Vaccine

An "urgent preliminary report of Yellow Bill of fare information" issued by the Uk-based Evidence-Based Medicine Consultancy Ltd submitted to the Medicines and Healthcare Products Regulatory Agency (MHRA) states that "the MHRA now has more than plenty prove on the Yellow Card arrangement to declare the COVID-19 vaccines unsafe for use in humans."

Like to the U.S. Vaccine Adverse Events Reporting System (VAERS), the MHRA describes the purpose of its Yellow Card system as providing "an early on alarm that the rubber of a medicine or a medical device may require further investigation."

The report, signed by Evidence-based Medicine Consultancy Ltd and EbMC Squared CiC Manager Dr. Tess Lawrie (MBBCh, PhD), says:

"we take searched the Yellow Carte reports using pathology-specific key words to group the data according to the following five [sic] broad, clinically relevant categories:
  • Bleeding, Clotting and Ischaemic ADRs
  • Allowed System ADRs
  • 'Pain' ADRs
  • Neurological ADRs
  • ADRs involving loss of Sight, Hearing, Voice communication or Scent
  • Pregnancy ADRs"

The report goes on to say:

"We are aware of the limitations of pharmacovigilance data and sympathise that information on reported Agin Drug Reactions should not be interpreted as pregnant that the medicine in question by and large causes the observed upshot or is unsafe to use. We are sharing this preliminary report due to the urgent need to communicate information that should lead to cessation of the vaccination rollout while a total investigation is conducted. Co-ordinate to the recent paper by Seneff and Nigh, potential acute and long-term pathologies include:
Pathogenic priming, multisystem inflammatory disease and autoimmunity
  • Allergic reactions and anaphylaxis
  • Antibody dependent enhancement
  • Activation of latent viral infections
  • Neurodegeneration and prion diseases
  • Emergence of novel variants of SARSCoV2
  • Integration of the spike protein gene into the human Dna
"Information technology is now apparent that these products in the blood stream are toxic to humans. An firsthand halt to the vaccination programme is required whilst a total and independent safety analysis is undertaken to investigate the total extent of the harms, which the UK Yellow Card information advise include thromboembolism, multisystem inflammatory disease, immune suppression, autoimmunity and anaphylaxis, as well as Antibiotic Dependent Enhancement (ADE)."

The report concludes:

"The MHRA at present has more than enough evidence on the Xanthous Card organization to declare the COVID-nineteen vaccines unsafe for employ in humans. Preparation should be fabricated to scale up humanitarian efforts to assist those harmed by the COVID-19 vaccines and to anticipate and improve 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.

"In that location are at least 3 urgent questions that need to exist answered by the MHRA:

  1. How many people have died inside 28 days of vaccination?
  2. How many people have been hospitalised within 28 days of vaccination?
  3. How many people have been disabled by the vaccination?"