COVID Vaccine Problems Media Articles
Below are key excerpts of revealing news articles on COVID vaccine problems from reliable news media sources. If any link fails to function, a paywall blocks full access, or the article is no longer available, try these digital tools.
George Garvey, along with several other individuals (collectively, Petitioners) are former NYC Department of Sanitation workers who got fired for their failure to get vaccinated or obtain an approved exemption. They filed a lawsuit pursuant to Article 78 of the New York Civil Practice Law and Rules. They sued NYC, the NYC Department of Health and Mental Hygiene, the NYC Department of Sanitation, the NYC Commissioner of the NY Department of Health and Mental Hygiene and the Mayor of NYC (collectively, Respondents). Judge Ralph J. Porzio issued an order essentially dismissing the Respondent’s arguments and accepting most of the Petitioners’ arguments. The order commanded that all terminated Petitioners be reinstated on October 25, 2022 and collect back pay from their date of termination. The court held that the vaccination mandate was unlawful. First, it was arbitrary and capricious. The court ... argued that it treated similarly situated people differently without providing evidence to support the unequal treatment. Athletes, performers and artists could be exempted from the vaccination requirement, but the Petitioner could not. The court noted that the Petitioners could continue working while their exemption requests were being processed. Therefore, the court felt that the vaccination mandate was never about public safety. Because if it was, any unvaccinated workers would have immediately been placed on leave until a decision concerning their requests for a coronavirus vaccine exemption.
Note: For more along these lines, see concise summaries of deeply revealing news articles on government corruption and coronavirus vaccines from reliable major media sources.
In July 2021 the US Food and Drug Administration (FDA) quietly disclosed findings of a potential increase in four types of serious adverse events in elderly people who had had Pfizer’s covid-19 vaccine: acute myocardial infarction, disseminated intravascular coagulation, immune thrombocytopenia, and pulmonary embolism. Little detail was provided, such as the magnitude of the increased potential risk, and no press release or other alert was sent to doctors or the public. Eighteen days later, the FDA published a study planning document (or protocol) outlining a follow-up epidemiological study intended to investigate the matter more thoroughly. This recondite technical document disclosed the unadjusted relative risk ratio estimates originally found for the four serious adverse events, which ranged from 42% to 91% increased risk. More than a year later, however, the status and results of the follow-up study are unknown. The agency has not published a press release, or notified doctors, or published the findings ... or updated the vaccine’s product label. Cody Meissner, a paediatrician and member of the FDA’s Vaccines and Related Biological Products Advisory Committee, said ... "One of the great problems was the suppression of opposing voices to various recommendations and that’s going to cause extraordinary harm ... everyone is aware that there are going to be side effects from any vaccine and as time goes by, we’re going to find out more and more about those side effects."
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Pfizer's plan to as much as quadruple U.S. prices for its COVID-19 vaccine next year is beyond Wall Street's expectations and will spur its revenue for years despite weaker than anticipated demand for the new booster shot so far, analysts said. The drugmaker, which developed and sells the vaccine with Germany's BioNTech, said on Thursday evening that it is targeting a range of $110 to $130 a dose for the vaccine once the United States moves to a commercial market next year. Analysts said the move could lead to price hikes by rivals. The companies have varied the pricing during the pandemic, with wealthy countries paying the most for the shots and the poorest countries the least. Wells Fargo analyst Mohit Bansal said the new pricing range for the vaccine could add around $2.5 billion to $3 billion in annual revenue for Pfizer. "This is much higher than our assumption of $50 per shot," Bansal wrote in a research note. Global vaccine access group the People’s Vaccine Alliance, which has pushed for Pfizer to allow cheaper copies of the vaccine to be made, called the proposed price hike "daylight robbery." The price range announced by Pfizer represented a more than 10,000% markup over what experts have estimated it costs the vaccine makers to produce the shots.
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No, you’re not crazy. Yes, they claimed the vaccines would prevent transmission. One of the most bizarre lies being told this week in response to Pfizer executive Janine Small’s testimony to EU Parliament is that, actually, the Covid vaccines were never supposed to stop the spread of the virus. Asked by Dutch MEP Rob Roos whether the company had tested its vaccine on “stopping the transmission of the virus” before it rolled out globally, Ms Small said “no” because “we had to really move at the speed of science to really understand what is taking place in the market”. In a viral Twitter video which has now been viewed more than 12 million times, Mr Roos described the response as “scandalous”, arguing “millions of people worldwide felt compelled to get vaccinated because of the myth that ‘you do it for others’”. Mr Roos said the admission removed the entire basis for vaccine mandates and passports which “led to massive institutional discrimination as people lost access to essential parts of society”. The public was told repeatedly, for months, both explicitly and implicitly, that the vaccines would prevent transmission. They’re all on tape saying it. US President Joe Biden, for example, said in July 2021 that “you’re not going to get Covid if you have these vaccinations”. CDC director Rochelle Walensky said in March 2021 that “vaccinated people do not carry the virus”. In Australia, politicians ... held millions of people hostage for months, lecturing and threatening them to get vaccinated to regain their “freedoms”.
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The U.S. Centers for Disease Control and Prevention, facing a Freedom of Information Act lawsuit seeking a vast trove of data about the safety and side-effects of the COVID-19 vaccines, made a pledge in August. The agency in court papers said that on or before Sept. 30, it would post on its website a "public use" set of data from about 10 million people who signed up for its "v-safe" program -- a smartphone-based system that periodically sends people text messages and web surveys to monitor potential side effects from the Pfizer, Moderna and Johnson & Johnson COVID-19 vaccines. But the CDC missed its deadline. In the meantime, the CDC handed over the v-safe data (minus personal identifying information) to the plaintiff in the FOIA case, the Informed Consent Action Network, or ICAN, a Texas-based nonprofit. ICAN crunched the numbers on its own and came up with some statistics that its lawyer says appear to be "alarming." According to ICAN, 7.7% of the v-safe users - 782,913 people - reported seeking medical attention via a telehealth appointment, urgent care clinic, emergency room intervention or hospitalization following a COVID-19 vaccine. About 25% of v-safe users said they experienced symptoms that required them to miss school or work or prevented them from doing other normal activities, according to ICAN's "dashboard" that summarizes the results. In addition to the dashboard summary, ICAN on its website has made the underlying dataset available for public download.
Note: These are very significant numbers, yet other than this Reuters report, the media is largely silent about this very important data. For lots more on this important development with access to the data, see this webpage. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
In response to a lawsuit filed by Siri & Glimstad LLP on behalf of the Informed Consent Action Network (ICAN), the CDC has released the first set of data from its v-safe program. V-safe is a smartphone-based program created by CDC specifically for Covid-9 vaccines. It allows users to register and provide health check-ins after receiving a Covid-19 vaccine. Out of the approximate 10 million v-safe users, 782,913 individuals, or over 7.7% of v-safe users, had a health event requiring medical attention, emergency room intervention, and/or hospitalization. Another 25% of v-safe users had an event that required them to miss school or work and/or prevented normal activities. There were also 71 million symptoms reported in the pre-populated fields. This is an average of more than 7 symptoms reported per v-safe user. Reported symptoms include, for example, over 4 million reports of joint pain. While around 2 million of these joint pain reports were mild, over 1.8 million were for moderate joint pain and over 400,000 were for severe joint pain. There were also around 13,000 infants under 2 years of age registered in v-safe. Among these infants, over 33,000 symptoms were reported, with the most common symptoms being irritability, sleeplessness, pain, and loss of appetite. The data also reflects a disproportionate amount of negative health impacts, including medical events, following the Moderna vaccine versus the Pfizer vaccine and shows a disproportionate number of negative events reported by women versus men.
Note: For lots more on this important development with access to the data, see this webpage. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Not long after the rollout of coronavirus vaccines last year, women around the country began posting on social media about what they believed was a strange side effect: changes to their periods. Now, new research shows that many of the complaints were valid. A study of nearly 20,000 people around the world shows that getting vaccinated against covid can change the timing of the menstrual cycle. Vaccinated people experienced, on average, about a one-day delay in getting their periods, compared with those who hadn’t been vaccinated. The data for the study, published Tuesday in the British Medical Journal, was taken from a popular period-tracking app called Natural Cycles and included people from around the world, but most were from North America, Britain and Europe. The researchers used “de-identified” data from the app to compare menstrual cycles among 14,936 participants who were vaccinated and 4,686 who were not. The data showed that vaccinated people got their periods 0.71 days late, on average, after the first dose of vaccine. However, people who received two vaccinations within one menstrual cycle experienced greater disruptions. In this group, the average increase in cycle length was four days, and 13 percent experienced a delay of eight days or more. Many people on social media have complained of longer, heavier and more-painful periods after getting vaccinated. Preliminary findings from a different study suggest that getting a coronavirus vaccine sometimes may cause heavier periods.
Note: This news article states, "men who contract COVID-19 may experience a temporary reduction in fertility." Yet this Guardian article, titled "No data linking Covid vaccines to menstrual changes, US experts say" quotes an expert claiming, "I suspect the awful people who invented this lie saw the reports of menstrual irregularities post Covid-19 vaccine online and decided to warp it for their campaign of chaos. No, the Covid-19 vaccine is not capable of exerting reproductive control via proxy. Nothing is. This is because it is a vaccine, not a spell."
Last year, Michel Goldman, a Belgian immunologist and one of Europe’s best-known champions of medical research, walked into a clinic near his house, rolled up his sleeve, and had a booster shot delivered to his arm. Michel was having night sweats, and he could feel swollen lymph nodes in his neck. It was cancer of the immune system—lymphoma. Michel understood this meant he’d soon be immunocompromised by chemotherapy. He had just a narrow window of opportunity in which his body would respond in full to COVID vaccination. Having received two doses of Pfizer the prior spring, Michel quickly went to get his third. Within a few days, though, Michel was somehow feeling even worse. His night sweats got much more intense, and he found himself—quite out of character—taking afternoon naps. Most worryingly, his lymph nodes were even more swollen than before. Scans ... showed a brand-new barrage of cancer lesions. It looked like someone had set off fireworks inside Michel’s body. More than that, the lesions were now prominent on both sides of the body, with new clusters blooming in Michel’s right armpit in particular, and along the right side of his neck. When Michel’s hematologist saw the scan, she told him to report directly to the nearest hospital pharmacy. He’d have to start on steroid pills right away. Such a swift progression for lymphoma in just three weeks was highly unusual. As he followed these instructions, Michel felt a gnawing worry that his COVID booster shot had somehow made him sicker.
Note: A study of this case was published in Frontiers in Medicine. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Denmark is currently not offering booster vaccine doses against COVID-19 to people under 50, said the guidelines published on the Danish Health Authority's website. The guidelines added that people below 50 years of age were not at a particularly higher risk of developing serious COVID-19 symptoms. "In addition, younger people aged under 50 are well protected against becoming severely ill from covid-19, as a very large number of them have already been vaccinated and have previously been infected with covid-19, and there is consequently good immunity among this part of the population," the country's health authority said. The Danish health authority said it was likely that many people will contract COVID-19 in autumn and winter months. "With the autumn vaccination programme, we aim to prevent serious illness, hospitalisation and death," it said, advising people to take appropriate precautions. Denmark had become the first country in the world to pause its broad vaccination programme starting May 15 this year. “Spring has arrived, vaccine coverage in the Danish population is high, and the epidemic has reversed,” the Danish Health Authority was quoted as saying by CNBC. “Therefore, the National Board of Health is now ending the broad vaccination efforts against Covid-19 for this season." Pausing broad inoculation only meant people were no longer invited for vaccination but everyone was allowed to complete their vaccination course.
Note: Read the policy on the website of the Danish health authority. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
When Covid-19 struck ... four organizations took on roles often played by governments — but without the accountability of governments. While nations were still debating the seriousness of the pandemic, the groups identified potential vaccine makers and targeted investments in the development of tests, treatments and shots. And they used their clout with the World Health Organization to help create an ambitious worldwide distribution plan. The largest and most powerful was the Bill & Melinda Gates Foundation, one of the largest philanthropies in the world. Then there was Gavi, the global vaccine organization that Gates helped to found to inoculate people in low-income nations, and the Wellcome Trust, a British research foundation with a multibillion dollar endowment that had worked with the Gates Foundation in previous years. Finally, there was the Coalition for Epidemic Preparedness Innovations, or CEPI, the international vaccine research and development group that Gates and Wellcome both helped to create in 2017. The organizations spent at least $8.3 million lobbying the U.S. and E.U., according to an analysis of lobbying disclosures. Now, critics are raising significant questions about the equity and effectiveness of the group’s response to the pandemic — and the serious limitations of outsourcing the pandemic response to unelected, privately-funded groups.
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The updated Covid vaccine boosters, a reformulated version targeting the BA.5 omicron subvariant [will] be the first Covid shots distributed without results from human trials. Because the Biden administration has pushed for a fall booster campaign to begin in September, the mRNA vaccine-makers Pfizer-BioNTech and Moderna have only had time to test the reformulated shots in mice, not people. That means the Food and Drug Administration is relying on the mice trial data — plus human trial results from a similar vaccine that targets the original omicron strain, called BA.1 — to evaluate the new shots. Federal health officials hope that the new vaccines will provide stronger protection over the existing booster shots, which still target the original coronavirus strain. But the lack of data in humans means officials likely won’t know how much better the new shots are — if at all — until the fall booster campaign is well underway. The FDA’s decision to move forward without data from human trials is a gamble, experts say, threatening to further lower public trust in the vaccines should the new boosters not work as intended. The U.S. is still on its first iteration of the Covid vaccines, and the mRNA technology has only been in widespread use since late 2020. The agency is making “huge assumptions” in its consideration of the new Covid boosters, [Dr. Paul] Offit said, adding that it’s possible the new shots may not be any more effective than the existing vaccines.
Note: Read a revealing article with critical information about the new mRNA boosters. To further inquire into this complex topic, explore concise summaries of news articles on coronavirus vaccines and Big Pharma corruption from reliable major media sources.
The European Medicines Agency (EMA) is recommending Novavax's COVID-19 vaccine carry a warning of the possibility of two types of heart inflammation. The heart conditions - myocarditis and pericarditis - should be listed as new side effects in the product information for the vaccine, Nuvaxovid, based on a small number of reported cases, the EMA said. Novavax said no concerns about heart inflammations were raised during the clinical trials of Nuvaxovid and that more data would be gathered. "We will work with the relevant regulators to assure our product information is consistent with our common interpretation of the incoming data," U.S. vaccine developer Novavax added. In June, the U.S. Food and Drug Administration flagged a risk of heart inflammation from the Novavax vaccine. Myocarditis and pericarditis were previously identified as rare side effects, mostly seen in young men, from groundbreaking messenger RNA (mRNA) vaccines made by Moderna and the Pfizer and BioNTech alliance. The EMA said on Wednesday it had asked Novavax to provide additional data on the risk of these side effects. Last month, the EU agency identified severe allergic reactions as potential side effects of the vaccine. Novavax was hoping that people who have opted not to take Pfizer and Moderna's vaccines would favour its shot because it relies on technology that has been used for decades. However, only around 250,000 doses of Nuvaxovid have been administered in Europe.
Note: For more, see this informative article. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
They waved signs that read “Defeat the mandates” and “No vaccines.” They chanted “Protect our kids” and “Our kids, our choice.” “I wish I’d woken up to this cause sooner,” said one protester, Lisa Longnecker, 54. “But I can’t think of a single more important issue. It’s going to decide how I vote.” Longnecker and her fellow objectors are part of a potentially destabilizing new movement: parents who joined the anti-vaccine and anti-mask cause during the pandemic, narrowing their political beliefs to a single-minded obsession over those issues. Their thinking hardened even as Covid-19 restrictions and mandates were eased and lifted, cementing in some cases into a skepticism of all vaccines. Nearly half of Americans oppose masking and a similar share is against vaccine mandates for schoolchildren, polls show. But what is obscured in those numbers is the intensity with which some parents have embraced these views. While they once described themselves as Republicans or Democrats, they now identify as independents who plan to vote based solely on vaccine policies. The extent of activity is evident on Facebook. Since 2020, more than 200 Facebook groups aimed at reopening schools or opposing closings have been created in states including Texas, Florida and Ohio, with more than 300,000 members. Another 100 anti-mask Facebook groups dedicated to ending masking in schools have also sprung up in states including New Jersey, New York and Connecticut, some with tens of thousands of members.
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Sen. Rand Paul (R-KY) has been heavily criticized by those on the Left for fighting back against mask and vaccine mandates. He was censored by Big Tech and vilified by Democratic politicians. Consider the recent admission by Dr. Deborah Birx regarding the efficacy of the COVID-19 vaccines. Birx, the former White House COVID response coordinator, stated in an interview with Neil Cavuto on Fox News that she knew the vaccines wouldn't stop infections. Birx's comments align with what Paul was saying last year regarding the vaccines and the sycophantic nature in which Democrats were pushing them on the public. "I knew these vaccines were not going to protect against infection," Birx said. "I think we overplayed the vaccines, and it made people then worry that it's not going to protect against severe disease and hospitalization. It will. But let's be very clear: 50% of the people who died from the omicron surge were older, vaccinated." Consider Paul's comments in an exchange with Department of Health and Human Services Secretary Xavier Becerra last September. Paul challenged Becerra on the efficacy of vaccines compared to natural immunity. At the time, Paul was one of only a few people who challenged those in charge. Some even claimed Paul's words were causing people to die. As it turns out, Paul was right, and they were wrong. "The science is against you on this. The science is clear. Naturally acquired immunity is as good as a vaccine," Paul said.
Note: Watch the revealing interview where Dr. Birx makes these comments. Note that Birx is promoting Paxlovid for which the gov’t pays $530 per person and is offering free of charge. So who do you think pays for this ultimately? And who profits? The official narrative on COVID is falling apart as shown in the evidence in this great article. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Dr. Anthony Fauci, White House Press Secretary Karine Jean-Pierre, other Biden administration officials and five social media companies have 30 days to respond to subpoenas in a lawsuit alleging collusion to suppress freedom of speech. Discovery requests were served to ask for information and documents from ... NIAID, CDC, ... Surgeon General Vivek Murthy, and Nina Jankowicz, who led the DHS Disinformation Governance Board until it was disbanded. Also requested were any communications to any social media platform relating to the “Great Barrington Declaration,” [which] was published in response to COVID-19 policies that recommended “focused protection,” an approach to reaching herd immunity by allowing those at minimal risk of death to live normal lives by building up immunity through natural infection while protecting those at highest risk. A media release from [Missouri Attorney General Eric] Schmitt ... stated information requested was identifying all communications with any social media platform relating to content modulation and/or misinformation. It requests all communications with Mark Zuckerberg from Jan. 1, 2020, to the present. “In May, Missouri and Louisiana filed a landmark lawsuit against top-ranking Biden Administration officials for allegedly colluding with social media giants to suppress free speech on topics like COVID-19 and election security,” Schmitt said. “Earlier this month, a federal court granted our motion for expedited discovery. We will fight to get to the bottom of this alleged collusion and expose the suppression of freedom of speech by social media giants at the behest of top-ranking government officials.”
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"It's like a horror movie I'm being forced to watch and I can't close my eyes," one senior FDA official lamented. That particular FDA doctor was referring to two recent developments inside the agency. First, how, with no solid clinical data, the agency authorized COVID vaccines for infants and toddlers, including those who already had COVID. And second, [how] the FDA bypassed its external experts to authorize booster shots for young children. That doctor is hardly alone. At the NIH, doctors and scientists complain to us about low morale and lower staffing: The NIH's Vaccine Research Center has had many of its senior scientists leave over the last year, including the director, deputy director and chief medical officer. The CDC has experienced a similar exodus. "There's been a large amount of turnover. Morale is low," one high level official at the CDC told us. "Things have become so political, so what are we there for?" Another CDC scientist told us: "I used to be proud to tell people I work at the CDC. Now I'm embarrassed." Why are they embarrassed? First, they demanded that young children be masked in schools. On this score, the agencies were wrong. Compelling studies later found schools that masked children had no different rates of transmission. Next came school closures. The agencies were wrong – and catastrophically so. Poor and minority children suffered learning loss with an 11-point drop in math scores alone and a 20% drop in math pass rates. Then they ignored natural immunity. Wrong again.
Note: Why are so few media reporting on this most important news? For more along these lines, see concise summaries of deeply revealing news articles on government corruption and the coronavirus from reliable major media sources.
Hundreds more people than usual are dying each week in England and Wales with Covid not to blame for the majority of deaths. Latest data from the Office for National Statistics (ONS) show there were 1,540 excess deaths in the week ending June 24 but only around 10 per cent were due to coronavirus. Health experts have called for an urgent investigation into what is behind the excess mortality, with fears that the pandemic response, lack of access to healthcare and even the cost of living crisis, may be to blame. Prof Paul Hunter ... at the University of East Anglia, said some of the excess could be people whose health was weakened by Covid. But he warned that there may be other more complex factors at play. “Some might also be down to other impacts of the pandemic, such as problems in accessing health care, delayed referrals for treatment and then things related to the restrictions we lived under, such as reduced activity and sedentary lives,” he said. “I think the reality is going to be quite complex but it’s something we do need to be aware of and actually try and understand." The ONS reported 752 excess deaths in the home in the latest week, 30 per cent more than usual, and more than hospitals and care homes put together.
Note: Not one word in this article about an obvious suspect in this excess mortality - the COVID injections. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines and health from reliable major media sources.
On June 18, the U.S. Centers for Disease Control and Prevention (CDC) officially recommended Pfizer and Moderna COVID-19 vaccines for all children between the ages of 6 months and 5 years. While the Food and Drug Administration (FDA) is the agency responsible for authorizing emergency use of vaccines, it’s the CDC that crafts subsequent messaging, makes specific recommendations, and prioritizes who can, should, or should not get vaccinated. In her briefing, CDC Director Rochelle Walensky strongly urged all parents of the nearly 20 million American children in this age group to vaccinate them as soon as possible. There remains ... no solid consensus among physicians about the importance of vaccinating healthy children against COVID-19. In a Food and Drug Administration (FDA) meeting on June 28, Pfizer Vice President for Viral Vaccines Kena Swanson even acknowledged that “there is no established correlate” between antibody levels and protection from disease. Approval for the COVID vaccines in infants and toddlers is based on two trials that used changes in antibody levels as an estimate of efficacy, but did not assess protection from severe disease, hospitalization, or multisystem inflammatory syndrome in children (MIS-C), important outcomes that parents worry about. Additionally, neither trial met the 50% efficacy requirement established by the FDA for approval of adult COVID vaccines. More puzzling is the fact that ... the pediatric vaccines now being administered target an outdated variant.
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Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases and President Biden's chief medical adviser, recently revealed he is experiencing a rebound of his Covid-19 infection after taking the antiviral medication Paxlovid. Fauci described the "interesting course" his own infection had taken on Tuesday during an appearance at Foreign Policy's Global Health Forum. "I turned positive about two weeks ago, with very minimal symptoms. When they increased, given my age, I went on Paxlovid for five days," Fauci said. Fauci, 81, credited the drug with keeping him out of the hospital. After five days on the drug, he tested negative. He had three consecutive days of negative tests. On the fourth day he tested positive again. "It was sort of what people are referring to as a Paxlovid rebound," he said. The CDC issued a health alert to doctors on May 24, advising that Covid-19 symptoms sometimes come back, and that may just be how the infection plays out in some people, regardless of whether they're vaccinated or treated with medications like Paxlovid. In Fauci's case, he said his symptoms got worse when they returned after treatment. "Over the next day or so I started to feel really poorly, much worse than in the first go around," he said. His doctors prescribed another course of Paxlovid. "I went back on Paxlovid, and right now I am on my fourth day of a five-day course of my second course of Paxlovid. Fortunately, I feel reasonably good. I mean, I'm not completely without symptoms, but I certainly don't feel acutely ill."
Note: So two Pfizer shots and two boosters couldn’t keep Fauci from getting COVID not once, but twice. And he says the reason he managed to avoid the hospital is not because of the four shots, but because of the new antiviral he is promoting. This certainly is an “interesting course” as he himself describes it. So how effective are these many injections so strongly promoted by Fauci, the CDC and others. For more along these lines, see concise summaries of deeply revealing news articles on the coronavirus from reliable major media sources.
New York City teachers want a third federal judge off their pandemic vaccine case over potential stock ownership conflicts, this time for what they say are stakes in Pfizer and Johnson & Johnson. The teachers asked Judge Naomi Reice Buchwald in the Southern District of New York to recuse herself from their challenge to the city’s Covid-19 vaccine mandate for education workers after she was assigned to the case. Two other judges at the Manhattan court were off the case after the teachers requested they recuse themselves for similar holdings. The moves come as judicial stock holdings are under increased scrutiny. A Wall Street Journal report that found at least 131 judges heard cases in which they or a family member had a stock conflict prompted a new federal law requiring judicial financial disclosures be publicly accessible online. Judge Valerie E. Caproni, the initial judge on the case, recused after the teachers asked her to disqualify herself because of investments in Pfizer. According to her financial disclosure, the teachers said Caproni held between $50,000 and $100,000 in Pfizer stock at the end of 2020. The case was reassigned to Judge Edgardo Ramos, who the teachers also asked to recuse for his holdings in Pfizer, AstraZeneca, and other companies. The case was then reassigned to Buchwald after one day. Buchwald held Pfizer stock and Johnson & Johnson stock at the end of 2020, the teachers said, citing her financial disclosure.
Note: For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
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