Breaking: MHRA Chief Exec Jumps Ship After MPs Call For Investigation Into Failure to Flag Covid Jab Side Effects.

An all-party group believe Medicines and Healthcare products Regulatory Agency (MHRA) were aware of heart and clotting issues in February 2021 but did not highlight the problems for several months. The Telegraph reported today that MPs have said that the medical regulator failed to sound the alarm over Covid vaccine side effects and should be investigated. The group warned that the MHRA Yellow Card reporting system – which encourages patients and doctors to flag-up medicine side effects – “grossly” underestimates complexities, and in some instances picks up just one in 180 cases of harm. Also today, June Raine, Chief Executive of the agency has announced that she will be standing down after spending 5 years in the position.

The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible for approving drugs and devices and monitors side effects caused by treatments. But the all-party parliamentary group (APPG) on pandemic response and recovery, an influential group of MPs, has raised “serious patient safety concerns”. It has claimed that “far from protecting patients” the regulator operates in a way that “puts them at serious risk”.

The Chief Executive

Dame June said:

“It has been an enormous privilege to have led the MHRA through a time of change which is unprecedented in UK medical products regulation. I am especially proud that during the last 5 years the Agency has built a new vigilance system, strengthened international and national partnerships, and delivered regulation which has enabled groundbreaking innovation, from gene therapy for sickle cell disease and the world’s first Covid vaccine, to being close to eradicating polio, and from medical device software to AI diagnostics.”

“It has been an honour to lead an agency which has patient safety as its top priority and makes a difference to the lives of everyone in the UK.”

“While I am stepping back from my MHRA role, I hope still to be involved in contributing to patient safety and public health in other ways.” Source

Clearly the Chief Executive is delusionaal the vigilance system was rendenred not fit for purpose under Raine’s watch, but she remained in the post for the five years ignoring the thousands of Covid jab deaths and harms. thus enabling their continuation. The Chief executive should not be anywhere near a public health role, but yes, she was right in saying that she “made a difference to the lives of everyone in the UK”

MHRA Aware of Heart and Clotting Issues Since March 2021

The Telegraph reported “Some 25 MPs across four parties have written to the health select committee asking for an urgent investigation. In reply, Steve Brine, the health committee chairman, has said an inquiry into patient safety is “very likely”. 

In a letter to Mr Brine, the APPG said that there was reason to believe that the MHRA had been aware of post-vaccination heart and clotting issues as early as February 2021, but did not highlight the problems for several months.

Denmark and several other European countries suspended the AstraZeneca vaccine over clotting fears in March 2021, but the MHRA only published safety advice on April 7, by which time 24 million people had been vaccinated.

The watchdog also saw a “signal” for the heart problems myocarditis and pericarditis in February 2021, but did not include the conditions in safety updates until June 2021, MPs said.

“In effect, the MHRA licences medical products as safe knowing it lacks the processes to properly monitor adverse events,” the APPG wrote.

“In the case of Covid-19 vaccines, given the comparatively novel technology and record manufacturing speed, could the MHRA have even properly scrutinised the licensing data or known the short term safety?

“Historically trust and confidence in vaccines and vaccine safety has been high in the UK, but it seems that the experience of the Covid-19 vaccines has undermined this and by association trust in the regulator and the pharmaceutical industry.

“Now more than ever a wide-reaching and in-depth review is needed.”

Underestimates complexities

The group also warned that the MHRA Yellow Card reporting system – which encourages patients and doctors to flag-up medicine side effects – “grossly” underestimates complexities, and in some instances picks up just one in 180 cases of harm.

An analysis by Stockport NHS Foundation Trust found that in the North West of England, 1,058 people had been admitted to hospital with stomach bleeds caused by anticoagulant medication over five years, yet just six Yellow Card reports were made during the period.

Side effects from drugs account for one in every 16 hospital admissions in Britain, and cost the NHS more than £2 billion each year.

But trials are often too small to pick up adverse reactions, particularly when they are driven by rare genetic mutations, meaning it is vital to continue monitoring drugs in the community.

The MHRA recently said it would investigate why blood thinners were causing dangerous side effects in between two and five per cent of patients.

The APPG said it was also concerned that MHRA regulation of medicine was funded by the pharmaceutical industry and said the body had shifted from focusing on scrutiny to trying to help drugs get approved.

‘Watchdog to the enabler’

Dame June Raine, the chief executive of the MHRA, who announced she would be stepping down last week, has previously said the agency was transitioning from “watchdog to the enabler,” a phrase which MPs said warranted its own investigation.

Graham Stringer MP, co-chair of the APPG on pandemic response and recovery, said:

“The MHRA oversees a failing system that is slow to act, causing harm to patients and beset with conflicts of interest.

“We cannot allow it to continue. That’s why we have written to the health select committee calling for an urgent investigation into the MHRA.”

The APPG said that concerns raised directly with the MHRA had been met with “an habitually dismissive and evasive response”.

Dame June  said: “We have made significant steps to put patients at the heart of all our work.

“These include incorporating patient views and lived experience into our safety reviews; involving patients in the early stages of planning medicines development and building a new responsive reporting system for patients to tell us about any adverse incidents. We have also led on legislative changes to strengthen surveillance for medical devices and medicines, meaning patient safety is embedded firmly into law.

“Our progress so far in making changes based on meaningful patient involvement gives us a solid base to build upon as we continue on this important journey.”

“We are committed to enabling innovation that brings transformative medical products safely to patients.’’

From Dr. Tess Lawrie:

“If you have been harmed in any way by the Covid injections, you may wish to send June Raine a Notice of Liability before she leaves office. Raine received our urgent report on the Covid ‘vaccines’ in June 2021.
Despite this, she continued to enable the mass deployment of these inadequately tested, experimental and fundamentally unsafe Covid-19 injections without informed consent on the people of the UK, including on our little children, pregnant women and our most vulnerable” – Tess Lawrie.

The urgent report follows below:

Urgent Preliminary Report of Yellow Card Data.

The Yellow Card System is an early warning system where doctors and individuals can report side effects that they suspect correspond with a medicine they have received. It is a vital way of monitoring the safety of medicines and can also identify any issues that have not yet been detected.
The Yellow Card Report was sent from Ebmcsquared to Dr. June Raine, the Chief Executive of the Medicines and Healthcare products Regulatory Agency (MHRA), on 9th June 2021, highlighting the high number of vaccine adverse event reports on the system between 4th January 2021 and 26th May 2021. A reply was received from Dr. Raine on 22nd July 2021. In the letter, she expresses the opinion that “some events may have happened coincidentally, regardless of vaccination”. We have posted this reply below for public interest.
With the announcement of the need for booster shots, it would appear that the vaccines are not as effective as once hoped. This reinforces the need to make available safe, effective early treatments, for which much guidance has been provided from experts – http://www.bird-group.org.
Ebmcsquared has now sent an updated Yellow Card Report to Dr. Raine on 9th August 2021, which evaluates the Yellow Card data up until end of June 2021.

This work has been supported by money raised by the public and assistance from the ukfreedomproject.org.

Member of the WHO

The investigation is a long time coming, but unfortunately, Raine will get off scott free as at same time that she was Chief Exec of MHRA Medicines & Healthcare products Regulatory Agency, she was also an unpaid member of member of the World Health Organisation WHO Committee on Safety of Medicinal Products. Therefore, she is now more likely to be offered another role working for the globalists rather than be reprimanded.

A full FOI shows the WHO memership https://www.whatdotheyknow.com/request/june_raine_emails#outgoing-1309992