The UK government’s regulator has revealed that a study of official data found that 13.7% of people who received Covid “vaccines” suffered adverse events considered to be “medically serious.”
The findings of the study were revealed in a report from the Medicines Healthcare Products Regulatory Agency (MHRA) – the UK’s equivalent of the U.S. Food and Drug Administration (FDA).
The study for the MHRA report was conducted by a team of researchers at the agency’s Patient Safety Monitoring, Safety, and Surveillance Department, led by Deputy Director Phil Tregunno.
The researchers analyzed official government data from the Yellow Card Vaccine Monitor (YCVM).
Their findings were published in the medRxiv medical journal.
This safety system was established by the UK MHRA to facilitate active monitoring of adverse reactions following Covid vaccination.
The data can be used to further characterize safety in populations under-represented in clinical trials.
In this latest study, a set of randomly selected individuals were invited to register.
They were actively contacted to seek further information on the vaccines received and adverse events they experienced.
The researchers present demographics of patients recruited and summaries of reported data alongside detailed analyses of the cohort.
The study found a substantial 13.7% of the total sample experienced a “medically serious” event after receiving a Covid “vaccine.”
Out of 36,604 persons registered in the study database, 30,281 were reported to be vaccinated with at least one dose of a Covid injection.
The researchers followed up on participants on a median [IQR] period of 184 days [14-367].
Of the total 30,281 individuals in the vaccinated group, 15,764 (52.1%) reported experiencing at least one adverse reaction, a substantially high number.
Tregunno and colleagues report that all of these, however, “were expected acute reactions, and only 4,134 (13.7%) reported an event considered medically serious.”
However, 13.7% is a seriously high number for experiencing adverse events deemed “medically serious,” yet the researchers seem to downplay the finding.
A total of 19 reports of spontaneous abortion were tabulated.
The majority of these reports were reported in association with a 1st dose of COVID-19 vaccination (n=11), 7 with the Pfizer BioNTech mRNA vaccine, 3 with AstraZeneca, and 1 with Moderna mRNA.
A tragic case of fetal death was reported alongside a spontaneous abortion, and this was reported in association with a 1st dose of AstraZeneca.
Reporting of menstrual disorders appeared stimulated by media interest, as seen in spontaneous reporting systems.
Data on the incidence of tinnitus were used to support regulatory action on this signal.
It should be noted that the study didn’t include individuals who were killed by the shots.
The news comes after an explosive statement from the former vice president of Pfizer.
As Slay News previously reported, Dr. Mike Yeadon has given an explosive testimony and blown the whistle on the true motivations behind the company’s Covid mRNA “vaccines.”
The former Pfizer executive is a professional research scientist with over 30 years of experience in the pharmaceutical industry and biotechnology.
According to Yeadon, the Covid mRNA injections were “designed intentionally” as tools to depopulate the human race.
In addition, the doctor alleges that COVID-19 was fabricated as an illness in order to push the “vaccines” onto the public.
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Meanwhile, U.S. regulators at the FDA have just given the green light to advance a new “self-amplifying” mRNA “vaccine” for “bird flu.”
The new “vaccine” is being developed by Arcturus Therapeutics, a Bill Gates-funded company specializing in mRNA-based pharmaceuticals.
READ MORE – FDA Advances Bill Gates’ ‘Replicon’ mRNA Bird Flu ‘Vaccine’