Doctors Sue FDA, Allege Crusade Against Ivermectin ‘Unlawfully Interfered’ With Their Ability to Treat Patients
The Defender | June 6, 2022
Three physicians are suing the U.S. Food and Drug Administration (FDA) for launching what they allege is a “crusade” against ivermectin as a treatment for COVID-19 that “unlawfully interfered” with the doctors’ ability to practice medicine.
In a lawsuit filed June 2, Drs. Robert L. Apter, Mary Talley Bowden and Paul E. Marik argued the FDA acted outside of its authority by directing the public, including health professionals and patients, to not use ivermectin — even though the drug is fully approved by the FDA for human use.
The suit, filed in the U.S. District Court, Southern District of Texas, Galveston Division, also names the U.S. Department of Health and Human Services (HHS), HHS Secretary Xavier Becerra and Robert Califf, acting FDA commissioner.
According to the complaint:
“The FDA generally cannot ban particular uses of human drugs once they are otherwise approved and admitted to the market, even if such use differs from the labeling — commonly referred to as ‘off-label’ use.
“The FDA also can not advise whether a patient should take an approved drug for a particular purpose. Those decisions fall within the scope of the doctor-patient relationship.
“Attempts by the FDA to influence or intervene in the doctor-patient relationship amount to interference with the practice of medicine, the regulation of which is — and always has been — reserved to states.”
The plaintiffs said their lawsuit isn’t about whether ivermectin is an effective treatment for COVID-19. It’s about who determines the appropriate treatment for each unique patient and whether the FDA can interfere with that process.
In their complaint, they site an FDA publication, “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19,” and tweets from the FDA — including one implying that ivermectin is intended only for animals — among examples of the FDA discouraging the use of ivermectin.
The plaintiffs also argued if the FDA is allowed to interfere with the practice of medicine now, using the pandemic as a cover, “this interference will metastasize to other circumstances, destroying the carefully constructed statutory wall between federal and state regulatory powers, and between the FDA and the professional judgment of health professionals.”
“This lawsuit, brought by three eminently qualified physicians, is a welcome development,” said Mary Holland, Children’s Health Defense president and general counsel.
Holland told The Defender :
“These doctors rightfully assert that the FDA, assisted by corporate media, have unlawfully interfered in the doctor-patient relationship and the appropriate treatment for individual patients. Regulating the doctor-patient relationship is an area of well-established state, not federal, law.
“I hope these plaintiffs will enjoin the FDA from continuing to restrict access to ivermectin and from penalizing healthcare practitioners who use this licensed drug for their patients.”
The plaintiffs: well-respected in their field, high success rate treating COVID patients
Apter, who is licensed to practice medicine in Arizona and Washington and has a COVID-19 patient survival rate of more than 99.98%, was referred to the Washington Medical Commission and Arizona Medical Board for disciplinary proceedings for prescribing ivermectin to treat COVID-19.
In a press release, Apter said, “If doctors are freed to treat patients according to their best judgment and unprejudiced evaluation of the medical literature, many thousands more deaths and serious disabilities will be averted.”
Apter said the FDA’s pronouncements against the use of ivermectin “have been the basis for disciplinary actions against doctors, interfere with the doctor-patient relationship, and have had a severe chilling effect on the use of life-saving medication for a deadly disease.”
In the lawsuit, Apter argued that government pressure, “largely through the FDA,” also led pharmacies — especially in large corporate chains — to refuse to fill ivermectin prescriptions for COVID-19, because that position is supported by the FDA.
Bowden, who according to the lawsuit has 40 years of experience in emergency medicine, began recommending ivermectin to treat COVID-19 in early 2020. She treated more than 3,900 patients for COVID-19, with a success rate of over 99.97%.
She said the FDA’s actions regarding ivermectin, specifically its directives to stop using the drug to treat COVID-19, harmed Bowden’s ability to practice medicine and treat patients.
Bowden’s employer, Houston Methodist Hospital, last year forced her to resign by suspending her privileges for spreading “COVID misinformation.”
Bowden said she is “fighting back — the public needs to understand what the FDA has done is illegal, and I hope this suit will prevent them from continuing to interfere in the doctor-patient relationship.”
In an interview earlier this year with The Defender, Bowden said she was all for the COVID vaccines when they first came out — it was only when she started seeing what was happening with all the breakthrough cases that she wondered, “Why am I seeing so many COVID cases among the fully vaccinated?”
Then her patients began having adverse reactions. “If I hadn’t seen that firsthand, I would still think the vaccine was the way to go,” she said.
As the pandemic evolved, Bowden developed protocols for preventing and treating COVID patients. She said she’s seen excellent results.
“The basis of it is ivermectin,” she said. “And also vitamins C and D, quercetin and zinc, and black seed oil. It’s nothing complicated — and it’s just like with anything in medicine — not one size fits all — protocols are guidelines.”
The controversy over prescribing ivermectin was initially “intimidating and isolating,” she said. “I thought I was a little bitty island in a huge ocean, and now I realize that I’m part of at least half a continent.”
Marik, author of more than 750 publications, was professor of medicine and chief of pulmonary and critical care medicine at Eastern Virginia Medical School (EVMS) in Norfolk, Virginia, from 2009 through 2021. He also served as a director of the intensive care unit at Sentara Norfolk General Hospital.
He developed a protocol for EVMS for treating COVID-19, called the EVMS COVID-19 Management Protocol, which included the MATH+ Protocol.
However, according to the lawsuit, Marik was forced to resign from his positions at EVMS and Sentara Norfolk General Hospital for promoting the use of ivermectin — “as well as other safe, cheap, and effective off-label FDA-approved drugs” — to treat COVID-19 following the FDA’s attempts to stop use of those drugs for that purpose.
Marik alleged in the lawsuit that refusing to allow patients to receive effective early treatment for COVID-19 “led to innumerable hospitalizations and deaths, and caused extreme distress for patients, their families, and health professionals.”
Boyden, Gray & Associates, a Washington, DC-based law firm, is representing the plaintiffs.
Ivermectin was developed in the 1970s as a veterinary medicine to treat parasitic diseases in livestock, but a decade or so later was hailed as a “wonder drug” and received approval for human use as a therapeutic against diseases such as river blindness — or onchocerciasis — and lymphatic filariasis, according to Newsmax.
Since 1987, it has been used safely in 3.7 billion doses worldwide. William Campbell and Satoshi Omura won the 2015 Nobel Prize in Physiology or Medicine for their research on the drug.
Studies show ivermectin is associated with lower COVID-19 death rates, but the FDA — with help from mainstream media — continues to state the drug is ineffective for treating COVID.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
Ghost Shot: Pfizer quietly admits it will never manufacture original FDA approved COVID vaccines
Company claims it is manufacturing Comirnaty product with new formula

By Jordan Schachtel | The Dossier | June 3, 2022
The August 23, 2021 FDA approval of Pfizer’s Comirnaty vaccine was a cause for celebration. Marked as a turning point in the battle against COVID19, the announcement was highly publicized by the Biden Administration with the clear intention to extinguish “vaccine hesitancy” and boost uptake.
It was celebrated as a cause for national relief, and many Americans arrived at their local pharmacies under the impression, via government and pharmaceutical propaganda, that they were receiving an FDA-approved COVID vaccine. Yet that legally distinct product, as we know it, never existed. And now we know, via Pfizer, that it will never exist.
For the uninitiated:
Comirnaty is a legally distinct product from the emergency use authorization (EUA) shots, and It has never made its way to market. For months on end, no such vaccine has ever become available. Those who received the “Pfizer shot(s)” have been injected with the emergency use authorization (EUA) version of the shots. See my piece in The Dossier for more info:
Shell Game? There remains no FDA approved COVID vaccine in the United States
The information operation succeeded. There was indeed an FDA approved vaccine, at least on paper, but you couldn’t get it.
When originally confronted with this ordeal, Pfizer labeled this issue an inventory question that had nothing to do with the legal distinction between an experimental EUA product and an FDA-approved vaccine. Up until just weeks ago, this was the statement up on the CDC website via Pfizer:
“Pfizer received FDA BLA license on 8/23/2021 for its COVID-19 vaccine for use in individuals 16 and older (COMIRNATY). At that time, the FDA published a BLA package insert that included the approved new COVID-19 vaccine tradename COMIRNATY and listed 2 new NDCs (0069-1000-03, 0069-1000-02) and images of labels with the new tradename.
At present, Pfizer does not plan to produce any product with these new NDCs and labels over the next few months while EUA authorized product is still available and being made available for U.S. distribution. As such, the CDC, AMA, and drug compendia may not publish these new codes until Pfizer has determined when the product will be produced with the BLA labels.”
In May, Pfizer updated its statement to mention a December 2021 licensed Comirnaty product, which was granted a license four months after the highly-publicized August FDA press release.
And just last week, Pfizer finally acknowledged that its original licensed product will never be distributed. In an unreported update on the CDC website, Pfizer told the agency:
“Pfizer received initial FDA BLA license on 8/23/2021 for its COVID-19 vaccine for use in individuals 16 and older (COMIRNATY). At that time, the FDA published a BLA package insert that included the approved new COVID-19 vaccine tradename COMIRNATY and listed 2 new NDCs (0069-1000-03, 0069-1000-02) and images of labels with the new tradename. These NDCs will not be manufactured. Only NDCs for the subsequently BLA approved tris-sucrose formulation will be produced.”
The key distinction between the originally approved formulation and the tris-sucrose formulation is that — according to manufacturers — the latter can be held for a much longer period of time outside of an ultra cold freezer. These freezers cost over $10,000 a piece and each unit uses as much energy per day as an average American household. Improper storage can render the mRNA unstable.
Notably, the clinical trials for the Pfizer shot were conducted without the modified tris-sucrose ingredient. Given the partisan nature of Pfizer, the corporate media, government health bureaucracies, and your correspondent’s lack of expertise in this area, it is unclear whether this is significant.
Another notable thing to look out for in the coming days and weeks is the possibility that the subsequently FDA approved product finally becomes available in the United States. In recent days, the CDC removed the language of “not orderable at this time” above the description of both Comirnaty and Moderna’s Spikevax.
Additionally, as reported by Uncover DC, the Defense Department appears to be in the early stages of ordering what it has interpreted as a legally required minimum of Comirnaty in order to continue its mRNA mandate of American service members.
Fauci’s COVID origins coverup spook has resurfaced to misdirect us about the origin of money pox
By Meryl Nass, MD | June 7, 2022
Andrew Rambaut (pronounced Rambo—and like Rambo, he is still in the ring, fighting for the globalists, when he should have taken his toys and slunk away long ago—after being beaten up as one of the stooges who produced the fake Nature Medicine paper on COVID’s origins) has long been associated with a group of virology spooks in Tony Fauci and Jeremy Farrar’s network. The field of evolutionary biology is supposed to tell you where new viruses have come from. But of course, it has been kidnapped to provide specious explanations when the biowarriors need to try and explain their concoctions as having natural origins.
Rambaut was also used to dispute the origins of HIV (as described in my friend Ed Hooper’s book The River ) while teamed up with Eddie Holmes, another Fauci flunkie, more than 20 years ago.
Republican members of Congress want to know what Fauci and his henchmen were up to when they concocted a fake natural origin for COVID, as revealed in the Fauci emails.
Rambaut was one of the 5 authors of that paper, and the paper was highly effective for a bit over one year at keeping a lid on COVID’s lab origin. As the members of Congress wrote:
Andersen and three other doctors on this teleconference [including Rambaut] later published a paper titled “the proximal origin of SARS-CoV-2 in Nature Medicine on March 17, 2020. This paper was highly influential in shaping our nation’s response to the pandemic. In the paper, the doctors concluded that “…we do not believe that any type of laboratory-based scenario is plausible.”[11]
… The Andersen paper led the narrative away from COVID-19’s potential lab origins. As Americans, we are deeply concerned by the appearance of discrepancies that largely influenced our understanding and approach to this virus. As Representatives of the American people, we owe it to them to seek and expose the truth about this virus’ origins wherever those efforts may lead.
Now Rambaut has popped up again, like a jack-in-the-box, to explain how the unexplainable 50 single nucleotide polymorphisms (SNP mutations) could have happened naturally. He has another bold theory! There was an evolutionary jump!
And Rambaut proffered yet another theory: the virus has been spreading in humans for years; we just didn’t notice it.
Below is a paper published by Portuguese researchers discusing the newly discovered mutations in money pox. They mention Rambaut’s theory, and Rambaut himself provides the first comment below the paper.
Spooks like Dr. Rambaut don’t do this dirty work for nothing. Just last month, he was made a fellow of the Royal Society.
From Wikipedia:
Science reported on 11 January 2020 that Rambaut was the first to publish the genome of the COVID-19 coronavirus after it was sent to him by Edward C. Holmes.[11][12] Holmes has said that it “took 52 minutes from receiving the code [from his Chinese colleague Professor Yong-Zhen Zhang] to publishing” on Virological.[13][14] The BBC Horizon episode The Vaccine stated: “When Chinese scientists published the genetic sequence of a mystery new virus on January 10th 2020, vaccine scientists around the world immediately sprang into action”.[15]
Rambaut was one of the authors of the scientific paper The proximal origin of SARS-CoV-2,[16] which concluded that “SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus”.
Rambaut is an attendee of the UK’s Scientific Advisory Group for Emergencies (SAGE).[17]
Perhaps someone else can look up his recent research grants. Were they from NIH or Wellcome? Being rewarded royally with other peoples’ money is another characteristic of the virology spook group.
Israeli regime openly calls on IAEA to censure Iran
Press TV – June 7, 2022
The Israeli regime is openly putting pressure on the United Nations’ nuclear watchdog to censure Iran’s peaceful nuclear energy program.
“We expect the IAEA (the International Atomic Energy Agency’s) Board of Governors to place a clear warning light in front of the regime in Tehran, and make it clear that if it continues in its defiant nuclear policy, it will pay a heavy price,” the regime’s Prime Minister Naftali Bennett said on Tuesday, addressing the Knesset (Israeli parliament), The Times of Israel reported.
The comments came a day after the board started a five-day meeting in Vienna.
The event is set to adopt an anti-Iran resolution, drafted by Britain, France, Germany, and the United States to accuse the Islamic Republic of withholding cooperation with the agency.
Various media reports and official sources have warned about the existence of the Israeli regime’s footprints across the process that has led to the emergence of the draft resolution.
Raising even more suspicion was a Friday flying visit to the occupied territories by the IAEA’s Secretary-General Rafael Grossi, and his meeting there with Bennett, with some reports even sounding the alarm about the watchdog and Tel Aviv’s “collusion” against Iran.
“He (Grossi) arrived for a snap visit in Israel, and I made Israel’s stance clear — that we are operating and will continue to maintain our freedom of action to act against Iran’s nuclear program as long as necessary… nothing ties our hands,” Bennet said.
The Israeli regime has, over years, conducted several sabotage operations against Iran’s nuclear facilities and assassinated at least seven Iranian nuclear scientists.
The regime’s vicious anti-Iran campaign comes while Tel Aviv, itself, continues to be the sole possessor of nuclear arms in the Middle East region, with a stockpile of hundreds of atomic warheads. Due to the cover provided by the US and Europeans, however, the regime has refused to open up its nuclear sites to the IAEA’s inspectors and join the Nuclear Non-Proliferation Treaty (NPT).
“When it comes to nuclear weapons, we live in a world of double standards,” Frank N. von Hippel, an American physicist, who is a professor and co-director of the Program on Science and Global Security at Princeton University, told Press TV.
“This unequal situation cannot persist indefinitely: Either we get rid of nuclear weapons or nuclear weapons will get rid of us,” he added.
Biden Rocks the Middle East
Partitioning Syria may be on the way

BY PHILIP GIRALDI • UNZ REVIEW • JUNE 7, 2022
That dwindling band of observers that continues to express concern over the catastrophe that constitutes United States foreign policy under President Joe Biden have come to realize how the Ukraine situation is being used as cover for interventions and other similar mischief in other parts of the world. Recent reporting, for example, reveals that the Biden Administration has decided “to reestablish a persistent US military presence in Somalia to enable a more effective fight against al-Shabaab” in spite of the fact that “there is absolutely no constitutional authority for President Biden to send troops into Somalia or drop bombs on Somalia.” Nor does al-Shabaab represent a threat to Americans or American interests.
To be sure, the emphasis on Ukraine has a certain cogency as it is particularly dangerous and could lead to nuclear devastation in a situation where intervention by the United States was not only unwarranted but also unresponsive to any actual national interest of threat. And escalate it will if the White House continues on its current path. Ukrainian government sources are now stating that the United States is preparing to destroy the Russian Black Sea fleet to end the blockade of Ukraine’s ports. The commander of US forces in Europe General Christopher Cavoli seems to be confirming that report when he refers to the preparation of “military options” to help export Ukrainian grain.
One might suggest that such a move could just be enough to start World War III and World War III would almost certainly turn nuclear very quickly. Some might consider that taking a deliberate step that would inevitably escalate into destruction of the entire planet as we know it just might be a foreign policy mistake on the part of the President Joe Biden Administration but I’m sure the chairborne warriors down at Foggy Bottom would disagree, pointing out that nothing would make old Vladimir Putin run and hide faster than a barrage of harpoon missiles imbibed with his breakfast tea.
And, of course, there’s more. There’s always more. The focus on Ukraine in the US and international media combined with a stream of befuddling malapropisms coming out of the White House has obscured what is going on in other corners in the world, where Washington is also flexing its biceps in full knowledge that a manageable war or two will surely help one’s favorability rating come elections in November.
And there is always Israel. The Israeli army and police have recently been shooting dead Palestinian teenagers on a nearly daily basis, and that comes on top of the killing of Palestinian-American journalist Shireen Abu Akleh a month ago. Israel’s Defense Minister Benny Gantz was in Washington two weeks ago to meet and greet and one might suspect that he just might have been in town inter alia to express some apology for his army’s assassination of Abu Akleh, but that would be to misunderstand the bilateral relationship. In reality, when Israel shouts “jump” the Biden Administration responds “how high, sir?”
Also in the Middle East and also related to Israel, the US State Department has gone into a hissy fit over the May 26th Iraqi parliament’s unanimous vote to make illegal all “normalization” ties with Israel. State was quick to react, in contrast to its torpor dealing with most issues, but it was Israel involved, not just “most issues.” A statement was issued saying “The United States is deeply disturbed by the Iraqi Parliament’s passage of legislation that criminalizes normalization of relations with Israel [while also] jeopardizing freedom of expression and promoting an environment of antisemitism…” Ah yes, the old anti-semitism canard surfaces yet again!
There are also several interesting stories relating to Syria, which continues to be a hotspot because Israel wants to maintain its ability to freely bomb targets that it describes as “terroristic” or connected to arch enemy Iran. The bombing has continued regularly since the Ukraine situation started and has hardly ever been reported in the US media. And, yet again, there is more to the story in terms of US involvement. First of all, Russia reacted to the lukewarm Israeli support for its invasion of Ukraine. An Israeli attack on targets in Syria last week was met by a S-300 missile fired by Russian army manned air defenses. Up until now, Moscow has refrained from attempting to shoot down Israeli warplanes, but the missile was clearly a warning of what might be coming if Israel persists in its attacks.
Also relating to Syria, it is ironic that the US has accused Russia of war crimes over its intervention in Ukraine while at the same time continuing its own illegal occupation of Syria. And it has its own war crimes record. Last week the Pentagon announced that it had completed its investigation into an attack in Syria on March 18, 2019 that killed some presumed ISIS guerrillas as well as four civilians while wounding fifteen others. The Pentagon press secretary John Kirby said the Defense Department had determined that that the airstrike “did not violate the laws of warfare or the rules of engagement. Neither the ground forces commander nor anyone involved in carrying out the airstrike ‘acted inappropriately or acted with malicious intent’ or ‘deliberately wanted to and sought out to kill civilians.’” In an earlier investigation concluded last December, the Pentagon said “it would not hold anyone accountable for a drone strike also in Syria in late-August that killed 10 civilians, including seven children. A review of the strike concluded it was a ‘tragic mistake’ that was the result of ‘execution errors.’”
And there are also credible reports that the United States is preparing to de facto partition Syria, to create a separate state run by its Kurdish allies in the country’s northeast that would be under Washington’s protection and would include a garrison of American troops. Such a move would, of course, be completely illegal and is in fact eerily reminiscent of the alleged “war crimes” that the US is claiming regarding Russia for its attempted partition of Ukraine. Interestingly, the planning has not been reported in the mainstream media, yet another instance of the Ukraine crisis serving as cover to drown out all background noise and provide the US with opportunities to increase its meddling in places like the Middle East on behalf of feckless allies like Israel and Saudi Arabia.
Ironically, when the United States initially intervened in Syria, it claimed to do so to fight the terrorist group Islamic State in Syria (ISIS). Subsequently, it cooperated with an al-Qaeda affiliate while close ally Israel had a similar arrangement with ISIS itself. The Kurds and both ISIS and al-Qaeda are all believed to be involved in the theft and sale of Syrian oil. Now the US, which also has been stealing the oil, is seeking something like a permanent presence to solidify its control over Syrian resources.
Interestingly, the planning by Washington to create a sub-state or autonomous region in the north east of Syria was revealed by no less than State Department number three Victoria Nuland at a recent conference held in Morocco. Nuland, who was the driving force behind regime change in Ukraine in 2014, described the Syria development as a “stabilization” activity. The new entity would include Syria’s major oil producing region, which is currently being exploited by Washington and its “allies,” as well as much of the country’s arable land.
Washington has already applied unprecedented punitive sanctions on the parts of Syria controlled by the Russians and President Bashar al-Assad, to include the so-called Caesar Syrian Civil Protection Act’s secondary sanctions that punish anyone trying to avoid the restrictions placed by Washington. Former US Ambassador to Syria James Jeffrey put it this way “And of course, we’ve ratcheted up the isolation and sanctions pressure on Assad, we’ve held the line on no reconstruction assistance, and the country’s desperate for it. You see what’s happened to the Syrian pound, you see what’s happened to the entire economy. So, it’s been a very effective strategy….” He also added “My job is to make it a quagmire for the Russians.”
To circumvent the existing sanctions, the new mini-state would therefore be granted economic viability by making it sanction free as an inducement for foreign investment and development of settlements largely inhabited by Kurds associated with the United States. A “general license” will be issued to facilitate investment and other economic activity. The US will commit $350 million to the project, which is being carried out with the cooperation of the Turkish authorities controlling their own militias along the border. By securing the north east of Syria, Washington would also be able to maintain and protect the illegal US Al-Tanf military base in the south-east of the country bordering Jordan. Al-Tanf blocks the creation of a contiguous “Resistance Axis” from Iran to Lebanon and ultimately to Palestine, thereby maintaining “Israeli security” in the region. As is all too frequently the case, Israeli interests always come first in the minds of Washington politicians.
Philip M. Giraldi, Ph.D., is Executive Director of the Council for the National Interest, a 501(c)3 tax deductible educational foundation (Federal ID Number #52-1739023) that seeks a more interests-based U.S. foreign policy in the Middle East. Website is councilforthenationalinterest.org, address is P.O. Box 2157, Purcellville VA 20134 and its email is inform@cnionline.org.
Grading the uses of the Defense Production Act during COVID Mania
By Jordan Schachtel | June 6, 2022
With President Biden beginning this week by invoking the Defense Production Act (this time, to build solar panels) we figured it’s time to take a look at what happened to the DPA during COVID Mania, and explore how it has been used (abused) since March of 2020.
For starters:
The Defense Production Act is a federal law that was enacted in 1950 after the commencement of the Korean War.
The explanation of the bill, via Congress, goes as follows:
“To establish a system of priorities and allocations for materials and facilities, authorize the requisitioning thereof, provide financial assistance for expansion of productive capacity and supply, provide for price and wage stabilization, provide for the settlement of labor disputes, strengthen controls over credit, and by these measures facilitate the production of goods and services necessary for the national security, and for other purposes.”
In short, these are emergency powers granted to the executive with a precedent for being enacted during an actual war. These powers allow the president to compel private companies to work with the government on developing material goods that are supposed to be used for national security purposes.
During COVID Mania, the DPA has been routinely abused for our manufactured national emergency.
Let’s take a look at how the DPA has been utilized to “fight the virus.”
- March 27, 2020: President Trump defines ventilators and PPE as “essential to the national defense,” and orders GM to start producing ventilators. The move came with bipartisan insistence. We later discovered that ventilators were possibly killing COVID patients.
Grade: F - April 2, 2020: President Trump invokes the DPA to compel several American companies to produce N95 masks. Masks don’t work, though.
Grade: Hysteria Sells - April 28, 2020: President Trump issues an executive order via the DPA to combat food insecurity and “to ensure a continued supply of protein to Americans.”
Grade: Shrug Emoji - January 21, 2021: President Biden invokes the DPA to pursue a “sustainable public health supply chain.”
Grade: Total Scam - March 2, 2021: Biden uses the DPA to give money to Merck so that they can produce more Johnson & Johnson COVID injections
Grade: Facepalm Emoji - September 2021: Biden invokes the DPA to supply fire hose materials to California, citing the climate hoax, because Gavin Newsom’s regime did not effectively manage California’s forests.
Grade: Avoidable Crisis - May 18, 2022: Biden uses the DPA to import baby formula from overseas because American supply became catastrophically short.
Grade: Cringeworthy - June 6, 2022: Biden issues DPA to advance the climate hoax narrative and give government funds to solar panel companies that otherwise would go bankrupt due to the unproductive nature of their businesses.
Grade: Boondoggle
Biden declares US energy emergency

Samizdat | June 6, 2022
President Joe Biden has blamed Russia for another crisis, saying the US might not be able to generate enough electricity to meet consumer demand partly because of Moscow’s military offensive against Ukraine.
The president declared an energy emergency on Monday, saying national security and quality of life are jeopardized by potential shortfalls in power supplies. He invoked the Defense Production Act – originally part of an industrial mobilization effort in response to the Korean War – to spur domestic production of solar panels and other forms of “clean” energy to boost power supplies.
“Multiple factors are threatening the ability of the United States to provide sufficient electricity generation to serve expected customer demand,” Biden said in his emergency declaration. “These factors include disruptions of energy markets caused by Russia’s invasion of Ukraine and extreme weather events exacerbated by climate change.”
Increased reliance on renewable energy sources has been blamed for disruptions to power service in such states as California and Texas. Solar and wind power are intermittent, so periods of high demand aren’t always matched by supplies. For instance, wind turbines froze up during an historic winter freeze last year in Texas, contributing to blackouts that caused 246 deaths and at least $195 billion in damage.
Biden’s emergency declaration included a two-year exemption from tariffs on solar panels from four Southeast Asian countries. The proposed tariffs had been blamed for delaying major solar projects in the US. About three-fourths of the solar modules installed in the US are imported from Southeast Asia.
The president has blamed Russia for record US fuel prices and a surge in inflation to a 40-year high. He’s also attributed a looming global food crisis to the Russia-Ukraine conflict.
US may lift ban on Iranian oil – Vitol
Samizdat | June 6, 2022
The Biden administration might let more sanctioned Iranian oil flow into the global markets in an attempt to rein in fuel prices at home amid the run-up to the midterm elections in the US, according to a major independent crude trader.
“If the midterms are dominated by the need to get gas prices lower in America, turning a somewhat greater blind eye to the sanctioned barrels flowing out is probably something you might expect to see,” Mike Muller, the head of Asia at Vitol Group, told Dubai-based Gulf Intelligence on Sunday.
Gasoline prices have doubled in the US since President Joe Biden was inaugurated in January last year, according to last week’s data from the non-profit American Automobile Association (AAA). Global crude prices have been rallying in recent months, fueled by restrictions on Russian exports. On Monday, crude hit $120 a barrel as Saudi Arabia hiked prices for Asia.
The Trump administration reimposed sanctions on Iran’s oil, petrochemicals, shipping and other sectors in 2018 due to concerns over the country’s nuclear program. Talks between Tehran and world powers stalled in March and, according to Muller, the window of opportunity for the Biden administration to reach an agreement with Tehran has almost closed, but it could allow the transportation of Iranian crude anyway. In April, the US seized Iranian oil carried by a Russian tanker. Iran currently exports most of its oil to China.
Iranian nuclear chief: IAEA’s Grossi lacks serious will to find Tehran’s ‘accurate’ answers convincing
Press TV | June 6, 2022
The head of the Atomic Energy Organization of Iran (AEOI) says Tehran has given accurate answers to questions posed by the International Atomic Energy Agency (IAEA), but the Agency bases its reports on the information provided to it by the enemies of Iran.
In an interview with Al Jazeera network on Monday, Mohammad Eslami said the director general of the IAEA, Rafael Grossi, lacks serious will to describe Iran’s answers to the Agency’s queries as convincing.
“The International Atomic Energy Agency relies on the intelligence reports [provided by] our enemies, topped by Israel,” Iran’s nuclear chief said.
Eslami made the remarks after the IAEA chief, in his introductory statement to the Board of Governors’ meeting on Monday, once again repeated his anti-Iran rhetoric, alleging that since February 23, 2021, the Agency’s “activities have been seriously affected by Iran’s decision to stop the implementation of its nuclear-related commitments under the JCPOA, including the Additional Protocol.”
Grossi claimed, “Iran has not provided explanations that are technically credible in relation to the Agency’s findings at three undeclared locations in Iran.” Grossi’s allegation, however, came after his meeting with Eslami and the adoption of the two sides’ joint statement on March 5, 2022.
The AEOI and the IAEA agreed, in continuation of their cooperation as stated in the Joint Statement of August 26, 2020, to accelerate and strengthen their cooperation and dialogue aimed at the resolution of the issues, read part of the joint statement.
Grossi’s remarks came despite frequent warnings by Iran that in case the Agency drifts away from its technical nature and makes a politicized decision related to Iran’s peaceful nuclear program, the country will respond in kind.
Elsewhere in his interview, Eslami pointed to the possible adoption of an anti-Iran resolution during the ongoing meeting of IAEA’s Board of Governors and said even if adopted, such a resolution would not create a new situation.
Advising the UN nuclear watchdog to block political influence on its decisions and abide by its own regulations, the AEOI’s head said, “The IAEA has not condemned attacks on our [nuclear] facilities and this is a big question mark.”
Over the past years and amid lack of sensitivity and proper attention on the part of the IAEA towards performing a responsible role in the area of protection of various countries’ peaceful nuclear activities, some malign activities, for which the Zionist regime has implicitly accepted responsibility, have afflicted some damage to our country’s nuclear facilities.
Although these activities have never had a decisive effect on the progress of Iran’s peaceful nuclear program, given the sensitivity that is inherent to the nature of nuclear work, adoption of new strategies in the structural, hardware, and software aspects have found a place on the AEOI authorities’ agenda so the nuclear facilities’ security can be completely ensured.
Eslami also rejected allegations that Iran is planning to build nuclear weapons, saying, “Nuclear weapons have no place in our strategies” and that all such allegations are nothing but spiteful accusations.
Asked about the IAEA’s access to information recorded by monitoring cameras it has installed in Iran’s nuclear facilities, Eslami said this issue depends on the fate of the ongoing talks in the Austrian capital on the revival of the 2015 Iran deal, officially known as the Joint Comprehensive Plan of Action (JCPOA).
“If other parties commit to all articles of that agreement, we are ready for full compliance with the accord,” Iran’s nuclear chief said.
Under the JCPOA, Iran accepted certain caps on its nuclear program in exchange for the removal of international sanctions.
The US, however, unilaterally abandoned the deal in 2018 and re-imposed crippling sanctions despite Tehran’s full compliance with its share of obligations.

