In response Lisa Groenewoud to her Publication

It is neither FOOD nor DRUG... How did the FDA have authority to imprison W. Reich?

Med Beds:

New Way of Healing! Med Bed, Quantum, Anti-Gravity, Concealed Technologies, Replicators & Perpetual Fountain of Youth – American Media Group (amg-news.com)

In 1900, a man named Wilhelm Reich invented a way to cure cancer, heart disease, arthritis, and thousands of other ailments, within a few 15-minute sessions of sitting in a box. How was this possible? The ‘box’ was a carefully crafted ‘orgone accumulator’ which concentrates the orgone energy or life energy “Chi / Prana”, and this has an incredible effect on patients. The FDA banned Wilhelm’s inventions and sentenced him to prison where he died in 1957.

I'm a research scientist in Private Practice Genetics & Genomics, Immunology & Infectious Disease, Biology, Integrated Biology & In

Pfizer, BioNTech Seek FDA Consent to Vaccinate Children Under Five Years Old - Geller Report

https://gellerreport.com/2022/12/pfizer-biontech-seek-fda-consent-to-vaccinate-children-under-five-years-old.html/?lctg=90994700

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Forwarded from
Ultra Pepe Deluxe (I'll never DM U to sell you Bitcoins...scammers).
(
Pepe Deluxe
)
https://www.pennlive.com/coronavirus/2022/12/pfizer-asks-fda-to-clear-updated-covid-19-vaccine-for-kids-under-5.html

Pfizer is asking U.S. regulators to authorize its updated COVID-19 vaccine for children under age 5 — not as a booster but part of their initial shots.

Children ages 6 months through 4 years already are supposed to get three extra-small doses of the original Pfizer COVID-19 vaccine — each a tenth of the amount adults receive — as their primary series. If the Food and Drug Administration agrees, a dose of Pfizer’s bivalent omicron-targeting vaccine would be substituted for their third shot.

just doesnt stop

TODAY IS THE LAST DAY!!!

No sugar coating: we're
brinking loss of homeopathy, a 220+ year record of safety/efficacy/cures.

PLEASE - 10 seconds to complete form. US resident not required.
The FDA regulated homeopathy since inception. It's written into legislation that created FDA. 2019 FDA drafted guidance to change homeopathy regulations. Guidance states all homeopathic medicines are unapproved new drugs/can’t be legally marketed/sold. Become legal through the new drug process designed for conventional drugs. Will fail since work VERY differently in body than chemical drugs. Draft guidance sent to White House to finalize and officiate. 90 day process for White House review. Americans for Homeopathy Choice meetimg canceled due to White House completed review/no changes. Suspiciously fast. Overwhelm FDA with concerns re: removing homeopathy from marketplace.
healthcare choice, please sign
https://homeopathychoice.org/tell-fda/#/20/

In response KrakenQrew _Zum to her Publication

They don't even have our best interest at heart...let alone the FDA....

Digital Warrior who took the Oath! Retired Caretaker of 3 Dogs! Beloved Father in Heaven, Deliver us from The Evil One!

"The FDA has also authorized 1169
revisions to EUA authorizations."

@SenateGOP @HouseGOP Can you
get a list of these changes?

Something tells me they're NOT in the
Best Interest of We The People.

#ULTRA-MAGA, Retired Navy and Patriot. The oath never expires as long as I'm alive. https://t.me/NakedMinotaur

In the Real World America

These Evil Demonic Individuals are trying to Poison and Kill our Children America

Pfizer Seeks FDA Authorization for Omicron Vaccine for Children Under 5
By Madeline Leesman December 05, 2022 5:30 PM
https://townhall.com/tipsheet/madelineleesman/2022/12/05/pfizer-seeking-authorization-for-omicron-vax-for-kids-under-5-yr-old-n2616754

Patriot loving truth and freedom. God wins. ❤️🙏 🇺🇸 #WWG1WGA 🐸

Pfizer Pushes For FDA Approval to Give Babies New Bivalent COVID-19 Shot
https://100percentfedup.com/pfizer-pushes-for-fda-approval-to-give-babies-new-bivalent-covid-19-shot/

In response Stephanie Foster to her Publication

Really should form coalitions and I am sure many do exist, grass roots, where fams could go in on cows, etc. together. AND LEGALLY sell deer. FDA is death admin from devils, MADE BY them, gotta rid ourselves of all that, GITMO again a very practical answer.

U.S. Navy Veteran. Investigative Researcher. Into The Fitness and Health Lifestyle. Lives in The North-East of The U.S.A.

• Sen. Ron Johnson: 'It's an Insane Policy' to Force Anyone to Take a Covid-19 Injection. "The bottom line here is the vaccine does not prevent infection — does not prevent transmission. So why would we make anybody take it?" asked Johnson.

"The fact of the matter is there are safety signals that anybody who's looking at CDC and NIH and FDA data might have cause for concern about. Now, part of our problem here is that the FDA, the CDC, and the NIH have not been honest. They have not been transparent." Plandemic Secrets:

https://greatawakening.world/plandemic1

• "Foot-Long Blood Clots" From mRNA, Says Pathologist Dr. Ryan Cole w/ Dr Kelly Victory – Ask Dr. Drew

• Operation Warp Speed: Millions of Americans Die Suddenly: https://www.naturalnews.com/2022-12-02-operation-warp-speed-millions-americans-died-suddenly.html

⌚ T̨͈͗̌ͥr̴̨̦͕̝ư̡͕̭̇ḿ̬̏ͤͅp̞̈͑̚͞s̠҉͍͊ͅ W̯ͤ̾ͣ͝o̯̱̊͊͢r̴̨̦͕̝l̙͖̑̾ͣḑ̴̞͛̒ 2024 -⒄ #𝐌𝐀𝐆𝐀 ➊➐➐➏ ╰┈➤ CheckMate .·:*¨༺ #𝕎𝕎𝔾𝟙𝕎𝕎𝔸 ༻¨*:·.

🤬🤬🤬
Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine in Children Under 5 Years

NEW YORK and MAINZ, Germany, December 5, 2022 — Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that the companies have submitted an application to the U.S. Food and Drug Administration (FDA) for emergency use authorization (EUA) of their Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine as the third 3-µg dose in the three-dose primary series for children 6 months through 4 years of age. With the high level of respiratory illnesses currently circulating among children under 5 years of age, updated COVID-19 vaccines may help prevent severe illness and hospitalization.

https://investors.biontech.de/news-releases/news-release-details/pfizer-and-biontech-submit-application-us-fda-emergency-use-1/

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