Hydroxychloroquine has a long history of use for the prevention of malaria. It has been considered to be a very safe drug for several decades. The “off label” policy of the FDA allows doctors to prescribe medications for any condition, as they see fit. An approved drug does not need additional approvals for a doctor…
If you are feeling pressured to take a vaccine, DO NOT QUIT YOUR JOB! Make your boss fire you. Please see the statement from America’s Front Line Doctors about this. As of August 23, 2021, the Pfizer-BioNTech inoculation is now approved under the brand name Comirnaty. The Comirnaty/Pfizer-BioNTech Fact Sheet for Healthcare Providers Administering Vaccine…
NCVIA’s purpose was to eliminate the potential financial liability of vaccine manufacturers due to vaccine injury claims in order to ensure a stable market supply of vaccines, and to provide cost-effective arbitration for vaccine injury claims. The Justice Department was put in charge of the compensation program in an unprecedented arrangement. Vice President George H.…
The BWATA extended the scope of bio-warfare materials regulation to include private individuals and non-state organizations. Drafted by Francis Boyle. Loophole: Sec. 2(b) has a “peaceful purposes” clause. SEC. 2. PURPOSE AND INTENT. (a) PURPOSE.—The purpose of this Act is to— (1) implement the Biological Weapons Convention, an international agreement unanimously ratified by the United…
Ivermectin is an anti-parasite medication. Ivermectin is used to treat infections in the body that are caused by certain parasites. — The Vigilant Fox 🦊 Sources:
From the patent: The present invention provides the amino acid and nucleotide sequences of a CCV spike gene, and compositions containing one or more fragments of the spike gene and encoded polypeptide for prophylaxis, diagnostic purposes and treatment of CCV infections. — Patent US6372224B1 This is the patent for the spike protein virus, a vaccine…
The Model State Emergency Health Powers Act is prepared by The Center for Law and the Public’s Health at Georgetown and Johns Hopkins Universities for the Centers for Disease Control and Prevention [CDC] The MSEHPA (Model State Emergency Health Powers Act) which was passed by many states in 2002, included provisions that would allow state…
A helper cell for producing an infectious, replication defective, coronavirus (or more generally nidovirus) particle cell comprises (a) a nidovirus permissive cell; (b) a nidovirus replicon RNA comprising the nidovirus packaging signal and a heterologous RNA sequence, wherein the replicon RNA further lacks a sequence encoding at least one nidovirus structural protein; and (c) at…
Disclosed herein is a newly isolated human coronavirus (SARS-CoV), the causative agent of severe acute respiratory syndrome (SARS). Also provided are the nucleic acid sequence of the SARS-CoV genome and the amino acid sequences of the SARS-CoV open reading frames, as well as methods of using these molecules to detect a SARS-CoV and detect infections…
The invention provides compositions and methods that are useful for preventing and treating a coronavirus infection in a subject. More specifically, the invention provides peptides and conjugates and pharmaceutical compositions containing those peptides and conjugates that block fusion of a coronavirus, such as the SARS virus, to a target cell. This blocking mechanism prevents or…
Abstract Background Syndromic surveillance uses health-related data that precede diagnosis and signal a sufficient probability of a case or an outbreak to warrant further public health response. Objective While most syndromic surveillance systems rely on data from clinical encounters with health professionals, I started to explore in 2004 whether analysis of trends in Internet searches…
Dartmouth-Hitchcock Medical Center thought it had an outbreak of whooping cough. Nearly 1,000 staff members were given a PCR test. 142 of them came back positive. Later, more definitive testing was done. Not a single case of whooping cough was confirmed with the definitive test. Instead, it appears that the staff probably had ordinary respiratory…
Disclosed herein is a newly isolated human coronavirus (SARS-CoV), the causative agent of severe acute respiratory syndrome (SARS). Also provided are the nucleic acid sequence of the SARS-CoV genome and the amino acid sequences of the SARS-CoV open reading frames, as well as methods of using these molecules to detect a SARS-CoV and detect infections…
The present invention relates in part to amino acid sequences that are directed against and/or that can specifically bind to an envelope protein of a virus, as well as to compounds or constructs, and in particular proteins and polypeptides, that comprise or essentially consist of one or more such amino acid sequences. — Patent US9193780B2…
Grant Final Report: Review of Vaccine Adverse Event Reporting System (VAERS) determines that fewer than 1% of vaccine adverse events are reported. Even if we assume that the COVID-19 situation has created increased awareness of VAERS, we can assume that adverse reactions are still grossly underreported. If nothing has changed, this means that statistics derived…
The CDC is not the only one considering this possibility. Check out item 42.10 from the “AWS [Amazon Web Services] Service Terms, Last Updated: September 2, 2021”: 42.10. Acceptable Use; Safety-Critical Systems. Your use of the Lumberyard Materials must comply with the AWS Acceptable Use Policy. The Lumberyard Materials are not intended for use with life-critical…
The provision is part of H.R.4310 – National Defense Authorization Act for Fiscal Year 2013 passed by the 112th Congress (2011-2012). I suppose we were too smart to pass the Smith-Mundt Modernization Act of 2012 but not smart enough to block it as part of the National Defense Authorization Act for Fiscal Year 2013. Sources:…
On behalf of the U.S. government, often the military, Daszak scours the globe for animal pathogens and brings them back to the lab to be catalogued, investigated and manipulated. $ Award Amounts: $3.7M Grant description: Understanding the risk of bat coronavirus emergence But this is just one project. A search of the system showed 37…
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They were assessing “gain-of-function” studies. Some call this “chimeric research” because it involves the mixing of DNA from various species. According to Marc Lipsitch, and Thomas Inglesby: The purpose of this research funding pause is to complete “a robust and broad deliberative process … that results in the adoption of a new [U.S. Government] gain-of-function…
Sometime in 2015, most likely: Someone at the NIH approved money to be used for research at the Wuhan lab. The timing would suggest that this was done to skirt the 2014 congressional moratorium on gain of function research. For the last year and a half, questions have been raised about how and why EcoHealth…
The Wuhan National Biosafety Laboratory’s (WNBL) BSL-4 lab was constructed as a result of an agreement between the PRC and France that was signed after the 2003 SARS pandemic. Construction was completed in 2015, but due to delays the BSL-4 space did not become operational until early 2018. This is an addition to an existing…
The workshop was “Rapid Medical Countermeasure Response to Infectious Diseases: Enabling Sustainable Capabilities Through Ongoing Public- and Private-Sector Partnerships.” In it, Peter Daszak gave a presentation, “Ranking risk for zoonotic potential of novel viruses.” In this speech, he was quoted as saying, Until an infectious disease crisis is very real, present, and at an emergency…
The present invention provides a live, attenuated coronavirus comprising a variant replicase gene encoding polyproteins comprising a mutation in one or more of non-structural protein(s) (nsp)-10, nsp-14, nsp-15 or nsp-16. The coronavirus may be used as a vaccine for treating and/or preventing a disease, such as infectious bronchitis, in a subject. — Patent US10130701B21 Sources:…
This executive order helped set the stage to be able to ban travel from countries affected by COVID-19. By the time that the virus showed up, the precedent was set to be able to ban travel. Source:
This executive order helped set the stage to be able to ban travel from countries affected by COVID-19. By the time that the virus showed up, the precedent was set to be able to ban travel. Source:
A method is provided for processing and displaying biometric data of a user, either alone or together (in synchronization) with other data, such as video data of the user during a time that the biometric data was acquired. The method includes storing biometric data so that it is linked to an identifier and at least…
An eligible investigational drug is an investigational drug: For which a Phase 1 clinical trial has been completed That has not been approved or licensed by the FDA for any use For which an application has been filed with the FDA or is under investigation in a clinical trial that is intended to form the primary basis…
On September 12, 2019 the WIV’s online, public database of samples and virus sequences was taken offline in the middle of the night between 2:00AM and 3:00AM local time. The database contained more than 22,000 entries consisting of sample and pathogen data collected from bats and mice. The database contained key information about each sample,…
On March 13, 2020, it was reported that the first case of someone in China suffering from Covid-19, the disease caused by the novel coronavirus, can be traced back to November 17. Sources:
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His post: 7 confirmed cases of SARS were reported [to hospital] from Huanan Seafood Market. For this, he was reprimanded for leaking and publishing untrue information. He was made to sign a letter of admonition promising not to do it again. Sources: Related:
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Charles Lieber, the chair of Harvard University’s Department of Chemistry and Chemical Biology, was arrested. He was accused of lying about his contact with the Chinese program, Thousand Talents Plan, which the U.S. has previously flagged as a serious intelligence concern. He invented the virus sized transistors. Sources: Related: See also, on this site: Harvard…
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The Lancet published a Statement in Support of the Scientists, Public Health Professionals, and Medical Professionals of China Combatting COVID-19. These are the people who signed the statement. Many of them have an economic stake in the jabs. Charles Calisher: Colorado State University, Fort Collins, CO, USA Dennis Carroll: Scowcroft Institute of International Affairs, Texas…
Rx Only No descriptive printed matter, advertising and promotional materials, relating to the use of your product may represent or suggest that this test is safe or effective for the detection of SARS-CoV-2. The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of…
It’s not COVID-19 that’s killing Americans. It is Remdesivir poisoning causing acute kidney failure, pulmonary edema, flooding their lungs with water and they’re drowning them to death, which is why they’re requiring, supposedly, to vent these people. And that’s what’s killing these people, is Remdesivir poisoning, not COVID-19. Now, how do I know this? Amazingly,…
Operation Warp Speed (OWS) was a public–private partnership initiated by the United States government to facilitate and accelerate the development, manufacturing, and distribution of COVID-19 vaccines, therapeutics, and diagnostics. Moncef Slaoui and Gen. Gustave Perna were named as leads for Operation Warp Speed. Pres. Trump has always emphasized that acceptance of the vaccines is voluntary. They are not to…
A method is provided for acquiring and transmitting biometric data (e.g., vital signs) of a user, where the data is analyzed to determine whether the user is suffering from a viral infection, such as COVID-19. The method includes using a pulse oximeter to acquire at least pulse and blood oxygen saturation percentage, which is transmitted…
Stephen Hahn is Commissioner of the Food & Drug Administration when this happens. An exception is made for treating hospital patients. The rationale for this action is based on the Surgisphere studies that were retracted on June 2, 2020. The retraction took place prior to the date of the revocation of EUA for HCQ. This…
Note that Dr. Carrie Madej made this video well before the jab rollouts. Dr. Madej claims to have first-hand knowledge of the intentions behind technology included in the inoculations, and she has had this knowledge for a long time. If her statements about her history are true, then the comments she makes about the technology…
Note especially the bottom of page 69 where it talks about Occupational Exposures–encounters between vaccinated and non-vaccinated. These are references to potential shedding issues. Sources: Related: See also, on this site: Study finds increased death rate for children of jabbed parents
Bill Gates and Anthony Fauci endorse REGEN-COV. Sources:
System and methods for anonymously selecting subjects for treatment against an infectious disease caused by a pathogen. The system comprises a plurality of electronic devices comprising instructions to generate an ID and, when in proximity of another such electronic device, one or both electronic devices transmit/receive the ID to/from the other electronic device. Then, a…
The study presented in the Emergency Use Authorization based its efficacy assessment on the results of PCR tests, which we now know are unreliable and prone to errors. Page 41 includes additional data about people who actually got sick after the inoculation. Significantly more people got sick in the test group after vaccination than in…
Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), when the Secretary of HHS declares that an emergency use authorization is appropriate, FDA may authorize unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or…
Notice in this CDC post that it says “will be” rigorously evaluated for safety. Two months later at the time this is posted, after many have been injected with it, evaluation is still in the future. Source: See also, on this site: The CDC modifies its assurances about mRNA “vaccines”
This new designation upgraded the status of ivermectin from “against” to “neither for nor against”, which is the same recommendation given to monoclonal antibodies and convalescent plasma, both widely used across the nation. — Front Line COVID-19 Critical Care Alliance (FLCCC), January 15, 2021 So that paragraph on the NIH page now reads: There is…
The CDC keeps a database: Vaccine Adverse Event Reporting System (VAERS). The VAERS is a voluntary system. Only a fraction of actual adverse reactions are reported here. Symptom 2021 2015-2019 per year Rate increase (X Factor) Blue toe syndrome 10 0.0 INFINITE Pulmonary embolism 946 2.0 473.0 Deep vein thrombosis 740 2.8 264.3 Thrombosis 2255…
Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), when the Secretary of HHS declares that an emergency use authorization is appropriate, FDA may authorize unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or…
Someone noticed the following when reviewing the August 27, 2021, report from the CDC. The CDC published some data that had been received from Los Angeles. The following can be found on page 3 below the spreadsheet data: * Persons were considered fully vaccinated ≥14 days after receipt of the second dose in a 2-dose…
Dr. Charles Hoffe reports that 62% of his patients show evidence of micro-clots within one week of vaccination. This means that the blood clots are not rare. The majority of people are getting blood clots that they have no idea that they are even having. These clots are microscopic and block circulation at the capillary…
The correct date for this post is somewhat unclear, but we’ll just go with this one. As of March 1, 2021, the American Red Cross had this on their “Can I Donate after Receiving a COVID-19 Vaccine?” page: Can I donate COVID-19 convalescent plasma if I have received the vaccination? At this time individuals who…
As of May 1, 2021, CDC transitioned from monitoring all reported vaccine breakthrough cases to focus on identifying and investigating only hospitalized or fatal cases… The following is the new standard for testing breakthrough cases: For cases with a known RT-PCR cycle threshold (Ct) value, submit only specimens with Ct value ≤28 to CDC for…
The CDC changed what they are counting. As of May 1, 2021, CDC transitioned from monitoring all reported vaccine breakthrough cases to focus on identifying and investigating only hospitalized or fatal cases due to any cause. This shift will help maximize the quality of the data collected on cases of greatest clinical and public health…
“They are using magnetic fields through different chemicals to actually concentrate the RNA, the mRNA, into people’s cells. … It’s part of the lipid nanoparticle, and it’s a super delivery system. There are places in your body that other synthetic DNA or RNA should not be going, and yet this approach forces the material, the…
As of April 2021, four adenovirus vector vaccines for COVID-19 have been authorized in at least one country: The Oxford–AstraZeneca vaccine uses the modified chimpanzee adenovirus ChAdOx1 Sputnik V uses human adenovirus serotype 26 for the first shot and serotype 5 for the second. The Johnson & Johnson vaccine uses serotype 26. Convidecia uses serotype 5. Research article excerpt: During the last months many countries have…
June 2021: Highlights We report on a patient with a single dose of vaccine against SARS-CoV-2. He developed relevant serum titer levels but died 4 weeks later. By postmortem molecular mapping, we found viral RNA in nearly all organs examined. However, we did not observe any characteristic morphological features of COVID-19. Immunogenicity might be elicited,…
The following was stated in an open letter posted on medisolve.org: From: Dr. Tess Lawrie (MBBCh, PhD), Director, Evidence-based Medicine Consultancy Ltd and EbMC Squared CiC To: Dr. Raine, Medicines and Healthcare Products Regulatory Agency Statement on page 7 of letter: “The MHRA now has more than enough evidence on the Yellow Card system to…
Innova’s kit includes a nasal swab and a lateral flow test strip, which in less than a half-hour produces colored lines to display a positive reading, similar to a pregnancy test. However, the FDA said that false-negative and false-positive results may lead to delayed diagnoses, inappropriate treatment and the further spread of the virus. Though…
FDA revises fact sheets for Moderna and Pfizer-BioNTech COVID-19 vaccines regarding heart risks. Excerpt: Today, the FDA is announcing revisions to the patient and provider fact sheets for the Moderna and Pfizer-BioNTech COVID-19 vaccines regarding the suggested increased risks of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the tissue surrounding the heart) following vaccination. For each…
If you are feeling pressured to take a vaccine, DO NOT QUIT YOUR JOB! Make your boss fire you. Please see the statement from America’s Front Line Doctors about this. Federal law does not prohibit public agencies and private businesses from requiring COVID-19 vaccines that are under emergency use authorization, the Department of Justice concluded in an opinion. The Department…
Attorney Thomas Renz claims to have a signed affidavit from a whistleblower who says one of the US medical statistics systems shows 45,000 dead from the vaccines. When someone signs a legal affidavit, they can go to jail if they are found to have lied, so this is a very serious claim. If I understand…
The CDC will end the Emergency Use Authorization for the RT-PCR test for SARS-CoV-2 on December 31, 2021. This alert was issued to give labs time to find other tests to use. CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Such assays…
A Pfizer document mentioning graphene oxide was included in the February 2023 document dump. Whether the jabs contain graphene oxide is no longer speculation. We are no longer depending on laboratory science to show us that the jabs contain graphene oxide. This is now documented by Pfizer. Graphene oxide in the jabs is now an…
Sources: Related: See also, on this site: Reiner Fuellmich interviews Dr. Bryan Ardis Dr. Vladimir Zelenko publishes his COVID-19 treatment protocol. French Peer-Reviewed Study: Our Treatment Cured 100% Of Coronavirus Patients Amazing Polly elucidates the difference between “patient based” and “evidence based” health care As I ponder stories like those above, I am struck by…
As of August 23, 2021, the Pfizer-BioNTech inoculation is now approved under the brand name Comirnaty. The Comirnaty/Pfizer-BioNTech Fact Sheet for Healthcare Providers Administering Vaccine clearly states that pre-authorization Pfizer-BioNTech vaccine and the Comirnaty vaccine are equivalent. Any objections based on the experimental status of this vaccine are now moot. The argument now becomes whether…
The following transcript came from this source and is reproduced here with minor corrections. I have interspersed the transcript text with the facts as I know them. I do not have information to support every single point, but I can support most of them to some degree. My name is Dr. Sean Brooks, PhD, Oxford.1…
I am still working on setting up these links as events on the timeline. But since some of you really need this information now, I’m making it available now. There is going to be considerable shifting of information as I work on setting up the timeline. All of the fully decorated links will be kept,…
All calculations below use death statistics. These calculations use data from government sources. Some analyses are being done using numbers from all-cause deaths, which have increased significantly. One of these analyses is shown in Statistics and Calculation #5. Under Statistics and Calculation #4, I also show a chart of relative risks compared to other causes…
There is a rumor going around that the approval is for the name change. After looking at the Approval Letter from the FDA’s Comirnaty and Pfizer-BioNTech COVID-19 Vaccine page, it does appear to be the licensing letter for the inoculation. This is apparent in the terms used, which are different from those in an Emergency…
Marion Gruber is the Signatory Authority listed on the Emergency Use Authorization. Marion Gruber, director of the FDA’s Office of Vaccines Research & Review, and deputy director Phil Krause will exit the agency in October and November, respectively, according to a letter shared with CNBC by FDA spokeswoman Stephanie Caccomo. A former senior FDA leader…
If you go online right now and do a search on Joe Rogan, you will find article after article from the mainstream media about how Joe Rogan is an idiot because he took horse dewormer. The fact is that Joe Rogan took ivermectin formulated for humans that was prescribed to him by a medical doctor. …
It’s a sad day when we need a post like this, but apparently it has come to that. Unfortunately, you’ve got to understand that we’re at a point now that where they’re murdering people. The lawyers have been rendered in some cases impotent. — Thomas Renz Hospitals receive money when people die. Unfortunately, there are…
August 26, 2021: Vaccine: A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease. Vaccines are usually administered through needle injections, but can also be administered by mouth or sprayed into the nose. Vaccination: The act of introducing a vaccine into the body to produce immunity…
With numbers like these, no one can rightly claim that the jabs work. With each jab, people risk adverse events, some of which are extremely serious and could last a lifetime. These jabs do not pass any cost/benefit analysis, unless it is for the companies that produce them, perhaps. But even that may in time…
The “Wrap Up” Smear, as explained by Rep. Nancy Pelosi, works as follows: Demonize your political opponent by telling the public lies about them. The press reports the lies as if they were true. You use the press reports as validation that your lies are true. It would seem that this same tactic is being…
This was enough of a revelation to warrant its own post, plus I include another factor in the limitation of health care we are seeing with COVID-19. Probably the most important thing to know is that in many cases, your general practitioner does not write the orders for your care while you are in ICU. …
Sources: Post date is date Part 1 was posted on YouTube. Videos are listed in the order they appear on YouTube. I prefer to post videos from sites other than YouTube because YouTube postings seem to be a bit “fragile” these days, but my chosen site does not have all of the videos yet. I…
