The Novavax vaccine also has a substantially lower rate of side effects than the authorized mRNA vaccines. Last week’s data showed that about 40 percent of people who receive Novavax report fatigue after the second dose, as compared with 65 percent for Moderna and more than 55 percent for Pfizer. Based on the results of Novavax’s first efficacy trial in the U.K., side effects (including but not limited to fatigue) aren’t just less frequent; they’re milder too. That’s a very big deal for people on hourly wages, who already bear a disproportionate risk of getting COVID-19, and who have been less likely to get vaccinated in part because of the risk of losing days of work to post-vaccine fever, pain, or malaise. Side effects are a big barrier for COVID-vaccine acceptance.
The more old-school vaccine from Novavax combines ease of manufacture with high efficacy and lower side effects. For the moment, it’s the best COVID-19 vaccine we have.
Isn’t that pretty much what they said about the Johnson & Johnson potion...
Just before many countries halted its use?
When will it be available?
To think that I owned two thousand shares of that stock at $1.13....*&^#@*
With the high survival rate of covid, I’ll pass on any vaccine.
Uh let me think.......NO.
If the woke corporate is pushing it, I don't trust it.
If the media is pushing it, I don't trust it.
So, no.
It’s the Atlantic so proceed with caution.
The second part of the biological warfare waged on the whole world.
This is crimes against humanity.
Trust us. Because we care.
BWAHAHAHA!!!!!
Yeah, right.
When Biden’s “strike force” come through I’ll just let them know that I’m waiting on this new, “far superior and safer”, vaccine.
Compared to how long it has taken the Novavax vaccine to be created, the mRNA Vaccines have come at Warp Speed—Thanks to President Trump. That is the beauty of mRNA technology.
The CIMAvax-EGF vaccine developed by Cuba to fight lung cancer will have a new life in the form of a mRNA vaccine. Even before the pandemic began, Memorial Sloan Kettering researchers had already been working to use mRNA vaccine technology to treat cancer. A potential treatment for pancreatic cancer is now in clinical trials. I guess some day people will be telling cancer patients to stay away from the mRNA cancer vaccine because they might get a little dizzy.
FYI:
“If the World Health Organization has been captured by Big Pharma and is putting out information that goes against medical science, then public health is at grave risk
While the WHO insists large randomized controlled trials (RCTs) must be completed before ivermectin can be recommended, RCTs actually are not the gold standard in terms of scientific evidence. Meta-analyses are
A meta-analysis of 24 RCTs clearly demonstrates that ivermectin produces large statistically significant reductions in mortality, time to clinical recovery, and time to viral clearance
Ivermectin distribution campaigns have also resulted in rapid population-wide decreases in morbidity and mortality, which indicate that ivermectin is effective in all phases of COVID-19
While the WHO and world governments are willing to roll the dice when it comes to the novel COVID shots, they insist on ridiculously high standards of safety and effectiveness when it comes to off-patent drugs that have decades of safe use
Trust is the coin of the realm. And Deep State, Big Pharma, Big Med, Big Tech et al are flat busted.
Nurse Blows the Whistle on the Medical Industry: ‘They’re Not Offering Informed Consent’
Seems to me that trying to halt the spread or eliminate the virus is becoming akin to stopping the common cold. Nothing works for long and does not make you immune.
There are legitimate reasons not to take any experimental vaccine.
Especially when there’s a possibility the supposed cure is much more dangerous than the disease itself.
Very much since no one knows the 2nd or 3rd order effects and won’t know for 2-3 years.
The vaccine industry is pure evil and fraudulent
1970s
67 Killed measles vaccine is discontinued in the United States.
1967 General vaccination program for Mumps begins in the United States.
1967 Science magazine (10/20/67) features article on Joshua Lederberg of the Department of Genetics, Stanford University School of Medicine. Lederberg notifies the scientific world that ‘live viruses (as in vaccines) are genetic messages used for the purpose of programming human cells’ and ‘we already practice biological engineering on a rather large scale by use of live viruses in mass immunization campaigns’
1970 Due to the increasingly mild nature of whooping cough (Pertussis), infant deaths cease from naturally acquired Pertussis in Sweden. Deaths associated with vaccine continue. Sweden stops Pertussis vaccination in 1970.
1970 A study by Pittman reveals Pertussis vaccine can induce hypoglycemia due to increased production of insulin. (Ref: DPT shots). Study is corroborated in 1978 by Hannick and Cohen and by Hennessen and Quast in West Germany. Result: Pertussis and DPT vaccines can cause diabetes.
1972 British Journal of Psychiatry #120 reveals that ‘psychotic disorders may be caused by viral infections.’ (Ref: viruses induced by vaccines).
1972 WHO begins its “Special Programme” in human reproduction with programs for both male fertility control through vaccines and female fertility control.
1972 the World Health Organization (WHO) Bulletin No.47 refers to creation of an immune virus and suggests that a useful way to study the effects would be “to put it into a vaccination program and observe the results.” It is theorized that WHO used the smallpox vaccination program in Central Africa for this study, since the spread of HIV infection coincides precisely with the most intense and recent smallpox vaccination campaigns. Information on the Central African countries most infected with HIV precisely matches WHO figures indicating the number of people vaccinated in these areas. The virus requested would selectively destroy the T-cell system. (1972 Federation Proceedings of WHO).
1973 The field of genetic engineering is opened by advances in scientific research, making way for creation of recombinant micro-organisms and new viral structures in the laboratory. The U.S. military applies the technology to its chemical and biological weapons program, claiming overtly that such work is ‘to develop defensive vaccines’.
1974 British researcher George Disk estimates that there are 80 cases of severe neurological complications from Pertussis vaccine annually. Over 33% of these children died and another 33% were left with brain damage. Dick maintains he is not convinced that the community benefit from the vaccine outweighs the damage.
1974 The Association of Parents of Vaccine Damaged Children is formed in Britain, & pressures the government to study adverse reactions to Pertussis vaccine.
1974 Henry Kissenger writes a classified “National Security Study Memorandium 2000: Implications of worldwide population growth for U.S. security and overseas interest (NSSM 200)” which identifies India, Bangladesh, Pakistan, Nigeria, Mexico, Indonesia, Brazil, the Philippines, thailand, Egypt, Turkey, Ethiopia and Columbia as targets for initial population reduction. The Philippine Supreme Court found that 3 million Philippians between 12 and 45 years of age were given this vaccine. Native American Woman and Black women in the US received this vaccine. Sterility rates in Native American Women in the US is over 35%. Sterility rates in Black Women in the US is over 25%.
1975 Federal Drug Administration Bureau of Biologics concludes that Diphtheria toxoid (vaccine) is ‘not as effective an immunizing agent as might be anticipated.’ They admit that Diphtheria may occur in vaccinated people, and note that ‘the permanence of immunity induced by the toxoid is open to question.’
1975 Japan stops using Pertussis vaccine following publicity about vaccine-related deaths.
1976 FDA Pertussis vaccine specialist Charles Manclark comments ‘Pertussis vaccine is one of the most troublesome products to produce and assay. It has one of the highest failure rates of all products submitted to the Bureau of Biologics for testing and release. Approximately 15-20% of all lots which pass manufacturer tests fail to pass the tests of the Bureau.’
1976 According to a letter from the British Association for Parents of Vaccine Damaged Children, published in the British Medical Journal of February 1976, ‘two years ago we started to collect details from parents of serious reactions suffered by their children to immunizations of all kinds. In 65% of the cases referred to us, reactions followed ‘triple’ vaccinations. The children in this group total 182 to date. All are severely brain damaged, some are paralyzed, and 5 have died during the past 18 months. Approximately 60% of reactions (major convulsions, collapse, screaming) happened within 3 days and all within 12 days.
1976 Dr. Jonas Salk, creator of the polio vaccine, says that analysis indicates that the live virus vaccine in use since the 1960’s is the principle, if not sole cause of all polio cases since 1961.
1976 More than 500 people receiving flu vaccinations become paralyzed with Guilain-Barre Syndrome.
December 1976 No epidemic of Swine flu surfaces despite rapid approval and response to perceived threat following 1 death of a solder at Ft. Dix, NJ. Swine Flu inoculation program shut down after risk of death and polio like syndrome from the vaccination is found to be almost 12 times greater in vaccinated than un-vaccinated people. 5% of people afflicted die, 10% are crippled or maimed for life.
http://www.haverford.edu/biology/edwards/disease/viral_essays/warnervirus.htm
1977 A Blue Ribbon Panel is convened to investigate the reason for the drop in the general IQ of the United States. Seventy-nine theories were advanced, but none of them satisfactorily explained the drop in mental capacity of the US population. The idea that vaccines could be part of the problem was not brought up. Y.L. Warten, 1977. (The Prussian education system is also part of the problem, for those volkschuelen).
1977 The British government is pressured by the publicity following the new data about Pertussis and DPT vaccinations.
1977 The University of Glasgow in Scotland, Department of Community Medicine, Dr. Gordon Stuart, publishes a study analyzing 160 cases of adverse reaction and neurotoxicity following DPT vaccination. In 65 of those cases, reactions to DPT shots included convulsions, hyperactivity and severe mental defect. In a stern statement, Stuart says, ‘it seems likely that most adverse reactions are unreported and/or overlooked.’
1977 The British government conducts the National Childhood Encephalopathy Study (NCES) which tests the connection between vaccinations and neurological disease.
1977 (Mar) Jonas and Darrell Salk warn live virus vaccines produce same disease.
1978 According to Charlotte Parker of the University of Texas Department of Microbiology, the nature of the organism Bordetella Pertussis means that different lots of vaccine made from the same strains sometimes show different properties.
1978 In the United States, the FDA finances and conducts a study at UCLA from January 1, 1978 to December 15, 1979 called ‘Pertussis Vaccine Project: Rates, Nature and Etiology of Adverse Reactions Associated with DPT Vaccine’. The results of the study were published in Pediatrics in November.
1978 In England, Griffith studies pertussis vaccine reactions in children, noting a case in which a boy experiences brain damage 3 days after vaccination and dies 27 days later due to injection of triple vaccine.
1981 The unpublished contractors ‘Final Report’ was submitted to the FDA on March 18, 1980 (a year earlier) and contained revealing data. The study found a higher incidence of adverse reactions to the DPT shot than any previously reported in literature. After the study had run nine months, the FDA convened a Pertussis Symposium, at which it was revealed that ‘the most striking finding in this preliminary analysis is the high frequency of persistent crying, episodes of convulsions and collapse following DPT immunization.’ Because of these findings, the study was curtailed from the planned examination of 50,000 vaccinations to only 17,000. The UCLA FDA study also found that systemic reactions in the central nervous system were present in 50% of the vaccinations. Because of this potentially damaging information, the FDA placed an arbitrary time limit of 48 hours within which reactions had to occur, despite ongoing data which indicates that serious reactions occur after that time limit, in order to limit the statistical data and conceal the extent of the problem from the population. (See 1981).
1985 WHO Vaccines for smallpox and tetanus are laced with female reproductive hormones to induce permanent sterility to “eliminate 150 million excess Sub-Saharan Africans” according to WHO documents.