#FDA confirms, the mRNA vaccines are causing statistically severe risk of #myocarditis in 18-39 year olds!
> Risk Ratio is between 2x-24x higher than controls.
> Controls are not unvaccinated individuals, but they are comparing rates of days 0-7 to days 22-42 in vaccinated.
> This means that real risk is likely even higher, since real controls are missing.
Source: Vaccines and Related Biological Products Advisory Committee – 6/7/2022
@USMortality
> Risk Ratio is between 2x-24x higher than controls.
> Controls are not unvaccinated individuals, but they are comparing rates of days 0-7 to days 22-42 in vaccinated.
> This means that real risk is likely even higher, since real controls are missing.
Source: Vaccines and Related Biological Products Advisory Committee – 6/7/2022
@USMortality
Three months ago the #FDA approves the first genetically engineered #cows for the market, bred with #CRIPSR tech.
These cows are supposed to be "bred for climate change" and heat resistant.
Now you're telling me 5,000 cows died last week, "due to a heat wave"?? (which looked like total b.s.)
I bet those dead "heat wave" cows are going to be used to sell the new GMO cow technology..... You see what I'm saying?
@jordansather
These cows are supposed to be "bred for climate change" and heat resistant.
Now you're telling me 5,000 cows died last week, "due to a heat wave"?? (which looked like total b.s.)
I bet those dead "heat wave" cows are going to be used to sell the new GMO cow technology..... You see what I'm saying?
@jordansather
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Three #FDA Advisors Resign over Agency's Approval of Shoddy New #Alzheimer's Drug
In November 2020, an independent panel slammed Aduhelm, a new Alzheimer's drug just approved by the FDA. When asked if there was supportive evidence for the use of this drug, zero out of the seven panel members said yes.
"The drug, Aduhelm, a monthly infusion priced at $56,000 per year, was approved this week despite weak evidence that it helps patients," reported The New York Times.
Full Episode: https://thehighwire.com
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In November 2020, an independent panel slammed Aduhelm, a new Alzheimer's drug just approved by the FDA. When asked if there was supportive evidence for the use of this drug, zero out of the seven panel members said yes.
"The drug, Aduhelm, a monthly infusion priced at $56,000 per year, was approved this week despite weak evidence that it helps patients," reported The New York Times.
Full Episode: https://thehighwire.com
Follow @VigilantFox 🦊
Rumble | Substack | Support | Socials
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New #safe and #effective injection for #pregnant women approved by #FDA
– At Today's FDA VRBPAC Meeting to Review #Pfizer's Maternal #RSV Vaccine, Dr. Paul Offit Got Into a Tense Exchange w/ the FDA and Pfizer
Offit: "GSK also had a maternal vaccine program. Their vaccine was almost identical to this vaccine...they had a problem with premature births...If GSK has truly abandoned a program on an almost identical vaccine...it does need to be addressed."
Pfizer: "There's the real opportunity then to look at this...when we have larger numbers of women being vaccinated to determine whether or not there is in fact any sort of a signal...We can investigate that again post-approval."
https://twitter.com/TheChiefNerd/status/1659313234212450307
https://childrenshealthdefense.org/defender/fda-recommends-pfizer-rsv-vaccine-pregnant-women/
@ChiefNerd
– At Today's FDA VRBPAC Meeting to Review #Pfizer's Maternal #RSV Vaccine, Dr. Paul Offit Got Into a Tense Exchange w/ the FDA and Pfizer
Offit: "GSK also had a maternal vaccine program. Their vaccine was almost identical to this vaccine...they had a problem with premature births...If GSK has truly abandoned a program on an almost identical vaccine...it does need to be addressed."
Pfizer: "There's the real opportunity then to look at this...when we have larger numbers of women being vaccinated to determine whether or not there is in fact any sort of a signal...We can investigate that again post-approval."
https://twitter.com/TheChiefNerd/status/1659313234212450307
https://childrenshealthdefense.org/defender/fda-recommends-pfizer-rsv-vaccine-pregnant-women/
@ChiefNerd
The #FDA Wants People To Report “Misinformation”
In a recent announcement, the US Food and Drug Administration (FDA) has revealed the launch of a webpage designed to address and curtail what it says is the spread of misinformation related to health and medical topics online. This initiative, known as the “Rumor Control” page invites users to report instances of perceived misinformation on the internet, particularly on social media platforms
https://reclaimthenet.org/the-fda-wants-people-to-report-misinformation
In a recent announcement, the US Food and Drug Administration (FDA) has revealed the launch of a webpage designed to address and curtail what it says is the spread of misinformation related to health and medical topics online. This initiative, known as the “Rumor Control” page invites users to report instances of perceived misinformation on the internet, particularly on social media platforms
https://reclaimthenet.org/the-fda-wants-people-to-report-misinformation
Reclaim The Net
The FDA Wants People To Report “Misinformation”
Join Reclaim The Net.
#FDA says soda sweetener #aspartame is safe, disagreeing with #WHO finding on possible #cancer link
🤡
https://www.cnbc.com/2023/07/14/fda-says-aspartame-is-safe-disagrees-with-who-on-possible-cancer-link.html
🤡
https://www.cnbc.com/2023/07/14/fda-says-aspartame-is-safe-disagrees-with-who-on-possible-cancer-link.html
CNBC
FDA says soda sweetener aspartame is safe, disagreeing with WHO finding on possible cancer link
The FDA said the studies that World Health Organization experts relied on to make this conclusion had "significant shortcomings."
BOMBSHELL: Ivermectin Is Now OK To Treat COVID! – Says The FDA
Now that the pharmaceutical industry has made its hundreds of billions from vaccines, and despite an all out smear campaign the agency itself participated in, the Food & Drug Administration has approved the drug Ivermectin as a treatment for COVID. So it turns out that, according to the FDA, it’s OK even if you’re not a horse for you to take Ivermectin to treat your COVID. That’s what you call a win-whinny.
Guest host Craig “Pasta” Jardula, along with Jimmy Dore and Americans’ Comedian Kurt Metzger discuss why Ivermectin had to be so severely demonized during the early days of the pandemic but now can be approved in such a cavalier fashion.
#Ivermectin #covid #BigPharma #FDA
Now that the pharmaceutical industry has made its hundreds of billions from vaccines, and despite an all out smear campaign the agency itself participated in, the Food & Drug Administration has approved the drug Ivermectin as a treatment for COVID. So it turns out that, according to the FDA, it’s OK even if you’re not a horse for you to take Ivermectin to treat your COVID. That’s what you call a win-whinny.
Guest host Craig “Pasta” Jardula, along with Jimmy Dore and Americans’ Comedian Kurt Metzger discuss why Ivermectin had to be so severely demonized during the early days of the pandemic but now can be approved in such a cavalier fashion.
#Ivermectin #covid #BigPharma #FDA
Court Revives Doctors' Lawsuit saying FDA Overstepped its Authority with Anti-Ivermectin Campaign
#fda
#fda
FLCCC Alliance
FLCCC Alliance Statement on Court’s Reversal of Case Against DHHS for Telling the Public to “Stop it” Regarding Taking Ivermectin…
WASHINGTON, D.C. – Yesterday, the Fifth Circuit Court of Appeals reversed a lower court's ruling that “sovereign immunity” protects the Food and Drug Administration (FDA) from any wrongdoing or harm in telling the public to stop taking ivermectin, a safe…
The #FDA is playing a new game with the COVID vaccines. Instead of allowing the #DOD and other agencies to get wrapped up in lawsuits surrounding the use of #EUA and FDA authorization (since we're no longer under an emergency order and they never had any intention of producing the FDA authorized drug for liability reasons), the new labels don't say anything. If you dig a little further, you can see the last page on Dailymed says it's an "unnaproved drug."
According to the FDA, “Unapproved prescription drugs pose significant risks to patients because they have not been reviewed by FDA for safety, effectiveness or quality. Without FDA review, there is no way to know if these drugs are safe and effective for their intended use, whether they are manufactured in a way that ensures consistent drug quality or whether their label is complete and accurate.
https://twitter.com/samosaur/status/1699859009560252726
According to the FDA, “Unapproved prescription drugs pose significant risks to patients because they have not been reviewed by FDA for safety, effectiveness or quality. Without FDA review, there is no way to know if these drugs are safe and effective for their intended use, whether they are manufactured in a way that ensures consistent drug quality or whether their label is complete and accurate.
https://twitter.com/samosaur/status/1699859009560252726
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Great deal!
3 for 1 never tested before combo! For free!
#FDA in the US is approving a COVID-19 booster as part of a trio of vaccines slated to be released with the goal of avoiding a "tripledemic"🤣 of COVID, RSV and flu this fall.
Go ahead and demand proof about how they know it's safe or effective, CIA and the department of war may have them
3 for 1 never tested before combo! For free!
#FDA in the US is approving a COVID-19 booster as part of a trio of vaccines slated to be released with the goal of avoiding a "tripledemic"🤣 of COVID, RSV and flu this fall.
Go ahead and demand proof about how they know it's safe or effective, CIA and the department of war may have them
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#FOIA Documents Reveal the COVID Plandemic Was a #DoD Operation Dating Back to Obama
"The #Pentagon controlled the COVID-19 program from the very beginning and everything we were told was political theater to cover it up right down to the #FDA vaccine approval"
Join ➣ 👉@COVID19VACCINEVICTIMSANDFAMILIES
#foreknowledge #ww3 #safe #effective
"The #Pentagon controlled the COVID-19 program from the very beginning and everything we were told was political theater to cover it up right down to the #FDA vaccine approval"
Join ➣ 👉@COVID19VACCINEVICTIMSANDFAMILIES
#foreknowledge #ww3 #safe #effective
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#RFK: "The #FDA has just approved a shot, the new Covid shot for people all over the country....And that decision was utterly irresponsible because they've never done a study on it."
#trials #safe #effective
#trials #safe #effective
FDA Finds Safety Signal for COVID-19 Vaccination Among Toddlers
“Seizures/convulsions ‘met the statistical threshold for a signal’ in children aged 2 to 4 following receipt of a Pfizer COVID-19 vaccine and #children aged 2 to 5 following receipt of a Moderna COVID-19 vaccine, researchers with the #FDA and three large healthcare companies said in a new preprint study.
A safety signal is a sign that a health condition may be caused by vaccination, but further research is required to verify a link.
Overall, 72 cases of seizures/convulsions were recorded within seven days of a shot among toddlers and other young children. Most happened within three days of a shot.”
https://x.com/thechiefnerd/status/1714754028905586717
Full Story: https://bit.ly/48ZRIjf
@ChiefNerd
#safe #effective
“Seizures/convulsions ‘met the statistical threshold for a signal’ in children aged 2 to 4 following receipt of a Pfizer COVID-19 vaccine and #children aged 2 to 5 following receipt of a Moderna COVID-19 vaccine, researchers with the #FDA and three large healthcare companies said in a new preprint study.
A safety signal is a sign that a health condition may be caused by vaccination, but further research is required to verify a link.
Overall, 72 cases of seizures/convulsions were recorded within seven days of a shot among toddlers and other young children. Most happened within three days of a shot.”
https://x.com/thechiefnerd/status/1714754028905586717
Full Story: https://bit.ly/48ZRIjf
@ChiefNerd
#safe #effective
#FDA Fails to Address #DNA Adulteration Concerns
FDA’s Dr. Peter Marks resorts to gaslighting instead of facts in his response to Florida Surgeon General Inquiry
https://vigilantnews.com/post/fda-fails-to-address-dna-adulteration-concerns/
Follow @Vigilant_News
FDA’s Dr. Peter Marks resorts to gaslighting instead of facts in his response to Florida Surgeon General Inquiry
https://vigilantnews.com/post/fda-fails-to-address-dna-adulteration-concerns/
Follow @Vigilant_News
Vigilant News Network
FDA Fails to Address DNA Adulteration Concerns
FDA's Dr. Peter Marks resorts to gaslighting instead of facts in his response to Florida Surgeon General Inquiry
In a 2015 document, the #FDA defines #shedding as “the release of [viral or bacterial gene therapy products] ... from the patient through one or all of the following ways: excreta (feces); secreta (urine, saliva, nasopharyngeal fluids etc.); or through the skin (pustules, sores, wounds).”
https://www.zerohedge.com/political/covid-vaccine-shedding-real-fda-and-pfizer-documents-are-proof-clinicians
#safe #effective
https://www.zerohedge.com/political/covid-vaccine-shedding-real-fda-and-pfizer-documents-are-proof-clinicians
#safe #effective