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Human Genocide Alert
- Thread starter Roms
- Start date
although i was right to reject the jab for several wrong reasons which i have finally come to understand, i.e. gain of function is a mythology to invoke fear, a coronavirus can not pandemic since it mutates so fucking fast, sars-cov-2 did not spread across county lines, injecting anything into a muscle thinking that will improve respiratory immune function is just dumb ... all i can say is thank-you god ... grace is always unearned but always appreciated.
what i did get correct is that codon optimization is bad and good manufacturing in big batches is impossible ... just from the biology and engineering principles.
breaks my heart to see this nightmare play out, right in front of me. malthusians for the win! damn, they play the long game.
what i did get correct is that codon optimization is bad and good manufacturing in big batches is impossible ... just from the biology and engineering principles.
breaks my heart to see this nightmare play out, right in front of me. malthusians for the win! damn, they play the long game.
that looks incredibly weird. he shows no signs of distress to my eyes until a second before he collapses.
A million COVID vaccinated people died in England last year, compared to only 61,000 unvaccinated people
Antiilluminati TV December 11, 2023
Eine Million COVID-Geimpfte starben im vergangenen Jahr in England, verglichen mit nur 61.000 Ungeimpften
In den letzten zwei Jahren ist die Zahl der Todesfälle in England sprunghaft angestiegen, insbesondere unter den "vollständig geimpften" Personen gegen das Wuhan-Coronavirus (COVID-19). Neue Regierungsdaten zeigen, dass seit Anfang 2022 eine Million vollständig geimpfte Menschen in England...
telegra.ph
N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting - Nature
A study demonstrates that nucleotide modifications in mRNA-based therapeutics can lead to +1 ribosomal frameshifting during translation, yielding products that can trigger immune responses.
www.nature.com
Plandemic 3 VOSTFR
The Great Awakening est le troisième volet de la série Plandemic. Ce documentaire assemble les pièces interdites d'un puzzle pour révéler la grande image de ce qui se passe réellement en Amérique et a...
odysee.com
Top Expert Warns Public of America’s ‘Staggering’ Excess Deaths
By Frank Bergman
Top Expert Warns Public of America's 'Staggering' Excess Deaths - Slay News
A leading expert has appeared on national television to warn the American people about the "staggering" numbers of excess deaths that are being recorded across the country.
slaynews.com
US Mortality Rates Remain Increasing Long After COVID Pandemic; Why Are Americans Dying So Young?
US Mortality Rates Remain Increasing Long After COVID Pandemic; Why Are Americans Dying So Young?
A new study reveals that US mortality rates are far higher than peer nations, especially among young and working-age adults. Find out more about it in this article.
www.sciencetimes.com
Mary Talley Bowden MD
@MdBreathe
We now have 29 candidates and 23 elected officials from 14 states publicly stating the COVID shots must be pulled off the market. Over 17,000 physicians stand behind them. Please reward their courage with your support. (List is too long now for one post.) Candidates running for office:
@GhannonBurton
US Senate MS
@votemjs
US House NC HD13
@NateCain4WV
US House WV-2
@ReidRasner
US Senate in WY
@realTJRoberts
KY HD66
@DavidLowe4Texas
TX HD91
@Jack4TX99
TX HD99
@thejamesonellis
US House TX-2
@CarolineKaneTX
US House TX-7
@Julie_ClarkTX
US House TX-23
@Perez4Texas
TX HD133
@BiancaForTexas
TX HD128
@ByrnForTexas
TX HD71
@AndyHopperTX
TX HD64
@ShelleyLuther
TX HD62
@duke4texas
TX HD56
@WesleyVirdell
TX HD53
@AliciaForTexas
TX HD21
@tomgglass
TX HD17
@JayeforTXHD8
TX HD8
@Collier4Texas
TX HD5
@HulsintheHouse
TX HD1
@JustTheTweets17
TX159 Precinct Chair @DrHorwitz1A Rockwall TX Precinct Chair
@Nomoretweedles
AZ US Sen 24
@kupper4arizona
AZ LD25
@MaraMacie
FL HD5
@julie4butte5
Butte County Supervisor, CA, D5
@NHGOGAL
NH Laconia D5 Ask your congressmen if they will add their names to the list. Post this list on their timelines.
7:08 AM · Dec 20, 2023
·
15.3K
Views
@MdBreathe
We now have 29 candidates and 23 elected officials from 14 states publicly stating the COVID shots must be pulled off the market. Over 17,000 physicians stand behind them. Please reward their courage with your support. (List is too long now for one post.) Candidates running for office:
@GhannonBurton
US Senate MS
@votemjs
US House NC HD13
@NateCain4WV
US House WV-2
@ReidRasner
US Senate in WY
@realTJRoberts
KY HD66
@DavidLowe4Texas
TX HD91
@Jack4TX99
TX HD99
@thejamesonellis
US House TX-2
@CarolineKaneTX
US House TX-7
@Julie_ClarkTX
US House TX-23
@Perez4Texas
TX HD133
@BiancaForTexas
TX HD128
@ByrnForTexas
TX HD71
@AndyHopperTX
TX HD64
@ShelleyLuther
TX HD62
@duke4texas
TX HD56
@WesleyVirdell
TX HD53
@AliciaForTexas
TX HD21
@tomgglass
TX HD17
@JayeforTXHD8
TX HD8
@Collier4Texas
TX HD5
@HulsintheHouse
TX HD1
@JustTheTweets17
TX159 Precinct Chair @DrHorwitz1A Rockwall TX Precinct Chair
@Nomoretweedles
AZ US Sen 24
@kupper4arizona
AZ LD25
@MaraMacie
FL HD5
@julie4butte5
Butte County Supervisor, CA, D5
@NHGOGAL
NH Laconia D5 Ask your congressmen if they will add their names to the list. Post this list on their timelines.
7:08 AM · Dec 20, 2023
·
15.3K
Views
Breaking: Pfizer Whistleblower Brook Jackson’s Legal Team Filed Their Opposition for Pfizer’s Request to Dismiss in Federal Court Tonight
Excerpt From Their Filing: “Pfizer promised a vaccine to inoculate against and prevent the infection and transmission of Covid-19, one which was shown to meet the objective standards for Emergency Use Authorization as required by Congress. Pfizer’s contract with the Government required it to obtain such authorization from the FDA through honest reporting of its clinical trials.
Instead, Pfizer fabricated and falsified the reports and results, obtaining the authorization through fraud. What Pfizer delivered was a dangerous, ineffective drug that did not prevent transmission, infection or even therapeutically treat Covid-19, as honest reports to the FDA would have revealed.
Brook Jackson was the first to witness this directly at the clinical trial sites, raised her concerns directly with the defendants, but was fired instead.
The Pfizer “vaccines” fail to accomplish the principal benefits for which they were authorized and paid for: prevent infection with SARS-Cov-2 or stop transmission of Covid-19 from one individual to another. Data indicate the injections have "negative efficacy" -- the more doses a person receives, the more likely that person will get sick with Covid-19. Worse, Pfizer’s Covid-19 vaccines have staggering “downsides.”
Since the biologics were authorized, they have caused an alarming increase in spike-protein diseases, including heart and blood disorders, cancers, autoimmune diseases, neurological diseases, fertility disorders, and deaths.
Relator Jackson contends that well-controlled clinical trials of Pfizer’s Covid-19 vaccines would have revealed, prior to authorization, that the product failed to confer benefits and caused significant harm.
Furthermore, Ms. Jackson alleges Pfizer knew this and knew it could not legitimately obtain U.S. Food and Drug Administration (FDA) approval or authorization. Under the Emergency Use Authorization (EUA) statute, 21 U.S. Code § 360bbb–3(c), Congress required an objective basis to believe, based on the totality of scientific evidence available, that the “known and potential benefits” outweigh the “known and potential risks.”
Adequate and well-controlled clinical trials would have been a big part of the available scientific evidence. They would have revealed the lack of benefits for Pfizer’s Covid-19 vaccines and significant potential risks– foreclosing the FDA’s issuance of an EUA.
Relator Jackson alleged Pfizer abandoned the scientific method and the search for truth to induce FDA’s authorization of its modRNA biologic to enable it to sell the United States 100 million doses (for $1.9 billion). Ms. Jackson has alleged Pfizer engaged in fraud in the design, conduct, analysis and reporting of its clinical trials, and in statements it made to FDA.
In her Second Amended Complaint (SAC), Ms. Jackson details her knowledge of the particular circumstances in which Pfizer engaged in clinical trial fraud to induce FDA’s issuance of the EUA. Among other things, this includes a trial design to avoid disclosure on immunity and transmission; short-cutting the study to conceal negative efficacy and serious adverse events; manipulation of inclusion and exclusion determinations to reach predetermined results; unblinding of subject status and then falsely reporting the occurrence or non-occurrence of adverse events based on the subject’s disclosed status; and suppression of available alternatives.
Ms. Jackson saw this conduct first-hand as a Regional Director at Defendant Ventavia Research Group, which ran three test sites in Pfizer’s clinical trial. She pleads her own observations of material deviations from protocol as representative examples of the fraud committed by Pfizer.”
Excerpt From Their Filing: “Pfizer promised a vaccine to inoculate against and prevent the infection and transmission of Covid-19, one which was shown to meet the objective standards for Emergency Use Authorization as required by Congress. Pfizer’s contract with the Government required it to obtain such authorization from the FDA through honest reporting of its clinical trials.
Instead, Pfizer fabricated and falsified the reports and results, obtaining the authorization through fraud. What Pfizer delivered was a dangerous, ineffective drug that did not prevent transmission, infection or even therapeutically treat Covid-19, as honest reports to the FDA would have revealed.
Brook Jackson was the first to witness this directly at the clinical trial sites, raised her concerns directly with the defendants, but was fired instead.
The Pfizer “vaccines” fail to accomplish the principal benefits for which they were authorized and paid for: prevent infection with SARS-Cov-2 or stop transmission of Covid-19 from one individual to another. Data indicate the injections have "negative efficacy" -- the more doses a person receives, the more likely that person will get sick with Covid-19. Worse, Pfizer’s Covid-19 vaccines have staggering “downsides.”
Since the biologics were authorized, they have caused an alarming increase in spike-protein diseases, including heart and blood disorders, cancers, autoimmune diseases, neurological diseases, fertility disorders, and deaths.
Relator Jackson contends that well-controlled clinical trials of Pfizer’s Covid-19 vaccines would have revealed, prior to authorization, that the product failed to confer benefits and caused significant harm.
Furthermore, Ms. Jackson alleges Pfizer knew this and knew it could not legitimately obtain U.S. Food and Drug Administration (FDA) approval or authorization. Under the Emergency Use Authorization (EUA) statute, 21 U.S. Code § 360bbb–3(c), Congress required an objective basis to believe, based on the totality of scientific evidence available, that the “known and potential benefits” outweigh the “known and potential risks.”
Adequate and well-controlled clinical trials would have been a big part of the available scientific evidence. They would have revealed the lack of benefits for Pfizer’s Covid-19 vaccines and significant potential risks– foreclosing the FDA’s issuance of an EUA.
Relator Jackson alleged Pfizer abandoned the scientific method and the search for truth to induce FDA’s authorization of its modRNA biologic to enable it to sell the United States 100 million doses (for $1.9 billion). Ms. Jackson has alleged Pfizer engaged in fraud in the design, conduct, analysis and reporting of its clinical trials, and in statements it made to FDA.
In her Second Amended Complaint (SAC), Ms. Jackson details her knowledge of the particular circumstances in which Pfizer engaged in clinical trial fraud to induce FDA’s issuance of the EUA. Among other things, this includes a trial design to avoid disclosure on immunity and transmission; short-cutting the study to conceal negative efficacy and serious adverse events; manipulation of inclusion and exclusion determinations to reach predetermined results; unblinding of subject status and then falsely reporting the occurrence or non-occurrence of adverse events based on the subject’s disclosed status; and suppression of available alternatives.
Ms. Jackson saw this conduct first-hand as a Regional Director at Defendant Ventavia Research Group, which ran three test sites in Pfizer’s clinical trial. She pleads her own observations of material deviations from protocol as representative examples of the fraud committed by Pfizer.”
"spike-protein diseases"
what a tedious life you lead
William Makis MD@MakisMDRadiologist, Oncologist, Chief of Oncology at TWC http://makismd.substack.com Edmonton, Alberta makismd.substack.com
