The FDA Has Just Committed a Horrendous Crime Against Humanity
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The FDA Has Just Committed
A Horrendous Crime Against Humanity
1
On Monday, August 23, 2021 the FDA fraudulently "approved" "COMIRNATY." This product is not currently available in the United States. Other available vaccines are NOT yet approved, but merely authorized for emergency use. Any "mandates" that do not specify "COMIRNATY" are still illegal.
CLICK HERE FOR DETAILS and HERE
2
The FDA approved an injectable concoction that was designed to "protect" you against last year's coronavirus. The studies were conducted well before the onset of the "Delta Variant." No details of effectiveness against variants were provided.
3
For the sake of their clinical trials, Pfizer-BioNTech defined COVID-19 so that some of the most commonly experienced adverse events caused by their injection (such as fever, chills and muscle pain) could easily be confused with the symptoms of mild COVID-19. They conveniently did NOT include other symptoms such as fatigue, headache and joint pain in their definition of COVID-19.
4
All of the clinical trial data rely on the fraudulent RT-PCR tests which have been invalidated in several international court decisions.
5
The media is glossing over the FACT that according to the available data 99.9% of the people in the PLACEBO group did NOT catch COVID-19 and NO ONE in the PLACEBO group died of COVID-19. They fail to report that, in the clinical trials, the risk of dying from COVID-19 was ZERO.
6
The results of the clinical studies make it CLEAR that no lives were saved by the injections. None. Zilch. Nada.
7
Despite CLEAR EVIDENCE of much higher adverse event rates (see tables below) when compared to the placebo group and hundreds of thousands of voluntarily submitted reports of injury, it appears that existing VAERS data was not considered in the FDA decision to CLAIM that the Pfizer-BioNTech injectable bioweapon is safe.
8
The FDA also authorized that the expiration dates on the out-of-date, old vaccines could be extended 3 months in order to make use of old stockpiles. Really. They really did.
On Monday, August 23, 2021 the FDA fraudulently "approved" "COMIRNATY." This product is not currently available in the United States. Other available vaccines are NOT yet approved, but merely authorized for emergency use. Any "mandates" that do not specify "COMIRNATY" are still illegal.
CLICK HERE FOR DETAILS and HERE
2
The FDA approved an injectable concoction that was designed to "protect" you against last year's coronavirus. The studies were conducted well before the onset of the "Delta Variant." No details of effectiveness against variants were provided.
3
For the sake of their clinical trials, Pfizer-BioNTech defined COVID-19 so that some of the most commonly experienced adverse events caused by their injection (such as fever, chills and muscle pain) could easily be confused with the symptoms of mild COVID-19. They conveniently did NOT include other symptoms such as fatigue, headache and joint pain in their definition of COVID-19.
4
All of the clinical trial data rely on the fraudulent RT-PCR tests which have been invalidated in several international court decisions.
5
The media is glossing over the FACT that according to the available data 99.9% of the people in the PLACEBO group did NOT catch COVID-19 and NO ONE in the PLACEBO group died of COVID-19. They fail to report that, in the clinical trials, the risk of dying from COVID-19 was ZERO.
6
The results of the clinical studies make it CLEAR that no lives were saved by the injections. None. Zilch. Nada.
7
Despite CLEAR EVIDENCE of much higher adverse event rates (see tables below) when compared to the placebo group and hundreds of thousands of voluntarily submitted reports of injury, it appears that existing VAERS data was not considered in the FDA decision to CLAIM that the Pfizer-BioNTech injectable bioweapon is safe.
8
The FDA also authorized that the expiration dates on the out-of-date, old vaccines could be extended 3 months in order to make use of old stockpiles. Really. They really did.
IMPORTANT QUESTIONS:
Why did the FDA approve a "vaccine" for last years' version of SARS-COV-2 when practically ever American knows that it doesn't work against the Delta and variants?
(see: How COVID-19 variants evade immune response)
What EXACTLY is in this product (COMIRNATY)? Why is the detailed information regarding the nucleoside sequence that makes up the mRNA being injected being hidden?
Which version of the coronavirus's "spike protein" does COMIRNATY trigger the recipient's immune system to develop antibodies to?
Do those antibodies actually work against the more recent variants, or do those injection triggered antibodies actually make the disease worse through a process known as antibody dependent enhancement of COVID-19.
Where is the discussion of VAERS data?
Why is COVID-19 defined to EXACTLY match the most common side effects of the injection?
(see: How COVID-19 variants evade immune response)
What EXACTLY is in this product (COMIRNATY)? Why is the detailed information regarding the nucleoside sequence that makes up the mRNA being injected being hidden?
Which version of the coronavirus's "spike protein" does COMIRNATY trigger the recipient's immune system to develop antibodies to?
Do those antibodies actually work against the more recent variants, or do those injection triggered antibodies actually make the disease worse through a process known as antibody dependent enhancement of COVID-19.
Where is the discussion of VAERS data?
Why is COVID-19 defined to EXACTLY match the most common side effects of the injection?
Why is the fraudulent RT-PCR test used to determine COVID-19 "cases"?
Where is the animal study data?
Where is the toxicity study data?
Where is the carcinogenic study data?
Where is the pregnancy and nursing infant study data?
Where is the black box warning about myocarditis and pericarditis?
AND WHY IS THERE ABSOLUTELY NO MENTION OF WHETHER OR NOT THE "VACCINE" ACTUALLY REDUCED DEATHS DUE TO COVID-19?
BECAUSE THE "VACCINE" IS NOT DESIGNED TO SAVE LIVES.
IT IS A BIOLOGICAL WEAPON THAT IS DESIGNED TO DIS-REGULATE YOUR IMMUNE SYSTEM TO MAKE YOU A CUSTOMER-FOR-LIFE WITH A WIDE VARIETY OF MYSTERIOUS AILMENTS THAT ARE NOT PERMITTED TO BE ATTRIBUTED TO THE INJECTION.
For 100+ years, the medical, hospital, pharmaceutical industrial complex has conspired to make Americans the sickest people on planet earth. Their techniques are very sophisticated. I encourage you to wake up and see through their lies.
Scroll down and read the "FDA approval letter".
Read the "Fact sheet for health care providers".
Learn the things that they do not want you to know.
Make your own decisions.
Your body. Your choice.
Where is the animal study data?
Where is the toxicity study data?
Where is the carcinogenic study data?
Where is the pregnancy and nursing infant study data?
Where is the black box warning about myocarditis and pericarditis?
AND WHY IS THERE ABSOLUTELY NO MENTION OF WHETHER OR NOT THE "VACCINE" ACTUALLY REDUCED DEATHS DUE TO COVID-19?
BECAUSE THE "VACCINE" IS NOT DESIGNED TO SAVE LIVES.
IT IS A BIOLOGICAL WEAPON THAT IS DESIGNED TO DIS-REGULATE YOUR IMMUNE SYSTEM TO MAKE YOU A CUSTOMER-FOR-LIFE WITH A WIDE VARIETY OF MYSTERIOUS AILMENTS THAT ARE NOT PERMITTED TO BE ATTRIBUTED TO THE INJECTION.
For 100+ years, the medical, hospital, pharmaceutical industrial complex has conspired to make Americans the sickest people on planet earth. Their techniques are very sophisticated. I encourage you to wake up and see through their lies.
Scroll down and read the "FDA approval letter".
Read the "Fact sheet for health care providers".
Learn the things that they do not want you to know.
Make your own decisions.
Your body. Your choice.
Please watch
the videos below...
Pfizer-BioNTech's injectable bioweapon
has been rebranded as...
The name uses the prefix “co” to represent community, the “mirna” for mRNA, and the “ty” as a nod towards the end of both “community” and “immunity.”
The name "COMIRNATY" is supposed to make you think about the technology behind the vaccine, immunity and community at the same time.
Interestingly, COMIRNATY is trademarked in a category that includes some curious related categories.
| august_23_2021_approval_letter_-_comirnaty.pdf |
SCREENSHOTS FROM
THE LETTER
The "vaccine" was approved to prevent COVID-19, even though it is common knowledge that the "vaccine" does no such thing.
Page 1:
Page 1:
There is no "black box" warning. Pfizer-BioNtTech is merely required to "study" the occurrence of myocarditis and pericarditis until 2025.
Pages 6-8:
Pages 6-8:
Despite reports of 82% miscarriage rates in women who have received the "vaccine", Pfizer-BioNTech no "black box" warning is required. This critical safety issue will merely be studied until 2025.
Pages 9-10:
Pages 9-10:
The link on the last page of the approval letter is not working.
Page 11:
Page 11:
The FDA approval letter was sent to Pfizer-BioNTech by Mary Malarkey.
Mary A. Malarkey Director
(Named on the Pfizer-BioNTech approval letter)
Office of Compliance and Biologics Quality
Center for Biologics Evaluation and Research
240-402-9008
Mary.Malarkey@fda.hhs.gov
https://www.federalpay.org/employees/food-and-drug-administration/malarkey-mary-anne
https://www.linkedin.com/in/mary-malarkey-a8062998/
(Named on the Pfizer-BioNTech approval letter)
Office of Compliance and Biologics Quality
Center for Biologics Evaluation and Research
240-402-9008
Mary.Malarkey@fda.hhs.gov
https://www.federalpay.org/employees/food-and-drug-administration/malarkey-mary-anne
https://www.linkedin.com/in/mary-malarkey-a8062998/
Marion F. Gruber, PhD
(Named on the Pfizer-BioNTech approval letter)
Director
Office of Vaccines Research and Review
Center for Biologics Evaluation and Research
301-796-1856
Marion.Gruber@fda.hhs.gov
(Named on the Pfizer-BioNTech approval letter)
Director
Office of Vaccines Research and Review
Center for Biologics Evaluation and Research
301-796-1856
Marion.Gruber@fda.hhs.gov
Truth is stranger than fiction.
You simply cannot make this kind of stuff up.
DOWNLOAD ADDITIONAL DOCUMENTS
I will be analyzing these documents as soon as possible.
I will be analyzing these documents as soon as possible.
Another letter sent from the FDA to Pfizer-BioNTech.
| fda-letter-final_pfizer-loa-to-issue-with-bla-approval-08.23.21.pdf |
COMIRNATY Package Insert
| package_insert_-_comirnaty.pdf |
UPDATED PFIZER-BIONTECH FACT SHEET
FOR HEALTHCARE PROVIDERS
ADMINISTERING VACCINES
(VACCINATION PROVIDERS)
https://labeling.pfizer.com/ShowLabeling.aspx?id=14471
FOR HEALTHCARE PROVIDERS
ADMINISTERING VACCINES
(VACCINATION PROVIDERS)
https://labeling.pfizer.com/ShowLabeling.aspx?id=14471
| emergency_use_full_prescribing_info_hcp__fact_sheet_pfizer-b.pdf |
SCREENSHOTS
FROM THE FACT SHEET:
INGREDIENTS
Pages 33-34:
The Pfizer-BioNTech COVID-19 Vaccine is supplied as a frozen suspension in multiple dose vials; each vial must be diluted with 1.8 mL of sterile 0.9% Sodium Chloride Injection, USP prior to use to form the vaccine.
Each dose of the Pfizer-BioNTech COVID-19 Vaccine contains
30 mcg of a nucleoside-modified messenger RNA (modRNA) encoding the viral spike (S) glycoprotein of SARS-CoV-2.
What is the actual sequence of the RNA?
What is the actual structure of the protein that it will cause the body to generate?
IS THIS SPIKE PROTEIN CURRENTLY CIRCULATING AMONG THE GENERAL POPULATION OR ARE PEOPLE BEING "VACCINATED" AGAINST A PROTEIN THAT IS NO LONGER BEING SEEN IN THE MORE RECENT VARIANTS?
___
Each dose of the Pfizer-BioNTech COVID-19 Vaccine also includes the following ingredients (CLICK ON THE RED LINKS):
LIPIDS:
(0.43 mg (4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)
.05 mg 2[(polyethylene glycol)-2000]- N,N-ditetradecylacetamide
0.09 mg 1,2-distearoyl-sn-glycero-3-phosphocholine
and 0.2 mg cholesterol)
SALTS:
0.01 mg potassium chloride
0.01 mg monobasic potassium phosphate
0.36 mg sodium chloride
0.07 mg dibasic sodium phosphate dihydrate
6 mg sucrose.
The diluent (0.9% Sodium Chloride Injection, USP) contributes an additional 2.16 mg sodium chloride per dose.
CONTAMINANTS?:
Many people have documented their claims that vials of Pfizer-BioNTech's injectable bioweapon contain graphene oxide.
Pages 33-34:
The Pfizer-BioNTech COVID-19 Vaccine is supplied as a frozen suspension in multiple dose vials; each vial must be diluted with 1.8 mL of sterile 0.9% Sodium Chloride Injection, USP prior to use to form the vaccine.
Each dose of the Pfizer-BioNTech COVID-19 Vaccine contains
30 mcg of a nucleoside-modified messenger RNA (modRNA) encoding the viral spike (S) glycoprotein of SARS-CoV-2.
What is the actual sequence of the RNA?
What is the actual structure of the protein that it will cause the body to generate?
IS THIS SPIKE PROTEIN CURRENTLY CIRCULATING AMONG THE GENERAL POPULATION OR ARE PEOPLE BEING "VACCINATED" AGAINST A PROTEIN THAT IS NO LONGER BEING SEEN IN THE MORE RECENT VARIANTS?
___
Each dose of the Pfizer-BioNTech COVID-19 Vaccine also includes the following ingredients (CLICK ON THE RED LINKS):
LIPIDS:
(0.43 mg (4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)
.05 mg 2[(polyethylene glycol)-2000]- N,N-ditetradecylacetamide
0.09 mg 1,2-distearoyl-sn-glycero-3-phosphocholine
and 0.2 mg cholesterol)
SALTS:
0.01 mg potassium chloride
0.01 mg monobasic potassium phosphate
0.36 mg sodium chloride
0.07 mg dibasic sodium phosphate dihydrate
6 mg sucrose.
The diluent (0.9% Sodium Chloride Injection, USP) contributes an additional 2.16 mg sodium chloride per dose.
CONTAMINANTS?:
Many people have documented their claims that vials of Pfizer-BioNTech's injectable bioweapon contain graphene oxide.
It is not possible to determine whether or not the production of the "S antigen" elicits an immune response to the "S antigen" because the "S antigen" is a variable protein which is likely no longer in circulation within the general population. This injectable bioweapon is triggering an immune response to a protein to which people are no longer being exposed.
The studies are too old. If SARS-CoV-2 even exists, it has mutated more than enough to escape the antibodies that Pfizer-BioNTech's "vaccine" claims to trigger a response to.
This is a false and deceptive claim.
Clearly, the Pfizer-BioNTech "vaccine" does not "protect against COVID-19."
Page 34:
The studies are too old. If SARS-CoV-2 even exists, it has mutated more than enough to escape the antibodies that Pfizer-BioNTech's "vaccine" claims to trigger a response to.
This is a false and deceptive claim.
Clearly, the Pfizer-BioNTech "vaccine" does not "protect against COVID-19."
Page 34:
PAGE 1
To access future updates of this fact sheet, visit:
https://www.cvdvaccine.com/
https://www.cvdvaccine.com/
The expiration dates on existing products have been extended by 3 months.
???
???
PAGES 2-3
It is NOT okay to mix and match vaccines.
Page 4:
Page 4:
After dilution, each vial contains 6 doses, even though the package may state that it contains 5 doses. It is questionable that every vaccine provider clearly understands this discrepancy.
Pages 5-8:
Pages 5-8:
How many people have died or been permanently damaged by "vaccine" induced myocarditis and pericarditis?
Pages 8-9:
Pages 8-9:
No comment necessary.
Page 9:
Page 9:
It is HIGHLY unlikely that the drug stores and other "vaccine providers" are reporting adverse events suffered by the people who have received vaccines. The follow-up and tracking of patients' conditions by the people who administered the "vaccine" is nearly non-existent.
Page 11:
Page 11:
WHERE IS THE VAERS DATA?
WHERE IS THE DATA FROM V-SAFE?
Page 21:
WHERE IS THE DATA FROM V-SAFE?
Page 21:
SAFE???
It certainly seems that the Pfizer-BioNTech "vaccine" causes a substantially greater number of adverse reactions than placebo.
Pages 22-30:
Pages 22-30:
AGES 12-15
WHERE IS THE DATA
ON THE 16-17 YEAR OLDS?
AGES 18-55
AGES 56+
The New England Journal of Medicine reported that 82% of pregnant women who received the vaccine in their first trimester suffered miscarriages. This is absolutely a crime against humanity.
Page 32:
Page 32:
Page 33:
CLICK ABOVE FOR DETAILS
Pfizer-BioNTech's own data shows no evidence for use in immunocompromised individuals, but the FDA approves the "vaccine" for these people anyway??
Page 33:
Page 33:
The clinical trial data used to support the FDA approval appears to have been collected well BEFORE the emergence of the DELTA variant!
Page 35:
Page 35:
The DEFINITION of COVID-19 for the sake of these clinical trials only includes very mild symptoms and a RT-PCR test.
Page 36:
Page 36:
THE FOLLOWING
IS FROM
TRIAL SITE NEWS
IS FROM
TRIAL SITE NEWS
- The vaccines are more likely to kill you than save you. The clinical trial (gold-standard medical research) evidence to date shows the vaccine kills more people than it saves (including Pfizer’s own 6 month randomized study which demonstrated a 7% higher overall death rate for those administered the vaccine. The vaccine reduced COVID deaths by 50%, however this came at the cost of increasing deaths from cardiac arrest and other causes, so that the net benefit is negative, i.e., the vaccine is more likely to kill you than save you. For example, Pfizer’s own study showed deaths from COVID were reduced by a factor of 2, but this saving was more than offset by deaths from cardiac arrest which went up by 4X. This is not a good tradeoff. The safety data in VAERS compared with the CDC data on mortality for different age cohorts also confirms that the vaccines are more likely to harm than help.
- No autopsies have ever been done in the US on patients who die after getting the vaccine to determine if the vaccine contributed to the death. It is astonishing there are 13,068 death reports in VAERS without even a single autopsy being done in the US and nobody in academia, Congress, or the mainstream media has called for autopsies. Autopsies are a huge risk for them because if they are done, people will realize just how unsafe these vaccines really are.
- Pathology reports from one of the world’s top pathologists showed that at least 30% of the deaths within 2 weeks of vaccination were due to the vaccine. He was immediately criticized by people who never examined the bodies!?! Calls by the Federal Association of German Pathologists to require autopsies in vaccinated patients who have died have been ignored by the German authorities. They don’t want to find out the truth either because once people learn how deadly the vaccines are, nobody will want to be vaccinated.
- No analysis has been done of the obviously elevated neurological and cardiovascular events in the VAERS system (see table below). How can a safe vaccine cause all of these events to skyrocket vs. previous years?
- A broken formula for adverse-event signal detection keeps the CDC from detecting safety signals that would alert the CDC of a problem with the vaccines. The CDC will not meet with us to discuss this serious error. They have no interest in seeing safety signals, so maintaining an obviously broken system gives them all plausible deniability.
- A callous disregard for the health of our children. There are 18 deaths in VAERS for kids between 12 and 17. Five of those deaths are from cardiac arrest and none are from cancer. Yet the CDC says deaths from cancer are twice as likely than deaths from heart disease for teenagers. So the vaccine is clearly killing our kids by elevating cardiac arrests way above normal. Ignoring this is tragic. This UK article points out that just 1 in every 1.7 million children have died with Covid-19 in 18 months, while 1 in every 9 children suffered a serious adverse reaction to the Pfizer vaccine in the small and short clinical trial which left them unable to perform daily activities. Mothers should be absolutely furious about this data being hidden from them.
- Refusal to listen to scientifically qualified VAERS experts who had analyses showing the vaccines were extremely unsafe, including Dose 1 vs. Dose 2 causality analyses that clearly showed the vaccines were causing significant adverse events. Dose-dependency is a very clear sign of causality but the FDA and CDC refuse to look at the data.
- Failure to investigate clinical trial fraud such as 12-year-old Maddie de Garay, paralyzed in the Pfizer clinical trial, despite assurances by the head of the FDA that this would be investigated. The Pfizer clinical trial reported Maddie’s adverse event as abdominal pain with no mention of her severe neurological issues.
- An American death toll estimate of 150,000 can be calculated 5 different ways (and the FDA and CDC wouldn’t look at any of them).
- Lack of any safety data on original antigenic sin aka linked-epitope suppression and ADE. In short, these vaccines may make the disease worse, not better, and the FDA knows both of these are risks, but the FDA isn’t waiting for the data to find out. In addition, there was never a proper safety study that measured the amount, duration, and distribution of the cytotoxic spike protein in non-human primates.
- A safer, more effective alternative exists: early treatment. Early treatment protocols, such as the Fareed-Tyson protocol have more than a 99% relative risk reduction, work for all variants, and have negligible side effects making them safer and more effective than any vaccine. The NIH and FDA ignore these early treatments.
- Too many open questions about the vaccine that still need to be answered. Peter Doshi’s excellent op-ed in the BMJ points out that the list of concerns is now even longer than before, and the fact that the FDA did not seek input from the advisory committee as they had promised to do, is extremely troubling for a drug that is now being mandated.
- Use of censorship, rather than open public discussion, to help the public discover the truth about these vaccines. We have 16 experts covering all aspects of COVID. Nobody in the world from academia or any government agency will publicly engage with us on any topic related to vaccine safety. Instead, they censor us. What are they all afraid of?
However, the FDA doesn’t deserve all the credit. A number of other groups contributed to this remarkable “accomplishment”:
- The CDC ACIP members, charged with safety monitoring, refused to listen to any evidence that there might be a safety problem with the vaccines or a problem with their safety signal monitoring algorithm.
- Medical academia who refused to demand autopsies on people who died within 2 weeks after vaccination, refused to demand a death-stopping condition for the EUA, refused to look at the VAERS data, and refused to openly debate anyone with divergent views (such as our team). The Stanford team who did listen to our concerns said they could not dispute what we said but that it didn’t matter because the decision on mandating vaccination for students was made at a higher level.
- Medical journals who refused to publish papers that went against the narrative even after peer review and galley proofs were accepted.
- Mainstream media that ignored vaccine victims, including Maddie de Garay, even though this was clear clinical trial fraud. They refused to give any voice to qualified people such as Robert Malone and Peter McCullough.
- Social networks including YouTube, Facebook, and Twitter who did a marvelous job censoring anyone who has views that are different from the narrative espoused by the CDC, WHO, and US government. For example, when people in the Facebook vaccine side effects group started pointing out that the drug companies made it difficult-to-impossible to report adverse events in the Phase 3 clinical trials, Facebook removed the groups so that all evidence of clinical trial fraud would be covered up and so that vaccine victims would never discover that hundreds of thousands of other people had been disabled by the vaccines.
- Members of Congress and their staff for refusing to seriously listen to any constituent who brought up legitimate safety concerns with the vaccines that were backed with primary data. Rather than explain how the evidence presented could possibly be consistent with a safe vaccine, the Members and their staff simply told their constituents that they were wrong and refused to read the evidence presented to them.
Today, all of these groups are proud of what they have accomplished: a coordinated effort to suppress legitimate scientific evidence and dissent through censorship and intimidation and approve a vaccine that has caused enormous death and disability in America that has no scientific evidence whatsoever of an all-cause mortality benefit.
It’s a sad day in AmericaWe salute scientists and doctors who are not afraid to speak out like Dr. Robert Malone, Dr. Peter McCullough, Dr. Geert Vanden Bossche, Dr. Sucharit Bhakdi, Dr. Bret Weinstein, Dr. Byram Bridle, Dr. Chris Martenson, Dr. Ryan Cole, Dr. Charles Hoffe, Dr. Francis Christian, Dr. Sin Hang Lee, Dr. Jessica Rose, Dr. Tess Lawrie, as well as courageous journalists including Del Bigtree, Joe Rogan, and former NY Times reporter Alex Berenson, and others who are the real truth tellers here.
America should be listening to and embracing all of these people, not ignoring them.
Finally, here is a table of elevated adverse events that was extracted from the VAERS system. Anyone can replicate this table. The methodology is described starting on page 41 of this document. This is not a complete list. What this table shows is that this is the most deadly vaccine ever produced in modern times. Every cardio and neurological symptom we looked at was elevated. These events are consistent with the mechanism of action of the vaccines (causing a cytotoxic spike protein to be produced inside all organs).
No vaccine in recent times has a breadth of impact as wide as these vaccines.
Thanks to the FDA and others, we’ll now be mandating these very deadly vaccines for all our kids.
NAVIGATION:
SKY NEWS
DISCLAIMER:
THE INFORMATION
ON THIS WEBSITE IS FOR
INFORMATIONAL PURPOSES ONLY.
I AM NOT RECOMMENDING
THAT PEOPLE TAKE IVERMECTIN
OR ANY OTHER MEDICATION.
I AM RECOMMENDING
THAT EVERYONE SHARE THIS
INFORMATION WITH THEIR DOCTOR
SO THAT THEY CAN LEARN
MORE ABOUT IVERMECTIN.
CONSULT WITH YOUR PREFERRED
HEALTH CARE PROFESSIONAL
TO DETERMINE WHAT IS
BEST FOR YOUR HEALTH.
ON THIS WEBSITE IS FOR
INFORMATIONAL PURPOSES ONLY.
I AM NOT RECOMMENDING
THAT PEOPLE TAKE IVERMECTIN
OR ANY OTHER MEDICATION.
I AM RECOMMENDING
THAT EVERYONE SHARE THIS
INFORMATION WITH THEIR DOCTOR
SO THAT THEY CAN LEARN
MORE ABOUT IVERMECTIN.
CONSULT WITH YOUR PREFERRED
HEALTH CARE PROFESSIONAL
TO DETERMINE WHAT IS
BEST FOR YOUR HEALTH.
FINANCIAL DISCLOSURE:
I HAVE ABSOLUTELY
NO FINANCIAL STAKE
IN ANY BUSINESS
RELATED TO IVERMECTIN
OR COVID-19.
THIS IS A LABOR OF LOVE
THAT IS DONE
FOR THE GOOD OF ALL.
JAMES ROGUSKI
310-619-3055
.
This action is not currently available.
PLEASE SHARE THIS INFORMATION
WITH EVERYONE YOU POSSIBLY CAN.
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