@NHSEngland@OUHospitals@OxfordVacGroup@AstraZeneca Are you informing people that they have a very real risk of worse disease or death when they have the vaccine and are then exposed to the live virus before administration through ADE, or are you conveniently skipping over that info?
@NHSEngland@OUHospitals@OxfordVacGroup@AstraZeneca If clinical trial participants weren't generally being told about the possibility of increased risk of more severe disease post-vaccination, then is informed consent likely to be disastrously overlooked when delivering the vaccine rapidly to the populace?...
@NHSEngland@OUHospitals@OxfordVacGroup@AstraZeneca As far as I can determine through looking at the studies, a 'challenge' (introduction of the wild virus to trial participants to see if the vaccines were indeed effective) test was not used.
Inform yourself, because they won't inform you....
"... while the AstraZeneca form clearly discloses the specific risk of ADE, the disclosure is listed last among risks only in an attached information sheet. In all, the evidence from the Pfizer...
@NHSEngland@OUHospitals@OxfordVacGroup@AstraZeneca Moderna and Johnson & Johnson protocols for their COVID‐19 vaccine trials and the sample consent forms, when contrasted with the evidence for antibody‐dependent enhancement of disease presented by this report and widely available to any skilled practitioner in the field...
@NHSEngland@OUHospitals@OxfordVacGroup@AstraZeneca establishes that patient comprehension of the specific risk that receiving the COVID‐19 vaccine could convert a subject from someone who experiences mild disease to someone who experiences severe disease, lasting morbidity or even death is unlikely to be achieved by the informed
"Given the strong evidence that ADE is a non‐theoretical and compelling risk for COVID‐19 vaccines and the “laundry list” nature of informed consents, disclosure of the specific risk of worsened COVID‐19 disease from...
@NHSEngland@OUHospitals@OxfordVacGroup@AstraZeneca vaccination calls for a specific, separate, informed consent form and demonstration of patient comprehension in order to meet medical ethics standards."
@CMO_England Regulatory "checks and balances".
House of Commons Health Committee:
"The Secretary of State for Health
cannot serve two masters. The Department seems unable to prioritise the interests of
patients and public health...
... over the interests of the pharmaceutical industry. We therefore
recommend that sponsorship of the industry¹ pass from the Department of Health to the
Department of Trade and Industry."
¹ Now known as “responsibility for representing the interests of the industry".
This is why our 'government' were confident enough to purchase millions of doses of unapproved vaccines with tax payer money, well in advance of even the first trials being published...you always knew