UK: 35 People Deaf and 25 Blind After Taking mRNA Vaccine Jab
The Yellow Card scheme tracking potential vaccine injuries has flagged a combined 191,832 individual adverse events, or side effects, related to COVID vaccines.
LONDON, England, March 6, 2021 — Among the people in the UK who have taken the experimental mRNA COVID-19 vaccines, there have been 35 cases of deafness and 25 cases of blindness reported.
They derive the numbers from the U.K. Yellow Card vaccine reporting scheme, which is the British equivalent to the American Center for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS).
Both the Pfizer/BioNTech and Oxford/AstraZeneca mRNA COVID vaccines were given temporary authorization in the U.K. by the Medicines and Healthcare products Regulatory Agency (MHRA), the former in mid-December 2020, and the latter at the beginning of January 2021.
AstraZeneca’s vaccine performed consistently worse, accounting for 60% adverse events and 58% resulting in deaf and blind reports. Of the 402 fatalities, 197 were reported following the use of the Pfizer formula, and 205 after taking AstraZeneca’s vaccine.
It is also interesting to note that these vaccines had several side-effects during clinical trials, according to a post in The Observer.
How come do these adverse reactions persist then, even during the experimental phase as laid out by American Frontline Doctors (AFLD)?
According to Dr. Gold, “The Correct language is ‘critical’: Not COVID-19 ‘vaccines,’ but experimental biological agents”.
According to data published on February 22, an excess of debilitating side-effect is revealed and still, this has not alarmed officials at the MHRA, who maintain “no other new safety concerns have been identified from reports received to date.” They conclude from this that the “overall safety experience with both vaccines is so far as expected from the clinical trials.”
The regulator doubled down on supporting the jabs, stating that the “expected benefits of the vaccines in preventing COVID-19 and serious complications associated with COVID-19 far outweigh any currently known side effects,” including deafness, blindness, and death.
The MHRA Justified their position by citing the passive analytical nature of recordings on the Yellow Card Scheme: It is a self-reporting system. This means that none of the serious injuries, or even the deaths, are confirmed by a licensed doctor, giving the MHRA some leeway to declare that “the available evidence does not currently suggest that the vaccine caused the event.” Rather, the MHRA favours the use of the term “temporally-related” to describe the succession of adverse events from injection with the vaccine, which they describe as “events occurring following vaccination but may or may not be caused by the vaccine.”
John Stone of Children’s Health Defense noted that, despite the passive reporting system used by the MHRA, “the very distinct event profiles of two products [COVID-19] filtered through the same system after 15 million vaccine administrations [in the U.K.] would suggest that there is something to be investigated and explained.”
Regarding the use of the Pfizer vaccines in the U.S, following the award of “Emergency Use Authorization” by the Food and Drug Administration (FDA) in December. It is evidently clear that they have established a pattern of adverse results. In both the U.K. and the U.S., the use of the Pfizer vaccine has brought about similar results, accounting for most post-vaccination injuries in America. VAERS has recorded 19,907 cases of adverse events arising after taking a COVID-19 vaccine, 64% of which are linked to Pfizer’s mRNA vaccine, and 36% because of Moderna’s equivalent jab.
VAERS has reported 23 cases of complete deafness and 27 unilateral deafness in the U.S., with Pfizer’s jab making up 76% of complaints. Additionally, 29 cases of partial or complete blindness have been reported, over half of which followed the Pfizer vaccine.
Israel’s experimental mRNA program has returned poor results too, reporting a new analysis of vaccine-related deaths showing a dramatic rise in both young and elderly people dying after taking the Pfizer COVID-19 jab over those who have died after encountering the virus naturally.
After investigating the Israeli Health Ministry’s own data on the nation’s vaccine rollout, Dr., Hervé Seligmann, a member of the faculty of Medicine at Aix-Marseille University, and engineer Haim Yativ revealed that Pfizer’s mRNA experimental vaccine killed “about 40 times more [elderly] people than the disease itself would have killed” during a recent five-week vaccination period.
Among the younger class, the researchers discovered it compounds these numbers to death rates at 260 times what the COVID-19 virus would have claimed in the given time frame.