UK Doctors Call for Government Investigation of mRNA Covid Vaccines

Discussion in 'Coronavirus Pandemic Discussions' started by Kokomojojo, Jan 24, 2023.

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  1. Kokomojojo

    Kokomojojo Well-Known Member

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    How about that? The other shoe drops! Quick get your Vax ASAP!

    Doctors Speak out! :eekeyes: :winner:

    (Doctors for Patients UK)
    (DFPUK) — Many doctors, in the UK and internationally, have become increasingly concerned about the safety profile of Covid-19 vaccines and the continued rollout of these products to the public, including pregnant women and children. Several doctors in DFPUK have submitted multiple Yellow Card reports of adverse events to the MHRA, and have signed letters to the JCVI, MHRA, the RCOG, Prime Minister and others to express their concerns, but have seen little or no response or action taken.

    Doctors for Patients UK (DFPUK) was launched in September 2022 and has become a fast-growing group of UK doctors who are dedicated to practising ethical, evidence-based, patient-centred medicine. Our group was borne out of increasing concerns that core principles of medical ethics are being disregarded, such as the oath to “First do no harm”, respect for individual bodily autonomy and the need to obtain full and informed consent for all medical interventions.

    https://worldcouncilforhealth.org/news/news-releases/uk-doctors-investigation-c19-vaccines/

    Vax me!

    Vax me quickly!

    I want my daily jab!

    Discuss!
     
    Last edited: Jan 24, 2023
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  2. Kokomojojo

    Kokomojojo Well-Known Member

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    Specifically, EMA had major concerns over unexpectedly low quantities (around 55%) of intact mRNA in batches of the vaccine developed for commercial production.

    It is an issue relevant not just to Pfizer-BioNTech’s vaccine but also to those produced by Moderna, CureVac, and others, as well as a “second generation” mRNA vaccine being pursued by Imperial College London.

    In an email dated 23 November, a high ranking EMA official outlined a raft of issues. In short, commercial manufacturing was not producing vaccines to the specifications expected, and regulators were unsure of the implications on safety and efficacy.

    EMA responded by filing two “major objections” with Pfizer, along with a host of other questions it wanted addressed.

    Ultimately, on 21 December, EMA authorised Pfizer-BioNTech’s vaccine and a report published on its website, noted, “the quality of this medicinal product, submitted in the emergency context of the current (covid-19) pandemic, is considered to be sufficiently consistent and acceptable.”

    However, it’s unclear how the agency’s concerns were satisfied, writes Tinari.

    The BMJ asked Pfizer, Moderna, and CureVac, as well as several regulators, what percentage mRNA integrity they consider acceptable for vaccines against covid-19.

    None offered any specifics, and in subsequent correspondence, EMA, US Food and Drug Administration (FDA), and Canadian medicines regulator Health Canada all stated that specific information related to the acceptability criteria is confidential.

    Pfizer also declined to comment on what percentage mRNA integrity it is aiming for, nor would it address questions about the cause of the unexpectedly low percentage mRNA integrity in certain batches, leaving open the question of whether it could happen again.

    Moderna declined to respond to any of The BMJ’s questions, while CureVac told The BMJ that “it is too soon to give details.”

    https://www.bmj.com/company/newsroo...-of-mrna-molecules-in-some-covid-19-vaccines/
     
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  3. Eleuthera

    Eleuthera Well-Known Member Donor

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    Related is the coverage yesterday on Full Measure with interviews of a handful of doctors and nurses from Houston Methodist Hospital. Sorry for no link, I'm unable to get to it on internet, but the piece was great.

    Those medical professionals who refused the shot mandate at Houston Methodist told quite a story.
     

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