by Rhoda Wilson, Expose News:
In the UK, we have the right to request information from any public body and get answers. WhatDoTheyKnow is a non-governmental website that helps us make a Freedom of Information (“FoI”) request and publishes all the requests and responses online.
We were curious to know if our public health bodies were testing samples of batches of covid vaccines administered in the UK to ensure the ingredients were as they have publicly declared. So, we conducted a quick search.
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A simple search for ““vaccine batches”” on WhatDoTheyKnow, returns 50 results with some FoIs sent to multiple institutions. To view a list of these 50 FoIs the search words entered into the website’s search box are enclosed in double quotation marks (e.g., “search term”) to refine the search.
A search for “vaccine batches” not enclosed in quotation marks returns 200 results, although this will include results for both of the single words “vaccine” and “batches” as well. The word “batches” could be used to describe almost anything so many of the results will be unrelated to vaccines, let alone covid vaccines.
Below is a list of the FoIs relating to covid vaccine ingredients selected from the first two pages of results using the search term “vaccine batches” (without quotation marks). We’ve reordered the FoIs so that they are listed in ascending date order.
Some of the FoIs are lengthy, so we have shown little more than a brief one-line extract from each. A hyperlink to the specific FoI is contained in the institution’s name.
In our list, for each of the FoIs, we begin with the title of the FoI followed by the date the request was made, the institution the request was made to, what the request asked (in italics), the response and the status (in bold type). Please note the status of the request is completed by the requestor and not the institution the information is being requested from.
The Medicines and Healthcare products Regulatory Agency (“MHRA”) is the regulator of medicines, medical devices and blood components for transfusion in the UK. “We rigorously use science and data to inform our decisions, enable medical innovation and to make sure that medicines and healthcare products available in the UK are safe and effective,” MHRA states.
One of its responsibilities is to “educate the public and healthcare professionals about the risks and benefits of medicines, medical devices and blood components, leading to safer and more effective use.”
A number of the 16 FoIs below were requests made to the MHRA. Even though this is merely a quick overview, MHRA’s responses, or lack thereof, are quite revealing and indicate they do not “rigorously use science and data” to ensure healthcare products available in the UK are safe and effective. If they are not rigorously using science and data, how are they able to educate the public and healthcare professionals about the risks and benefits of products that fall under their responsibility?
1. Percentage of Placebo’s in Vaccine Rollout, 18 April 2021, Public Health Scotland
Can you confirm if, and how many placebo vaccines, by percentage or ratio, have been administered to the public in the vaccine rollout for Scotland?
Public Health Scotland does not hold the information outlined in your request.
Placebo vaccines have not been administered as part of the vaccine rollout programme in Scotland and are only administered as part of consented clinical trials. Furthermore, Public Health Scotland has not been directly involved in clinical trials for either the Astra Zeneca or Pfizer vaccinations.
Successful
2. Covid vaccines and saline, 19 April 2021 and 21 April 2021, NHS England and Public Health Scotland
How many of the batches contained saline, and how many doses of saline on average per batch?
NHS England: There are no “doses” of saline – it is contained, in a small amount, within each vaccine.
Public Health Scotland: Public Health Scotland does not hold the information outlined in your request.
Partially successful and Awaiting classification
3. Which medicines that are currently being used in England, contain graphene oxide or derivatives of graphene oxide, 5 October 2021, Medicines and Healthcare Products Regulatory Agency
Which medicines that are currently being used in England, contain graphene oxide or derivatives of graphene oxide?
And please specify if any of the ingredients of any medicines are not published due to trade secrets.
Do you obtain independent laboratory reports to confirm the ingredients or do you rely on the drug manufacturer?
Please let me have a copy of the independent laboratory reports detailing the analysis of the ingredients of the Pfizer, Moderna, AstraZeneca, and Johnson & Johnson Covid-19 “vaccines.”
No licensed medicines or those under emergency use in England contain graphene.
All excipients are published.
No licensed medicines or medicines under emergency use authorisation in England contain either graphene oxide or derivatives of graphene oxide.
There are no “trade secret” ingredients which are not published.
All vaccines authorised and deployed in the UK have been subject to rigorous checks by the MHRA, including individual batch testing and site inspections, even where those sites are outside the UK.
Regarding your request for the independent laboratory reports detailing the analysis of the ingredients of the Pfizer, Moderna, AstraZeneca, and Johnson & Johnson Covid-19 vaccines, MHRA neither confirms nor denies that it holds information falling within the description specified in your request.
Information not held (Note: an internal review was requested.)
4. Contaminants in the UK Covid experimental vaccines, 12 January 2022, Medicines and Healthcare Products Regulatory Agency
Can you please clarify if routine independent batch testing of sample vials is invasive (i.e. it involves testing of the actual content of the vials) and, if so, who holds the related images and data, if not you?
We have already responded about visual inspection and it is not an invasive test.
Long overdue
5. Manufacturing tolerances and Quality Assurance of COVID-19 vaccines, 21 February 2022, Medicines and Healthcare Products Regulatory Agency
[Please provide] full manufacturing specifications of the contents of all Covid-19 vaccines licenced by MHRA.
This information would be exempt under Section 41 and Section 43 of the Freedom of Information Act.
Refused (Note: an internal review was requested to no avail.)
