An independent medical research company in the UK recently wrote a letter to the country’s Medicines and Healthcare Products Regulatory Agency (MHRA) to warn about the negative health effects of COVID-19 vaccines.
Penned by Dr. Tess Lawrie (MBBCh, Ph.D.), Director of Evidence-based Medicine Consultancy Ltd and EbMC Squared CiC, the letter makes its case using the UK’s own vaccine adverse event reporting database.
Directed towards Dr. June Raine, Chief Executive of the (MHRA), Dr. Lawrie declared the warning “urgent” and noted the EbMC Squared CiC is an independent group with no conflicts of interest.
By reaching out to the government agency, Dr. Lawrie hoped to “draw attention to the high number of covid-19 vaccine-attributed deaths and ADRs that have been reported via the Yellow Card system between the 4th January 2021 and the 26th May 2021. In total, 1,253 deaths and 888,196 ADRs (256,224 individual reports) were reported during this period.”
The Yellow Card system is the UK government’s “system for collecting and monitoring information on safety concerns such as suspected side effects or adverse incidents involving medicines and medical devices,” including COVID vaccines.
The research group divided their findings into the six categories of adverse drug reactions (ADR) seen below.
A. Bleeding, Clotting and Ischaemic ADRs – 856 deaths
B. Immune System ADRs – 171 deaths
C. ‘Pain’ ADRs – 4 deaths
D. Neurological ADRs – 186 deaths
E. ADRs involving loss of Sight, Hearing, Speech or Smell – 0 deaths
F. Pregnancy ADRs – 164 deaths
For each of the categories listed above, the group detailed how many fatalities were attributed to the specific adverse reaction and how many vaccinated people suffered from each complication.
SEE THE FULL REPORT BELOW
The report mentions the UK’s Yellow Card system provides limited data, unlike the World Health Organization’s (WHO) pharmacovigilance database which explained the majority of ADR’s occurred in individuals aged 18 to 44 years and 45 to 64 years.
The paper states, “The vast majority (72%) of reported ADRs have occurred among women. Unfortunately, we have been unable to examine the UK Yellow Card data according to age and gender due to lack of data availability.”
The doctors also note that they only looked through five months of data in order to finish research in a timely matter and that the high number of death and complications found proves the experimental vaccines are dangerous to humans.
“Due to the need for expedience, we have not detailed all ADRs in this preliminary report” the paper explains. “The existing Yellow Card data covering just under a five-month period indicate that the extent of morbidity and mortality associated with the COVID-19 vaccines is unprecedented.”
The researchers also ask the UK government to investigate whether the novel vaccines “may be causing gene mutations among recipients, as suggested by the occurrence of usually extremely rare genetic disorders, such as Paroxysmal Extreme Pain Disorder (PEPD).”
“Are these ADRs occurring in babies of vaccinated pregnant women, or spuriously among vaccinated adults?” Dr. Lawrie asks.
“The MHRA now has more than enough evidence on the Yellow Card system to declare the COVID-19 vaccines unsafe for use in humans,” the research group wrote. “Preparation should be made to scale up humanitarian efforts to assist those harmed by the COVID-19 vaccines and to anticipate and ameliorate medium to longer-term effects.”
“As the mechanism for harms from the vaccines appears to be similar to COVID-19 itself, this includes engaging with numerous international doctors and scientists with expertise in successfully treating COVID-19,” the doctors added.
Additionally, the group asks the MHRA to answer the following urgent questions.
1. How many people have died within 28 days of vaccination?
2. How many people have been hospitalized within 28 days of vaccination?
3. How many people have been disabled by the vaccination?
Time will tell if the UK agency responds to the research group’s request.
In related news, this past weekend the European Medicines Agency’s (EMA) safety committee identified another rare blood condition after people taking AstraZeneca’s COVID-19 vaccine and warned people over 60 should avoid the Astrazeneca vaccine.