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"Tried to post this. . Blocked and the initial message I got was the News posting message Golden Age of Gaia. .c 0 m. So they are blocking everything. Not just msm news sites. So currently listening to Gene on Hyperdrive and lots going on in Peru. . What's everyone's thoughts or what does anyone know about this Could this be true Genes clip also below, it's a 3 hr clip, I'm 30 mins in, it's great , just talking about everything , no painful interruptions of advertising that Rick seems to be doing on B2T - anyone else noticed that ? I actually stopped on the Decodes half way through on that channel because it's overload on the Backstage , and all other advertising that he's now doing . . Update I'm an HR into link below . . It's brilliant"
Glen Stevens MY LIST OF VACCINE INGREDIENTS 2-Phenoxyethanol 2-Phenoxyethanol (2-PE) is a compound widely used in many industries as a preservative. It is found in insect repellents, topical antiseptics, dyes, inks, and resins. In vaccines, 2-phenoxyethanol it is added as a germicide and used as an alternative to thiomersal. Listed as a “very toxic material,” exposure may lead to kidney, liver, blood and central nervous system (CNS) disorders. It is harmful or fatal if swallowed. In experimental animals, damage to the reproductive tract and development have been seen. Additives are used in the manufacture of vaccines to prevent changes in the solution under adverse conditions, such as freeze-drying or heat. They help to prevent the antigens from adhering to the side of the vial. Vaccines also contain several reagents that are derived from animals. Excipients are considered to be pharmacologically inactive substances used as a carrier for the active ingredients. In many cases, an “active” substance is mixed with an excipient to be more easily absorbed into the body. Even though they are considered to be inert – they often are NOT, and can have metabolic interactions. Johns Hopkins maintains a full, updated list of vaccine excipients which can change from time to time. Aluminum, in the form of aluminum hydroxide, aluminum phosphate or alum has been commonly used as an adjuvant in many vaccines since the 1920s. Chapter 21 of the US Code of Federal Regulations [610.15(a)] limits the amount of aluminum in biological products, including vaccines, to 850 mcg per dose. The amount of aluminum in vaccines ranges from 85 mcg to 500 mcg per dose. Aluminum heightens the inflammatory response to the vaccine and is said to enhance the antigenicity of some vaccines, increasing the antibody response. After nearly 100 years of use, the true mechanism of action of how aluminum enhances vaccine responses is still unknown. Aluminum compounds are contained in the following vaccines: diphtheria-tet-anus-pertussis (DTaP, Tdap), Haemophilus Influenza (Hib), Pneumococcal (PCV), Hepatitis A, Hepatitis B, Human Papillomavirus (HPV), Meningitis B (MenB) Anthrax, & Rabies vaccines. Current amounts of aluminum are not adjusted to the body weight of an infant. A 2018 study confirmed on Day 1 of life, infants receive 17 times more aluminum than would be allowed if doses were adjusted per body weight. Aluminum adjuvants have been associated with severe local reactions such as erythema, subcutaneous nodules, and contact hypersensitivity. It has been determined that aluminum can be transported into the brain, leading to inflammation and possibly Alzheimer’s.
CONTINUATION OF VACCINE INGREDIENTS. Antibiotics are used in vaccines to prevent bacterial contamination during the manufacturing process. Antibiotics commonly used are gentamycin, kanamycin, neomycin, streptomycin, polymyxin B, chlortetracycline, and amphotericin B. All of these antibiotics can stimulate allergic reactions.
FluMist: Hypersensitivity to gentamicin, gelatin, or arginine; children and adolescents 2 to 17 y of age receiving aspirin therapy or aspirin-containing therapy.
Allergy to neomycin What is neomycin and where is it found? It is also used as a preservative in some vaccines. February 2008 – Pharmacovigilance of vaccines. “Thus pharmacoepidemiology studies are necessary to confirm the alerts identified by spontaneous reporting. ADRs can be specific, related to the antigen of an attenuated alive virus vaccine (lymphocyte meningitis after anti-mumps vaccine) or non-specific, related to a component different from the antigen (aluminum hydroxide involved in the “macrophagic myofasciitis”, allergic reactions to neomycin, latex, egg or gelatine). Importance of Pharmacovigilance of vaccines is illustrated.” Tuberculosis or TB (short for tubercle bacillus) is a common, and in many cases a lethal, infection caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. Tuberculosis typically attacks the lungs, but can also affect other parts of the body. It is spread through the air when people who have an active TB infection cough or sneeze. Most infections are asymptomatic and latent, but about one in ten latent infections eventually progresses to active disease which, if left untreated, kills more than 50% of those so infected. The classic symptoms of active TB infection are a chronic cough with blood-tingedsputum, fever, night sweats, and weight loss (the latter giving rise to the formerly prevalent term “consumption”). Infection of other organs causes a wide range of symptoms. Diagnosis of active TB relies on radiology (commonly chest X-rays), as well as microscopic examination and microbiological culture of body fluids. BCG Vaccine The only current vaccine available against tuberculosis (TB), Bacille Calmette-Guérin (BCG), created in 1921. According to the WHO, the vaccine has “variable protective efficacy.” Even thought BCG is unreliable in protecting against pulmonary TB, which accounts for most of the disease burden worldwide, this vaccine is given at birth to infants in most countries around the world. WHO recommends vaccinating infants with BCG as it provides protection against severe extra-pulmonary (non-lung) forms of pediatric TB, a rare and unusual form of the infection. “Further work is needed on the cost-benefit ratio of BCG as opposed to that of other approaches to control. One argument favoring the discontinuation of BCG is based on the advantages of testing pregnant women.” CDC Publications TB tests (pdf) – “Mantoux Tuberculin Skin Test. TST is administered by injection. Tuberculin is made from proteins derived from inactive tubercle bacilli •Most people who have TB infection will have a reaction at the injection site. Syringe being filled with 0.1 ml of liquid tuberculin are injected between the layers of skin on the forearm.
CONTINUATION OF VACCINE INGREDIENTS. Bovine extracts are cow-derived products used in vaccine manufacture. Cow products used include Amino acids Glycerol, Detergents, Gelatin, Enzymes, Blood. Cow tallow derivatives used in vaccine manufacture include glycerol. Gelatin and some amino acids come from cow bones. Cow skeletal muscle is used to prepare certain complex vaccine media. Many difficult to grow microorganisms required the addition of serum from blood to the growth media. Vaccine Excipient & Media Summary, Part 2 Included in U.S. Vaccines, by Vaccine Spongiform Encephalopathy and Immunizations What is Bovine Spongiform Encephalopathy (BSE)? Which bovine derived materials are used in vaccine manufacture? [BSE (bovine spongiform encephalopathy) is a progressive neurological disorder of cattle that results from infection by an unusual transmissible agent called a prion. The nature of the transmissible agent is not well understood. It is commonly known as Mad Cow Disease.] Transmissible spongiform encephalopathies (TSE) “There is increasing concern about the troubling possibility that blood or blood products, vaccines and other pharmaceutical products could spread the agent of variant CJD (vCJD) worldwide, especially in countries where BSE has not yet been reported. Bovine derived materials involved in the production of vaccines and other pharmaceutical products could represent a way of potential transmission of the disease.” [The FDA is fully aware that bovine cell substrates can become contaminated with adventitious viruses that are potentially deadly. In a 2004 FDA memo, the FDA states that, “the use of immortalized, neoplastic human cells to develop [vaccines] raises theoretical concerns with regard to possible contamination with TSE/BSE agents.” TSE is Transmissible Spongiform Encephalopathy, a condition that includes a group of rare degenerative brain disorders characterized by tiny holes in the brain tissues, giving a “spongy” appearance when viewed under a microscope. When this condition occurs in cows it is called Bovine Spongiform Encephalopathy, commonly known as “mad cow disease.” In a study published in 2004, researchers found that any cell line could potentially support the propagation of TSE agents.] Flublok [Influenza Vaccine] is a sterile, clear, colorless solution of recombinant hemagglutinin (HA) proteins from three influenza viruses for intramuscular injection. It contains purified HA proteins produced in a continuous insect cell line that is derived from cells of the fall army worm, Spodoptera frugiperda, and grown in serum-free medium composed of chemically-defined lipids, vitamins, amino acids, and mineral salts. Each of the three HAs is expressed in this cell line using a baculovirus vector (Autographa californica nuclear polyhedrosis virus), extracted from the cells with Triton X-100 and further purified by column chromatography. The purified HAs are then blended and filled into single-dose vials” FDA approval: For active immunization against disease caused by influenza virus subtypes A and type B contained in the vaccine. Flublok is approved for use in persons 18 through 49 years of age Flublok Quadrivalent Product Information and Supporting Documents Package Insert – Flublok Quadrivalent Found 386 cases where Vaccine is FLUR4 and Manufacturer is PROTEIN SCIENCES CORPORATION
CONTINUATION OF VACCINE INGREDIENTS. Formaldehyde is used to inactivate bacterial products for toxoid vaccines (tetanus and diphtheria) and to weaken unwanted viruses and bacteria that might contaminate the vaccine during production. In 2011, formaldehyde was added to the list of known carcinogens. Material Safety Data Sheet Formaldehyde 37% solution MSDS Report on Carcinogens, Thirteenth Edition (2014) Formaldehyde Current methods used to inactivate living pathogens in vaccine production involve the use of chemical agents such as formaldehyde or beta-propiolactone to chemically modify the genetic material of the pathogen. However, there is substantial evidence that both of these agents are human and animal carcinogens. For example, studies in rats exposed to formaldehyde by inhalation have shown that formaldehyde induces squamous-cell carcinoma of the nasal cavity. Additionally, formaldehyde has been shown to be genotoxic in vitro and in vivo. Both genotoxicity and cytotoxicity play an important role in the carcinogenicity of formaldehyde. Although the concentration of formaldehyde in vaccines is typically low (below 0.02%), this represents up to 50-100 micrograms of formaldehyde per injected dose in many vaccines…Particularly dangerous is the amount of formaldehyde that is injected into infants and small children during the course of multiple vaccinations. While the amount of formaldehyde in each vaccine dose is low, the combined amount can become substantial.” Comment: According to Manuel’s Web, 0.02% is 0.2 mg or 200 mcg, making the sum total of formaldehyde in anthraxvaccines even larger and more disconcerting. Vaccines that contain formaldehyde include nearly all pediatric and adult flu shots; all forms of pediatric and adolescent pertussis vaccines (DTaP and the teen version, Tdap); and injectable polio vaccines (IPV) vaccines. Vaccines given under special circumstances also contain formaldehyde: tetanus boosters (dT, DT and TT), Japanese encephalitis vaccine, rabies vaccines and anthrax vaccine (given as six doses). Let’s add up the amount of formaldehyde injected into children by the time they are five years of age. Assuming they get all doses of all recommended vaccines on time and according to the 2012 vaccination schedule:
Total: 1,795 mcg = 1.795 milligrams Through sloppy and negligent math, lawmakers and manufacturers failed to identify that infants received as much as 87.5 micrograms of mercury (thimerosal) by six months of age. Again, through sloppy and negligent math, lawmakers and manufacturers fail to throw up a red flag regarding the large amount of formaldehyde injected into young bodies with developing brains, neurological systems and organs. April 19, 2016 – Effect of different detoxification procedures on the residual pertussis toxin activities in vaccines“Due to multilevel reaction mechanisms of chemical detoxification that act on different molecular sites and with different production processes, it is difficult to define a molecular characteristic of a pertussistoxoid.”…”Different types of vaccines, detoxified by formaldehyde, glutaraldehyde or by both, have different residual functional and individual baseline activities. Of the vaccines tested, PT toxoid detoxified by formaldehyde had the lowest residual PTx ADP-ribosyltransferase activity.” October 2014 – Effect of Formaldehyde Inactivation on Poliovirus “Inactivated polio vaccines, which have been used in many countries for more than 50 years, are produced by treating live poliovirus (PV) with formaldehyde. However, the molecular mechanisms underlying virus inactivation are not well understood.”…”We show that inactivation with formaldehyde has an effect on early steps of viral replication as it reduces the ability of PV to bind to hPVR, decreases the sensitivity of PV to convert to 135S particles, and abolishes the infectivity of its viral RNA.” October 30, 2012 – Formaldehyde Impairs Learning and Memory Involving the Disturbance of Hydrogen Sulfide Generation in the Hippocampus of Rats “In the limbic system, the hippocampus plays a critical role in learning and memory (Morris et al. 1982). Increasing studies showed that inhaled FA exposure negatively affects the ability of spatial learning and memory in rats (Pitten et al. 2000; Malek et al. 2003; Ahmed et al. 2007; Lu et al. 2008; Liu et al. 2010), suggesting that FA has harmful effects on hippocampal functions. July 9, 2012 – Histomorphological and ultrastructural changes of the placenta in mice exposed to formaldehyde “In addition, in the FA-treated animals, a severe accumulation of cytoplasmic droplets in the II and III trophoblastic layers of the placenta were seen. In conclusion, this study may suggest that the exposure to FA during the organogenesis period at doses of 7–28 ppm induces toxic changes in the placental structure. These changes disrupt placental functions and leads to a decrease in the fetal weight.” February 28, 2012 – Title: Inactivating pathogens with oxidizing agents for vaccine production (patent) “Although the concentration of formaldehyde in vaccines is typically low (below 0.02%), this represents up to 50-100 micrograms of formaldehyde per injected dose in many vaccines (for example, Anthrax vaccine produced by Bioport Corp. contains 100 microgram/ml formaldehyde as a preservative) and poses a potential hazard due to the number of vaccinations a person receives over the course of a lifetime. Particularly dangerous is the amount of formaldehyde that is injected into infants and small children during the course of multiple routine childhood vaccinations. While the amount of formaldehyde in each vaccine dose is low, the combined amount can become substantial.” August 2011 – Safety and efficacy evaluation of TRUE TEST panels 1.1, 2.1, and 3.1 in children and adolescents. “Positive reactions noted in more than 10% of the children were to nickel sulfate (29.7%), p-tert-butylphenol formaldehyde resin (16.8%),”
CONTINUATION OF VACCINE INGREDIENTS. Influenza vaccines have been manufactured from eggs to manufacture since the 1940s. Insect cell-derived influenza vaccines are a new alternative to egg-derived vaccines. Three different approaches to using insect cell-derived influenza vaccines have been established that could contribute to future influenza vaccine supply and development. [Traces of these cells end up in the final vaccine product. Certain flu shots include insect particles and insect DNA.] January 16, 2013 – FDA approves new seasonal influenza vaccine made using novel technology “The U.S. Food and Drug Administration today announced that it has approved Flublok, the first trivalent influenza vaccine made using an insect virus (baculovirus) expression system and recombinant DNA technology. Flublok is approved for the prevention of seasonal influenza in people 18 through 49 years of age.” December 7, 2012 – Head-to-Head Comparison of Three Vaccination Strategies Based on DNA and Raw Insect-Derived Recombinant Proteins against Leishmania “Killed vaccines have generally been immunogenic yet ineffective. Recombinant protein-based vaccines have achieved moderate protection in mice and dogs, but they often need to be formulated with an adjuvant, which complicates the process for getting marketing authorization, particularly in human medicine. Naked DNA vaccines have also been tested reaching different degrees of protection in rodents, but they have often proved inadequate in providing protection in non-murine models.” October 1, 2011 – Insect cells as factories for biomanufacturing. “Insect cell culture, coupled with the lytic expression capacity of baculovirus expression vector systems (BEVS), constitutes a powerful platform, IC-BEVS, for the abundant and versatile formation of heterologous gene products, including proteins, vaccines and vectors for gene therapy.” September 9, 2011 – Application of Baculovirus-Insect Cell Expression System for Human Therapy. “In the review special attention is given to the development of new virus-like particles (VLPs) potential vaccines which represent a novel class of subunit vaccines that are able to stimulate efficiently cellular and humoral immune responses against viral agents. Apart from production of vertebrate proteins or VLPs “on demand” in insect cells, a new exciting field of using baculovirus as gene delivery system to vertebrate cells was recently open which has a great potential for future uses of baculovirus as effective gene therapy vector.” August 18, 2011 – Norovirus VLPs and rotavirus VP6 protein as combined vaccine for childhood gastroenteritis. “Live oral RV vaccines are already part of routine childhood immunization in many countries, but may be associated with low risk of intussusception and other potential risks associated with live vaccines. NoVcapsid-derived virus-like particles (VLPs) are in early phase clinical trials, but there is no vaccine available yet. We suggest that there is a need for non-live vaccines against both enteric pathogens. We have combined NoV GII-4 VLPs and human RV recombinant VP6 (rVP6) protein produced by recombinant baculovirus (BV) expression system in insect cells and used this combination vaccine to immunize BALB/c mice parenterally.” August 2011 – Baculovirus-Produced Influenza Virus-like Particles in Mammalian Cells Protect Mice from Lethal Influenza Challenge. “Influenza virus-like particles (VLPs) are effective vaccines against influenza infection, which can be produced either in insect cells by recombinant baculovirus (BV) infection or in mammalian cells by DNA plasmid transfection. However, VLPs produced from baculovirus/insect cells are difficult to purify due to baculovirus contamination; VLPs produced by plasmid transfection are limited by scale-up capability.” August 2011 – The preparation of human papillomavirus type 58 vaccine and exploring its biological activity and immunogenicity in vitro. July 2011 – Large-scale production and purification of VLP-based vaccines. “This system is very versatile: multiple recombinant baculoviruses containing the required genes of interest for the production of different viral proteins and multi-cistronic vectors with different promoters/enhancers can be used to infect insect cells(e.g., Spodoptera frugiperda 9, Sf21 or Hi5) to express large amounts of the required viral proteins and assemble these multimeric units into the correspondent VLP.” July 2011 – Arbovirus vaccines; opportunities for the baculovirus-insect cell expression system. “The baculovirus-insect cell expression system is a well-established technology for the production of heterologous viral (glyco)proteins in cultured cells, applicable for basic scientific research as well as for the development and production of vaccines and diagnostics. Arboviruses form an emerging group of medically important viral pathogens that are transmitted to humans and animals via arthropod vectors, mostly mosquitoes, ticks or midges.” January 11, 2010 – Insect cells could cut vaccine production to 10 weeks Vaccines could be produced in less than 10 weeks from first isolation of the RNA sequence by using insect cell derived influenza VLP’s according to research which has implications for H1N1 and H5N1. December 1, 2009 – Caterpillar Flu Vaccine Delayed The FDA wants further evidence that the novel approach is completely safe. “It has the potential to scale up rapidly, to deal with new strains of influenza such as this year’s H1N1, and to help stem a pandemic tide. However, a U.S. Food and Drug Administration advisory panel voted in late November not to approve the technology, which involves growing key vaccine ingredients inside caterpillar cells instead of in chicken eggs, as is currently done.” July 1, 2009 – Dangers of HPV Vaccine Production in Plants, Microbes, and Viruses The Cervarix vaccine available commercially is produced by GlaxoSmithKline using a baculovirus vector propagated in an insect cell line. Baculoviruses are soil inhabiting viruses that infect insects. Baculovirus expression vectors propagated in insect cells were originally hampered by the appearance of many interfering baculovirusese with chromosomal deletions, which arise as an intrinsic property of the native baculovirus. The intrinsic deletions in the viral chromosome may provide a source of diversity as the virus faces environmental challenges. Such instability is undesirable in producing vaccines. Some progress has been achieved in making more stable baculovirus expression vector lines. Nevertheless, regulators and the vaccine producer have not made public comment about the genetic stability of the baculovirus lines producing Cervarix vaccine, nor the fact that baculovirus is capable of infecting mammalian cells and tissues. If the GM baculovirus infects mammalian cells and tissues in vivo, they would also transfer transgenes to those infected cells as gene therapy experiments have demonstrated since 2001. Baculovirus can also serve as a gene delivery vector for stem cell and bone tissue engineering. October 1, 2008 – FluBlok: A Next Generation Influenza Vaccine Manufactured in Insect Cells (pdf) April 10, 2007 – Bypassing Eggs, Flu Vaccine Grown in Insect Cells Shows Promise October 18, 2005 – Baculovirus expression vectors for the production of viral proteins February 1999 – An experimental marker vaccine and accompanying serological diagnostic test both based on envelope glycoprotein E2 of classical swine fever virus (CSFV). 1997 – Virus-like particle vaccines for mucosal immunization. 1996 – Virus-like Particles as a Rotavirus Subunit Vaccine(full text) “Rotavirus subunit vaccines are being evaluated for use in humans. The virus-like particles (VLPs) for these vaccines are produced in insect cellscoinfected with combinations of baculovirus recombinants expressing bovine RF VP2 and simian SAll VP4, VP6, or VP7 rotavirus proteins.”
CONTINUATION OF VACCINE INGREDIENTS. MF59 is an oil-in-water emulsion of squalene, polyoxyethylene sorbitan monooleate (polysorbate 80, also called Tween 80) and sorbitan trioleate.
Squalene is a natural organic compound originally obtained for commercial purposes primarily from shark liver oil, although plant sources are now used as well, including amaranth seed, rice bran, wheat germ, and olives. Yeast cells have been genetically engineered to produce commercially useful quantities of “synthetic” squalane, which is similar to squalene. commercially sometimes referred to as Tween 80,
Sorbitan trioleate, also known as Polysorbate 85, has various industrial applications such as antioxidant, emulsifier and surfactant. Sorbitan tristearate is a nonionic surfactant. It is variously used as a dispersing agent, emulsifier, and stabilizer, in food and in aerosol sprays. As a food additive, it has the E number E492. Brand names for polysorbates include Alkest, Canarcel, and Span. The consistency of sorbitan tristearate is waxy; its color is light cream to tan.
MF59 adjuvant was developed by Chiron Corp., a company acquired by Novartis. MF59 is approved in Europe and is found in several vaccines, such as an influenza vaccine manufactured by Novartis. It has also been licensed to other companies and is being actively tested in vaccine trials.
CONTINUATION OF VACCINE INGREDIENTS. Measles, also known as rubeola, is a viral respiratory infection. Symptoms include fever, cough, runny nose, red eyes and a generalized rash. The characteristic measles rash begins several days after the onset of the fever. The rash is said to “stain”, changing color from red to dark brown before it disappears. The measles rash lasts for up to eight days. While classic measles is sometimes confused with rubella, the infections are unrelated. Rubella is also called 3-day measles or German measles. The rubella rash can look like many other viral rashes. It appears as either pink or light red spots, which may merge to form evenly colored patches. The rash can itch and can last up to 3 days. As the rash clears, the affected skin occasionally sheds in very fine flakes. The primary medical danger of rubella is the infection of pregnant women in their first trimester because it can cause congenital rubella syndrome. Mumps, caused by the mumps virus, typically starts with a few days of fever, headache, muscle aches, tiredness, and loss of appetite, and is followed by swelling of salivary glands. There is no specific treatment for mumps. Mumps can cause inflammation of the testicles called orchitis. At highest risk are post-pubertal men. Only about 10% of cases are bilateral, therefore the risk of infertility is rare. Varicella, Chickenpox (varicella) is a common illness that causes an itchy rash and red spots or blisters (pox) all over the body. Until the release of the chickenpox vaccine in 1995, it was a common childhood illness, usually manifesting in children 7 to 9 years of age. Chickenpox usually isn’t a serious health problem in healthy children. But a child with chickenpox needs to stay home from school. The vaccine was actually developed so that parents would not have to miss work to care for their ill child. After you have had chickenpox, you are not likely to get it again. But the virus stays in your body long after you get over the illness. Long term immunity has always been maintained in adults by re-exposure to the virus during an episode of chickenpox in their children or grand children. Now, long-term immunity is waning in millions of adults. If the virus becomes active again, it can cause a painful viral infection called shingles. In response, Zostavax, the vaccine for shingles, was developed. March 22, 2019 – GSK’s MMR vaccine safe, effective for US infants “We believe that if MMR-RIT (Priorix, GlaxoSmithKline) is licensed, it could provide a valid option to prevent measles, mumps and rubella in U.S. children,” Klein told Infectious Diseases in Children. “Plus, it could also help to reduce the potential risks of a vaccine shortage.” January 8, 2018 – Building capacity for active surveillance of vaccine adverse events in the Americas: A hospital-based multi-country network “The study evaluated the associations between measles-mumps-rubella vaccines and two well-recognized adverse events: Immune thrombocytopenic purpura (ITP) and aseptic meningitis. The regional network contributed 63 confirmed ITP and 16 confirmed aseptic meningitis eligible cases to the global study, representing, respectively, 33% and 19% of the total cases. To ensure long-term sustainability and usefulness to investigate adverse events following new vaccine introductions in low and middle-income countries, the network needs to be strengthened with additional sites and integrated into national health systems.” January 8, 2018 – Enhancing global vaccine pharmacovigilance: Proof-of-concept study on aseptic meningitis and immune thrombocytopenic purpura following measles-mumps containing vaccination “The World Health Organization (WHO) selected 26 sentinel sites (49 hospitals) distributed in 16 countries of the six WHO regions. Incidence rate ratios (IRR) of 5.0 (95% CI: 2.5–9.7) for ITP following first dose of measles-containing vaccinations, and of 10.9 (95% CI: 4.2–27. for AM following mumps-containing vaccinations were found. The strain-specific analyses showed significantly elevated ITP risk for measles vaccines containing Schwarz (IRR: 20.7; 95% CI: 2.7–157.6), Edmonston-Zagreb (IRR: 11.1; 95% CI: 1.4–90.3), and Enders’Edmonston (IRR: 8.5; 95% CI: 1.9–38.1) strains. A significantly elevated AM risk for vaccines containing the Leningrad-Zagreb mumps strain (IRR: 10.8; 95% CI: 1.3–87.4) was also found.” November 7, 2017 – County-level assessment of United States kindergarten vaccination rates for measles mumps rubella (MMR) for the 2014–2015 school year “The lack of local MMR data prevents identification of areas with low vaccination rates that would be vulnerable to the spread of disease. We collected county-level vaccination rates for the 2014–2015 school year with the objective of identifying these regions. … We found that county data can reveal vaccination trends that are unobservable from state-level data, but we also discovered that the current availability of county-level data is inadequate. Our findings can be used by state health departments to identify target areas for vaccination programs. September 7, 2017 – Effectiveness of a Third Dose of MMR Vaccine for Mumps Outbreak Control “Students who had received a third dose of MMR vaccine had a lower risk of mumps than did those who had received two doses, after adjustment for the number of years since the second dose. Students who had received a second dose of MMR vaccine 13 years or more before the outbreak had an increased risk of mumps. These findings suggest that the campaign to administer a third dose of MMR vaccine improved mumps outbreak control and that waning immunity probably contributed to propagation of the outbreak. (Funded by the Centers for Disease Control and Prevention.)” August 25, 2017 – Consistency Study of GlaxoSmithKline (GSK) Biologicals’ MMR Vaccine (209762) (Priorix®) Comparing Immunogenicity and Safety to Merck & Co., Inc.’s MMR Vaccine (M M R®II), in Children 12 to 15 Months of Age “Sponsor: GlaxoSmithKline Information provided by (Responsible Party): GlaxoSmithKline” May 25, 2017 – Antibody persistence in children aged 6–7 years one year following booster immunization with two MMR vaccines applied by aerosol or by injection “We performed clinical and serological follow-up of participants in a previous study of Mexican children aged 6–7 years, in which participants were randomized to four groups receiving, by aerosolized or by injection, the MMR SII vaccine (Serum Institute of India), or the MMR II (Merck Sharp & Dhome). We evaluated the antibody persistence by PRN test for measles and by ELISA for rubella and mumps. The occurrence of clinical events was evaluated via periodic visits of a nurse team to children’s schools and homes.” … “Conclusion Under conditions of no endemic transmission for measles and rubella, and of low circulation of mumps virus, school-aged children remained seropositive to the three viruses one year following booster immunization.
CONTINUATION OF VACCINE INGREDIENTS. Monosodium glutamate, or MSG, is the sodium salt of the chemical glutamic acid. It is used to enhance the flavor of food. Monosodium glutamate is commonly found in Chinese food, seasonings, salad dressings and boxed foods, like macaroni and cheese and rice mixes. MSG belongs to a class of chemicals called excitotoxins, substances believed to cause brain damage and damage the central nervous system. Excitotoxins can affect the hypothalmus portion of the brain, which controls important bodily functions such as growth, sleep patterns, puberty and even appetite. Some studies suggest long-term negative effects such as brain tumors, obesity, sleep disturbances and reproductive issues. The health disturbances from MSG have been known for more than 30 years. Hidden names for MSG Vaccines that contain MSG or potentially contain L-glutamine:
CONTINUATION OF VACCINE INGREDIENTS. Pertussis, referred to as whooping cough, is an upper respiratory infection caused by the bacterium, Bordetella pertussis (written in studies as B. pertussis). Pertussis presents as a deep and harsh cough that is worse at night and does not include fever. While the infection usually lasts 6 weeks, the severity can vary widely – from nothing more than a runny nose to a very severe, persistent barking cough. Pertussis tends to be more serious in children under six months of age due to the very small size of their trachea (wind pipe.) Whooping cough can affect people of any age. Anyone who has a persistent cough lasting more than 30 days should be suspected of having pertussis. Pertussis vaccines have several forms and several manufacturers. Whole cell pertussis vaccines (DTwP) have been used since the 1940s and is still used in foreign countries. Since 2002, the U.S. has used exclusively acellular pertussis vaccines (DTaP). In 2005, a new pertussis vaccine was released for adolescents and adults (Dtap). Acellular pertussis vaccines – “There is as yet no consensus about the antigenic composition of an ideal acellular pertussis vaccine. Acellular pertussis vaccines currently available from different manufacturers should be considered as different and unique products because of the presence of one or more different components…These individual antigens may be derived from different strains of Bordetella pertussis and have been purified by different methods. For these reasons the protective efficacy in humans of various manufacturers’ products may be based on different mechanisms, which complicates the direct comparison of the protective activity of various products and new formulations by means of simple laboratory tests. Indeed, no unequivocal immunological correlates of protection against pertussis have yet been demonstrated, nor has a generally accepted animal model to predict clinical efficacy been validated. Comment: This is a very important paper and essentially admits that they have no idea how the pertussis vaccine works, and that the components are not known to “protect.“ December 8, 2018 – Burden of Children Hospitalized With Pertussis in Canada in the Acellular Pertussis Vaccine Era, 1999–2015 (full text) “Prematurity and female sex were significantly associated with increased risk for death (5-fold and 3.5-fold increase, respectively).” Potential conflicts of interest.
M. S. is and has been an investigator on research grants received from Pfizer, Merck, and Variation Biotechnologies, Inc; all monies have been paid to his institution, and he has received no personal payments.
S. A. H. has received grants and contracts for research from Sanofi Pasteur and GlaxoSmithKline, both producers of aP vaccine.
October 8, 2018 – Reactogenicity and immunogenicity of tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccine (Tdap) in pregnant and nonpregnant women “374 pregnant and 225 nonpregnant women were vaccinated. Severe local or systemic reactions or “any” fever were uncommon (≤3% for both groups). Moderate/severe injection-site pain was significantly higher in pregnant (17.9%) versus nonpregnant (11.1%) women, but did not prompt a healthcare visit. Proportions of other moderate/severe or any severe reactions were not significantly higher in pregnant compared to nonpregnant women. Moderate/severe (including pain) and severe reactions were not significantly higher in pregnant women receiving repeat versus first-time Tdap.” Potential conflicts of interest
KME was on a Data and Safety Monitoring Board for a Novartis funded influenza vaccine in children and received research funding for studies of Group B streptococcus vaccine in pregnant women produced by Novartis.
GKS is on a Data and Safety Monitoring Board for a GlaxoSmithKline funded RSV vaccine study in pregnant women. She has received research funding for studies of Group B streptococcus vaccine in pregnant women produced by Novartis and for RSV vaccine in pregnant women produced by Novavax.
KBF has received research funding for studies of Group B Streptococcus vaccine in pregnant women produced by Novartis and for RSV and CMV surveillance among pregnant women and their infants by Pfizer and Regeneron.
EBW has received funding from CSL, GlaxoSmithKline, Merck, Novartis, Novavax, and Pfizer to conduct clinical research studies. He has received support from Novartis as a member of a Data Safety Monitoring Board and from Merck as a consultant. The other authors report no conflict of interest.”
CONTINUATION OF VACCINE INGREDIENTS. Polysorbate 80, also known as Tween80, is an amber-colored, viscous liquid with a slightly bitter taste. It is used primarily as an emulsifier in food products, cosmetics, vitamins, medicines, and vaccines. According to Emulsifiers.org, “When water and oil are mixed together and vigorously shaken, a dispersion of oil droplets in water – and vice versa – is formed. When shaking stops, the phases start to separate. However, when an emulsifier is added to the system, the droplets remain dispersed, and a stable emulsion is obtained.” Polysorbate 80 aids in dissolving ingredients that would not otherwise dissolve or fully dissolve. Polysorbate 80 is using in many medications and has been used to carry drugs and nanoparticles into the brain. Polysorbate 80 and the effect on infertility: Baby female rats were injected with polysorbate 80 at days 4-7 after birth. It accelerated the maturing of the rats and caused changes to the vagina and womb lining, hormonal changes, ovary deformities and degenerative follicles. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea and had degenerative follicles. Material Safety Data Sheet POLYSORBATE 80 MSDS October 29, 2012 – Assessment report Immunological differences of pandemic vaccines (review of hypothesis on Pandemrix and development of narcolepsy) “The authors suggest that their data show that children who developed narcolepsy after Pandemrix vaccination developed an altered immune response, and that polysorbate 80 is an immunologically active substance in the H1N1 antigen suspension of Pandemrix. They hypothesize that polysorbate 80 in H1N1 antigen suspension of Pandemrix revealed new epitope(s) in the viral protein(s), and the antibodies against these epitopes cross-reacted with narcolepsy associated autoantigens.” May 2012 – Hypersensitivity reaction to human papillomavirus vaccine due to polysorbate 80. “A 17-year-old girl reported generalized urticaria, eyelid angioedema, rhino-conjunctivitis, dyspnea and wheezing 1 hour after third intramuscular administration (injection) of quadrivalent human papillomavirus vaccine (Gardasil). She was treated with antihistamine, and corticosteroids with prompt relief of rhinitis and dyspnoea, while urticaria and angioedema lasted 24 hours. Intradermal test with Gardasil, which contains polysorbate 80 (PS80), resulted positive, while skin tests with the bivalent vaccine were negative. Prick test performed with PS80 resulted positive in the patient and negative in ten healthy controls. The CD203 basophil activation test result was negative for PS80 at all the tested dilutions and specific IgE was not found. As flu vaccine was recommended, the authors’ skin tested two flu vaccine, one containing PS80 (Fluarix, GSK), which resulted positive and another flu vaccine with no adjuvant or preservative (Vaxigrip, Sanofi Pasteur MSD), which gave negative results. The patient then received Vaxigrip without adverse reactions.” September 1, 2008 – Anaphylaxis following quadrivalent human papillomavirus vaccination (pdf) “Quadrivalent HPV (Gardasil) vaccine contains polysorbate 80 as a stabilizer. Polysorbates are commonly used as solubilizers, stabilizers and emulsifiers in cosmetics and medical preparations. Polysorbate 80 could be a potential trigger of nonallergic (“anaphylactoid”) anaphylaxis. There have been a number of reports of anaphylaxis or generalized hypersensitivity reactions occurring following the receipt of drugs that have implicated polysorbate 80 as the cause. August 30, 2008 – Polysorbate 80 and Histidine, a marriage of disaster by Cynthia Janak. (many scientific links). January 2008 – Evaluation of developmental neurotoxicity of polysorbate 80 in rats. “The developmental neurotoxicity of polysorbate 80 (PS80) was evaluated. Rats were given drinking water containing polysorbate 80 (PS80) [at a range of concentrations] on day 0 of pregnancy through day 21 after delivery. Pregnant rats were allowed to deliver spontaneously. Potential adverse effects of pre- and post-natal exposure on the development and function of the nervous system in offspring of rats given PS80 were examined. Maternal body weight was lowered at 7.5%. The number of pups born was lowered at 7.5%. Histopathological examinations of the brain revealed no toxicological changes. Lowered body weight was observed in male and female offspring. February 2007 – Alternative drug formulations of docetaxel: a review “Docetaxel (trade name Taxotere) is a chemotherapy medication used mainly for the treatment of breast, ovarian, prostate, and non-small cell lung cancer. Docetaxel is associated with the occurrence of unpredictable (acute) hypersensitivity reactions and cumulative fluid retention. These side-effects have been attributed, in part, to the presence of polysorbate 80 and have consequently initiated research focused on the development of a less-toxic, better-tolerated polysorbate 80-free formulation of docetaxel.” Comment: Polysorbate 80 causes serious side effects in oral medications and a substitute is sought. But when it causes serious reactions in a vaccine, the association is ignored.
This Category includes information about Human Cells (historically from aborted fetal tissue) used for the production of vaccines. Cell substrates are the actual cells used to produce vaccines. Cell substrates can be of human or animal origin (including insect) and/or unicellular organisms, such as bacteria or yeast. Cell substrates are categorized as primary cells (derived directly from an animal source (such as eggs) and that are not stored as cell banks), diploid cells (stored as cell banks prior to use in vaccine manufacture), or continuous cells (cells that are grown a certain way so that they divide forever; called “immortal” because they do not die – which, by definition, is a cancer cell). Cell line categories with specific pages in the Library include: ♦HeLa Cells – developed from human epithelial cells used since 1951 ♦ MRC-5 Cells – developed in 1966 from lung tissue taken from a 14 week aborted fetus ♦PER.C6 – developed by Crucell from aborted, embryoic retinal cells ♦WI-38 – developed in 1962 from lung tissue taken from 12 week aborted fetus Additional cell lines are being tested experimentally and are included on the page “Human Cells Lines, Experimental“
The Hegelian Dialectic is a framework to guide our thoughts and actions to a predetermined solution.
The government creates or exploits a problem blaming it on others
The people react by asking the government for help willing to give up their rights
The government offers the solution that was planned long before the crisis
Historical Evidence of Problem Reaction Solution Nero Burnt Rome, Blamed it on the Christians and then Savagely Butchered Them. Nero Claudius Caesar 37-68 CE, University of Texas History, in 64 CE, a fire swept through Rome, burning for a week and destroying a large portion of the city. According to some sources, when he found that he did not have enough land to build his palace, he set fire to the city a second time. It is at this point that he is said to have "played his fiddle [lyre] while Rome burned." To avert suspicion, he blamed the fires on the Christians and proceeded to kill them in horrendous ways. Nero persecutes Christians in Rome, Rutgers University History, Neither human effort nor princely largesse nor divine appeasement was able to dispel the scandal that the fire which burned much of Rome in 64 CE was believed to have been commanded by the emperor Nero. So, to do away with the rumor, Nero substituted as culprits those who were commonly called "Christians," who were hated because of their absurdities. And he inflicted them with the most extraordinary punishments. The USS Maine Sank in Havana Harbor Launching the US into the Spanish American War. Sinking of the USS Maine Resulting in the Spanish American War US Navy Official Website, the Spanish American War 21 April to 13 August 1898, was a turning point in the history of the United States, signaling the country's emergence as a world power. The blowing up of the battleship USS Maine in Havana harbor on the evening of 15 February was a critical event on the road to that war. The U.S. Navy Department immediately formed a board of inquiry to determine the reason for Maine's destruction. When the Navy's verdict was announced, the American public reacted with predictable outrage. The destruction of Maine did not cause the U.S. to declare war on Spain, but it served as a catalyst, accelerating the approach to a diplomatic impasse. In addition, the sinking and deaths of U.S. sailors rallied American opinion more strongly behind armed intervention. The Resinking of the Battleship Maine, Historical Museum of Southern Florida, there is no mystery about the second sinking of the United States battleship Maine. It occurred on March 16, 1912, four miles outside Havana harbor, and was witnessed by thousands. They raised it and sank it in deep waters. Adolf Hitler was elected Chancellor President and then Burnt the Reichstag , German Parliament Building. He then declared Himself Furor Dictator and Promised Utopia. Hitler Declared Martial Law and Suspended All Basic Human Rights. Reichstag Fire, Encyclopedia Britannica Reichstag fire, burning of the Reichstag parliament building in Berlin, on the night of Feb. 27, 1933, a key event in the establishment of the Nazi dictatorship and widely believed to have been contrived by the newly formed Nazi government. To turn public opinion against its opponents and to assume emergency powers, his propaganda minister, Joseph Goebbels, is supposed to have devised the scheme. On Feb. 28, 1933, the day after the fire, Hitler's dictatorship began with the enactment of a decree "for the Protection of the People and the State," which dispensed with all constitutional protection of political, personal, and property rights. Holocaust Timeline The Nazification of Germany University of South Florida, on February 27 1933, the Reichstag building went up in flames. Nazis immediately claimed that this was the beginning of a Communist revolution. This fact leads many historians to believe that Nazis actually set, or help set the fire. Others believe that a deranged Dutch Communist set the fire. The issue has never been resolved. This incident prompted Hitler to convince Hindenburg to issue a Decree for the Protection of People and State that granted Nazis sweeping power to deal with the so called emergency. This laid the foundation for a police state. In 1962, the government wanted to change public opinion to create a pretext for war with Cuba. The Joint Chiefs of Staff created a plan that they named the "Northwoods Document", to commit a series of terrorist acts against America and blame it on the Cuban government. One of the scenarios included blowing up a civilian airplane. U.S. terror plan called Cuba invasion pretext, the Baltimore Sun, U.S. military leaders proposed in 1962 a secret plan to commit terrorist acts against Americans and blame Cuba to create a pretext for invasion. The ouster of Communist leader Fidel Castro, according to a new book about the National Security Agency. U.S. Military Wanted to Provoke War With Cuba - ABCNEWS.com, in the early 1960s, America's top military leaders reportedly drafted plans to kill innocent people and commit acts of terrorism in U.S. cities to create public support for a war against Cuba. The Actual Northwoods documents. Pentagon Proposed Pretexts for Cuba Invasion in 1962 George Washington University, National Security Archive, this document, titled “Justification for U.S. Military Intervention in Cuba” was provided by the JCS to Secretary of Defense Robert McNamara on March 13, 1962, as the key component of Northwoods. Bombing of Alfred P. Murrah Federal Building in Oklahoma City. Other Examples of Problem Reaction Solution, the Stock Market Crash of 1929, The Federal Reserve was created in 1913. Evidence shows that it manipulated the market resulting in the greatest transfer of wealth to the 'Rich" in the history of the world. Then of course, we should never forget Septmber 11, 2001 - 911, which happened exactly 11 years, to the day, after George H W Bush made his New World Order Speach declaring the fifth objective. The UN Plot to Confiscate Civilian Weapons - Weapons Control, your Choices and your Responsibilities FAIR USE NOTICE: Title 17 U.S.C. Section 107, this material is distributed without profit for Research and Educational Purposes. Menu is at the Top, Sitemap is Here. Front-line New World Order Whistle Blowers - Learn the Faces Free Book in PDF - Steps Toward the Mark of the Beast