COVID Vaccine Profits Surge for US Pharmaceutical Companies, Boosted by the Spread of Delta; Causing Pfizer/BioNTech to Change its 2021 Sales Forecast to $33.5 Billion and Moderna's to $19.5 Billion

In June, analysts estimated the global market for the vaccines could be worth $70bn (£50bn) this year, but the figure could be even higher as the Delta variant of coronavirus spreads and scientists debate whether people will need booster shots. Pfizer and Moderna will take the lion’s share of global Covid vaccine profits. The firms are charging $30-plus a person for the required two shots in Europe and the US, while Britain’s biggest drugmaker, AstraZeneca, and the US’s Johnson & Johnson (J&J) have pledged to provide theirs on a not-for-profit basis until the pandemic ends.

From [HERE] and [HERE] Two US companies, Pfizer and Moderna, have raised the prices of their Covid-19 vaccines after data from clinical trials showed their mRNA formula was more effective than cheaper vaccines from Britain’s AstraZeneca and the American drugs maker Johnson & Johnson.

AstraZeneca and Johnson & Johnson have pledged to provide their doses on a not-for-profit basis until the pandemic ends.

Pfizer/BioNTech

Sales worth $11.3bn (£8bn) were made by Pfizer in the first half of this year from the Covid-19 jab that it developed with Germany’s BioNTech. In July it lifted its 2021 sales forecast to $33.5bn.

BioNTech expects to make revenues of nearly €16bn (£13.5bn) from the vaccine this year, as its first-half net profit jumped to almost €4bn from €142m a year earlier.

The two firms have agreed to supply up to 1.8bn doses to the EU from December up to 2023, on top of 600m doses previously ordered this year. The US government has ordered 700m up to April next year for Americans, as well as 500m for donations to the poorest nations.

Pfizer and BioNTech are aiming to produce 3bn jabs this year and 4bn next year. They are now charging the EU €19.50 per jab, up from €15.50 in the first procurement deal, the Financial Times reported. The UK is also reportedly paying more than previously, about £22 a shot for 35m doses for next year’s autumn booster campaign.

Pfizer’s chief executive, Albert Bourla, recently explained the tiered pricing. “This means wealthier nations would pay about the cost of a takeaway meal for each dose … middle-income countries would pay roughly half that price … and to low-income countries we were offering them doses at cost.”

Moderna

This company generated nearly $6bn of sales from its Covid-19 vaccine in the first half of the year, achieving a $4bn net profit – the first half-year profit since the firm was founded in Massachusetts in 2010.

Moderna has signed $20bn worth of vaccine contracts this year, including that for 17m doses to the UK, 460m to the EU and 500m to the US. It expects to produce up to 1bn jabs this year, followed by 2bn-3bn in 2022.

It has charged the US government (which helped fund the development of the vaccine) up to $16.50 a dose, and has sold it for $22 to $37 outside the US. Last week the company also said that sales under the Covax vaccine initiative to low-income countries were “considerably lower than the price to the US government”. The firm has reportedly lifted the price it charges the EU to $25.50 a dose from about $19 in its first deal.

[MORE]

AstraZeneca

Revenue of $1.2bn was achieved by AstraZeneca from the vaccine it developed with the University of Oxford in the first half of the year. So far it has shipped 1bn doses globally and is aiming to produce a total of 2bn-3bn jabs this year. The UK government is in negotiations with AstraZeneca to order a new version of its vaccine adapted to tackle variants of the coronavirus. Results from clinical trials are expected later this year.

The AstraZeneca jab is the cheapest of the main Covid-19 vaccines, priced at just $2.15 a dose in the company’s contract with the EU, rising to just over $5 a shot elsewhere.

However, the EU has not ordered any more doses after the vaccine was linked with rare blood clots. AstraZeneca’s chief executive, Pascal Soriot, said last month that “at some point in the future” the company would raise its prices, adding: “We cannot be a non-profit forever, but we will never intend to make large profits.”

Novavax

Denmark has ordered 280,000 doses of Novavax’s Covid-19 vaccine for $5.8m – roughly $20.90 per dose – as part of an EU deal with the US company. The European Commission said last week it would buy up to 200m doses of the vaccine, which is yet to be approved by the EU’s drugs regulator.

Israel, where 80% are Vaccinated, Suffers Another COVID Surge; Providing Empirical Evidence that "Vaccines" Don't Stop the Spread and are More About Corporate Profit and Government Control than Health

FROM [HERE]

From [HERE] After becoming one of the first countries to open up thanks to a widespread Covid-19 vaccination campaign, Israel is again on guard, this time against the spread of the Delta variant of the coronavirus.

Mask mandates are back, including requirements to mask up for large outdoor gatherings. Many venues require people to show proof of vaccination, a negative Covid-19 test or proof of recovery from the virus. People returning from most countries have to quarantine for at least a week, even if they are fully vaccinated. Over-60s are being offered a third, booster shot of Pfizer Inc.’s vaccine, and the government is planning to offer it to younger recipients with the hopes it can suppress the rise of cases of severe illness.

Health officials are warning that Israel could face a fourth lockdown during the Jewish holiday season in September if the country doesn’t deliver more booster shots and improve on its wider vaccination rate; 60% of the total population are fully vaccinated, making up around 80% of adults.

Meanwhile, Recorded coronavirus infections remain low in the West Bank and Gaza, with only 2,723 active cases. But health officials warn that relatively little testing is being done, meaning that the virus could be spreading widely undetected. However, there are no reports of Palestinian hospitals being in crisis due to COVID. [MORE]

A little over a month ago, day-to-day life in Israel was quickly getting back to normal. People were dining indoors or attending concerts without needing the so-called green pass, a digital certificate stored on phones to show the holder is fully vaccinated. But the more contagious Delta variant is forcing a change in tack, in a test case for what could happen elsewhere, including countries with high vaccination rates.

“That window when we weren’t concerned about things was so brief,” said Rena Magun, 61 years old, who co-runs a tourism and Jewish events-planning business with her husband in Jerusalem. 

Ms. Magun said when she sent an invite to her friends for a meal last week she was careful to emphasize it would take place outside on the porch.

Her business has been badly damaged as families hoping to celebrate bar or bat mitzvahs with their children in Israel have been forced to reschedule the trips up to four times already since March 2020.

“It’s absolutely devastating,” Ms. Magun said.

She said she had decided to get the third Pfizer shot once she was sure it was safe. “I’m gonna get that booster so I can go back to feeling like Superman,” she recalled telling herself.

Other countries with similarly high vaccination rates, notably the U.K., have seen a wave of Delta infections, but hospital admissions have remained low and are falling, according to official data through early August.

Israeli health experts are watching closely for indications that Israel will follow the U.K.’s trajectory. If not, it could be a worrying sign for other countries.

There has been a jump in Israel in cases of severe illness caused by the virus since the start of August, doubling to 400 in a population of 9 million, with 240 of those patients already having been vaccinated. Patients over 50 years old account for 90% of the severe cases, Prime Minister Naftali Bennett said Tuesday.

“I ask every Israeli citizen over 50 to be very careful in the coming weeks,” he said.

Though the number of severe cases remains low, the rate of growth has raised concerns. Hospitals are preparing for an influx of patients similar to the early days of the pandemic, with a seven-day average of nearly 4,000 new coronavirus cases now being recorded daily.

To head off the outbreak and prevent larger numbers of vaccinated Israelis falling ill, Israel last month became one of the first countries to begin offering a third Pfizer dose to people 60 years old and over—without any clinical evidence that it would be effective. The decision came after preliminary data made available to medical experts advising Israel’s government showed that protection against severe illness for vaccinated people in the age group had dropped to 81% from 97% in mid-April.

1st Responders Union Suit Against the Hawaii Vaccine Mandate Claims that 45,000 People Have Died within 72 Hours of Getting Vaccine. Says Vaccines Don't Stop the Spread or Immunize People

 From [HERE] and [HERE] Representatives for Hawaii union members taking legal action against the state’s COVID vaccine mandate held a news conference at attorney Michael Green’s office on Thursday. Approximately 1,200 first responders are part of the class action lawsuit.

The attorneys announced that they plan to file the lawsuit on Friday in order to try to stop the mandate which takes effect Monday, Aug. 16. This one is on behalf of police officers, firefighters and other first responders.

One of the lawyers representing the emergency responders recently listed data backing their decision to forego taking the experimental Covid jabs.

“The tests we’ve seen around the country from doctors are showing that almost 45,000 people that got these vaccinations were dead in 72 hours,” attorney Michael Green said at a Thursday press conference.

“They’re just asking for the chance to choose,” said attorney Shawn Luiz. “It’s a personal, autonomous, healthcare decision, and everyone should make their own choice, whether or not they want to take a vaccine or not.” 

“I have to choose between that career that I’m committed to or put in an experimental drug that I don’t know what it’s gonna do to me in my body, or I got to give all that up,” said Capt. Kaimi Pelekai of the Honolulu Fire Department.

Pelekai says the City just sent county workers a letter saying they either have to get vaccinated or show proof of religious or medical exemption by Monday — or they could lose their job. KHON2 is asking the City about the letter.

When the governor announced the mandate last week, he said unvaccinated workers have the option of getting tested weekly. Representatives for the union members in the class action lawsuit say this is a violation of their collective bargaining agreement, and it runs into a whole set of problems for the workers.

“If they can’t prove the testing because they’re waiting for their free tests and they’re going to be home without pay. So it’s almost the same result as being fired. You’re having a large majority of our first responders off the street without pay and being punished,” said attorney Kristin Coccaro.

“The heavy-handedness that we are now seeing is shocking to the conscious for Hawaii especially, and there’s got to be a voice,” said Green.

The City confirmed the letter that was sent to workers and released a statement from the Honolulu Mayor Rick Blangiardi saying, “I stand behind the decision to protect City employees, their families and our communities, while also reducing the number of positive COVID-19 cases.”

A spokesman for the state attorney general says, “The State is confident that its vaccine and testing policy is lawful and constitutional.”

Although there are a number of free testing sites, those who are unable to go to them will have to pay for their own. Exemptions will be provided, but it is still not clear how those will be determined. Those who do not comply, however, could lose their job.

During the press conference, Honolulu Fire Captain Kaimi Pelekai also spoke in an emotional testimony describing the pressure of having to choose between the shot and losing his job.

“I have to choose between that career that I’m committed to or put in an experimental drug that I don’t know what it’s gonna do to me in my body, or I got to give all that up,” Pelekai said. “I spent the last 20 years of my life and 37 years watching my dad do this job, and because I didn’t want to put an experimental drug in my body, I got to give that all up?”

The Vested Interests' Emergency COVID Clogic and Believabilia: ‘Vaccinations Don't Stop the Spread of COVID. Nevertheless, the Unvaccinated Must Get Vaccinated to Stop COVID From Spreading’

CDC Study shows 74% of People Infected in Massachusetts Covid Outbreak were Fully Vaccinated. Nevertheless, Dependent Media Makes Believe that Only Unvaccinated Persons Spread COVID.

From [HERE] One of the most nagging questions about the COVID-19 pandemic for public health authorities, policymakers and the public was whether the vaccines stop transmission.

New Centers for Disease Control and Prevention data show that in breakthrough cases of the highly transmissible delta variant, the answer is no. The newly released report showing that vaccinated people can still be superspreaders. [MORE]

The viral load of vaccinated people with breakthrough cases is the same as in unvaccinated people, the CDC said Friday.

About three-fourths of people infected in a Massachusetts Covid-19 outbreak were fully vaccinated against the coronavirus with four of them ending up in the hospital, according to new data published by the Centers for Disease Control and Prevention.

The new data, published in the U.S. agency’s Morbidity and Mortality Weekly Report, also found that fully vaccinated people who get infected carry as much of the virus in their nose as unvaccinated people, and could spread it to other individuals.

“This finding is concerning and was a pivotal discovery leading to CDC’s updated mask recommendation,” CDC Director Dr. Rochelle Walensky said in a statement. “The masking recommendation was updated to ensure the vaccinated public would not unknowingly transmit virus to others, including their unvaccinated or immunocompromised loved ones.”

The CDC reversed course on its prior guidance and recommended fully vaccinated Americans who live in areas with high Covid infection rates resume wearing face masks indoors. The guidelines cover about two-thirds of the U.S. population, according to a CNBC analysis.

While the delta variant continues to hit unvaccinated people the hardest, some vaccinated people could be carrying higher levels of the virus than previously understood and are potentially transmitting it to others, Walensky told reporters. She added the variant behaves “uniquely differently from past strains of the virus.”

Nevertheless the dependent media continues to parrot incorrect propaganda that only unvaccinated spread COVID. Last week Joe Rogan pointed out this stupid hypocrisy on his podcast. Rogan pointed to studies sent to him by doctors showing vaccines that don’t kill the host and still allow transmission, like Covid vaccines, can let virulent strains spread.

Essentially, Rogan claimed the data sent to him by doctors and scientists shows the vaccinated, not the unvaccinated are responsible for the surge in Delta variant cases as mainstream media continuously states.

“You have to have a vaccine passport to go to a restaurant, gym, to any place where people gather. And, meanwhile, the biggest percentage of people who haven’t been vaccinated are people of color"

From [HERE] During Friday’s edition of The Joe Rogan Experience, the top podcast host and comedian called out vaccine passports being rolled out around the country and exposed how Covid vaccines could actually create new, more powerful variants.

Describing New York’s vaccine passport system, Rogan said, “You have to have a vaccine passport to go to a restaurant, to a gym, to any place where people gather. And, meanwhile, the biggest percentage of people who haven’t been vaccinated are people of color.”

Rogan noted that the state’s Democrat Governor Andrew Cuomo virtue signals as a politician who stands up for immigrants and people of color.

“Those are the people who don’t have vaccines and now you’re precluding them from going to gyms and restaurants, and what about all the people working the restaurants?” he asked.

TARGETED AND PRESUMED UNVACCINATED BY SKIN COLOR until proven otherwise.  In Nazi Germany , as part of the destruction process of the Jews, the Nazi's marked Jews with a star. Without the stars (and meticulous recordkeeping) there was no way to tell who was a semite and who was not. Nazi's created an elaborate system of movement restrictions and identification measures that included personal Jew identification cards, passports marked with a J, assignment of names and the outward marking of persons with a yellow star. Jews were only allowed to appear in public when wearing the Jewish star. [MORE]

According to Raul Hilberg: "the whole identification system, with its personal documents, specially assigned names, and conspicuous tagging in public, was a powerful weapon in the hands of the police. It was a control measure in that it enabled the police to pick up any Jew, anywhere, anytime. [MORE]

In this MORE ORGANIZED, UPDATED OPERATING system (OS) of racism/white supremacy there is no need for any such star - non-whites are targeted by skin color [MORE] and [MORE] and [HERE].

Next, the top podcast host went over studies sent to him by doctors showing vaccines that don’t kill the host and still allow transmission, like Covid vaccines, can let virulent strains spread.

Essentially, Rogan claimed the data sent to him by doctors and scientists shows the vaccinated, not the unvaccinated are responsible for the surge in Delta variant cases as mainstream media continuously states.

Joe also recognized America as the first successful experiment in self-governance in human history before saying we are currently moving closer to a dictatorship thanks to vaccine passports and travel restrictions.

The UFC commentator also noted that over 70% of those dying from Covid are obese, asking why leaders aren’t pushing Americans to eat healthier and work out to prevent severe cases.

Now that the Haitian President is Out of the Way Mass Vaccinations Have Begun in Haiti. Jovenel Moïse Didn't Refuse Offers for Real Vaccines; He Rejected mRNA "Vaccines." Is that Why He was Murdered?

From [HERE] In the wake of one of the most devastating moments in Haiti's arduous history, there has been a bright spot.

One week after Haiti's president was assassinated, the country's first shipment of COVID-19 vaccines finally arrived.

President Jovenel Moïse was allegedly shot a dozen times in his private residence on July 7. Prior to his murder Haiti, the poorest nation in the Western hemisphere, was the only nation that hadn’t vaccinated a single resident against Covid-19.

Haiti was among the 92 poor and middle-income countries offered doses under the Covax Facility. But the government initially declined AstraZeneca PLC shots, citing side effects and widespread fears in the population.

“Haiti did not reject the offer of vaccines from Covax,” Haiti Ministry of Health General Director Laure Adrien said in a telephone interview. “All we asked was that they change the vaccine they were providing us.” [MORE] and [MORE]

Despite the political chaos, social disruption and a national "state of siege" that followed the killing, Haiti has now launched a mass COVID-19 immunization drive for health care workers and people over age 65. Haiti is one of the last countries in the world to make the vaccine available.

NPR says “The big question now is whether Haiti can overcome the political instability and high levels of distrust among the general public to actually get people vaccinated.“

The Pan American Health Organization (PAHO) warned in a memo in July that the volume of issues on Haiti's plate could leave it vulnerable to a devastating COVID-19 outbreak. The population is taking few precautions against the virus. Hardly anyone is vaccinated. And resistance to the vaccine is high. According to a survey conducted in June by UNICEFand the University of Haiti, only 22% of adults were open to getting it. The hesitancy is driven in part by people not viewing COVID-19 as a threat and in part by concerns amplified by social media about side effects. 

The PAHO memo adds, "The security situation could deteriorate even further and hurricane season has started."

Deaths attributed to COVID-19 in Haiti remain low. Officially, just over 500 Haitians have died of COVID-19 so far in the pandemic — half the number of fatalities that occurred in the first month of Haiti's devastating cholera outbreak in 2010.

By all accounts, these numbers are underestimates; testing is even far less frequent in Haiti.

Pape says random antibody screenings of patients at the Gheskio clinic show that many Haitians have already been exposed to COVID-19. 

"The majority of my patients — the poor people — they are getting infected," he says. "Sometimes they have symptoms but not enough to require hospitalization or even ventilation care."

Many don't seek medical care for COVID-19 at all — because they can't afford to go to a clinic or because their symptoms are mild or nonexistent.

Pape says new variants of the virus, especially the alpha variant that was first identified in the U.K., have led to more severe cases in Haiti. So far, the so-called the delta variant hasn't been documented, but the country doesn't have the capacity to test for it.

However, the New Humanitarian explained that Haiti has been spared high COVID-19 death tolls  largely due to the fact that more than half of Haiti’s 11 million population are under the age of 24. Conversely, the Dominican Republic – which shares the same island – has seen more than 3,226 deaths and 246,299 cases, many linked to its booming tourism industry.   

EU Regulator says Among Other Side Effects; the J & J Vaccine may Cause Easy/Excessive Bleeding, Dizziness and Tinnitus and AstraZeneca can Cause Nerve Inflammation, Pain and Difficulty Walking

From [HERE] Johnson & Johnson’s single-shot COVID-19 vaccine is linked to cases of low blood-platelet counts, the European Medicines Agency said on Friday.

The regulator’s drug safety committee, PRAC, said it reached the conclusion after assessing available evidence from scientific literature, as well as cases of suspected side effects reported to the drugmaker and to European and U.S. regulators. It didn't note in its statement how many cases it had observed. 

This specific condition, known as immune thrombocytopenia, occurs when the number of blood platelets — which are needed for clotting — falls because the immune system mistakenly attacks them.

The committee recommended updating the vaccine information to include immune thrombocytopenia as a possible side effect and warning health care staff and vaccine recipients of this risk.

In addition, the committee called for adding dizziness and tinnitus to the list of possible side effects after concluding that some reported cases are also linked to the vaccine.

Separately, PRAC has requested further data from AstraZeneca to assess whether its two-dose adenovirus vaccine is linked to cases of Guillain-Barré syndrome, a rare immune disorder causing nerve inflammation, pain and difficulty walking. 

At its last meeting, the committee recommended warning medics and recipients to be aware of this disease, but it has requested further data from the drugmaker "to clarify whether further updates to the product information and the risk management plan are necessary."

Drug Overdose Deaths are At All-Time High Due to the Spread of Fentanyl/Opioids Made by the Same Profiteers Getting Rich off COVID Vaccines. Whites Account for most Deaths but Deaths Rose among Blacks

From [HERE] and [HERE] Drug-overdose deaths in the U.S. surged nearly 30% in 2020 amid the COVID-19 pandemic. 

The estimated 93,331 deaths from drug overdoses last year, a record high, represent the sharpest annual increase in at least three decades, and compare with an estimated toll of 72,151 deaths in 2019, according to provisional overdose-drug data(link is external) released by the Centers for Disease Control and Prevention (article available here(link is external)).

“That is a stunning number even for those of us who have tracked this issue,” said Brendan Saloner, associate professor of health policy and management at the Johns Hopkins Bloomberg School of Public Health. “Our public health tools have not kept pace with the urgency of the crisis.”

The surge, the 2020 data show, was driven largely by a proliferation of fentanyl, a powerful synthetic opioid whose use has spread across the nation. The pandemic amplified the epidemic of overdoses, bringing on social isolation, trauma and job losses, according to addiction experts and treatment providers. Overdose deaths began rising in the fall of 2019 with the spread of fentanyl, but really took off starting in March 2020, when pandemic-driven shutdowns and physical-distancing measures set in. “It’s really one of those things where 2020 turbocharged something that was already wildly out of control,” Dr. Saloner said.

Fentanyl, which is 50 times more potent than heroin, is now frequently mixed into other widely used illicit drugs, often when the user is unaware. “Fentanyl is poisoning our drug supply,” said Monique Tula, executive director of the National Harm Reduction Coalition, an organization that advocates for people who use drugs and trains the harm reduction workforce.

An estimated 57,550 people died of overdoses from synthetic opioids, primarily fentanyl, an increase of more than 54% over 2019, according to Robert Anderson, chief of the mortality statistics branch at the CDC’s National Center for Health Statistics. “Definitely fentanyl is the driving factor,” he said. Overdose deaths from opioids overall rose nearly 37%, according to the CDC data.

Deaths from overdoses of methamphetamine and cocaine also rose, the CDC said.

“I can remember thinking 30,000 was an astounding number,” said Dr. Anderson. “Now we’re three times that. It’s crazy.” Final overdose death data will likely be released in December, he said.

The deaths from drug overdoses form a twin public health crisis with Covid-19 and show how the human toll of the pandemic extends well beyond the estimated 377,883 U.S. deaths involving that disease last year. Covid-19 was the third-leading cause of death in the U.S. in 2020, after heart disease and cancer, according to preliminary mortality data. Unintentional injuries, which include drug overdoses, were the fourth-leading cause.

Overdose deaths are helping to drive down U.S. life expectancy, which may have suffered the largest drop last year since 1943, during World War II.

The CDC is expected to report preliminary 2020 life-expectancy data next week.

Many people who were receiving treatment for drug addictions or wanted it were unable to get it in the early weeks or months of the pandemic, or faced disruptions or changes in service, treatment providers say. Job losses or deaths of family and friends created stress and trauma, while office and business closures reduced social interaction, depriving some of coping mechanisms they rely on. Some people ended up homeless, on the street, where they have had trouble accessing treatment, Ms. Tula said.

While white people account for most drug-overdose deaths, they have risen in recent years among Black people.

In Minnesota, the drug-overdose death rate for Black people was nearly twice that of white people in 2019, according to a report from the Minnesota Department of Health. Mary DeLaquil, author of the report and an epidemiologist with the department, said that while those data aren’t available yet for 2020, she doesn’t expect an improvement. “I feel fairly confident saying it’s not going to go down in 2020,” she said. “In Minnesota and nationally, we are seeing drug overdoses rise across the board.”

The rising death toll points to a need for urgent, comprehensive measures to address the crisis, public health and treatment experts said.

State and local governments are seeking more than $26 billion from opioid manufacturers and distributors in lawsuits that seek to recover the costs of fighting the epidemic.

In general, the governments allege that the pharmaceutical industry pushed opioids to be prescribed and distributed beyond what was medically necessary, creating widespread addiction that led to higher abuse of street opioid drugs such as heroin and illicit fentanyl. The companies say they sold or distributed a legal product that was prescribed by doctors necessary for pain management.

After years of delay, three trials are under way in New York, California and West Virginia.

Some cases have settled recently. Johnson & Johnson agreed in June to pay $230 million to the state of New York to resolve an opioid lawsuit.

New York, Massachusetts and 13 other states signed on to a settlement this month with OxyContin maker Purdue Pharma LP and its owners, the Sackler family.

The governments should use the settlement money they are expected to receive for treatment and prevention programs, including investments to help reduce disparities in communities of color, Ms. Tula said.

Video Shows Side Effects of "Vaccine" and People Passing Out at Vax Centers after Getting Injected

Investor, Hype Man and Chief Medical Advisor Anthony Fauci Warns that ‘COVID is Going to Get Worse.’ But More "Vaccinations" Mean More Profit So Its a Win-Win for Profiteers

From [HERE] The Biden administration’s chief medical adviser said he didn’t believe the U.S. would return to lockdowns but warned that “things are going to get worse” as a more contagious variant of the coronavirus has led to a surge of new cases.

“We are looking, not I believe, to lockdown but we are looking to some pain and suffering in the future because we are seeing the cases go up,” Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, said Sunday on ABC’s “This Week.” He added, “The solution to this is, get vaccinated.”

The latest statistics from the U.S. Centers for Disease Control and Prevention show a 64.1% increase in Covid cases over the week ended July 30 compared with the previous week, or an average of 66,606 cases a day. The CDC reported a current seven-day average of 6,071 new admissions of hospital patients with Covid-19, a 44% increase over the average for the week of July 16-22. CDC Director Rochelle Walensky previously has said that more than 97% of Covid patients entering the hospital nationwide were unvaccinated.

As of July 26, the CDC had reported fewer than 1,000 Covid-related deaths among vaccinated individuals. More than 164 million people in the U.S. have been fully vaccinated.

Dr. Fauci and other top medical officials pleaded on several Sunday talk shows for Americans to follow the newest government guidelines—that everyone in areas with high Covid-19 infection rates wear a mask, regardless of vaccination status. They also urged the nearly 100 million eligible Americans who hadn’t received a vaccine to get one.

Liberal Comedian Jimmy Dore Complains about His Lingering Vaccine Side Effects such as Brain Inflammation but Dependent Media Ignores Him b/c Criticism of "the Vaccine" is Prohibited by Uncle Brother

From [HERE] Comedian Jimmy Dore described side effects he’s experiencing more than four months after being injected with two doses of Moderna’s experimental Covid jab.

Speaking to Joe Rogan last week, Dore justified why he got the jab despite a general distrust of the establishment, explaining, “People are like, ‘Why [did you take it]? You trust the government?’ No I don’t trust the government. ‘You trust Big Pharma?’ No, I don’t trust Big Pharma, I trust my doctor.”

Dore described how he and others he knows who took the jab experienced similar symptoms post-vaccination; however, his symptoms have never fully gone away.

“So I had body aches, flu-like fever, joint aches, body pain. I had a stiff neck,” Dore said, adding he also experienced “waves of exhaustion.” 

The former Young Turks contributor also complained about the censorship faced by those who attempt to expose or speak about vaccine side effects.

“I tweeted just to let everybody know, ‘Hey, this is my reaction to the vaccine,’ and…people started to come [at] me and call me like, ‘Anti-vax.’ I’m like, ‘No, I got the vax, I got it.’ When people have a reaction to an experimental vaccine that is not FDA approved you’re supposed to not suppress the reaction, you’re supposed to ask people what the reactions are so we can make the vaccines better.”

Dore later said he takes medication to treat brain inflammation, which he says he now has as a result of the spike proteins contained in the vaccine.

Dore’s vaccine injury admissions on The Joe Rogan Show come after he documented the symptoms on his podcast in June, where he claimed a cardiologist told him of other patients experiencing similar vaccine-related side effects.

Renowned IP Underwriter and Analyst Provides Patent Documentation that COVID was Created by NIAID (US Gov) and that the "Vaccine" is an Injected Biological Weapon, Patented Prior to the 2020 Outbreak

• The Fauci/COVID-19 Dossier

Dr. David E. Martin is the Founder and Chairman of M·CAM Inc., an international leader in innovation finance, trade, and intangible asset finance. M.CAM is a Virginia-based company that underwrites lending on intellectual property, earning a fee from the lender, usually a bank, and in most cases the right to sell on the IP if the company defaults. [MORE] Martin is the developer of the first innovation-based quantitative index of public equities and is the Managing Partner of the Purple Bridge Funds. He is the creator of the world’s first quantitative public equity index – the CNBC IQ100 powered by M·CAM. He is also a respected financial analyst. [MORE]

In the video above Attorney Reiner Fuellmich interviews Dr David Martin for the German Corona Investigative Committee. [MORE] He has provided citations for all the references he uses in the video which are also documented [HERE] and [HERE]. Other references, such patent information, are verifiable [HERE] and [HERE] and [HERE].

A full transcript of the interview is below:

Our firm has been the world’s largest underwriter of intangible assets used in finance in 168 countries, so in the majority of the countries around the world. Our underwriting systems include the entire corpus of all patents, patent applications, federal grants procurement records, e-government records, etc. We have the ability to not only track what is happening and who is involved in what’s happening but we monitor a series of thematic interests for a variety of organizations and individuals as well as for our own commercial use, because as you probably know we maintain three Global Equity indices which are the the top performing large-cap and mid-cap equity indices worldwide. So our business is to monitor the innovation that’s happening around the world and specifically to monitor the economics of that innovation, the degree to which financial interests are being served, corporate interests are being dislocated etc. So our business is the business of innovation and its finance.

As you know we have reviewed the over 4,000 patents that have been issued around SARS Coronavirus and we have done a very comprehensive review of the financing of all of the manipulations of coronavirus which gave rise to SARS as a subclade of the beta coronavirus family. We took the reported gene sequence which was reportedly indicated as such by the ICTV (the International Committee on Taxonomy of Viruses) of the World Health Organization. We took the actual genetic sequences that were reportedly novel and reviewed those against the patent records that were available as of the spring of 2020. And what we found are over 120 patented pieces of evidence to suggest that the declaration of a novel coronavirus was actually entirely a fallacy. There was no novel coronavirus. There are countless very subtle modifications of coronavirus sequences that have been uploaded but there was no single identified novel coronavirus at all. As a matter of fact, we found records in the patent records of sequences attributed to novelty going to patents that were sought as early as 1999. So not only was this not a novel anything, it’s actually not been novel for over two decades.

Up until 1999 the topic of coronavirus was uniquely applied to veterinary sciences. The first vaccine ever patented for coronavirus was actually sought by Pfizer. The application for the first vaccine for Coronavirus which was specifically a Spike protein — so the exact same thing that allegedly we have rushed into invention — the first application was filed January 28th 2000 — 21 years ago. So the idea that we mysteriously stumbled on the way to intervene on vaccines is not only ludicrous, it is incredulous because Timothy Miller, Sharon Klepfer, Albert Paul Reed, and Elaine Jones on January 28th 2000 filed what ultimately was issued as U.S. patent 637-2224, which was the spike protein virus vaccine for the canine coronavirus, which is actually one of the multiple forms of coronavirus. But as I said the early work up until 1999 was largely focused in the area of vaccines for animals. The two animals receiving the most attention were probably Ralph Baric’s work on rabbits, and the rabbit cardiomyopathy that was associated with significant problems among rabbit breeders; and then canine coronavirus in Pfizer’s work to identify how to develop a spike protein. [These] target candidates give rise to the obvious evidence that says that neither the coronavirus concept of vaccine nor the principle of the coronavirus itself as a pathogen of interest with respect to the spike protein’s behavior is anything novel at all. As matter fact it’s 22 years old on based on patent files.

What’s more problematic and what is actually the most egregious problem is that Anthony Fauci and NIAID (National Institute of Allergy and Infectious Diseases) found the malleability of coronavirus to be a potential candidate for HIV vaccines, and so this is actually not a natural progression of a zoonotic modification of coronavirus. As a matter of fact, very specifically in 1999 Anthony Fauci funded research at the University of North Carolina Chapel Hill specifically to create — this comes directly from a patent application filed on April 19th, 2002 — you heard the date correctly, 2002 — where NIAID built an infectious replication-defective coronavirus specifically targeted for human lung epithelium. In other words we [U.S. NIAID] made SARS and we patented it on April 19th, 2002 before there was ever any alleged outbreak in Asia. Which [outbreak] as you know followed that by several months, that patent issued as US patent 727-9327. That patent clearly lays out in very specific gene sequencing the fact that we knew that the ACE-2 receptor, the ACE-2 binding domain for the s-1 spike protein and other elements of what we have come to know as this scourge pathogen, was not only engineered but could be synthetically modified in the laboratory using nothing more than gene sequencing technologies, taking computer code and turning it into a pathogen or an intermediate of the pathogen. And that technology was funded exclusively in the early days as a means by which we could actually harness coronavirus as a vector to distribute HIV vaccine.

My organization was asked to monitor biological and chemical weapons treaty violations in the very early days of 2000. You’ll remember the anthrax events in September of 2001. And we were part of an investigation that gave rise to the Congressional inquiry into not only the anthrax origins but also into what was unusual behavior around Bayer’s ciprofloxacin drug, which was a drug used as a potential treatment for Anthrax poisoning. And throughout the fall of 2001 we began monitoring an enormous number of bacterial and viral pathogens that were being patented through NIH, NIAID, and the US Armed Services Infectious Disease Program, and a number of other agencies internationally that collaborated with them. And our concern was that coronavirus was being seen as not only a potential manipulable agent for potential uses as a vaccine vector, but it was also very clearly being considered as a biological weapon candidate. So our first public reporting on this took place, prior to the SARS outbreak in the latter part of 2001. So you can imagine how disappointed I am to be sitting here twenty years later having 20 years earlier pointed out that there was a problem looming on the horizon with respect to coronavirus. But after the alleged outbreak — and I will always say alleged outbreak — because I think it’s important for us to understand that coronavirus as a circulating pathogen inside of the viral model that we have is actually not new to the human condition and is not new to the last two decades. It’s actually been part of the sequence of proteins that that circulates for quite a long time.

in PHOTO LEGEND HANK AARON WHO DIED 2 WEEKS AFTER GETTING INJECTED WITH A PLAY VACCINE. ACCORDING TO FUNKTIONARY: vaccinated - infected with poisons. (See: Antibiotics)

vaccination - mandatory infection--typically administered by agents of Corporate State in their public schools of indoctrination camps. How can unvaccinated children endanger other children who are immunized?

But the alleged outbreak [of SARS-1] that took place in China in 2002 going into 2003 gave rise to a very problematic April 2003 filing by the United States Center for Disease Control and Prevention. And this topic is of critical importance to get the nuance very precise, because in addition to filing the entire gene sequence on what became SARS coronavirus, which is actually a violation of 35 U.S. Code Section 101 — you cannot patent a naturally occurring substance. The 35 U.S. Code Section 101 violation, what is patent number 7220852, now that patent also had a series of derivative patents associated with it. These patent applications were broken apart because they were of multiple patentable subject matter. These include U.S. Patent 465-9270-3p which is actually a very interesting designation, U.S. Patent 7776521. These patents not only covered the gene sequence of SARS coronavirus but also covered the means of detecting it using RT-PCR. Now the reason why that’s a problem is, if you actually both own the patent on the gene itself and you own the patent on its detection, you have a cutting-edge advantage to being able to control 100% of the provenance of not only the virus itself but also its detection — meaning you have entire scientific and message control. And this patent sought by the CDC was allegedly justified by their public relations team as being sought so that everyone would be free to be able to research coronavirus. The only problem with that statement is it’s a lie. And the reason why it’s a lie is because the Patent Office not once but twice rejected the patent on the gene sequence as unpatentable because the sequence was already in the public domain. In other words prior to CDC’s filing for a patent the Patent Office found 99.9% identity with the already existing coronavirus recorded in the public domain.

And over the rejection of the Patent Examiner and after having to pay an appeal fine in 2006 and 2007, the CDC over[came] the Patent Office’s rejection of their patent, and ultimately in 2007 got the patent on SARS Coronavirus. So every public statement that CDC has made that said that this was in the public interest is falsifiable by their own paid bribe to the Patent Office. And to make matters worse, they paid an additional fee to keep their application private. Last time I checked, if you’re trying to make information available for the public to research, you would not pay a fee to keep the information private. I wish I could have made up anything I just said, but all of that is available in the public patent archive record which any member of the public can review. The United States Patent Office has not only the evidence but the actual documents which I have in my possession now.

This is critically important because fact-checkers have repeatedly stated that the novel coronavirus designated as SARS-CoV-2 is in fact distinct from the CDC patent. And here is both the genetic and the patent problem. If you look at the gene sequence that is filed by CDC in 2003, again in 2005, and then again in 2006, what you find is identity in somewhere between 89 to 99% of the sequence overlaps that have been identified in what’s called the novel subclade of SARS-CoV-2. What we know is that the core designation of SARS coronavirus which is actually the clade of the beta coronavirus family, and the subclade that has been called SARS-CoV 2, have to overlap from a taxonomy point of view. You cannot have SARS designation on a thing without it first being SARS. So the disingenuous fact-checking that has been done, saying that somehow or another CDC has nothing to do with this particular patent or this particular pathogen, is beyond both the literal credibility of the published sequences, and it’s also beyond credulity when it comes to the ICTV taxonomy, because it very clearly states that this is in fact a subclade of the clade called SARS coronavirus.

Now what’s important is on the 28th of April — and listen to the date very carefully because this date is problematic — 3 days after CDC filed the patent on the SARS coronavirus in 2003, 3 days later Sequoia Pharmaceuticals — a company that was set up in Maryland — Sequoia Pharmaceuticals on the 28th of April 2003 filed a patent on antiviral agents of treatment and control of infections by coronavirus. CDC filed three days earlier and then the treatment was available 3 days later. Just hold that thought for a second. Sequoia Pharmaceuticals and ultimately [Ablig] Pharmaceuticals became rolled into the proprietary Holdings of Pfizer, [Crysel], and Johnson & Johnson, So ask yourself a simple question: How would one have a patent on a treatment for a thing that had been invented three days earlier? The patent in question, the April 28th 2003 patent 715-1163, issued to Sequoia Pharmaceuticals has another problem. The problem is it was issued and published before the CDC patent on coronavirus was actually allowed. So the degree to which the information could have been known by any means other than insider information between those parties is zero. It is not physically possible for you to patent a thing that treats a thing that had not been published. Because CDC had paid to keep it secret. This, my friends, is the definition of criminal conspiracy, racketeering, and collusion. This is not a theory, this is evidence. You cannot have information in the future inform a treatment for a thing that did not exist. It is a RICO case and the RICO pattern which was established in April of 2003 for the first coronavirus was played out to exactly the same schedule when we see SARS-CoV show up, when we have Moderna getting the spike protein sequence by phone from the Vaccine Research Center at NIAID prior to the definition of the novel subclade. How do you treat a thing before you actually have the thing?

Before you actually have the thing on the 5th of June 2008 — which is an important date because it is actually around the time when DARPA, the Defense Advanced Research Program in the United States, actively took an interest in coronavirus as a biological weapon — June 5th 2008 [Ablig], which as you know is now part of Sanofi, filed the series of patents that specifically targeted what we’ve been told is the novel feature of the SARS-CoV-2 virus, and you heard what I just said, this is the 5th of June 2008 they found the specific sequence they targeted, what was called the poly-basic cleavage site for SARS-CoV the novel spike protein in the ACE-2 receptor binding domain which is allegedly novel, to SARS-CoV-2, and all of that was patented on the 5th of June 2008. And those patents in sequence were issued between November 24th of 2015 which was U.S. Patent 919-3780, so that one came out after the gain-of-function moratorium. That one came after the MERS outbreak in the Middle East but what you find is that then in 2016, 2017, 2019 a series of patents all covering not only the RNA strands but also the subcomponents of the gene strands were all issued to [Ablig] and Sanofi and then we have Rubius Therapeutics, we have Children’s Medical Corporation, we have countless others that include Ludwig-Maximilians-University, Protein Science Corporation, Dana-Farber Cancer Institute, University of Iowa, University of Hong Kong, Chinese National Human Genome Center in Shanghai, all identifying in patent filings that ranged from 2008 until 2017 every attribute that was allegedly uniquely published by the single reference publication. The novel coronavirus reveals quote ‘natural insertions at the S1, S2 cleavage site of the spike protein and possible recombinant origin of the SARS-CoV-2 virus, the paper that has routinely been used to identify the novel virus.

Unfortunately if you actually take what they report to be novel, you find 73 patents issued between 2008 and 2019 which have the elements that were allegedly novel in SARS-CoV-2 specifically as it relates to the poly-basic cleavage site ACE-2 receptor binding domain, and the spike protein, so the clinically novel components of the clinically unique, clinically contagious virus [were already in those 73 patents]. There was no outbreak of SARS because we had engineered all of the elements of that, and by 2016 the paper that was funded during the gain-of-function moratorium that said that the SARS coronavirus was poised for human emergence — written by none other than Ralph Baric — was not only poised for human emergence, but it was patented for commercial exploitation. A statement made in 2015 by [Eco-Health Alliance Director] Peter Daszak reported in the National Academies of Science Press publication February 12th 2016, and I’m quoting ‘We need to increase public understanding of the need for medical countermeasures such as a pan-coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process‘ end quote. Let me repeat the quote: ‘We need to increase public understanding of the need for medical countermeasures such as a pan-coronavirus vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process‘ end quote.

There wasn’t a lab leak. This was an intentional by weaponization of spike proteins to inject into people to get them addicted to a pan-coronavirus vaccine. This has nothing to do with a pathogen that was released, and every study that has ever been launched to try to verify a lab leak is a red herring. And there’s really nothing that is new in this, zero. These patents on everything clinically novel, 73, [were] all issued before 2019. To prove that this was actually not a release of anything, because patent 727-9327, the patent on the recombinant nature of that lung targeting coronavirus, was transferred mysteriously from the University of North Carolina Chapel Hill to the National Institutes of Health in 2018. Now here’s the problem with that under the Bayh-Dole Act, the U.S. Government already has what’s called a march-in right provision. That means if the U.S. Government has paid for research they are entitled to benefit from that research at their demand or at their whim. So explain why in 2017 and 2018 suddenly the National Institutes of Health have to take ownership of the patent that they already had rights to, held by the University of North Carolina Chapel Hill. And how did they need to file a Certificate of Correction to make sure that it was legally enforceable because there was a typographical error in the grant reference in the first filing so they needed to make sure that not only did they get it right but they needed to make sure every typographical error contained in the patent was corrected on the single patent to develop the Vaccine Research Institute’s mandate which was shared between the University of North Carolina Chapel Hill in November of 2019 and Moderna in November of 2019, when UNC Chapel Hill and NIAID and Moderna began the sequencing of a spike protein vaccine a month before an outbreak ever happened, you have all the evidence.

The script for this was written first January 6th 2004, in Bioterrorism, Emerging Infectious Diseases, Antimicrobial Therapeutics, and Immune Modulators. Moderna introduced the notion of what they called The New Normal which became the branded campaign that was adopted by the World Health Organization, the Global Preparedness Monitoring Board which was the Board upon which the Chinese Director of Center for Disease Control, Elias of the Gates Foundation, and Anthony Fauci sat together on that Board of Directors. But the the first introduction of The New Normal Campaign, which was about getting people to accept a universal pan-influenza pan-coronavirus vaccine, was actually adopted January 6th 2004 so it’s it’s been around quite quite a long time.

Moderna knew that it was going to be placed in the front of the line with respect to the development of a vaccine in March of 2019, and this is a very important date because in March of 2019, for reasons that are not transparent, they suddenly amended a series of rejected patent filings, which is a very bizarre behavior, but they amended a number of patent filings specifically to make reference to a deliberate or accidental release of coronavirus. So in March 2019 [with] the amended failed patent applications, [they] begin the process of a coronavirus vaccine development. And they began dealing with a very significant problem that they had which was they relied on technology that they did not own. Two Canadian companies Arbutus Pharmaceuticals and Acuitas Pharmaceuticals actually own the patent on the lipid nanoparticle envelope that’s required to deliver the injection of the mRNA fragment. And those patents have been issued both in Canada and in the U.S. and then around the world. Moderna knew that they did not own the rights and began trying to negotiate with Arbutus and Acuitas to make the lipid nanoparticle patented technology available to be put into a vaccine. And we know, before that in November they entered into a research and cooperative research and development agreement with UNC Chapel Hill with respect to getting the spike protein to put inside of the lipid nanoparticle so that they actually had a candidate vaccine before we had a pathogen allegedly that was running around. What makes that story most problematic beyond the self-evident nature of it is that we know that from 2016 until 2019 at every one of the NIAID advisory Council Board meetings, Anthony Fauci lamented the fact that he could not find a way to get people to accept the universal influenza vaccine, which was his favorite target — he was trying to get the population to engage in this process.

And what becomes very evident with Peter Daszak (Eco-Health Alliance), UNC Chapel Hill and others and then most specifically by March of 2019 in the amended patent filings by Moderna, we see that there is an epiphany that says what if there was an accidental or an intentional release of respiratory pathogen. And what makes that particular phrase problematic is it is exactly recited in the book A World At Risk which is the scenario that was put together by the World Health Organization in September of 2019. So months before there’s an alleged pathogen, [this book from WHO] says that we need to have a coordinated global experience of a respiratory pathogen release which by September 2020 must put in place a universal capacity for public relations management, crowd control, and the acceptance of a universal vaccine mandate. That was September of 2019 and the language of an intentional release of a respiratory pathogen was written into the scenario that quote ‘must be completed by September 2020‘.

The ACE-2 receptor was already described in the patents before 2019. Specifically the ACE-2 receptor targeting mechanism for SARS coronavirus is in publications going back to 2008, in the weaponization conferences that took place in Slovenia in Europe, all across Europe, and all across the DARPA infrastructure. We’ve known about that since 2013 and its isolation and amplification, add to this 70 amendments that merge the two. The failed [Moderna] patent applications were essentially revitalized in March of 2019, to include the ‘deliberate release of a respiratory pathogen‘ language. Their [patenting] process is similar to other pharmaceutical companies where they ever-green applications and continually modify applications to enjoy the earliest priority dates available. But that’s why you have to go back and look at the amendment of the application records to find out when the actual amendment language is put in place. Any assertion that this pathogen is somehow unique or novel falls apart on the actual gene sequences which are published in the patent record and then more egregiously falls apart in the fact that we have Peter Daszak himself stating that we have to create public hype to get the public to accept the medical countermeasure of a pan-coronavirus vaccine. And what makes that most ludicrous is the fact that as we know World Health Organization had declared coronavirus kind of a dead letter — they said that that we had eradicated coronavirus as a concern. So why having eradicated it in 2007 and 2008, why did we start spending billions of dollars globally on a vaccine for a thing that had been eradicated by declaration in 2008? That falls into the zone of incredulity, to say the least.

The entirety of the evidence then is that this is a tool — the coronavirus and the vaccines, this is a tool and the interest of DARPA in creating a biological weapon out of this. This is a tool for everything else that latches onto this, including population control. This was seen as a highly malleable bio-weapon. There is no question that by 2005 it was unquestionably a weapon of choice. Unfortunately very well-meaning people get trapped into conversations about whether we’re having a vaccine for a virus. The fact of the matter is we’re not. We are injecting a spike protein mRNA secret mRNA sequence which is a computer simulation; it’s not derived from nature, it’s a computer simulation of a sequence which has been known and patented for years. And what we know is that that sequence is reported across phone conversations that took place between Moderna and the [NIH] Vaccine Research Center. The story that this is somehow prophylactic or preventative flies in the face of 100% of the evidence because the evidence makes it abundantly clear that there has been no effort by any pharmaceutical company to combat the virus. This is about getting people injected with the known-to-be-harmful spike protein. So the cover story is that if you get an expression of a spike protein you’re going to have some sort of general symptomatic relief but the fact of the matter is there has never been an intent to vaccinate a population as defined by the vaccination universe [namely, to prevent infection].

When Anthony Fauci tried desperately to get some of his quote ‘synthetic RNA vaccines’ [for HIV] published he had his own patents rejected by the Patent Office, and I want to read what the patent office told him when NIAID’s own Anthony Fauci thought that he could get an mRNA-like vaccine patented as a vaccine. And here’s the quote: ‘These arguments are persuasive to the extent that an antigenic peptide stimulates an immune response that may produce antibodies that bind to a specific peptide or protein, but it is not persuasive in regards to a vaccine.‘ This is the Patent Office. The immune response produced by a vaccine must be more than merely some immune response, it must also be protective as noted in the Patent Office action. ‘The art recognizes the term vaccine to be a compound which prevents infection. Applicant has not demonstrated that the instantly claimed vaccine meets even the lower standards set forth in the specification let alone the standard definition for being operative. In regards therefore claims five, seven, and nine are not operative.‘ As the anti-HIV vaccine which is what he was working on is not patentable utility. So Anthony Fauci himself was told by the Patent Office themselves that what he was proposing as a vaccine does not meet the patentable standard, the legal standard, or the clinical standard.

This is the problem going back to the very beginning of what’s alleged to be a pandemic. We do not have any evidence that the gene sequence alteration had any clinical significance whatsoever, There has not been a single paper published by anyone that is actually established that anything novel since November of 2019 has clinical distinction from anything that predates November of 2019. The problem with the 73 patents that I described is that those 73 patents all contain what was reported to be novel in December and January of 2019 and 2020 respectively, so the problem is that even if we were to accept that there are idiopathic pneumonias, even if we were to accept that there are some sets of pathogen induced symptoms, we do not have a single piece of published evidence that tells us that anything about the subclade SARS-CoV-2 has clinical distinction from anything that was known and published prior to November 2019 in 73 patents dating to 2008.

Influenza did not leave the human population. Influenza was a failed decade-long pan-influenza vaccine mandate that was desperately desperately desperately promoted by governments around the world. They failed and they decided if influenza doesn’t deliver on the public promise of getting everybody to get an injection, let’s change the pathogen.

US Judge Postpones (Again) Suit Over COVID Conditions at Dallas Jail. Inhumane Authorities Failed to Provide Soap, Cleaning supplies, Food, blankets and had Shortages of Basics like Toilet Paper

From [HERE] In late April 2020, shortly after the start of the COVID-19 pandemic, the American Civil Liberties Union (ACLU) of Texas and its partners filed a federal class-action lawsuit against Dallas County Sheriff Marian Brown in U.S. District Court for the Northern District of Texas.

The lawsuit was continued again in July.

Representing nine plaintiffs, the filing comes in light of more than 30 individuals in the jail testing positive for COVID-19 back then. The lawsuit accuses Sheriff Brown and her department of failing to take proper action in order to protect incarcerated people from the novel virus.

Ideare Bailey, one of the nine plaintiffs, testified that when he was arrested for property theft and landed in the Dallas County Jail on April 6, he was not provided with a mask despite being forced to live in close proximity in a dormitory with 60 other people. He also had no feasible way to stay apart from the men coughing in the dorm.

When Bailey inevitably got sick, the medical staff not only refused to take his temperature until three whole days later but also were negligent of his aftercare after his positive COVID-19 diagnosis.

Allegedly, they only gave Bailey a mask soon after he tested positive and just gave him Tylenol to cope with the side effects. They did not administer insulin for his diabetes nor check his oxygen levels.

Other plaintiffs have also spoken out on how during the pandemic the jail did not provide access to soap and cleaning supplies, had a constant shortage of food and blankets, and were inconsistent in giving out basic supplies like toilet paper.

The lawsuit is asking the District Court to immediately remove medically at-risk people from jail and ensure that the jail establishes proper health protocol to combat the virus spread, such as providing sufficient cleaning supplies, testing regularly, and enforcing physical distancing.

At the filing of the lawsuit, Alison Grinter of the NGAN Legal Advocacy Fund stated that the COVID-19 pandemic “will spread faster and hit harder in our jails and [the court] must take action now to prevent needless deaths.”

Terri Burke – former executive director of ACLU of Texas – also commented, “People’s lives are at stake … and [we are] asking the court to take immediate action. We [must make] sure that our vulnerable loved ones in jail don’t get left behind and have a way out.”

However, reality often does not meet expectations.

The case has been pending for more than a year now and a trial was initially scheduled to take place on July 27. But, citing the need for the court to shuffle through an increasing backlog of motions, U.S. District Judge Ada Brown ordered the postponement of the upcoming trial and has yet to set a new date.

In light of this delay, objections have obviously erupted from ACLU of Texas and advocates of their lawsuit.

ACLU of Texas staff attorney Brian Klosterboer stated that “this is a lawsuit that could be resolved if the county takes some small steps to keep people safe in jail” and the million dollars spent fighting the lawsuit could have gone into actually solving the growing health crisis in the jail.

Jails and prisons are generally accepted as one of the most dangerous places amidst the pandemic as the outbreak of the virus is much stronger in their facilities. Dallas County Jail is no exception because during November last year, it was already one of the worst hotspots for the disease in the country.

A study by the Lyndon B. Johnson School of Public Affairs at the University of Texas found that incarcerated people in Texas jails and prisons tested positive at a rate of 490 percent higher than the state’s general population.

Evidently, according to an ACLU of Texas statement earlier this month, the situation in the Dallas County Jail has not improved much since the filing of the lawsuit in that it “still does not provide comprehensive testing for COVID-19 … [and even] failed its annual inspection for the first time in years … due in part to a failure to provide soap and hygiene products [to detainees].”

As of May 2021, it has also purportedly administered vaccines to, at most, just 25 percent of the jail’s population.

Japanese Company, Shionogi, has Started Human Trials of the First Once-a-day Pill for COVID. Pill Aims to Neutralize the Virus 5 days after a Patient takes it w/o Vaccine

From [HERE] A Japanese company has started human trials of the first once-a-day pill for Covid-19 patients, joining Pfizer Inc. PFE 0.51% and Merck MRK 1.32% & Co. in the race to find treatments for the disease.

Osaka-based Shionogi 4507 3.20% & Co., which helped develop the blockbuster cholesterol drug Crestor, said it designed its pill to attack the Covid-19 virus. It said the once-a-day dosing would be more convenient. The company said it is testing the drug and any side effects in trials that began this month and are likely to continue until next year.

Shionogi is months behind Pfizer and Merck, which have started later-stage tests of pills to treat Covid-19. Pfizer has said its twice-daily pill could be ready to hit the market as soon as this year. It is preparing to enroll more than 2,000 patients in a test of the antiviral pillcombined with a booster antiviral drug against a placebo.

All three companies aim to fill one of the biggest gaps in fighting the pandemic. Vaccines remain effective at preventing serious illness from known strains of the Covid-19 virus including the contagious Delta strain, studies have shown. But some people don’t want to get vaccinated, and cases can occur for those who do get their shots. 

Existing treatments, including Gilead Sciences Inc.’s infused antiviral drug remdesivir, generally have to be administered in hospitals and work only some of the time. Other drugs that can be given in hospitals include monoclonal antibody drugs such as one made byRegeneron Pharmaceuticals Inc. and the steroid dexamethasone.

Drugmakers are looking for a pill that those who get a positive Covid-19 test could take at home while their symptoms are mild. Such medicines already exist for influenza, includingRoche Holding AG’s Tamiflu and Shionogi’s Xofluza, although they don’t work for all patients and might be prescribed too late to do much good. Xofluza is marketed in the U.S. by Roche.

“Our target is a very safe oral compound, like Tamiflu, like Xofluza,” said Isao Teshirogi, Shionogi’s chief executive officer. He said Shionogi’s Covid-19 pill aims to neutralize the virus five days after a patient takes it.

Dr. Teshirogi said Shionogi expects to enroll 50 to 100 healthy subjects in its trial in Japan. A larger trial comparing the drug with a placebo in Covid-19 patients could begin in Japan later this year, he said.

The failure rate for drug trials is generally high. Any side effect, even a relatively mild one such as nausea, could make a Covid-19 pill impractical for home use. It isn’t yet known whether getting rid of the virus in patients would translate into reducing serious complications such as low oxygen that land people in the hospital, researchers working on Covid-19 treatments said. [MORE]

Pfizer and BioNTech Raise Price on COVID Vaccines Sold to US Government from $19 to $24 a Shot on Latest Purchase of 200 Million Vaccines. So Far US has Bought 1 Billion Doses

From [HERE] The U.S. has purchased 200 million additional Covid-19 vaccine doses from Pfizer Inc.PFE 0.51% and partner BioNTech SE, BNTX 0.35% at a higher price than previous deals.

The U.S. is paying about $24 a dose, according to Pfizer, up from the $19.50 that the government paid in its earlier deals to supply the country. The deal brings the total purchased from the U.S. to 1 billion doses.

The companies said they expect to deliver 110 million of the additional doses by the end of the year, with the rest by the end of next April. Pfizer said the U.S. has the option to acquire an updated version of the vaccine targeting variants, should they be available and authorized by regulators. Pfizer is testing one targeting the Beta variant, which was first identified in South Africa. 

“The price for this order accounts for the additional investment necessary to produce, package and deliver new formulations of the vaccine, as well as the increased cost associated with delivering the vaccine in smaller pack sizes to facilitate delivery at individual provider offices, including pediatricians,” a Pfizer spokesman said in a statement.

White House press secretary Jen Psaki confirmed that the Biden administration’s purchase could be used to inoculate children or serve as booster shots should health regulators deem them necessary.

“We’ve always prepared for every scenario,” Ms. Psaki said, noting that the additional shots will be delivered between the upcoming fall and the spring of 2022.

Officials from the Food and Drug Administration and Centers for Disease Control and Prevention have yet to say that booster shots are necessary. Pfizer said earlier this month it would seek clearance from U.S. regulators to distribute a booster shot of its Covid-19 vaccine. 

More than 86 million people in the U.S. ages 12 and up have received the two-dose shot, the most among the three shots cleared by regulators for use, according to federal figures.

Johnson and Johnson Hits the Jackpot w/COVID: Vaccine Should Notch $2.5 Billion in Revenue for the Year, according to Chief Financial Officer

From [HERE] Greater demand for medical devices, drugs and consumer-health products helped boost sales and profit for Johnson & Johnson JNJ 1.06% in the latest quarter, a sign people are returning for healthcare services they deferred earlier in the pandemic.

Sales of J&J’s medical devices climbed 63% year over year, the company said Wednesday. Higher sales of the company’s skin-care and beauty products helped lift J&J’s consumer-health revenue by 13% compared with a year earlier.

The New Brunswick, N.J.-based company, a bellwether for the healthcare industry because its products span several categories, logged sales of $23.31 billion—a 27% increase year over year—and adjusted earnings of $2.48 a share.

Wall Street analysts had forecast adjusted earnings of $2.29 a share and revenue of $22.49 billion, according to FactSet.

Shares of Johnson & Johnson were largely flat Wednesday.

J&J executives expressed confidence the return to healthcare use would continue, saying they didn’t expect the spread of the Delta variant of the coronavirus would have an impact.

“Our outlook for the rest of the year really remains strong for our sector regardless of what happens with emerging variants and any continued blips as it relates to Covid,” said Jennifer Taubert, who runs J&J’s pharmaceuticals business.

Ashley McEvoy, J&J’s medical devices chief, said hospitals appear better than earlier in the pandemic at handling any surges in Covid-19 cases while keeping elective surgeries going. Yet she said some hospitals in the U.S. are beginning to delay elective procedures as Covid-19 cases mount.

The company raised its guidance for full-year performance. J&J forecast sales of $93.8 billion to $94.6 billion and adjusted earnings of $9.60 to $9.70 a share, up from the maximums from its previous forecast of $91.6 billion and $9.57 a share.

J&J said sales of its Covid-19 vaccine, which generated $164 million in revenue in the second quarter, would pick up during the latter parts of the year. The shot should notch $2.5 billion in revenue for the year, most of it in the fourth quarter, Chief Financial Officer Joseph Wolk said.

CBPP Study Says COVID has Exacerbated “Socialist Distancing" btw Whites and Non-Whites as Black/Latino Households Still Disproportionately Lack Sufficient Food and are Unable to Pay Rent/Daily Needs

From [HERE] While employment is rising and strains on household budgets have eased in recent months, the employment rate remains low and millions still report that their households did not get enough to eat or are not caught up on rent payments. We are able to track the extent of the nation’s progress against hardship thanks to nearly real-time data from several sources on the ongoing economic crisis.

Key hardship indicators show strong improvement since December, Census Bureau data show, aided by job growth and government benefits. Hardship rates fell especially fast after the enactment of the American Rescue Plan on March 11, which included $1,400 payments for most Americans as well as other assistance to struggling households. (See Figure 1.) Nonetheless, 20 million adults live in households that did not get enough to eat, 11.5 million adult renters are behind on rent, and some of the progress from late March appears to be waning.

The impacts of the pandemic and the economic fallout have been widespread, but remain particularly prevalent among Black adults, Latino adults,[1] and other people of color. These disproportionate impacts reflect harsh, long-standing inequities — often stemming from structural racism — in education, employment, housing, and health care that the current crisis has exacerbated. Households with children also continue to face especially high hardship rates. Considerable evidence suggests that reducing childhood hardship and poverty would yield improvements in education and health, higher productivity and earnings, less incarceration, and other lasting benefits to children and society.[2]

Report is [HERE]

According to FUNKTIONARY:

Socialist distancing – the ever-expanding and increasing disparity between the haves and the have-nots until the Socialist (i.e., monopoly capitalist) Welfare State becomes the Farewell State—farewell to your rights, your family, friends and even your life through Plandemics (Coronavirus), $camdemics (Corporate State turned Surveillance and Nanny State), 5G bio-weaponized eugenics, starvation, vaccinations, civil unrest, genocide and other nefarious LWO (Last World Order) activities that will greatly reduce the world’s population by 2030. Before Social Distancing, we were experiencing the effects of “Socialist Distancing”...the ever-widening separation between the “haves” (holders) and the “have-nots” (held-back) due to “monopoly capitalism” (centralization of credit in the hands of the State) which by wide academic recognition is the core attribute of communism / socialism, in fact, it is the 5th plank of the Communist Manifesto. The litmus test to any political system is what is used as “money” and who controls (monopolizes) its “issuance.” Labels just don’t cut it. Think deeper...learn to access the underlying reality behind the truth veneer you’ve been conditioned to hold or have been told. (See: Plandemic, $camdemics, Vaccines, Coronavirus, “Monopoly Capitalism,” Exchange, Economics, Matrix Capitalism, Political Money, GEO-Dollars, The Farewell State, Trapitalism, Cultural Induction & COVERT-19)

'Because We Said So' Not Good Enough for Everybody: Surgeon General Mad About Covid Misinformation but Fails to Dispel Claim that Vaccines Carry Substantially Serious Side Effects and May Cause Death

From [HERE] Joe Biden’s administration renewed its assault on social media companies allegedly spreading Covid-19 misinformation on Sunday, as new infections continued to surge across the entire US.

Vivek Murthy, the US surgeon general who has accused companies including Facebook of “poisoning information” about coronavirus vaccines, said they were not doing enough to check the online proliferation of false claims.

“The reality is that misinformation is still spreading like wildfire in our country aided and abetted by technology platforms,” he said on Fox News Sunday.

“I’m worried about what is to come because we are seeing increasing cases among the unvaccinated in particular. It’s so important people have the information they need about the vaccine … it is our fastest, most effective way out of this pandemic.” [MORE]

Last month a medical study that appeared on the National Library of Medicine website called "The Safety of COVID-19 Vaccinations — We Should Rethink the Policy" explained that the COVID vaccines are effective but carry significant risk of death and serious side effects. The doctors who authored the study, Harald Walach Rainer (Poznan University of the Medical Sciences, Pediatric Hospital in Poland ) J. Klement (Department of Radiation Oncology, Leopoldina Hospital, Germany) and Wouter Aukem (Independent Data and Pattern Scientist, Brinkenbergweg, The Netherlands), explain that ‘governments should rethink their vaccination policies in light of the deadly risks involved.’

The study was removed from the internet last week and replaced with a version that has “retracted” stamped across it. The original is posted here. The abstract states:

COVID-19 vaccines have had expedited reviews without sufficient safety data. We wanted to compare risks and benefits. Method: We calculated the number needed to vaccinate (NNTV) from a large Israeli field study to prevent one death. We accessed the Adverse Drug Reactions (ADR) database of the European Medicines Agency and of the Dutch National Register (lareb.nl) to extract the number of cases reporting severe side effects and the number of cases with fatal side effects. Result: The NNTV is between 200–700 to prevent one case of COVID-19 for the mRNA vaccine marketed by Pfizer, while the NNTV to prevent one death is between 9000 and 50,000 (95% confidence interval), with 16,000 as a point estimate. The number of cases experiencing adverse reactions has been reported to be 700 per 100,000 vaccinations. Currently, we see 16 serious side effects per 100,000 vaccinations, and the number of fatal side effects is at 4.11/100,000 vaccinations. For three deaths prevented by vaccination we have to accept two inflicted by vaccination. Conclusions: This lack of clear benefit should cause governments to rethink their vaccination policy.