The Athens Health Department Helped Ohio University and Others Lie about FDA Approval

First lets summarize what we know. Comirnaty was approved by the FDA, at the time of writing this it is unavailable in America. Spikevax was more recently approved by the FDA, it is also not available in America.

This means providers can continue to distribute and use Emergency Use Authorized (EUA) vaccines, while patients may believe they are receiving an FDA approved vaccine. The chart below summarizes the differences for a patient who takes an FDA approved vaccine or an EUA vaccine.

Approved or Authorized?ApprovedAuthorized
Can you sue for damage
caused by the vaccine?		YesNO
Source https://crsreports.congress.gov/product/pdf/LSB/LSB10443 and https://childrenshealthdefense.org/defender/mainstream-media-fda-approval-pfizer-vaccine/

So once again to be very clear if you take a Emergency Use Authorized vaccine and even if it kills you, YOU CAN NOT hold anyone liable for the damages caused to you.

This is why it has been frequently reported by the press that Pharmaceutical companies will not give their products to people who actually can sue them.

https://www.reuters.com/legal/government/refugees-lack-covid-shots-because-drugmakers-fear-lawsuits-documents-2021-12-16/

A lot of people may wonder, If the Pharma companies are doing this to protect themselves from lawsuits, how do they get everyone else including healthcare providers to go along with it? A recent release of 1,000+ pages from the Athens County/City Health Department may help shed some light on how this Big-pharma created misinformation is spread in a healthcare setting.

Misinformation at the County Level

I want to start with some of the most blatant misinformation I have ever seen. November 3rd, 2021 Athens county held a COVID EMA (Emergency Management Agency) Brief. Keep in mind to today February 8th 2022 COMIRNATY is the only FDA approved vaccine made by Pfizer and it is only for people 16+ STILL.

In the COVID EMA Brief someone made a slide that said the Pfizer vaccine was FDA approved on November 1st, 2021 for kids 5-11. This is blatantly false.

Whoever made the presentation must have heard about this November 1st, because what really happened is on October 29th, 2021 the FDA Emergency Use Authorized the Pfizer-BioNTech COVID-19 vaccine for kids 5-11. It DID NOT receive approval and IS STILL NOT APPROVED. The FDA couldn’t make this any clearer.

https://www.fda.gov/news-events/press-announcements/fda-authorizes-pfizer-biontech-covid-19-vaccine-emergency-use-children-5-through-11-years-age

The source that was linked on the presentation even says it is “emergency use”. The source did use the word “approved” misleadingly. The difference between FDA approved and EUA authorized is not complicated but Pharma funded news sources like HealthDay continue to mislead and cause confusion for monetary gain.

This presentation was shared with who knows how many people throughout Athens county. How many providers took this false information and shared it with patients? One thing we do know for sure is that Gillian Ice received this presentation.

Another Email from the Health Department sent on September 28th, 2021 about a month after the FDA announced COMIRNATY’s approval shows they knew the available vaccines were Emergency Use Authorized, they never bothered to send the COMIRNATY fact sheet since no one ever had any COMIRNATY to give.

These fact sheets from the email all make it VERY clear, all available COVID vaccines are EMERGENCY USE AUTHORIZED

The health department likes to do the same thing Gillian Ice does and act like the “Legally Distinct” vaccines are actually the same exact thing.

In this email Jack Pepper of the Athens country Health department repeats the lie that the FDA approved Pfizer for 5-11 year old’s. Once again, what actually happened is the FDA Emergency Use Authorized the Pfizer-BionNTech COVID-19 Vaccine for kids ages 5-11, it was never approved and still is not. Using this incorrect vocabulary is unethical, and if the excuse is these people aren’t smart enough to understand the difference between FDA authorization and approval, they sure as hell should not be in a position to make health recommendations for others.

It seems the health department was getting a lot of questions about the details of the vaccine that the health department was struggling to answer. If health officials did not lie and cause confusion about the vaccines, maybe Health department employees could actually answer the questions from concerned patients. This email was sent to try and help them answer these questions.

Attached to the email is an interesting document from the CDC. The CDC makes the statement “Vaccines are not interchangeable” which was the case before COVID. They explain in some cases interchangeability is now allowed. I wonder what case that is.

The Health department also received This Document from FEMA. FEMA provides funding for mostly everything related to COVID as long as the Health Department follows orders and doesn’t get out of line actually trying to save lives.

fema-health-departmentDownload

Lets focus on the vaccination section, since the government continues to act like vaccines are the only treatment for COVID, Maybe vaccine funding will help us understand. The Federal Government uses are tax dollars to pay for all COVID vaccine doses no questions asked. Other costs are also eligible for more funding if they do what they are told by “established vaccine protocols”.

Once again this extra funding applies to almost everything vaccine related. FEMA even provides fund for “Onsite emergency medical care to address adverse reactions to vaccinations or other emergency medical care needs that may arise while administering COVID-19 vaccinations.”

Someone applied to be the Public Health Emergency Preparedness coordinator. The Athens health department followed up after their to ask if they will remove their name from consideration if the COVID vaccine is required for employment.

The person who was interviewed said they would not take the vaccine and would withdraw their name if that was a condition of employment. They would rather not get the job than take the vaccine, just an interesting find.

There are thousands of pages from this release and we will be releasing more soon. Check out our File Cabinet to see all full source documents.

Nobody Is Getting Vaccines Or Boosters Anymore, Demand has Cratered

Even with children 5 and over now eligible, the total number of doses administered in the United States every day is well under 1 million. That figure is barely above the July 2021 lows, before the Biden administration tried and failed to force its big-company vaccine mandate through.

Let’s look at where America is at overall in regards to vaccinations first.

200 Million+ Vaccinated

88 Million+ Boosted

75.4%+ Of Americans Vaccinated

95%+ of High Risk (over 65) Vaccinated

source: CDC Vaccination Dashboard

The amount of people in America receiving their first dose of the vaccine is the lowest it has been since the second day the Vaccines were distributed to the public. Everyone who wants to get vaccinated, clearly has got vaccinated. Mandating vaccines at this point only increases vaccine hesitancy.

The Share of American’s becoming fully vaccinated has also slowed significantly, allowing the world on average to catch up.

More third shot “boosters” are administered currently than either first or second doses, But demand for boosters is also plunging.

Boosters may be less popular now because it has become clear that over-boosting with these mRNA vaccines is correlating with increased COVID deaths. We are following a similar trend to Israel who is even more BOOSTED than the United States.

Another Interesting piece of data being overlooked is the difference between people with dose 1 and dose 2. As you can see the older you are the less likely you are not to get a second dose after your first.

https://www.mayoclinic.org/coronavirus-covid-19/vaccine-tracker/

Looking at it deeper we see the 75+ age group is an outlier, What could explain why so many people over 75 didn’t get a second dose? 18-24 Year old people also had a large amount of people not get a second dose of the vaccine.

Source: https://www.mayoclinic.org/coronavirus-covid-19/vaccine-tracker/

Well the CDC shares some data that could explain this gap, according to them these 2 age groups have seen 2 surges in COVID deaths since the vaccination’s were distributed. Keep in mind over 75% of 18 to 24 year old’s are vaccinated and over 99% of people 75+ are vaccinated. So it is possible the difference is accounted for by people who were killed by COVID (or from the vaccine and counted as a COVID death).

https://covid.cdc.gov/covid-data-tracker/#rates-by-vaccine-status

But the CDC shows death rates for the unvaccinated still being much higher? This is explained in the footnotes of the CDC‘s page. If someone tests positive within 14 days of of their first dose and then die at anytime later they are counted as an unvaccinated COVID death. once again remember both these groups are highly vaccinated and 75+ is over 99% vaccinated. This is how the CDC manipulates the data to promote vaccination.

See Footnotes: https://covid.cdc.gov/covid-data-tracker/#rates-by-vaccine-status

According to the CDC Side effects after the second shot may be more intense than the ones experienced after the first shot. They also say this is normal, I personally don’t remember having more intense side effects from any other vaccine dose I have received.

https://www.cdc.gov/coronavirus/2019-ncov/vaccines/expect/after.html

Both Spikevax.com and Comirnaty.com say people who had previous reactions to vaccines and COVID vaccines should not take the another dose. Which is weird since the CDC said reactions are normal and means it’s “working”. Both pages also say the vaccines may not actually protect you interestingly.

https://spikevax.com/
https://www.comirnaty.com/

When we look at the CDC’s Vaccine Adverse Event Reporting system (VAERS) we see there are over a million adverse events, so approximately 1 million people SHOULD NOT get another dose of these vaccines because of adverse effects.

https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&VAX=COVID19

According to the CDC VAERS database COVID Vaccine related deaths are also highest among the 75+ age group, which also is the group with the largest difference between 1st and second doses.

https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&VAX=COVID19&DIED=Yes

Quick Fact: Moderna’s website Spikevax.com even says The Moderna COVID-19 Vaccine Is Emergency Use Authorized

if you visit Spikevax.com you will see a notice right at the top of the page that says “The Moderna COVID-19 Vaccine has not been approved by the FDA, but has been authorized for emergency use by FDA“. I’m just not sure how much more clear it can be, but some people still deny this patent fact that NO FDA APPROVED VACCINE IS AVAILABLE in the United States.

https://www.modernatx.com/covid19vaccine-eua/recipients/

As discussed in FDA reissues EMERGENCY USE AUTHORIZATION FOR Moderna Vaccine, Approves “Spikevax” this behavior of ignoring the reality of the legal differences in the vaccines was expected. This is part of Big Pharma’s Pyramid scheme. It is just sad to see so many people falling for it.

Gillian Ice is a supporter of this misinformation. She knows these vaccines are legally distinct but continues to mislead students to believe they can get an APPROVED vaccine. Which they can not get because no FDA approved vaccine is available in America.

She claims The FDA approval changes Spikevax “from Emergency Use Authorization (EUA) to full approval”, But Spikevax was never Emergency Use Authorized, the “Moderna COVID-19 vaccine” was Emergency Use Authorized and it still is.

Page 7 of The Letter of Authorization for Spikevax clearly admits Spikevax and COMIRNATY are not available in the United States as of 1/31/22. COMIRNATY has been approved since August, why else would Pfizer continue to produce the EUA vaccine and still have no FDA approved COMIRNATY available unless it was for the liability protection?

Below is a video of Gillian Ice trying to dance around admitting COMIRNATY is not available.

Question Starts at 40 Minutes. The following transcript is Auto-generated by YouTube with some corrections.

Moderator: all right thank you we next we have Cameron

Cameron: uh yeah so I just had a question about the vaccine. does the university have any type access to the FDA approved Pfizer COMIRNATY vaccine, or is it all just the emergency use authorized BioNTech Vaccine

Gillian Ice: so the vaccine that we have is um, first of all we’re not administering the vaccine the health department is administering the vaccine. Our community health programs is administering the vaccine. they have the Pfizer vaccine which is equivalent to the COMIRNATY vaccine, and the FDA has provided that information, which I believe you have.

This misinformation is DANGEROUS. If someone is hurt by an Emergency Use Authorized Vaccine the Pharma companies and providers have full liability protection.

The FDA Approved Spikevax Despite NO DATA showing it is at all effective against Omicron, Why?

Since we are going to talk about Spikevax we once again need to make it very clear that Spikevax and the Moderna COVID-19 Vaccine do have VERY IMPORTANT differences.

There is a significant legal distinction between products authorized under EUA and those fully licensed by the FDA. According to the FDA there is NO FDA APPROVED COVID VACCINE AVAILABLE IN AMERICA.

https://www.fda.gov/media/144636/download

EUA products are experimental under U.S. law. Under the Nuremberg Code and federal regulations, no one can force a human being to participate in this experiment.

Specifically, under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), “authorization for medical products for use in emergencies,” it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines.

That’s an issue military members, unable to find any vaccination sites that offer the fully licensed Comirnaty vaccine, cited in various lawsuits challenging vaccine mandates.

Notably, on Nov. 12, 2021, a federal judge rejected an argument by the U.S. Department of Defense, in defending the military’s vaccine mandate, that the Pfizer Comirnaty and Pfizer-BioNTech vaccines are “interchangeable.”

U.S. law also requires the EUA designation be used only when “there is no adequate, approved and available alternative to the product for diagnosing, preventing or treating such disease or condition.”

This means that, in legal terms, all EUA products should be withdrawn once alternative products have received full approval.

Perhaps the most significant legal distinction, however, pertains to the legal protections afforded vaccine manufacturers, depending on how their product is classified.

Under the 2005 Public Readiness and Preparedness (PREP) Act, EUA-approved vaccines enjoy a significant liability shield. Specifically, vaccine manufacturers, distributors, providers, and government officials involved in the policymaking, approval, and distribution process are immune from any legal liability.

Under such regulations, the only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct.

No such lawsuit has ever succeeded.

Conversely, fully licensed vaccines, such as Spikevax and Comirnaty, do not have a liability shield, and are instead subject to the same product liability laws as other products.

This means the Spikevax and Comirnaty vaccines could expose pharmaceutical companies to significant financial claims if individuals injured by the vaccines chose to sue the vaccine makers. This is why they remain unavailable.

The rush to get COVID vaccines authorized for all ages — a ploy to avoid liability? 

There’s another reason Pfizer and Moderna don’t want their fully licensed vaccines to be available yet — they’re waiting for the vaccines to be authorized, then licensed, for children as young as 6 months old.

Why? Because once a vaccine is fully licensed by the FDA, the only way its manufacturer can be shielded from legal liability is if the vaccine is added to the Centers for Disease Control and Prevention’s childhood vaccination schedule.

The National Childhood Vaccine Injury Act (NCVIA), passed into law in 1986, provides a legal liability shield to drugmakers if they receive full authorization for all ages and the vaccine is added to the mandatory schedule.

Reporting on the FDA’s approval of Spikevax, investigative journalist Jordan Schachtel wrote:

“Are Pfizer and Moderna waiting for full authorization for children’s shots to distribute Comirnaty and Spikevax to the masses? There’s plenty of litigators who have suggested that this is exactly what is going on in Big Pharma world.”

By creating the public perception that the Pfizer and Moderna EUA vaccines are fully approved, businesses, schools and other institutions are emboldened to impose vaccine mandates that violate existing law and allow the vaccines to be administered without informed consent.

It has also been argued that by relabeling the product, any previous data regarding vaccine injuries and side effects identified in association with the EUA vaccine are not counted in the safety studies for the approved vaccine.

FDA admits no safety data for Spikevax use among pregnant women or for Omicron

Beyond the legal questions raised by the FDA’s approval this week of Spikevax, the approval also raises safety questions.

For instance, the FDA admitted Spikevax was insufficiently tested on pregnant women, stating that “[a]vailable data on SPIKEVAX administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy.”

Furthermore, Spikevax was approved without having been tested for its ability to provide protection against the Omicron variant, which is reported to account for 99.9% of current U.S. COVID cases — it was approved only for providing protection against mutations that are no longer circulating.

And yet, the FDA cited the Omicron variant as the reason behind its decision to pull its EUA for monoclonal antibody products. The FDA claims that these products have not been shown to provide protection against the Omicron variant.

According to the CDC 99.9-100% of COVID cases are currently Omicron

https://covid.cdc.gov/covid-data-tracker/#variant-proportions

Quick Fact: The FDA has Recalled At Least 8 Different COVID Tests For Providing False Results

Since the COVID pandemic began the anti-science obsession with testing has created an entire new industry for scam artist and Pharmaceutical companies alike. The FDA even had to issue a warning about fake tests and vaccines, because of the large influx of people creating fake treatments and tests for profit. In the rush to be the first and most widely available tests many testing manufacturers have made mistakes, this has resulted in at least 8 tests being recalled through the FDA Safety Communications.

The 8 tests that have been recalled can be found below.

May 28th, 2021: FDA Recalls Lepu Medical Technology SARS-CoV-2 Antigen AND Leccurate Antibody Tests

According to the FDA these 2 tests were recalled because it “is likely a high risk of false results when using these tests. Neither test has been authorized, cleared or approved by FDA for distribution and use in the United States.”

June 10th, 2021: FDA Recalls Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test

According to the FDA this test was recalled because it presented a risk to public health and made false claims about the performance of the test.

October 25th, 2021: FDA issues warning about False Positive Results with Ellume COVID-19 Home Tests

According to the FDA this test has the potential to give patient a false positive results. a “false positive” is a test result that indicates that a person has the virus when they do not actually have it.

January 11, 2022: FDA recalls 2 LuSys Laboratories COVID-19 Tests

According to the FDA these 2 tests were recalled because there is likely a high risk of false results when using these tests.

January 28, 2022: FDA Recalls 2 Empowered Diagnostics COVID-19 Tests

According to the FDA both these tests have a risk of false results.

Gillian Ice: Public Misinformation Update for February 1st, 2022

Gillian begins her Feb. 1st, 2022 Public health update by admitting cases COVID cases are down significantly. She then offers an ultimatum that in person activities can return if we just do what she claims, she thinks works at preventing COVID. She even says its “The time for all of us to double down on prevention”. I’m sure its easy for her to tell students to double down on disruptive measures like wearing a mask while she works from home maskless.

Another “prevention” measure Gillian refuses admit has failed is mandated COVID vaccines. This semester was the first semester students were required to be vaccinated or receive an approved exemption and this was also by far the semester with the most COVID cases since the pandemic began. The 7 day average still remains higher as of January 28th than any previous peak. The vaccination rate was much lower and even zero for the first of the previous 3 surges.

Next Gillian tells a bold faced lie about the FDA’s approval of Spikevax. She claims The FDA approval changes Spikevax “from Emergency Use Authorization (EUA) to full approval”, But Spikevax was never Emergency Use Authorized. the “Moderna COVID-19 vaccine” was Emergency Use Authorized and it still is.

As we reported yesterday The FDA, Big Pharma, and people like Gillian are pulling the same bait and switch they did with COMIRNATY (which remains unavailable in the United States).

The FDA’s letter of approval clearly states this is not true and that “The products are legally distinct with certain differences”

From Page 3 of: https://www.fda.gov/media/144636/download

This is also clearly stated on the FDA fact sheet for healthcare providers which obviously Gillian either did not read or did read and is knowingly lying about.

The Moderna COVID-19 Vaccine is Emergency Use Authorized (EUA) for doses 1 & 2, as well as additional booster doses.

Spikevax is only FDA approved for doses 1 & 2, it is EUA for booster doses.

https://www.fda.gov/media/144637/download

Page 7 of The Letter of Authorization for Spikevax literally even admits Spikevax and COMIRNATY are not available in the United States as of 1/31/22. COMIRNATY has been approved since August, why else would Pfizer continue to produce the EUA vaccine and still have no FDA approved COMIRNATY available unless it was for the liability protection?

Which is why yesterday before Gillian sent this public health update I informed her and OU COVID Operations that COMIRNATY AND SPIKEVAX ARE UNAVAILABLE which is why the EMERGENCY USE AUTHORIZATION for the Moderna COVID-19 Vaccine was reissued.

Knowing Ohio University and Gillian ice would lie and pretend these vaccines are the same and claim the FDA approved Spikevax is actually available I posted on my personal Instagram yesterday calling out what COVID operations would do before they even did it, the lies are so bad they are predictable.

Image.jpeg

Gillian loves saying “fully approved” which is weird since the FDA does not use the term “fully approved”, because something is either Emergency Use Authorized or Approved, there is no half approval. You don’t have to believe me, do a CTRL+F search for “fully approved” or “full approval” on the FDA’s Spikevax page and documents.

You can even search the whole FDA website for “fully approved” or “full approval”, they have literally never used the term for anything, yet Gillian does repeatedly.

Which makes it obvious Gillian has heard this phrase from watching mainstream media who also uses the term. I would hope Gillian actually believes the Media’s (sponsored by Pfizer) lies and she’s not knowingly lying, but when I repeatedly inform her about the misinformation she’s spreading and she continues to spread the disinformation it is clear she has some type of motivation to mislead people about this.

This is not even the first time Gillian has been caught lying about FDA approval as we previously reported An OU Student Asked COVID Operations If They Could Receive The Only FDA APPROVED COVID Vaccine COMIRNATY. OU Could Not Provide an Answer. and reported in Gillian Ice and Ohio U Hid the Fact That Ohio University has NOT Administering FDA Approved Vaccines and KNEW that the Vaccine Mandate was Unlawful.

Gillian goes on the make the claim the unvaccinated are being hospitalized at higher rates.

To support her claim she used preliminary data from the CDC. She did not provide a link for the source because she doesn’t want you reading to deep into the CDC’s page.

The footnotes of this data admit some very interesting and important facts.

First the CDC admits anyone who is hospitalized while partially vaccinated or within the first 14 days of being fully vaccinated they are counted as an Unvaccinated hospitalization.

Lets make this very clear A FULLY VACCINATED PERSON HOSPITALIZED FOR COVID IS COUNTED AS UNVACCINATED WITHIN THE FIRST 14 days of vaccination.

Getting a booster also makes you count as unvaccinated for another 2 weeks.

So if you get a booster and a week later you are hospitalized from COVID you are still counted as unvaccinated.

The CDC’s footnotes even admit it may over-estimate first doses, under-estimate follow up doses and under-estimate the hospitalization rates for boosted people.

The CDC also admits anyone without record of vaccination is considered unvaccinated.

It is obvious this data is manipulated for the purpose of promoting vaccines through fear. Now that so many more vaccinated people are getting COVID, hospitalized for COVID, and even dying from COVID the CDC will probably stop reporting breakthrough data again as they have previously.

According to a report by the Boston Globe: the CDC declined to collect crucial information even when it had the power to do so, such as when it decided last year not to track breakthrough COVID cases that did not result in hospitalization or death.

“We have to know the totality of breakthrough incidents, and the CDC has not prioritized getting those raw numbers,” said Rivera, whose organization is working on tracking breakthrough cases. “It’s a huge disappointment.”

Jernigan said the agency limited its tracking of breakthrough cases to ensure it studies only cases in which the outcome is known. But outside experts say that has not yielded enough information.

“This has hampered our ability to come up with a public health recommendation, and tell the public, go and get a booster much earlier,” said Mokdad, the University of Washington professor.

Real-world data show most of infected are fully Vaccinated

Real-world data from areas with high COVID jab rates show the complete converse of what media, the CDC and White House officials are telling us. In addition to the British Technical Briefing No. 16, cited above, we have additional data from Israel, Scotland, Massachusetts and Gibraltar:

  • Aug.1, 2021, director of Israel’s Public Health Services, Dr. Sharon Alroy-Preis, announced half of all COVID-19 infections were among the fully vaccinated. Signs of more serious disease among fully vaccinated are also emerging, she said, particularly in those over the age of 60.

A few days later, Aug. 5, Dr. Kobi Haviv, director of the Herzog Hospital in Jerusalem, appeared on Channel 13 News, reporting that 95% of severely ill COVID-19 patients are fully vaccinated, and that they make up 85% to 90% of COVID-related hospitalizations overall. As of Aug. 2, 66.9% of Israelis had received at least one dose of Pfizer’s injection, which is used exclusively in Israel; 62.2% had received two doses.

  • In Scotland, official data on hospitalizations and deaths show 87% of those who have died from COVID-19 in the third wave that began in early July were vaccinated.
  • A CDC investigation of an outbreak in Barnstable County, Massachusetts, between July 6 through July 25, found 74% of those who received a diagnosis of COVID19, and 80% of hospitalizations, were among the fully vaccinated. Most, but not all, had the Delta variant of the virus.

The CDC also found that fully vaccinated individuals who contract the infection have as high a viral load in their nasal passages as unvaccinated individuals who get infected. This means the vaccinated are just as infectious as the unvaccinated.

  • In Gibraltar, which has a 99% COVID jab compliance rate, COVID cases have risen by 2,500% since June 1.

While those who benefit from keeping the pandemic going would like you to cower in fear at the thought of the Delta variant, there’s really no evidence that it’s any worse than the original. It’s more transmissible, yes, but far less dangerous, as its primary symptoms are that of a regular cold.

According to Harvard and Stanford professors, the actual number of Americans dying from or with COVID-19 are actually at an all-time low, so alarmism is uncalled for. Gillian Ice just want’s to scare people to promote Big Pharma’s vaccine, as she previously admitted in our press release OU Now Claims They are Not Enforcing The Vaccine Mandate. Here is Why They “Promoted Vaccination”

FDA reissues EMERGENCY USE AUTHORIZATION FOR Moderna Vaccine, Approves “Spikevax”

The FDA is pulling the same bait and switch they did with COMIRNATY (which remains unavailable in the United States). So lets make a few things very clear before the inevitable misinformation about Spikevax being available spreads. According to the FDA Spikevax has received FDA approval.

According to the FDA the Moderna COVID-19 vaccine REMAINS EMERGENCY USE AUTHORIZED.

Many will attempt to spread misinformation by claiming Spikevax and the Moderna COVID-19 vaccine are the same thing. The FDA’s letter of approval clearly states this is not true and that “The products are legally distinct with certain differences”

From Page 3 of: https://www.fda.gov/media/144636/download

This is also clearly stated in the FDA‘s fact sheets to vaccine providers which was updated the day of Spikevax Approval 1/31/22

The Moderna COVID-19 Vaccine is Emergency Use Authorized (EUA) for doses 1 & 2, as well as additional booster doses.

Spikevax is only FDA approved for doses 1 & 2, it is EUA for booster doses.

https://www.fda.gov/media/144637/download

Why have 2 legally distinct vaccines?

It is simple, the PREP act protects people like Big Pharma, Vaccine Providers, and more from legal liability if the vaccine or any other EUA product hurts or even kills you. Yes death is covered by PREP act Liability protection.

The PREP act covers many people, including Ohio University. While FDA approved vaccines can lose liability protection for many reasons including if a pandemic is declared over, EUA countermeasures are covered indefinitely.

This means Pfizer and Moderna can advertise their vaccines as “FDA Approved”, give patients the Emergency Use Authorized Vaccines, and protect themselves from all liability, While receiving millions and billions from the government.

It is probably safe to assume you wont see any Spikevax doses being administered for the primary series anytime soon. Neither Spikevax or COMIRNATY is shown on vaccines.gov vaccine finder.

According to the CDC Vaccines.gov displays the “types of COVID-19 vaccines available”. So it’s odd they wouldn’t list their FDA approved vaccines on the website if they were actually available, which they of course are not.

Page 7 of The Letter of Authorization for Spikevax literally even admits Spikevax and COMIRNATY are not available in the United States as of 1/31/22. COMIRNATY has been approved since August, why else would Pfizer continue to produce the EUA vaccine and still have no FDA approved COMIRNATY available unless it was for the liability protection?

The FDA acknowledges once again the mRNA vaccines are known to cause Myocarditis and pericarditis in the SPIKEVAX Information for Recipients and Caregivers.

https://www.fda.gov/media/155762/download

The Big Pharma pyramid scheme continues.

OU Now Claims They are Not Enforcing The Vaccine Mandate. Here is Why They “Promoted Vaccination”

After having a lawsuit filed against them and receiving multiple public records request for information that will show OU knowingly violated state laws to require EUA vaccinations, OU now claims they are not enforcing the COVID-19 vaccine mandate for those without vaccine exemptions.

So Why Would OU Announce The Vaccine Mandate in the first place?

Well according to the Post:

“Gillian Ice, special assistant to the president for public health operations, said the university is not enforcing the mandate as originally stated because of the university’s high vaccination rate. Ice said OU and the COVID Operations team will continue to promote vaccines. Carly Leatherwood, a university spokesperson, said that approach is “in line with other public institutions in the state.”

However, a few universities across the country are taking action against unvaccinated students and staff. Xavier University of Louisiana, University of Pittsburgh and the University of Virginia have said they will be unenrolling unvaccinated students who have not submitted exemptions. 

Ice said she considers the vaccine mandate a success because it encouraged many people who were not vaccinated to get the shot.”

https://www.thepostathens.com/article/2022/01/ohio-university-not-enforcing-covid-19-vaccine-mandate

So according to Gillian Ice the point of the mandate was to encourage people who weren’t vaccinated to get vaccinated, not to protect students from COVID, not to return classes to normal, but simply to “promote vaccines”.

Why would OU want to promote COVID vaccines?

As we recently discussed in “Here Is How Much The Federal Government Pays Hospitals to Prescribe Expensive Drugs instead of Cheap Proven Effective Treatments.” the federal government pays vaccine providers $40 for each dose they stick people with. CMS.gov implies only Emergency use Authorized vaccines are eligible for the $40 payment under this program.

which adds up with our recent reporting: COMIRNATY Is FDA Approved, The Pfizer-BioNTech COVID-19 Vaccine is Emergency Use Authorized, and An OU Student Asked COVID Operations If They Could Receive The Only FDA APPROVED COVID Vaccine COMIRNATY. OU Could Not Provide an Answer, and Gillian Ice and Ohio U Hid the Fact That Ohio University has NOT Administering FDA Approved Vaccines and KNEW that the Vaccine Mandate was Unlawful.

According to the CDC COMIRNATY products are not orderable or available in the United States. This means ALL COVID vaccines available are still EMERGENCY USE AUTHORIZED.

According to the CDC these are the requirements to participate as a COVID-19 Vaccination Program Provider:

This is also how the CMS defines Mass immunizers:

definitions-_-cmsDownload

As you may know OhioHealth is the healthcare provider for Ohio University.

CMS has a Medicare Provider lookup feature on their website.

OhioHealth is listed as a Medicare provider who charges Medicare-approved prices. Remember the Medicare approved price for COVID vaccines is $0 from the patient and $40 from CMS to the provider.

Vaccines.gov also lists 5 locations on the Ohio University campus where you can receive a COVID vaccine on Campus.

The Star recently asked Ohio University whether they were distributing Comirnaty or Pfizer’s EUA vaccine. Ohio University admitted that OhioHealth distributes their vaccines.

“They are being distributed in this area by the Athens City-County Health Department and OhioHealth,” Jim Sabin, a school spokesman said.

OhioHealth Confirmed COMIRNATY is not being distributed: “As of today’s stock, we are currently distributing the Pfizer vaccine that does not have the Comirnaty branding label,” Katie Logan, a spokeswoman for OhioHealth said by email.

This means either OhioHealth or Ohio University were receiving $40 from the Medicare COVID-19 Vaccine Shot Payment Program for EVERY EUA SHOT THEY PUT IN STUDENTS ARMS. Of course Gillian wanted to “promote vaccines”

According to the CDC COVID vaccines are paid for with government tax dollars. So providers aren’t the ones paying for the vaccines.

covid-19-vaccines-are-free-to-the-public-_-cdcDownload

Also according to the HRSA only the federal government or insurance companies can be billed for COVID vaccines. it also clearly states the reimbursement is for administration of the vaccine not the vaccine itself.

https://www.hrsa.gov/sites/default/files/hrsa/coronavirus/provider-covid-vaccine-factsheet.pdf

This would explain why Gillian Ice was so mad I accused Ohio University of receiving money MONTHS AGO for the vaccines that she ordered me to get a COVID test:

It also seems CMS pays providers for every COVID test as well, which may explain Ohio University’s obsession with testing everyone.

https://www.cms.gov/sites/default/files/2020-04/4.30.20%20COVID19%20Medicare%20Payment%20for%20Lab%20Services%20Graphic.PNG
https://www.cms.gov/sites/default/files/2020-04/4.30.20%20COVID19%20Testing%20Graphic.PNG

According to CMS schools can be Medicaid providers of COVID-19 screening testing covered under section 1905(a)(4)(F). So schools get reimbursed for the price of the test and they receive the CMS payment based on type of test.

Since 2020 the government has been providing funding to purchase tests as well as vaccines. Providers DO NOT pay for vaccines or tests but they are reimbursed.

According to the HRSA just like vaccines, testing reimbursements are for administration of tests, not the tests themselves, because providers don’t pay for the vaccines or tests either. OU is making nearly pure profit off each test.

https://www.hrsa.gov/sites/default/files/hrsa/coronavirus/provider-covid-vaccine-factsheet.pdf

So why is OU saying they are not enforcing the mandate?

This past Sunday 1/23/22 I submitted a Public Records request for the emails that will further prove my hypothesis that Gillian Ice and Ohio U Hid the Fact That Ohio University has NOT Administering FDA Approved Vaccines and KNEW that the Vaccine Mandate was Unlawful.

This is why just 3 days later 1/26/22 Gillian Ice began doing damage control and claiming the CLEARLY ILLEGAL vaccine mandate is not actually being enforced. The plaintiffs in our lawsuit and numerous other students have been harassed for months for being unvaccinated, as can be seen by Gillian Ice targeting me with COVID tests and threats in Emails:

Interestingly Ohio University’s 2021 financial statement shows gifts, grants, and contracts revenue has doubled since 2019 and now accounts for over 15% of OU’s total revenue.

Use this information to draw your own conclusions, but Gillian Ice admitting the Vaccine mandates purpose was to promote vaccines and Vaccine providers receiving $40 for each dose given seems to show a pretty clear story.

Never forget this is the same Ohio University that laid off workers and professors so they could give their administrators $100,000 bonuses just before the COVID pandemic began.

https://www.athensnews.com/news/campus/top-ohio-university-administrator-quietly-accepts-100k-bonus-amid-financial-turmoil/article_ee07c7bf-de1b-5ec3-8f8d-0e22a15499a5.html
Deb Shaffer Protester

Here Is How Much The Federal Government Pays Hospitals to Prescribe Expensive Drugs instead of Cheap Proven Effective Treatments.

To understand the scope of this problem you must first understand what is going on in the big picture. So first we will discuss 3 life saving drugs that have been proven effective against COVID-19, these 3 drugs have been relentlessly attacked by Big Pharma and the media because of how cheap they are.

For the COVID vaccines to receive Emergency Use Authorization (EUA) and even be allowed to be distributed at all there can NOT be any alternative treatments already approved and available. This is clearly stated on the FDA’s website and the FD&C Act.

So this is why it was so important for companies like Pfizer to convince the FDA and media to attack alternative treatments while the vaccines were being developed. So lets talk about those attacks.

hydroxychloroquine (HCQ)

The first time you probably heard about HQC was probably in 2020 when the president mentioned it being found to be effective in studies and the media immediately began attacking HQC and calling it a “fish tank cleaner” the only reason I mention this anti-science term the media used is because you will see its a pattern, the media clearly has a playbook and a defined set of attacks to use for this sort of thing.

Within the first 5 months of the pandemic the FDA quickly spread doubt about hydroxychloroquine effectiveness and even claimed it was causing new adverse reactions. Signaling they would not approve it or look further into it for approval, which keeps the future vaccines eligible for EUA. This was of course found by many studies to be untrue.

The single study the FDA used to justify these statements was soon after retracted.

However the science and over 300 studies have overwhelmingly found Hydroxychloroquine is very effective, unlike the media and FDA quickly rushed to claim.

effectiveness improves with earlier usage and improved dosing. Early treatment consistently shows positive effects. Negative evaluations typically ignore treatment time, often focusing on a subset of late stage studies. In Vitro evidence made some believe that therapeutic levels would not be attained, however that was incorrect, e.g. see [Ruiz].

Ivermectin

The first time you probably heard about Ivermectin is when Comedian Joe Rogan and NFL quarterback Aaron Rodgers publicly announced their doctors treated them with Ivermectin for COVID and found it very effective as many other studies already had at the time. The media quickly sprung into action to attack ivermectin, remember if an effective drug is discovered and approved Big Pharma’s vaccines can’t get an EUA. The media called Ivermectin a “horse dewormer” which technically it is also used for, but Horses also drink water, that doesn’t make water bad. The media knew they were spreading this misinformation to discourage people from using ivermectin, which has been found to be life saving.

CNN – “Joe Rogan has announced he has tested positive for Covid-19 and mentioned taking numerous medications to combat the virus, including the livestock drug ivermectin.”

What CNN failed to mention is many congressmen (over 200) including Democrats were also treated with Ivermectin for COVID.

The FDA also wasted no time attacking Ivermectin, making it very clear that while it was a safe drug with many uses, they claimed COVID was not one of them. Which was obviously found to be false by MANY studies, Ivermectin is effective and life saving. Of course once again this is because the COVID vaccines could not remain EUA if Ivermectin was proven effective and approved.

Once again the science and studies on Ivermectin are overwhelming clear, Ivermectin is safe and effective for treating COVID, and even more effective than HCQ

Monoclonal Antibodies (Bamlanivimab/etesevimab)

Antibodies are naturally made in our bodies to fight infection. Without antibodies, a virus can enter and infect a cell. With antibodies, however, when the virus tries to enter the cell, antibodies block the virus. Monoclonal antibodies (mAbs) are antibodies developed in a laboratory to help our bodies fight infection. Nearly 100 mAbs are already FDA-approved to treat health conditions including cancers and autoimmune diseases.

The FDA just today used the new variant as an excuse to halt monoclonal antibody treatments. This will delay new variant specific monoclonal antibody treatments and will also prevent anyone with a different variant like delta, which monoclonal antibody’s are very effective against, from getting them.

You may not know this, but Monoclonal antibodies were also used in Ohio and helped a lot of people. They can no longer be used in Ohio because pf the FDA’s decision.

Many studies have found Monoclonal antibodies effective, the FDA cited no data in making this recent decision.

Why would the media want to spread disinformation to help big pharma?

It’s pretty simple, Big Pharma is one of the biggest sponsors of mainstream media, they would rather lie for Big Pharma then hurt their Ad revenue.

Federal Payments for Giving Vaccines and Deadly Treatments

It is hard to fully explain this because it is obvious the hospital’s reason for forcing these deadly protocols is profit. No hospital administrator would turn down free money from the federal government. The reason the federal government is suppressing life saving drugs while paying hospitals to prescribe ones they know are deadly is more unclear, Big Pharma does have a long history of government lobbying so that would be the most likely explanation again.

Cash for Jabs

The federal Government through the Centers for Medicaid and Medicare Services established the Medicare COVID-19 Vaccine Shot Payment, you’ll notice COMIRNATY is not mentioned anywhere because it is unavailable in the United States.

The Federal Government currently pays $40 per every dose given in the United States. This is on top of the $24 the Government pays Pfizer per dose. So if you wanted to know the reason everyone else is pushing vaccines so hard when there are cheap alternatives available, it is because they are getting PAID to do it and to jab people with it!

Payments for Remdesivir and Convalescent Plasma (deadly)

Interestingly, the federal government and FDA have chose to promote and even once again pay hospitals for prescribing Remdesivir and Convalescent Plasma. These treatments aren’t just ineffective, they are expensive, and studies have found them to be DEADLY. The New COVID-19 Treatments Add-On Payment (NCTAP) was created to pay providers for using these deadly treatments.

Below is a chart of all applicable alternative treatment studies showing an overview of their effectiveness against COVID-19.

Remdesivir and Convalescent Plasma have been outlined in red

The 3 good treatments we talked about that the FDA has essentially banned have been outlined in green

The science and data is clear. HCQ, Ivermectin, and Monoclonal Antibodies are safe and effective. Remdesivir and Convalescent Plasma are NOT. Dr. Paul Marik recently shared concerning data that found Remdesivir can actually be DEADLY.

So why would the federal government attack effective safe treatments and promote and even pay doctors to prescribe ineffective and in some cases deadly drugs? This is once again a good question, the much higher prices of Remdesivir and Convalescent Plasma may give us some insight. Remdesivir and Convalescent Plasma are over double as expensive as Monoclonal Antibodies. Ivermectin and HCQ are EXTREMELY CHEAP.

Other suspicious decisions on payments for COVID

Medicare gives over $13,000 if a COVID-19 patient on Medicare is admitted

Medicare gives about $39,000 more if the patient goes on a ventilator

an analysis published April 7 by the Kaiser Family Foundation, a leading source of health information found.

Multiple studies have found ventilators actually make COVID patients worse like this peer reviewed study.

Experts even warned the ventilators were being overused. Were they being overused because of the incentive hospitals get for putting a COVID patient on a ventilator? Once again why would the federal government pay hospitals to use something the science shows is DEADLY? All while suppressing and attacking cheap, safe, and effective treatments.

Conclusion

Big Pharma and the Government love telling you the vaccine is free. They can achieve this because we are the product. As long as the “emergency” and the pandemic of fear continues Big Pharma has protections to make billions without any liability or consequence of lying and misleading. The government will keep paying hospitals to give bad drugs, which supports the fear of COVID. The fear of COVID will justify the government continuing to give Big Pharma millions. Big Pharma would have to be stupid to actually make a vaccine that ends this pandemic. It is the single greatest pyramid scheme of all time.

If it's free, You are not the customer-You are the Product

Pfizer Board Member and Previous FDA Director say it’s TIME TO END MANDATES

The surge in COVID-19 cases fueled by the Omicron-variant has slowed dramatically, with cases falling 12% over the past seven days, leaving experts to call for ‘divisive’ pandemic restrictions, like mask and vaccine mandates, to be phased out in the United States just as they recently were in the United Kingdom. 

America is averaging 682,374 cases per day, according to data from Johns Hopkins University (JH), a 12 percent drop over the past two weeks. 

Dr Scott Gottlieb, former director of the Food and Drug Administration (FDA) and current board member at Pfizer, says that the declining cases should be a signal to officials that it is time to start lifting some pandemic-related restrictions.

‘I think certainly on the east coast where you see cases declining dramatically we need to be willing to lean in and do that very soon I think as conditions improve we have to be willing to relax some of these measures with the same speed that we put them in place,’

He compares the current U.S. situation to that of the UK. Across the pond, Prime Minister Boris Johnson has set plans to drop all pandemic restrictions amid a drop in cases. Gottlieb said that America should soon follow, and pointed out masks in schools and vaccine mandates as particularly ‘divisive’ restrictions that he thinks should go. 

‘We haven’t described clear goalposts for when we’re gonna withdraw a lot of these measures and the two most contentious things right now in the U.S. are the masks among children in schools and the vaccine mandates,’ he said. 

He also added that in order for people to comply by Covid rules, health officials need to ‘have a flexible doctrine’ that changes as the situation of the pandemic does. 

Obviously this is because he will once again support mandates when they are making Pfizer and him money. He is essentially forced to admit these truths about mandates as damage control for Big Pharma’s own credibility and profits.