There has been a vast quantity of water under the bridge since this article first appeared in March 2021 as part of HART’s COVID-19: an overview of the evidence. Despite numerous unanswered questions to the regulators, and legal challenges, the ethical and legal precept of protecting children was dropped in the clamour to protect society as a whole.
Vaccine
First finding from Pfizer trials
A texan court ordered that the FDA release the documents used by the FDA to give emergency use authorisation for the Pfizer vaccine. The FDA asked if these documents could be kept hidden until 2076 but by August all will have been shared. Early analysis has demonstrated several concerning anomalies but crucially it has revealed that the efficacy data was not what was sold.
Second Open Letter to all members of the FDA vaccines committee
We are a group of health professionals and scientists from the UK, who submitted a letter to the FDA meeting in March regarding our concerns over the potential authorisation of Pfizer vaccine for children aged 6 months to 4 years and our letter is reattached today in readiness for your June meeting. No new evidence has come to light since our March letter, which gives any credibility to the necessity, safety or even efficacy of this vaccine for infants.
Another nudge to vaccinate children and for whose benefit?
When the JCVI considered covid vaccines for children in July 2021, they stated, “JCVI is of the view that the health benefits of universal vaccination in children and young people below the age of 18 years do not outweigh the potential risks.
The unintended consequences of COVID-19 vaccine policy
A recent article published in prestigious scientific journal BMJ global health has questioned the effectiveness of vaccination mandates during the Covid-19 pandemic and pointed out their unintended consequences.
Look Away Now: This Article Contains Dangerous Warning Signals
At the back end of February we wrote about the known problem of underreporting of adverse effects related to new and novel pharmaceutical products.
Meddling with modelling
This paper, published in the “peer-reviewed” Canadian Medical Association Journal, quite simply represents an amoral, unethical and utterly transparent attempt to use pseudoscientific modelling to fabricate a false narrative.
What is the MHRA up to now?
Not content with authorising the Pfizer vaccine for 12-15s last summer and more recently and even more controversially for 5-11s, they have now authorised the Moderna Spikevax for this young age group.
Open Letter: To all members of the FDA Vaccines Committee
Pfizer application for Emergency Use Authorisation of the mRNA Covid-19 vaccines in children aged 6 months to 4 years.
Doctors say ‘No’, politicians say ‘Go’. Stop the 5-to-11s ‘offer’
This is the heading of a crowdjustice appeal looking to challenge the government’s decision on vaccinating healthy primary school children. But given this is only an ‘offer’, is a legal challenge required?
Why the ongoing push for more vaccinations?
Since the arrival of the omicron variant, infection rates or positive cases have risen rapidly. Hospitalisations have also risen but it has been hard to disentangle admissions ‘with’ and admissions ‘for’ covid.
Reports of child deaths in the VAERS (US Vaccine Adverse Event Reporting System)
There have been 28 reports of deaths of children in the US Vaccine Adverse Event Reporting System within 6 weeks of a Covid vaccine. As is stated in each VAERS report, the submission of a report ‘does not mean that the vaccine caused or contributed to the adverse event’.
Are school premises suitable for vaccinations?
In a classic example of social media getting itself wrongly into a lather, a letter from a clinical director at Vaccination UK, addressed to ‘Dear Headteacher’ did the rounds, along with inappropriate invective.
How to measure vaccine harms
Drug harm reporting systems, like the MHRA’s yellow card system, are designed to alert the regulator to a potential issue. They are not designed to measure the size of the problem. If an issue is highlighted then the regulator has a responsibility to carry out an audit and see whether the incidence of the condition of concern has been higher than historical levels in the population who were vaccinated.
The story of patient 11281009 in the Pfizer trial
Some disturbing findings hidden in the reluctantly released data After a Texan court ordered the FDA to release the documents used to approve the covid vaccine the first 150 documents have now been published. These include the medical notes for a selection of patients at five different trial sites. Sonia Elijah has carried out part […]
Vaccine Damage: the human cost of rushed-to-market products
The existing mechanism for compensating those suffering vaccine damage was set up in 1979. If the vaccination caused ‘severe disablement’ (classed, somewhat callously, as being ‘60% disabled’), then one can become eligible for a one-off payment of £120,000, but only if you are able to undergo an excruciating and protracted battle with the authorities to have your claim accepted.
Children’s covid vaccines: it’s all about balance of risks…
Over many months, a group of experienced health professionals and academics have been writing to the MHRA and the JCVI regarding the vaccination of healthy children, with most of the letters posted on the HART website. In our most recent letter, the authors have called for a pause to the children’s vaccine rollout pending a thorough investigation of a number of safety concerns.
Vaccine Mandate revoked
On Tuesday 1 March, the government released the results of the consultation period, which unequivocally shows the lack of public support for this mandate, with 87% of respondents saying that they “feel strongly that the requirement should be revoked”.
