/qrb/ - QResearch Bunker

dough

https://fullchan.net/?0afba5ee2f7cdac1#CqKc1v9hRYW4F76v3jV9JCQJECUsTctbkn3fy1dFt7VH

https://controlc.com/74d96cea

baker standing down

G'nite and Godspeed, friends.

-OUT for now.

GHOST BREAD!

Welcome to 8san. An imageboard centered around free speech. User board creation is enabled!

https://8san.org/

Tor: http://a5gomggvi5n75w4llxspnkryrfyiqgcpe6g5kbmlk6dq5t27ujddhoyd.onion/

With love,

Q

>>85572

you need some colors yo

https://www.notonthebeeb.co.uk/post/what-is-really-in-the-c19-vaccines

WHAT IS REALLY IN THE C19 VACCINES?

A new report has just been released by The Scientists Club collating research on the real contents of the C19 'vaccines'.

This article features a few highlights - to read the full report please download the PDF at the end.

ANALYSIS: Environmental Scanning Electron Microscope coupled with an x-ray microprobe of an Energy Dispersive System

MODERNA

* A mixed entity (organic-inorganic) identified in a Moderna “vaccine”. It is a Carbon-based substrate where some nanoparticles are embedded. The nanoparticles are composed of Aluminium-Copper-Iron-Chlorine.

* Many foreign bodies were identified with a spherical morphology with some bubble-shaped cavities. They are composed of Silicon- Lead-Cadmium-Selenium. This highly-toxic composition reminds that of quantum dots (Cadmium selenide).

* A 100-micron entity that reminds that of graphene. It is composed of Carbon and Oxygen with contamination of Nitrogen, Silicon, Phosphorus, Chlorine.

* Carbon-based entities in a Moderna “vaccine” (see below) mixed with aggregates filled with Aluminium-silicate particles

PFIZER

* Sharp debris of 20micron of length identified in a Pfizer “vaccine”. It is composed of Carbon, Oxygen Chromium, Sulphur, Aluminium, Chloride, Nitrogen.

* A strange foreign body, surely engineered with strange holes on the surface. The white debris are composed of Carbon, Oxygen, Aluminium, Silicon, Calcium, Magnesium, Chlorine and Nitrogen.

* Debris identified in a Pfizer “vaccine”. The white 2-micron-long particle is composed of Bismuth, Carbon, Oxygen, Aluminium, Sodium, Copper, Nitrogen.

* An organic (Carbon-Oxygen-Nitrogen) aggregate with embedded nanoparticles of Bismuth-Titanium-Vanadium -Iron-Copper Silicon-Aluminium embedded in Pfizer “vaccine”

* The 50-micron long body (see image below) is a mysterious presence in a vaccine. It could be a trypanosoma parasites several variants of which are lethal’ (the bold italic text is missing form original {PDF)

JANSSEN

* Shows an organic-inorganic aggregate (see below) identified in a Janssen “vaccine”. The particles are composed of stainless steel and are glued together with a “Carbon-based glue”.

This aggregate is magnetic and can trigger biological problems inside the blood circulation due to possible interactions with other dipoles.

ASTRAZENECA

* An engineered aggregate of Iron-Chromium-Nickel (stainless steel) nanoparticles embedded identified in an Astrazeneca “vaccine”

>>85575

ZEUS11 USAF RC135 Rivet Joint done in Black Sea off Crimea wif it's NATO harassment program and sw

09-0016 USAF C-32A wn from JBA

SAM045 USAF G5 sw from Barnstable Muni. Airport ground stop of just under 2 hours

Gulf look

MOOSE81 USAF C-17 Globemaster and French AF CTM1573 Airbus A400M outta Paki

RCH884 USAF C-17 arriving at Ali Al Salem AB Kuwait from Ramstein departure earlier

Dutch AF MMF51 Airbus A330 inbound from Eindhoven Airport Belgium

morning

IMF's $650 billion reserves distribution is 'shot in arm' for global economy- Georgieva

The IMF will distribute about $650 billion in new Special Drawing Rights to its members on Monday, providing a “significant shot in the arm” for global efforts to combat the COVID-19 pandemic, Managing Director Kristalina Georgieva said.

The International Monetary Fund’s largest-ever distribution of monetary reserves will provide additional liquidity for the global economy, supplementing member countries’ foreign exchange reserves and reducing their reliance on more expensive domestic or external debt, Georgieva said in a statement. “The allocation is a significant shot in the arm for the world and, if used wisely, a unique opportunity to combat this unprecedented crisis,” she said. Countries can use the SDR allocation to support their economies and step up their fight against the coronavirus crisis, but should not use the fiscal space to delay needed economic reforms or debt restructuring, the IMF said in separate guidance document.

IMF member countries will receive SDRs the fund’s unit of exchange backed by dollars, euros, yen, sterling and yuan in proportion with their existing quota shareholdings in the fund. Georgieva said about $275 billion of the allocation will go to emerging market and developing countries, with some $21 billion to flow to low-income countries. Georgieva said the IMF was encouraging rich countries that receive SDRs to channel them to poorer countries that need them more. One key option is for wealthier countries to contribute SDRs to the IMF’s existing Poverty Reduction and Growth Trust for low-income countries, she said.

The IMF was also continuing to work on a possible Resilience and Sustainability Trust that could use channeled SDRs to help the most vulnerable countries with structural transformation, including dealing with climate change, she said. Another possibility, she said, could be to channel SDRs to support lending by multilateral development banks.The IMF’s last SDR distribution came in 2009 when member countries received $250 billion in SDR reserves to help ease the global financial crisis. To spend their SDRs, countries would first have to exchange them for underlying hard currencies, requiring them to find a willing exchange partner country.**

https://www.reuters.com/article/us-imf-reserves/imfs-650-billion-reserves-distribution-is-shot-in-arm-for-global-economy-georgieva-idUSKBN2FO18R

**hello currency swaps with the FRB

>>85593

>>85590

>>85592

o7

>>85588

2 moar AC's outta Paki

RAF NAG81XT C-17 Globemater and Belgian AF BAF640 Airbus A400M west

MOOSE81 continues to Al Udeid

Dutch AF MMF51 A330 heading in-eventually

India to monetise $81 billion worth of state assets over next 4 years

India plans to monetise 6 trillion rupees ($80.90 billion) worth of state assets over the next four years under a plan announced earlier in the 2021/2022 budget to boost infrastructure spending and spur economic growth in Asia’s third biggest economy.

The Indian government aims to hand already built assets such as gas pipelines, roads, railway stations and warehousing facilities among others over to the private sector to operate on a long-term lease, Amitabh Kant, chief executive of government think tank NITI Aayog, told a news conference. “The strategic objective of the programme is to unlock the value of investments in brownfield public sector assets by tapping institutional and long-term patient capital which can thereafter be leveraged for further public investments.” The top five sectors, estimated by their potential for monetisation, are roads, railways, power, oil and gas pipelines, and telecommunication. The government aims to monetise assets worth 880 billion in the current fiscal year that began in April, and a transparent mechanism would achieve “a fair value”, Kant said. Finance Minister Nirmala Sitharaman said the programme would give an impetus to economic growth.

Earlier this year, Prime Minister Narendra Modi’s administration announced a privatisation plan which would leave government ownership only in a few critical sectors. Although coronavirus lockdowns and the subsequent downturn have slowed the privatisation process, the government still hopes to raise 1.75 trillion rupees from such sales in the current fiscal year to March 2022. In the current fiscal year, the government expects to list state-run Life Insurance Corp. of India, and privatise state-run oil refiner Bharat Petroleum Corp Ltd. and state carrier Air India Ltd. Proceeds from privatisation are crucial for India, which witnessed a record fiscal deficit of 9.3% in the last fiscal year to March 2021, when the economy contracted by 7.3%.

By the end of the current 2021-22 fiscal year, the government aims to cut the fiscal deficit to 6.8% and revive economic growth to 10.5%.

https://www.reuters.com/article/india-privatisation/update-1-india-to-monetise-81-bln-worth-of-state-assets-over-next-4-years-idUSL4N2PU389

>>85600

yeah..wut they are taking "out" is the most concerning part.

Taliban Threatens Biden With "Consequences" If Afghan Evacuation Goes Past Aug. 31

Following another rambling, incoherent press conference from President Joe Biden on Sunday, a spokesman for the Taliban told Sky News early Monday that the Taliban would not permit the US to extend its evacuation efforts beyond Aug. 31.

The Taliban met with Sky News for an exclusive interview in Doha, and issued a stark warning about the withdrawal of troops from the country. Taliban spokesperson Dr. Suhail Shaheen said: "It's a red line. President Biden announced that on Aug. 31 they would withdraw all their military forces. So if they extend it that means they are extending occupation while there is no need for that."

He added that the deadline is "a red line."

"It's a red line. President Biden announced that on 31 August they would withdraw all their military forces...If the U.S. or U.K. were to seek additional time to continue evacuations - the answer is no. Or there would be consequences." "It will create mistrust between us. If they are intent on continuing the occupation it will provoke a reaction."

The response was elicited by a question about a possible extension, which itself followed comments from UK PM Boris Johnson, who said he would ask Biden to try and extend the pullout deadline. Unfortunately for both of them, the authority to do so is no longer in their hands. When asked about the people risking their lives to escape Afghanistan - including the people who clung to a plane as it took off, only to plummet to their deaths in gruesome footage that swiftly went viral - the Taliban spokesman said all people attempting to migrate were doing so for economic reasons, not fear of Taliban retribution, despite the many reports of Taliban members threatening Afghans who worked with the US and NATO, as well as their families. "All fake news," Dr Shaheen told Sky. "I can assure you there are many reports by our opponents claiming what is not based on realities." He added: "I assure you it is not about being worried or scared." "They want to reside in Western countries and that is a kind of economic migration because Afghanistan is a poor country and 70% of the people of Afghanistan live under the line of poverty so everyone wants to resettle in Western countries to have a prosperous life. It is not about [being] scared."

The Taliban spokesman also defended the Taliban's treatment of women and especially female students, saying they would be allowed to be educated, so long as they wear the Hijab. Dr Shaheen said: "They will lose nothing. Only if they have no hijab, they will have a hijab… women are required to have the same rights as you have in your country but with a hijab." When pressed, he was insistent: "Now, women teachers have resumed work. Lost nothing. Female journalists they have resumed their work. Lost nothing." Finally, asked about what he would say to the families of those who died fighting in Afghanistan, the Taliban spokesman showed little compassion. "They occupied our country. If we occupy your country. What you will say to me? What if I killed your people in your country what you will say?"

Then added that the past is the past, and it would be best for both sides to simply move on. "I think all people suffered a lot. Bloodshed. Destruction. Everything. But we say the past is the past. Part of our past history. Now we want to focus on the future." Around 10K to 15K Americans are still in the country now controlled by the Taliban, with thousands being evacuated every day. However, more than 50K Afghans who aided in the American effort are still stuck in the country, with many desperately calling American troops that they worked with, pleading for help.

But the Taliban has made it clear: no additional time will be ceded to the US and the West. Once Aug. 31 passes, Taliban will have near-complete control of Afghanistan, with the last pockets of resistance gathering int he Panjshir Valley.

https://www.zerohedge.com/geopolitical/taliban-threatens-biden-consequences-if-afghan-evacuation-goes-past-aug-31

>>85506 pb BOXER47 inbound to Kyiv last night (CONUS time)

Some high level Gov't AC's departing Kyiv, Ukraine

Dis is Merkel

German AF GAF833 Airbus ACJ319-133X departed Kyiv- Boryspil Int'l

Angela Merkel meets President Zelensky to discuss gas pipeline

German Chancellor Angela Merkel met President Volodymyr Zelensky to discuss the situation in eastern Ukraine and the Nord Stream 2 gas pipeline. Kyiv strongly opposes the pipeline, which runs between Russia and Germany. Ukraine says it will increase Europe's energy dependence on Russia and Moscow's geopolitical clout. Merkel called for Ukraine's existing transit deal with Russia to be extended beyond the expiration date of 2024. She also tried to reassure Zelensky and expressed her understanding of Kyiv's concerns. This is her last official trip to Ukraine as she prepares to step down next month, after nearly 16 years in office.

https://news.cgtn.com/news/2021-08-23/Angela-Merkel-meets-President-Zelensky-to-discuss-gas-pipeline-12XVQ8GSoKc/index.html

Slovenian AF LSV101 Falcon 2000, Hungarian AF Falcon 7X, Irish AF IRL258 Learjet 45, Italian AF IAM3105 Falcon 900 also departed from Boryspil Int'l Airport

Three of the Fed’s Wall Street Bailout Programs Vanish from Its Monthly Reports to Congress

Federal Reserve Chairman Jerome Powell and Fed Vice Chairman for Supervision, Randal Quarles, would desperately like to make three of the Fed’s emergency bailout programs to Wall Street disappear from further scrutiny by Congress or the American people. That’s because the specific details of those programs do not comport with the testimony that Powell and Quarles have provided at Congressional hearings throughout the pandemic. Both Powell and Quarles have told Congress that the mega banks were a source of strength during the pandemic. (The chart above shows what was really happening.)

The three emergency lending programs that the Fed would like to make vanish are the Primary Dealer Credit Facility (PDCF); the Commercial Paper Funding Facility (CPFF); and the Money Market Mutual Fund Liquidity Facility (MMLF). These are not only the most opaque of the Fed’s “official” bailout programs but they are also the first three emergency lending programs that the Fed stood up in 2020. The PDCF and CPFF were both announced on March 17, 2020 by the Fed. The MMLF was announced the very next day. For each of the other Fed emergency lending programs, those created under Section 13(3) of the Federal Reserve Act, the Fed has reported the transaction details, including the names of the recipients and dollar amounts received. But the Fed has withheld that information from Congress for these three programs – despite promising complete transparency.

Now, it seems the Fed wants to make these programs disappear altogether.

In its monthly 13(3) emergency lending reports to Congress, from January through May of this year, those three programs appeared with a lump sum total for what had been loaned out but no names of recipients or transaction details. Now, even the names of those programs have completely disappeared on the most recent June, July and August reports to Congress. Just how much money was sluiced to Wall Street under these programs? We know from the Fed’s H.4.1 weekly release of the line items on its balance sheet that as of April 8, 2020, just a few weeks after these three programs started, the Primary Dealer Credit Facility had ballooned to $33 billion in loans outstanding while the Money Market Mutual Fund Liquidity Facility had soared to $53 billion. The Commercial Paper Funding Facility (CPFF) grew far more slowly but gyrated in disconcerting fashion in its early days. According to the Fed’s weekly H.4.1 releases, as of May 20, 2020 the CPFF stood at $4.3 billion, but one week later, on May 27, it had almost tripled to $12.8 billion, strongly suggesting that one or more large financial institutions could not roll over their commercial paper because of some kind of taint attached to it. But the size of these three “official” emergency lending facilities pales in comparison to what the Fed had rolled out four months before COVID-19 had ever been heard of in the United States.

1 of 2

>>85608

2 of 2

On June 22, 2021 the House Select Subcommittee on the Coronavirus Crisis convened a hearing to take testimony from Powell regarding the Fed’s crisis relief efforts. During Powell’s opening statement, he testified as follows: “Our emergency lending tools require the approval of the Treasury and are available only in unusual and exigent circumstances, such as those brought on by the crisis.”

When the eyes of mainstream media are on the Fed, Powell is quick to say that the Fed can only make emergency loans with the approval of the Treasury. In fact, there was no Treasury approval, or Congressional oversight, when the Fed launched its repo loan bailouts of Wall Street beginning on September 17, 2019 – four months before the first reported case of COVID-19 in the United States. By January 27, 2020, the Fed’s ongoing repo loans to bail out Wall Street had reached a cumulative $6.6 trillion. According to the Fed’s own audited financial statements for 2020 and 2019, on its peak day in 2020 the Fed’s repo loan operation had $495.7 billion in loans outstanding to Wall Street versus $259.95 billion on its peak day in 2019. That’s a lot of Wall Street bailout money avoiding any oversight by Congress.

The American people have good reason to be skeptical of the Federal Reserve as a transparent operation as a result of how it stonewalled the public during and after its last big bailout of Wall Street from December 2007 through at least July of 2010. The Fed battled media outlets in court for years, refusing to turn over the names and dollar amounts of where the money went. When the Government Accountability Office (GAO) finally released the granular data from its audit of the Fed’s bailout programs in July of 2011, Senator Bernie Sanders’ office issued a press release stating the following: “The first top-to-bottom audit of the Federal Reserve uncovered eye-popping new details about how the U.S. provided a whopping $16 trillion in secret loans to bail out American and foreign banks and businesses during the worst economic crisis since the Great Depression…“The Fed outsourced virtually all of the operations of their emergency lending programs to private contractors like JP Morgan Chase, Morgan Stanley, and Wells Fargo. The same firms also received trillions of dollars in Fed loans at near-zero interest rates. Altogether some two-thirds of the contracts that the Fed awarded to manage its emergency lending programs were no-bid contracts. Morgan Stanley was given the largest no-bid contract worth $108.4 million to help manage the Fed bailout of AIG.”

But the GAO audit failed to include all of the Fed’s secret bailout programs. When the Levy Economics Institute added the additional lending facilities not included by the GAO, the total cumulative tally came to $29 trillion. The reality was that the Fed was attempting to cover up its own incompetence at supervising the mega banks on Wall Street. In the press release, Sanders was quoted as follows: “The Federal Reserve must be reformed to serve the needs of working families, not just CEOs on Wall Street.” Despite two unprecedented bailouts of Wall Street in 2007-2010 and again in 2019-2021, Congress has failed to strip the Fed of its supervisory role over the mega banks on Wall Street or its ability to create electronic money out of thin air to bail out the same banks, while hiding the details from the American people.

It’s time for all Americans to demand accountability from both the Fed and Congress because it’s the American taxpayer who is on the hook for the liabilities of the Fed.

https://wallstreetonparade.com/2021/08/three-of-the-feds-wall-street-bailout-programs-vanish-from-its-monthly-reports-to-congress/

Moar coming out after sunset

58-0009 USAF KC-135 tanker RCH864 USAF C-17 Globemaster followed by RAF NAG82XT Airbus A400M

RAAF BONDI71 C-17 Globemaster behind the inbound to Paki Dutch AF MMF51 Airbus A330

TORQUE12 USAF C-130 Hercules wn wif

CREEP57 USAF C-130 Hercules east

58-0085 east from Al Udeid AB

RCAF RACER24 C-17 Globemaster east from Kuwait

Belgian AF BAF640 Airbus A400M heading into SA after Paki exit

Donald J. Trump

Biden’s biggest mistake was not understanding that the Military has to be last out the door, not first out the door. Civilians and equipment go first and then, when everyone and everything is out, the Military goes. So simple, and yet it wasn’t done. Tragic!

https://t.me/s/real_DonaldJTrump

>>85612

Free-for-all!!

Mike Pompeo

@mikepompeo

·

54m

God bless our troops

📸: @AP

this pic makin the rounds

>>85616

1106

Q !xowAT4Z3VQ 04/09/2018 13:25:58 ID: 28003e

Archive Bread/Post Links: 967079 / 967752

Direct Link: 967752

Syria.

Hold until CONF.

MIL assets on the ground locked out of GZ.

ISRAEL strike harmed ability to prove events.

Clown report must be VERIFIED.

Troop unwind to STILL occur.

Have faith.

Trust POTUS.

Q

ANON USAF KC-135 tanker took off from Salt Lake City then switched to UTAH51 shortly after

>>85618

Germany Warns Situation At Kabul Airport Continues To Deteriorate After Latest Killings

Update (1155ET): German Foreign Minister Heiko Maas warned the press Monday that the situation outside the airport in Kabul has grown even more chaotic on Monday after a member of the Afghan national forces who was working as a guard outside the airport was killed, while several others were wounded.

Meanwhile, after the Taliban assured there would be no extension of the airlift deadline, UK PM Boris Johnson has nevertheless called for a virtual meeting of G-7 leaders on Tuesday to discuss the crisis, and the possibility of an extension. The US managed to evacuate more than 10K people over the past 24 hours, the administration confirmed Monday.

Meanwhile, on the ground in Kabul, some militants wanted by Islamabad have been freed from jail in Afghanistan, Pakistan’s interior minister said. The militants are from Tehrik-e-Taliban Pakistan (TTP), a group that has previously carried out attacks in Pakistan. The Taliban are also asking Iran to step up exports of fuel. Circling back to the latest word out of Germany, Maas said the government in Berlin is holding talks with the US and Turkey to plan for extending civilian operations at Kabul airport after the departure of US troops to enable further evacuations. This includes current negotiations with the Taliban. Mass also said the early-Monday firefight showed how dangerous the situation is. "The situation at the airport has only grown more chaotic over the last few hours,” Maas told reporters in Berlin on Monday. "The situation remains dangerous."

Outside Afghanistan, Kamala Harris is doing her best not to talk about the situation during her trip to Singapore. Heading into Monday afternoon in the US, new videos of a fire blazing at the airport are circulating on social media.

NOW - Fire erupts at #Kabul airport in Afghanistan.pic.twitter.com/GoscbdxRGr— Disclose.tv (@disclosetv) August 23, 2021

Another guard was killed Monday outside the International Airport in Kabul when a firefight broke out, leaving one member of the Afghan National Army dead, and three others wounded. Some members of the now-dissolved Afghan military are helping to guard the airport. News of the killing was revealed by the Germany military, which announced it via twitter early Monday morning in the US. No German soldiers were harmed in the skirmish, fortunately. It doesn't appear that any other NATO forces were harmed either. The firefight was instigated by unidentified gunmen.

https://www.zerohedge.com/geopolitical/afghan-killed-firefight-kabul-airport-resistance-forces-prepare-showdown-panjshir

Acting counterterrorism center head fired, according to former U.S. officials

March 19, 2020

The acting director of the National Counterterrorism Center was removed Wednesday in what insiders fear is a purge by the Trump administration of career professionals at an organization set up after 9/11 to protect the nation from further attacks, according to two former U.S. officials.

Russell E. Travers, a highly regarded intelligence professional with more than 40 years of government service, told colleagues he was fired by acting director of national intelligence Richard Grenell, said the former officials, who like others interviewed spoke on the condition of anonymity to discuss a sensitive matter.

Travers, who took up the acting position last August, had been resistant to pressure to make personnel cuts at the center, which has been undergoing a review of its mission and effectiveness.

Also removed at the NCTC was Travers’s acting deputy, Peter W. Hall, who is returning to the National Security Agency, the former officials said.

The surprise move came hours after President Trump announced his intent to nominate Pentagon Special Operations and counterterrorism official Christopher Miller to head the center. A deputy director will be named to serve as acting director pending Miller’s confirmation, said a spokesman for the Office of the Director of National Intelligence.

A spokeswoman for Grenell disputed that Travers was fired.

Travers “was offered the opportunity to move to a new role and chose to retire,” Assistant Director of National Intelligence for Strategic Communications Amanda Schoch said in a statement to The Washington Post. “Russ told Acting Director Grenell he wanted to retire and that he did not want another assignment.”

Said Schoch: “We are grateful for Acting Director Russ Travers’ many years of service to the American people. . . . Over the next few weeks we expect Russ to step out of his current position to prepare for retirement. . . . Russ’ willingness to step up and serve as the acting director of NCTC multiple times is an example of his commitment to serve this vital mission. He has given NCTC many years of great service.”

The removals have shocked Travers’s colleagues, who are upset at the treatment of someone so well-regarded, according to the two former officials.

One of the former officials said that Travers walked into a meeting on Wednesday expecting to brief Grenell on the center when he was told that he was out. He had no intention or desire to retire, they said.

In the meeting, Grenell told Travers he would like to know “how long it would take you to leave,” according to one of the former officials, who was briefed on the meeting. Travers replied that he would need “a few weeks” to complete the administrative work, the official recounted.

“They said, ‘Great, we’ll afford you the opportunity to retire,’ ” the former official said.

In a farewell note to the workforce Wednesday, Travers noted Trump’s plan to bring on Miller, lauded Miller’s experience and said the acting DNI wanted to “assemble a new team.” He sought to boost morale, noting the center’s accomplishments. “We have recently been the subject of an external evaluation by a group of national security luminaries that strongly validated the need for the center,” he wrote. “And most importantly, we have you — the finest workforce with whom I have ever been associated. I have no doubt that the center is postured for success going forward.”

Trump plans to tap Special Forces veteran to head counterterrorism center

read full article

https://www.washingtonpost.com/national-security/acting-counterterrorism-center-head-fired-according-to-former-us-officials/2020/03/19/fb33d516-6a02-11ea-b313-df458622c2cc_story.html

>>85616

Wondered if that was the baby they passed over the wall but this one is littler.

g'morning btw

>>85620 pb

fda.gov

FDA Approves First COVID-19 Vaccine

For Immediate Release:

August 23, 2021

Today, the U.S. Food and Drug Administration approved the first COVID-19 vaccine. The vaccine has been known as the Pfizer-BioNTech COVID-19 Vaccine, and will now be marketed as Comirnaty (koe-mir’-na-tee), for the prevention of COVID-19 disease in individuals 16 years of age and older. The vaccine also continues to be available under emergency use authorization (EUA), including for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.

“The FDA’s approval of this vaccine is a milestone as we continue to battle the COVID-19 pandemic. While this and other vaccines have met the FDA’s rigorous, scientific standards for emergency use authorization, as the first FDA-approved COVID-19 vaccine, the public can be very confident that this vaccine meets the high standards for safety, effectiveness, and manufacturing quality the FDA requires of an approved product,” said Acting FDA Commissioner Janet Woodcock, M.D. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated. Today’s milestone puts us one step closer to altering the course of this pandemic in the U.S.”

Since Dec. 11, 2020, the Pfizer-BioNTech COVID-19 Vaccine has been available under EUA in individuals 16 years of age and older, and the authorization was expanded to include those 12 through 15 years of age on May 10, 2021. EUAs can be used by the FDA during public health emergencies to provide access to medical products that may be effective in preventing, diagnosing, or treating a disease, provided that the FDA determines that the known and potential benefits of a product, when used to prevent, diagnose, or treat the disease, outweigh the known and potential risks of the product.

FDA-approved vaccines undergo the agency’s standard process for reviewing the quality, safety and effectiveness of medical products. For all vaccines, the FDA evaluates data and information included in the manufacturer’s submission of a biologics license application (BLA). A BLA is a comprehensive document that is submitted to the agency providing very specific requirements. For Comirnaty, the BLA builds on the extensive data and information previously submitted that supported the EUA, such as preclinical and clinical data and information, as well as details of the manufacturing process, vaccine testing results to ensure vaccine quality, and inspections of the sites where the vaccine is made. The agency conducts its own analyses of the information in the BLA to make sure the vaccine is safe and effective and meets the FDA’s standards for approval.

Comirnaty contains messenger RNA (mRNA), a kind of genetic material. The mRNA is used by the body to make a mimic of one of the proteins in the virus that causes COVID-19. The result of a person receiving this vaccine is that their immune system will ultimately react defensively to the virus that causes COVID-19. The mRNA in Comirnaty is only present in the body for a short time and is not incorporated into - nor does it alter - an individual’s genetic material. Comirnaty has the same formulation as the EUA vaccine and is administered as a series of two doses, three weeks apart.

“Our scientific and medical experts conducted an incredibly thorough and thoughtful evaluation of this vaccine. We evaluated scientific data and information included in hundreds of thousands of pages, conducted our own analyses of Comirnaty’s safety and effectiveness, and performed a detailed assessment of the manufacturing processes, including inspections of the manufacturing facilities,” said Peter Marks, M.D., Ph.D., director of FDA’s Center for Biologics Evaluation and Research. “We have not lost sight that the COVID-19 public health crisis continues in the U.S. and that the public is counting on safe and effective vaccines. The public and medical community can be confident that although we approved this vaccine expeditiously, it was fully in keeping with our existing high standards for vaccines in the U.S."

FDA Evaluation of Safety and Effectiveness Data for Approval for 16 Years of Age and Older

The first EUA, issued Dec. 11, for the Pfizer-BioNTech COVID-19 Vaccine for individuals 16 years of age and older was based on safety and effectiveness data from a randomized, controlled, blinded ongoing clinical trial of thousands of individuals.

To support the FDA’s approval decision today, the FDA reviewed updated data from the clinical trial which supported the EUA and included a longer duration of follow-up in a larger clinical trial population.

Specifically, in the FDA’s review for approval, the agency analyzed effectiveness data from approximately 20,000 vaccine and 20,000 placebo recipients ages 16 and older who did not have evidence of the COVID-19 virus infection within a week of receiving the second dose. The safety of Comirnaty was evaluated in approximately 22,000 people who received the vaccine and 22,000 people who received a placebo 16 years of age and older.

Based on results from the clinical trial, the vaccine was 91% effective in preventing COVID-19 disease.

More than half of the clinical trial participants were followed for safety outcomes for at least four months after the second dose. Overall, approximately 12,000 recipients have been followed for at least 6 months.

The most commonly reported side effects by those clinical trial participants who received Comirnaty were pain, redness and swelling at the injection site, fatigue, headache, muscle or joint pain, chills, and fever. The vaccine is effective in preventing COVID-19 and potentially serious outcomes including hospitalization and death.

Additionally, the FDA conducted a rigorous evaluation of the post-authorization safety surveillance data pertaining to myocarditis and pericarditis following administration of the Pfizer-BioNTech COVID-19 Vaccine and has determined that the data demonstrate increased risks, particularly within the seven days following the second dose. The observed risk is higher among males under 40 years of age compared to females and older males. The observed risk is highest in males 12 through 17 years of age. Available data from short-term follow-up suggest that most individuals have had resolution of symptoms. However, some individuals required intensive care support. Information is not yet available about potential long-term health outcomes. The Comirnaty Prescribing Information includes a warning about these risks.

Ongoing Safety Monitoring

The FDA and Centers for Disease Control and Prevention have monitoring systems in place to ensure that any safety concerns continue to be identified and evaluated in a timely manner. In addition, the FDA is requiring the company to conduct postmarketing studies to further assess the risks of myocarditis and pericarditis following vaccination with Comirnaty. These studies will include an evaluation of long-term outcomes among individuals who develop myocarditis following vaccination with Comirnaty. In addition, although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.

The FDA granted this application Priority Review. The approval was granted to BioNTech Manufacturing GmbH.

[The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.]

https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine

Just a reminder REGENERON is also FDA approved and it works great. Uses Amino Peptides to cure Covid…there are injection clinics setup all over the country. Use the below website to locate an treatment center near you. This is the “vaccine”/treatment/cure GEOTUS used and the one Gov. Ron DeSantis is rolling out across Florida…

Learn More About Regeneron

https://www.regeneron.com/

Find a Treatment Center

https://covid.infusioncenter.org/

Ron DeSantis Talks About Regeneron

https://rumble.com/vlin6n-interview-with-fl-gov-ron-desantis-on-oann-re-regeneron-covid-treatment.html

>>85635

JANET WOODCOCK DIG

History of controversial pro-Big Pharma decisions.

After Janet Woodcocks appointment by Biden as Acting FDA head:

January, 2021: "In a letter to the administration, 28 groups accused Dr Janet woodcock of presiding over "one of the worst regulatory agency failures in US history" as head of the FDA department responsible for approving new prescription opioids, the Center for Drug Evaluation and Research (CDER). Drug makers conspired to worsen the opioid crisis. They have blood on their hands. woodcock was named acting FDA commissioner by the new administration on the day Biden took office. The letter urged the president not to nominate her to permanently head the agency.

"In its opioid decision-making, Dr woodcock, and the division she supervised, consistently put the interests of opioid manufacturers ahead of public health, often overruling its own scientific advisors and ignoring the pleas of public health groups, state Attorneys General, and outraged victims of the opioid crisis," the letter said.

The letter accused Woodcock of "dereliction of duty" for allowing opioid manufacturers to spend years disseminating false claims that narcotic painkillers were less addictive and more effective than they really were, contributing to the rise of mass opioid prescribing and spread of an epidemic that has claimed more than 500,000 lives."

https://www.theguardian.com/us-news/2021/jan/28/fda-janet-woodcock-opioids-biden

RE Woodcock's support for Dsurvia, a fentanyl-like drug up for approval in May 2018:

Dr Raeford Brown head of the FDA cmte on drug safety, thought it was dangerous. But they voted on it when he was out of town:

In his absence, the committee had voted 10-3 to recommend approving Dsuvia, which likely influenced the FDA's final decision.

A few weeks later he was working from his home office in Lexington, Ky., when Dr. Janet woodcock, director of the Center for Drug Evaluation and Research at the FDA, called to tell him that Dsuvia had just been officially approved. "I told her that I thought that was a bad decision," Brown, an anesthesiology professor and clinician at the University of Kentucky, said in a recent interview. "I told her exactly why"....Just six months later, in May 2019, the FBI, in an intelligence bulletin marked "for official use only," warned that this new painkilling drug would likely exacerbate the nation's opioid crisis. https://www.yahoo.com/news/the-fbi-called-a-powerful-opioid-developed-for-the-military-a-public-threat-the-company-selling-the-drug-says-itll-save-lives-090041326.html

Woodcock's claims that WE ARE USING EVERY TOOL IN OUR TOOLBOX TO FIGHT THIS PANDEMIC

The FDA may allow vaccine makers to ease up on lengthy clinical trials once more is known about how the vaccines work against new variants.

The Food and Drug Administration has laid the groundwork for drugmakers to be able to react quickly to emerging coronavirus variants and get modified products to the public without the need for extended clinical trials.

"We are using every tool in our toolbox to fight this pandemic, including pivoting as the virus adapts," Dr. Janet woodcock, acting FDA commissioner, said in a statement Monday.

[LIAR LIAR PANTS ON FIRE]

http://www.tathasta.com/2021/02/fda-says-covid-vaccine-makers-can.html

Potential Covid Drug was BLOCKED by Woodcock bc it's not from Big Pharma: 4-10-21

Former President of the Philippines saved by a proven safe drug made by a small non-Big Pharma American company based in Vancouver WA. The drug is Leronlimab and is the experimental drug Charlie Sheen has taken for years for his HIV. It's been tested on over 800 HIV patients for a number of years with zero side-effects. That's right, ZERO SIDE EFFECTS. Leronlimab just completed successful Phase 3 trails with the US FDA but is being slow-walked by Janet woodcock and her Big Pharma ass-kissing cronies. They can't have a small pharma company come in and stop covid, make vaccines unnecessary, and box out their Big Pharma buddies. Here's a vetted link to the FB page of the son of the former Philippines president confirming that he was given Leronlimab and is now off ventilation and recovering.

https://m.facebook.com/story.php?story_fbid=1076306802893234&id=100015417732589&anchor_composer=false

Janet woodcock and the rest of the criminals at the FDA should be charged with mass murder and executed.

>>85645

C101 US Coast Guard G5 ne from Reagan National Airport

BOXER43 USAF C-40C inbound to JBA from overnight at Azores-Joao Paulo II Airport on San Miguel Island

>>84337 pb

this AC last seen having landed at Agadez, Niger on 0818

>>85648

FAMOTIDINE

Dry Bulk Shipping Rates Are Soaring and the Rally Looks Set

For a glimpse at how fast demand for commodities has rebounded in the wake of the coronavirus, look no further than the market for shipping them.

Monday marked the 10th consecutive increase for the Baltic Dry Index, a benchmark measure of commodity hauling costs that has surged to an 11-year high. “Earlier in the year, people thought this was a short-term spike in the market, but now people see it as more structural and longer term,” said Jan Rindbo, the chief executive officer of D/S Norden A/S, a 150-year-old Danish operator of more than 500 vessels. Demand for cargoes of raw materials like coal and iron ore has jumped this year, outpacing an expansion of the fleet as economies recover from the ravages of the pandemic. Exacerbating tight vessel supply, Covid-related disruptions have cut how many ships are available, tilting the market further in favor of owners.

The Baltic Dry hit 4,147 points on Monday, the highest since May 2010. Rates for Capesize carriers jumped 2% to $50,708, the strongest market since at least 2014, according to the Baltic Exchange. Forward contracts are pointing to continued bullish expectations. Seaborne trade in iron ore trade is forecast to climb 4% to 1.56 billion tons this year, the largest annual jump since 2017, according to data from Clarkson Research Services Ltd., a unit of the world’s largest shipbroker.

Wider dry bulk trade is expected to rise 4.2% year-on-year in 2021 and by 1.7% in 2022. Fleet growth is likely to lag behind the increase in cargoes, with capacity expanding by 3.3% this year, and 1.4% growth next, the Clarkson data show.

https://www.bnnbloomberg.ca/dry-bulk-shipping-rates-are-soaring-and-the-rally-looks-set-1.1643363

NYC Orders 150,000 Teachers & School Staff To Either Get Vaccinated Or Find A New Job

Mere minutes after the FDA announced that it had finally approved Pfizer's coronavirus jab for all patient's over the age of 16, NYC announced a new, revised vaccine mandate for all NYC public school teachers: either get the jab, or go find somewhere else to work.

That's right: according to the new mandate, NYC teachers, as well as principals, other administrators, custodians and central-office staff will no longer have the option of submitting to weekly testing instead of getting the vaccine. The new mandate will impact some 148,000 employers (NYC is home to the largest school district in the country, with more than 1MM students, who we suspect will all be required to get the vaccine once it's approved for their age groups).

As the NYT explained, education staffers are the first group of city workers to face a full vaccine mandate. The announcement also opens the door to a broader vaccine mandate of city workers, which the mayor said Monday the city was considering. Last month, Mayor Bill de Blasio issued a mandate for city workers that allowed for those unvaccinated to submit for weekly coronavirus testing.

"We know this is going to help ensure that everyone is safe," Mr. de Blasio said during a news conference on Monday, adding that city schools had extremely low virus transmission last year. The mandate, the mayor said, will help the city "build on that success."

While the mayor's push is likely to prove unpopular with many rank-and-file members; the city's teacher's unions, and unions representing other DoE staff, have signed off on the new mandate (though they're still negotiating about what might happen to workers who continue to refuse). UFT President Michael Mulgrew acknowledged that the city had the legal right to impose the mandate, but he told reporters details were still being hashed out.

The city announced last month that any teacher who failed to comply with both the vaccination requirement, and the required weekly testing for those who didn't get the jab, would be suspended without pay.

"While the city is asserting its legal authority to establish this mandate, there are many implementation details, including provisions for medical exceptions, that by law must be negotiated with the U.F.T. and other unions, and if necessary, resolved by arbitration," Mr. Mulgrew said in a statement.

https://www.zerohedge.com/political/nyc-orders-150000-teachers-school-staff-either-get-vaccinated-or-find-new-job

Conspiracies pay: MSNBC’s Rachel Maddow signs deal to start own production company

MSNBC Host Rachel Maddow has signed a multiyear deal with the network to create a media empire of books, series, documentaries and podcasts. Peddling conspiracy theories, it seems, pays off.

News of Maddow’s deal was broken by Axios on Monday. On top of ‘The Rachel Maddow Show,’ the liberal host will run a production company pumping out “books, documentaries, movies, TV series and podcasts.” According to Axios’ report, WarnerMedia (including Warner Bros. and CNN), Disney (including ABC and ESPN), Netflix and Spotify were all looking to sign Maddow, but her own network won out in the bidding war.

Axios’ source described Maddow as "a purveyor of great storytelling,” and Maddow certainly liked to weave elaborate yarns during the tumultuous years of Donald Trump’s presidency. It just didn’t matter that many of them were outright lies.

Maddow was a diehard proponent of the ‘Russiagate’ conspiracy theory, and saw Moscow’s meddling behind every one of America’s ills. She’s falsely accused RT of colluding with WikiLeaks to publish damaging information on Hillary Clinton, claimed that Russia could “flip the switch” and shut down the US power grid, called Trump’s short-lived Secretary of State Rex Tillerson a puppet of Vladimir Putin, suggested that the Russian president could hypothetically “give orders” to Trump, and accused the latter of literally setting aside campaign funds to pay for the services of “Russian hackers.”

None of this was true, and when right-wing news outlet OAN sued Maddow for calling them “literally paid Russian propaganda,” a US judge recognized this, ruling that no “reasonable viewer” could interpret Maddow’s Russiagate hysteria as “objective fact.” Her statement about OAN, the court ruled, was “opinion and rhetorical hyperbole.”

The release of the Mueller Report didn’t stop her peddling tall tales of collusion, even as normally sympathetically liberal news outlets called her “delusional” and commented that her reporting had “no sense of proportion or, honestly, responsibility.” Nor did Trump’s departure from office stem her breathless tales of Russian hacking and other Kremlin skulduggery plucked from thin air.

Despite peddling conspiracy theories that would make Alex Jones take a pause, Maddow is MSNBC’s top-rated host, and the number two host in her 9pm time slot, behind Fox News’ Sean Hannity.

Yet Alex Jones’ conspiracy theories have seen him banned from every major social media platform, while Maddow’s earned her a lucrative deal to start a media empire. In the words of CNN’s Brian Stelter, “Maddow defines the MSNBC brand more than any single host on CNN or, I'd even argue, Fox News.” What that says about MSNBC depends on just how much you buy into the conspiracy theories.

https://www.rt.com/usa/532845-maddow-msnbc-deal-conspiracy/

U.S. Holds This Year’s Largest Sale of Strategic Oil Reserves

The U.S. is holding its largest sale of oil from strategic reserves this year at a time when the outlook for fuel demand is darkening amid the resurgent Covid-19 virus.

The Energy Department plans to auction off 20 million barrels of crude, twice as much as it offered for sale 3 1/2 months ago. The oil will be delivered during the fourth quarter, when U.S. demand for gasoline and other fuels typically falters and refineries slow down oil purchases while they shut down equipment for repairs and maintenance.

The sale also comes after crude prices have dropped 15% since touching a 6 1/2-year high in early July as the spread of the delta variant threatens to derail the economic recovery and return to business as usual. Companies including BlackRock Inc. and Jefferies Financial Group Inc. are postponing plans to return workers to offices.

The reserve, created in 1975 to serve as an emergency stockpile, held 621 million barrels in four underground caverns as of Aug. 13, Energy Department figures showed.

Benchmark American crude futures rose almost 6% on Monday in New York amid a broader rally in commoditiues and equity markets.

https://www.bnnbloomberg.ca/u-s-holds-this-year-s-largest-sale-of-strategic-oil-reserves-1.1643358

Be ready.

https://twitter.com/USNavy/status/1429866577340555269

After cooling off for a bit we habs moar heading back in.

BUFF heading east from Al Udeid and looks like a topping of da tanks

GRIMM22 USAF B-52 Stratofortress and 61-0293 USAF KC-135 tanker east from Al Udeid AB

Looks like GRIMM22 topped off da tanks

French AF CTM1573 Airbus A400M back out from Al Dhafra AB

RCH884 USAF C-17 Globemaster departed Ali Al Salem AB Kuwait

RAF NAG87XT A400M up from Al Minhad AB Dubai

>>85666

chek't and rek't those ebil digits

>>85649

C101 US Coast Guard on final approach at Waterville, ME-LaFleur Airport from Reagan National depart

>>85673

https://phys.org/news/2018-08-natural-human-enzyme-biodegrade-graphene.html

Degradation of pristine graphene occurs in the human body when interacting with a naturally occurring enzyme found in the lung, announced Graphene Flagship partners; the French National Centre for Scientific Research (CNRS), University of Strasbourg, Karolinska Institute and University of Castilla–La Mancha (UCLM).

Graphene-based products, including flexible biomedical electronic devices, are being designed for interface with the human body within the Graphene Flagship. If graphene is to be used for such biomedical applications, it should be biodegradable and thus be expelled from the body.

To test how graphene behaves within the body, Alberto Bianco and his team at Graphene Flagship partner CNRS conducted several tests to determine whether and how graphene was broken down with the addition of a common human enzyme. The enzyme, myeloperoxidase (MPO), is a peroxide enzyme released by neutrophils, cells found in the lungs that are responsible for the elimination of foreign bodies or bacteria that enter the body. If a foreign body or bacteria is detected inside of the body, neutrophils surround it and secrete MPO, thereby destroying the threat. Previous work by Graphene Flagship partners found MPO to biodegrade graphene oxide. However the structure of non-functionalized graphene was thought to be more degradation resistant. To test this, Bianco and his team looked at the effects of MPO, ex vivo, on two graphene forms: single- and few-layer.

Bianco says, "We used two forms of graphene—single- and few-layer, prepared by two different methods in water. They were then taken and put in contact with myeloperoxidase in the presence of hydrogen peroxide. This peroxidase was able to degrade and oxidise them. This was not really expected, because we thought that non-functionalized graphene was more resistant than graphene oxide."

Rajendra Kurapati, first author on the study, from Graphene Flagship partner CNRS, said, "The results emphasize that highly dispersible graphene could be degraded in the body by the action of neutrophils. This would open the new avenue for developing graphene-based materials."

In-vivo testing is the next stage. Bengt Fadeel, professor at Graphene Flagship partner Karolinska Institute, says, "Understanding whether graphene is biodegradable or not is important for biomedical and other applications of this material. The fact that cells of the immune system are capable of handling graphene is very promising."

Prof. Maurizio Prato, leader of Work Package 4, said, "The enzymatic degradation of graphene is a very important topic, because in principle, graphene dispersed in the atmosphere could produce some harm. Instead, if there are microorganisms able to degrade graphene and related materials, the persistence of these materials in our environment will be strongly decreased. These types of studies are needed. What is also needed is to investigate the nature of degradation products. Once graphene is digested by enzymes, it could produce harmful derivatives. We need to know the structure of these derivatives and study their impact on health and environment."

Prof. Andrea C. Ferrari, Science and Technology Officer of the Graphene Flagship, and chair of its management panel, added, "The report of a successful avenue for graphene biodegradation is a very important step forward to ensure the safe use of this material in applications. The Graphene Flagship has put the investigation of the health and environment effects of graphene at the centre of its programme since the start. These results strengthen our innovation and technology roadmap."

>>85672

You can LARP as a horse and get horse Ivermectin instead.