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Pfizer has slashed its sales estimates for COVID antiviral Paxlovid by $7 billion and its COVID vaccine Comirnaty by $2 billion. It adds up to a 13% decline in projected revenue for the company in 2023. As the coronavirus outbreak has shifted to the endemic phase, drugmakers have warned of a drop in demand for COVID-19 products, with the impact coming into focus during the fall vaccination season. Pfizer has stepped up to the plate with an update, and its effects are staggering as the company has slashed its 2023 revenue projection by $9 billion. Pfizer now expects sales to...

...Combining results from a community-wide serological survey of 5,310 blood donors and volunteers with SARS-CoV-2 viral load data from city-wide wastewater surveillance, the researchers estimated, (i) vaccine effectiveness against all Omicron BA.2 infections conferred by two, three and four homologous doses of the Comirnaty or CoronaVac vaccines for 100 days after each dose and (ii) COVID-19 infection attack rate in Hong Kong from 1 January to 31 July 2022. The researchers developed two in-house ELISA assays detecting IgG antibodies to the nucleocapsid (N) or Open Reading Frame 8 (ORF8) protein of SARS-CoV-2, with the latter assay developed specifically to detect...

I'm currently going through web-based classes to be licensed as a pharmacy technician, and under the section educating me on all of the immunizations offered by our pharmacy, the COVID shots are listed. Comirnaty is one of them, but last I knew, the CDC said that none of the vials out for delivery were actually labeled, "Comirnaty." Does anyone have updated information on this? I would like to have it for my own knowledge. Thanks, FReepers!

Pfizer Quietly Admits it Will NEVER Manufacture the Vaccine that was FDA Approved – Will Produce New “Tris-Sucrose Formulation” mRNA Vaccine Instead By Julian Conradson Published June 9, 2022 at 4:30pm 52 Comments Share Tweet Gab Share Telegram Telegram Gettr Gettr It’s official – Pfizer’s “fully approved” and experimental mRNA vaccine, dubbed “Comirnaty,” was nothing more than a head-fake. Earlier this week, the notorious experimental vaccine maker quietly submitted an update to the CDC, admitting that its originally licensed “Comirnaty” vaccine will never be distributed for use. In other words, Pfizer has exclusively been supplying its version of the experimental...

ransomnote: The Expose is over the target and taking flak, banned and censored - even Paypal turned against them in an effort to deprive them of funding. Please pray that the Expose receive the funds it needs to keep serving the public.There are now four teams in New Zealand performing microscopic examinations in an attempt to establish what the so-called Covid vaccines contain and Dr. Robin Wakeling has gone public with his findings. He compares the Comirnaty (Pfizer-BioNTech) Covid injections to other vaccines and discusses the findings with Dr Mark Bailey. Dr. Robin Wakeling is a microbiologist and biodeterioration expert...

The tally for how much the federal government spent to combat COVID-19 is now estimated to be $5 trillion. It is more than the combined costs of World Wars I and II. The left is celebrating that politicians in Washington saved us. Really? From what exactly? Two years later, it is time for an honest assessment. Could things have worsened for the country if the government had spent nothing and done nothing? What would have happened if we had not shut down our businesses? Our churches, schools, and restaurants. Our parks, basketball courts, and playgrounds. Would the public have made...

Two FDA “approvals,” two shell games. On Monday, the FDA “approved” Moderna’s Spikevax COVID-19 vaccine for all US customers. Just like the Pfizer “approval” episode, this vaccine will not be able for anyone for an indefinite period of time. And according to the FDA, the shot was approved without being tested for Omicron, which accounts for 99.9% of current U.S. COVID cases. “Today, the U.S. Food and Drug Administration approved a second COVID-19 vaccine. The vaccine has been known as the Moderna COVID-19 Vaccine; the approved vaccine will be marketed as Spikevax for the prevention of COVID-19 in individuals 18...

The British Medical Journal (BMJ) is demanding pharmaceutical companies release raw COVID-19 vaccine data. BMJ Editors Peter Doshi, Fiona Godlee, and Kamran Abbasi published an editorial stating that “data should be fully and immediately available for public scrutiny” adding that much of the data from major vaccine manufacturers cannot be accessed because the vaccinations are not approved by the Food and Drug Administration. The FDA is only producing data for Pfizer’s vaccine as both Moderna and Johnson & Johnson’s vaccines are not approved by the FDA, despite the popular misconception that they are. Rather, the latter pair have “Emergency Authorization...

Pfizer and the U.S. Food and Drug Administration last week failed to directly address questions by two media outlets about whether Pfizer's Comirnaty vaccine is available in the U.S. [This is the core legal issue concerning government and employer vaccine mandates.]

AbstractBackground Age-specific incidence of acute myocarditis/pericarditis in adolescents following Comirnaty vaccination in Asia is lacking. This study aimed to study the clinical characteristics and incidence of acute myocarditis/pericarditis among Hong Kong adolescents following Comirnaty vaccination. Methods This is a population cohort study in Hong Kong that monitored adverse events following immunization through a pharmacovigilance system for COVID-19 vaccines. All adolescents aged between 12 and 17 years following Comirnaty vaccination were monitored under the COVID-19 vaccine Adverse Event Response and Evaluation Programme. The clinical characteristics and overall incidence of acute myocarditis/pericarditis in adolescents following Comirnaty vaccination were analysed. Results Between 14...

A federal district court judge rejected a claim by the U.S. Department of Defense that the Pfizer-BioNTech COVID-19 vaccine being administered under Emergency Use Authorization is interchangeable with Pfizer’s fully licensed Comirnaty vaccine. A federal district court judge has rejected a claim by the U.S. Department of Defense (DOD) that the Pfizer-BioNTech COVID-19 vaccine being administered under Emergency Use Authorization is interchangeable with Pfizer’s Comirnaty vaccine, which in August was fully licensed by the U.S. Food and Drug Administration (FDA).In an order issued Nov. 12 in Doe et al. v. Austin, U.S. Federal District Judge Allen Winsor of the U.S....

Direct from the Comirnaty package insert... https://www.fda.gov/media/151707/download 5.2 Myocarditis and Pericarditis Postmarketing data demonstrate increased risks of myocarditis and pericarditis, particularly within 7 days following the second dose. The observed risk is higher among males under 40 years of age than among females and older males. The observed risk is highest in males 12 through 17 years of age. Although some cases required intensive care support, available data from short-term follow-up suggest that most individuals have had resolution of symptoms with conservative management. Information is not yet available about potential longterm sequelae. The CDC has published considerations related to myocarditis...

STORY AT-A-GLANCEPfizer/BioNTech’s Comirnaty COVID shot was approved (licensed) by the U.S. Food and Drug Administration in late August 2021, but only for adults, and only when carrying the Comirnaty label. No other COVID shot has been FDA approved. However, Comirnaty is currently not available, and while the experimental, emergency use authorized (EUA) Pfizer shot is substituted for Comirnaty, the two products are clearly legally distinct and not the sameA licensed vaccine is not shielded from liability until or unless it’s added to the recommended childhood vaccination schedule by the CDC. So, if you were injured by Comirnaty, you could sue...

http://web.archive.org/web/20210922125540/https://www.fda.gov/media/150386/download Original text of 8/22 letter: “COMIRNATY (COVID-19 Vaccine, mRNA) is now licensed for individuals 16 years of age and older. There remains, however, a significant amount of PfizerBioNTech COVID-19 vaccine that was manufactured and labeled in accordance with this emergency use authorization. This authorization thus remains in place with respect to that product for the previously-authorized indication and uses (i.e., for use to prevent COVID-19 in individuals 12 years of age and older with a two-dose regimen, and to provide a third dose to individuals 12 years of age or older who have undergone solid organ transplantation, or who...

Finland has joined Sweden, Denmark and Norway in either banning or discouraging young adults or teens from getting the Moderna COVID-19 vaccine, because of the increased risk of myocarditis — heart inflammation.Dr. Hanna Nohynek, chief physician at the Finnish Institute for Health and Welfare, had told the media a decision was coming down Thursday. Finland's health authorities announced that men under 30 will not get the Moderna shot, and should get the Pfizer vaccine instead. Sweden banned Moderna for people under the age of 30, and Denmark did the same for people under 18. Instead of issuing a ban, Norway...

Senator Ron Johnson, R-Wisc., claimed that the U.S. still doesn't have an FDA-approved vaccine as he exposed what was really approved by the government agency on "Fox News Primetime."SEN. RON JOHNSON: We do not have an FDA-approved vaccine being administered in the U.S. The FDA played a bait and switch. They approved the Comirnaty version of Pfizer drugs. It’s not available in the U.S. They even admit it. I sent them a letter three days later going "What are you doing?" What they did is they extended the emergency use authorization for the Pfizer drug vaccine that’s available in the...

1. Fox News admits that Vax is more harmful to children than COVID citing VAERS.https://www.youtube.com/watch?v=zbpNboboDb0 and 2. Senator mentions on-air that Pfizer vaccine is NOT approved by the FDA.https://www.youtube.com/watch?v=5WGaAYVa80Y

The fervor in which our government and media have been pushing this untested, experimental gene therapy on the populous is as suspicious as it is concerning. But now they have the battle cry of its “FDA approved” so it’s completely safe! Oh is it? While the media ran with the story that the Pfizer show was “FDA approved” ….the truth is that it’s not. They never had a public forum to discuss the myriad of side effects and death, nor comple the stage 3 trials required for approval per the FDA’s own perimeters. What the FDA did “approve” however, was...

Vaccines and Related Biological Products Advisory Committee Meeting September 17, 2021 FDA Briefing Document Application for licensure of a booster dose for COMIRNATY (COVID-19 Vaccine, mRNA) https://www.fda.gov/media/152176/download

Study Shows Vaccine Will ENHANCE Delta InfectivitySTORY AT-A-GLANCEA group of Japanese researchers released research showing that the SARS-CoV-2 Delta variant “is poised to acquire complete resistance” to existing COVID-19 jabs When four common mutations were introduced to the Delta variant, Pfizer’s mRNA injection enhanced its infectivity, causing it to become resistant A Delta variant with three mutations has already emerged, which suggests it’s only a matter of time before a fourth mutation develops, at which point complete resistance to Pfizer’s jab may be imminent A number of experts have raised concerns that COVID-19 jabs and the mass vaccination program could...