who received the experimental mRNA shots experienced skin reactions, including hives, itchiness or hives caused by scratching. Skin reactions can be an “early warning radar for general immune response” issues.

New partnership between the UK and World Economic Forum (WEF) to ensure innovators have the environment needed to create and support the industries, products and services of the future.

Benjamin Singer, M.D., the Lawrence Hicks Professor of Pulmonary Medicine in the Department of Medicine and a Northwestern Medicine pulmonary and critical care physician and colleagues conducted a study using machine learning finding no evidence of cytokine storm in critically ill patients with COVID-19. Rather, the Illinois-led team at Northwestern finds that secondary bacterial infection of the lung (pneumonia) was extremely common in patients with COVID-19, affecting almost half the patients who required support from mechanical ventilation. It turns out cytokine storms were nowhere near as prevalent as was assumed according to this data. TrialSite contributor Peter McCullough, M.D., MPH December 13, 2023, in his Courageous Discourse https://petermcculloughmd.substack.com/p/secondary-bacterial-pneumonia-common?r=14jb45&utm_campaign=post&utm_medium=web&triedRedirect=true covered this topic reporting that inpatient COVID-19 protocol-driven care led to new findings by the National Institutes of Health Autopsy Consortium—secondary bacterial and in some cases invasive fungal infections not recognized clinically before death, were frequent.

NTD’s Lee Hall sits down with Hedley Rees, Managing Director of Pharmaflow, who has worked in the pharmaceutical industry for over 40 years.

Reviewing a Century of Vaccine Disasters and the Early Trailblazers who Fought Against Them

Reviewing a remarkably disingenuous "apology" and what actually caused the vaccine disaster

According to documents obtained by Children’s Health Defense, reports of injuries and deaths following COVID-19 vaccines — including a child injured by the Pfizer vaccine during a clinical trial and a fatal vaccine-induced case of myocarditis — reached NIH researchers, Dr. Anthony Fauci and others in 2021 and 2022.

‘We kind of got cancelled because no one wanted to talk about the potential that there was a problem from the vaccines,’ Dr. Robert Redfield said.

The Human Medicines Regulations state that celebrity endorsement of drugs is not allowed. So why are TV doctors in the pay of AstraZeneca promoting vaccines in the media, ask Tom Jefferson and Carl Heneghan.

"We kind of got cancelled because no one wanted to talk about the potential that there was a problem from the vaccines," Dr. Robert Redfield said.