Vaccine

An "urgent preliminary report of Yellow Bill of fare data" issued past the Britain-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 evidence on the Yellow Card system 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 Carte organization equally providing "an early alert that the safe of a medicine or a medical device may require farther investigation."

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

"we accept searched the Yellow Carte reports using pathology-specific key words to group the data according to the post-obit 5 [sic] broad, clinically relevant categories:
  • Haemorrhage, Clotting and Ischaemic ADRs
  • Allowed System ADRs
  • 'Pain' ADRs
  • Neurological ADRs
  • ADRs involving loss of Sight, Hearing, Speech or Odour
  • Pregnancy ADRs"

The report goes on to say:

"Nosotros are aware of the limitations of pharmacovigilance information and sympathize that information on reported Agin Drug Reactions should non be interpreted as pregnant that the medicine in question generally causes the observed effect 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 full investigation is conducted. According 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
"It is now credible that these products in the blood stream are toxic to humans. An immediate halt to the vaccination programme is required whilst a full and independent safety analysis is undertaken to investigate the full extent of the harms, which the UK Xanthous Card data suggest include thromboembolism, multisystem inflammatory disease, immune suppression, autoimmunity and anaphylaxis, as well every bit Antibody Dependent Enhancement (ADE)."

The report concludes:

"The MHRA at present has more than enough prove on the Xanthous Bill of fare system to declare the COVID-nineteen vaccines dangerous for use in humans. Training should be made to scale upwards humanitarian efforts to assist those harmed by the COVID-xix vaccines and to anticipate and ameliorate medium to longer term effects. As the mechanism for harms from the vaccines appears to exist similar to COVID-xix itself, this includes engaging with numerous international doctors and scientists with expertise in successfully treating COVID-nineteen.

"There are at least 3 urgent questions that need to exist answered past the MHRA:

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