Covid-19 Vaccines: Safety

Roger Gale Excerpts

Monday 24th October 2022 Westminster Hall

[Mr Richard Holden (North West Durham) (Con)]

My hon. Friend is making a good speech. My constituent Gareth Eve lost his wife Lisa Shaw when she was only 44, as a result of the AstraZeneca vaccine. He is not an anti-vaxxer. Although the debate is on the broad issue, does my hon. Friend agree that matters such as how families get compensation could be dealt with much better, even if he does not agree with a full public inquiry into the entire body of the issue? So many families, including that of my constituent, have been left waiting for that support for a very long time.

[Sir Roger Gale (in the Chair)]

Order. I appreciate that hon. Members wish to represent their constituents, but interventions must be interventions and not speeches.

[Elliot Colburn]

I am very sorry to hear of the case of my hon. Friend’s constituent, and I agree that we need to look at compensation and measures when things go wrong. No vaccine is without risk. No medicine is without risk, but that is the balance that we must weigh up when making decisions about our own health.

Let me return to the safety and efficacy of the vaccine, and how that is monitored. The core of this work is individuals self-reporting any adverse effects post vaccination, and active surveillance of particular groups of adverse events. That is well known as the yellow card scheme. I recently met representatives of the MHRA to be briefed on its vaccine safety surveillance strategy, which has four main pillars, the first of which is enhanced passive surveillance through observed versus expected analysis. The MHRA performs enhanced statistical analysis on data generated through the yellow card scheme to evaluate observed versus expected event reports in order to determine whether more events are occurring after vaccination than might be expected ordinarily. That assists the MHRA to identify when and where vaccine-related side effects are signalled.

Secondly, the MHRA conducts rapid cycle analysis and ecological analysis to supplement the yellow card scheme, which relies on direct reporting. The MHRA also analyses anonymised electronic healthcare records, particularly by way of the clinical practice research datalink Aurum dataset, which captures data from 13 million registered GP patients in the UK. It will track a range of theoretical side effects in order to detect safety signals. The MHRA also performs ecological analysis to monitor trends in high priority vaccination population cohorts—for example, increased trends among the elderly.

Thirdly, the agency performs targeted active monitoring; it has developed a new, voluntary follow-up platform for a randomly selected group of those vaccinated through the NHS. The group is contacted at set intervals to determine the frequency and severity of any vaccine side effects. Finally, there are formal epidemiological studies. The above methods detect signals and patterns but do not necessarily confirm vaccine causation. As such, where necessary, formal epidemiological studies are undertaken to solidify causal links.

As of 28 September 2022, in the UK, 173,381 yellow cards had been reported for Pfizer-BioNTech; 246,393 for AstraZeneca; 42,437 for Moderna; 14 for Novavax; and 1,848 for vaccines where the brand was not specified. For Pfizer, AstraZeneca and Moderna, the reporting rate is about two to five yellow cards per 1,000 doses administered.

The use of the yellow card scheme has been used as an example of why vaccines do not work, but it is important to note that the scheme is a self-reporting system. It cannot be used to prove a causal link between reported symptoms and potential damage caused. The reported reaction could have occurred regardless of the vaccine, or the person reporting could have no knowledge of the relationship between that symptom and the vaccine; it may have occurred even if the person had not been vaccinated altogether. I could get on the phone to the yellow card scheme right now and say that I have a side effect from a vaccine—I could completely make it up. The scheme has no verification process.

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[Several hon. Members rose—]

[Sir Roger Gale (in the Chair)]

Nobody from the Opposition Benches? No. I call Danny Kruger.

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[Several hon. Members rose—]

[Sir Roger Gale (in the Chair)]

We should be all right for time, but bear in mind that three people wish to speak, and I need to start the wind-ups at 5.30 pm.

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[Sir Christopher Chope]

My right hon. Friend is absolutely right. In the United States, they changed the definition of a vaccine. We have always understood a vaccine to mean someone receiving into their system something containing a small element of that which they were being vaccinated against, so that their system could react against it and protect them if they were later exposed to a large amount. But unlike those old vaccines, these vaccines do not use the raw material, so in many senses it is a misnomer to describe them as vaccines at all. That information is not really out there among the public any more than the fact that the booster vaccines have not been tested on humans at all during studies; they were tested only on mice. People are being used as victims for experimentation, and that is why they are getting worried.

Finally, Oracle Films’ film, “Safe and Effective: A Second Opinion”, is available on YouTube—I make no apology for the fact that I participate in that film—and sets out a different view on the safety of these vaccines. I am not saying we should ban all covid-19 vaccines and have a complete halt. What I am saying is that there is an urgent need for the Government to get to grips with this issue before more people are duped into having vaccines that they probably do not need, that will not do them any good and that will present risks to their health.

[Sir Roger Gale (in the Chair)]

Could I ask Mr Bridgen and Mrs Elphicke to confine their remarks to six minutes?

[Andrew Bridgen (North West Leicestershire) (Con)]

It is a pleasure to serve under your chairmanship, Sir Roger. I will try to curtail my remarks to six minutes.

This is a hugely important debate and it is overdue. Those people who have questioned the efficacy or safety of the vaccines have generally been cut down and cancelled. That is why this is so important. I do not claim to be any sort of expert, but my degree a long time ago was in genetics, behaviour and biochemistry. Science works by challenge, and the science behind the vaccines has not been allowed to be challenged.

A study published in The Journal of the American Medical Association, included 7,806 children aged five or younger who were followed for an average of 91.4 days after their first Pfizer vaccination. The study showed that one in 500 children under five years of age who received a Pfizer mRNA—messenger ribonucleic acid—covid vaccine were hospitalised with a vaccine injury, and one in 200 had symptoms ongoing for weeks or months afterwards. Will the Minister outline the Government’s current policy on vaccination and boosters, and our current policy for the vaccination of children?

Half a per cent. of the children—40 out of the 7,806—had symptoms that were still ongoing and of unknown significance at the end of the trial. That was during a two to four-month follow-up period, so 0.5% of the children had an adverse effect that lasted for weeks or months. In two cases, the symptoms were confirmed to have lasted longer than 90 days. Given that evidence, perhaps the Minister could explain why we are vaccinating healthy children who are at minimal risk from covid. Surely that is in breach of the Hippocratic oath to do no harm. We are not in a situation where we can ask young people to risk their lives to protect older people. In a civilised society, that cannot be the way it works.

According to The Independent in April, more than 1,200 claims have been made to the vaccine damages payment scheme, which entitles successful applicants to £120,000, as pointed out by my hon. Friend the Member for Christchurch (Sir Christopher Chope), if a causal link between vaccination and severe reaction culminating in injury or death is proven. Does the Minister recognise those figures? Sarah Moore, a lawyer who represents 95 families seeking claims, said that her clients felt “silenced and ignored”, adding that they cannot speak about vaccine harm or linked injuries without being accused of being anti-vax. What is the Minister’s view on victims being labelled as anti-vaxxers?

The Department of Health and Social Care commissions research through the National Institute for Health and Care Research. There is £1.6 million that has been allocated for a programme to understand the rare condition of blood clotting with low platelets following vaccination for covid-19. Does the Minister think that is sufficient? Is there a sufficient breadth of investigation considering all the things we are finding out about the vaccines? Where is the cost-benefit analysis by age group for the vaccines, given the risks that they carry, especially as the pharma companies are now admitting that vaccination does not impact on transmission? Did the Government know, when they mandated vaccines for care and NHS workers, that the vaccines had not been tested to find whether they prevented transmission?

The Florida department of health conducted an analysis through a self-controlled case series, which is a technique originally developed to evaluate vaccine safety. The analysis found that there is an 84% increase in the relative incidence of cardiac-related death among males aged 18 to 39 within 28 days following messenger ribonucleic acid vaccination. With a higher level of global immunity to covid-19, the benefit of vaccination is likely outweighed by that abnormally high risk of cardiac-related death among men in that age group. The recommendation now in Florida is that they do not vaccinate any male under the age of 40.

Florida’s surgeon general, Dr Joseph Ladapo, said:

“Studying the safety and efficacy of any medications, including vaccines, is an important component of public health. Far less attention has been paid to safety and the concerns of many individuals have been dismissed—these are important findings that should be communicated to Floridians.”

I suggest that such important findings should be transmitted to everyone who has had a vaccine or is contemplating a booster. I also had the pleasure of meeting Dr Aseem Malhotra at the APPG launch last week. He made a very strong case for the idea that up to 90% of adverse vaccine reactions are not even being reported.

Finally—I wish I had longer to speak—what is the Government’s analysis of the excess deaths that we are suffering in this country, across Europe and in the Americas? Even a casual glance at the data shows a strong correlation between vaccine uptake and the excess deaths in those regions. Surely we must have an investigation. Tens of thousands more people than expected are dying. This is really important, and if we do not get it right, no one will believe us, and trust in politicians, in medicine and in our medical system will be lost. [Interruption.]

[Sir Roger Gale (in the Chair)]

Order. I call Natalie Elphicke.