FDA Corruption in the Spotlight at ACIP

Many people tell me that RFK, Jr. is a lunatic even though they haven't bothered to watched any of his videos. Never read any of his words. Well, he appointed a bunch of competent doctors and medical researchers to ACIP and for the first time in memory, Big Pharma and the FDA are being put under the spotlight. Here, the FDA effectively admits regulatory capture. Pharma has been its boss-and the FDA hasn't been questioning Pfizer's corrupt research. Real research is now showing that spike protein wanders all over the body (and lingers, damaging hearts and other organs) and the so-called COVID vax is contaminated by DNA. FDA: We can solve that problem by putting our head in the sand. That will protect Pfizer, our boss.

I am so very grateful that RFK, Jr. has cleaned house, but you'd never know the good things that are happening if you rely on corporate media.

Mary Talley Brown, MD, is a doctor who had her license threatened for using her medical judgment to treat COVID patients (instead of jamming endless boosters into her patients):

This is the most important exchange from the ACIP meeting. FDA admits to @KMilhoanMDPhD it has not performed independent inspection of mRNA shots for DNA contamination, instead relying on Pfizer and Moderna’s data. Multiple independent studies have shown excess levels of DNA contamination in these products, and @US_FDA is aware but not taking action.

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Stays in the Deltoid?

Remember when the CDC assured us that the the mRNA would "stay in the deltoid"? New ACIP board member Robert Malone asked how Pfizer determined that. I'll translate part of Pfizer's answer: We used the least sensitive test and we worked in close consultation with the corrupt people at the FDA. The CDC quietly removed this "will stay in the deltoid" phrasing from its site around 2022–2023 without explanation. A short highly disturbing video. I'm so very glad we have Robert Malone sitting on the ACIP board to ask real questions.

And it's incredible how many things non-curious financially incentivized companies don't know.

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“Safe and Effective” Drugs

At least 100 drugs once considered "safe and effective" for their intended uses (based on clinical trial data submitted by manufacturers) have been taken off the market due to how dangerous they were. Well-known examples include Thalidomide, Vioxx and Bextra, which have caused tens of thousands of deaths and injuries.

The presenter in this video is Simone Gisondi, host of the podcast "The Health Confidential with Simone Gisondi."

Based on FDA and global regulatory data, here are 20 recently withdrawn drugs (sorted most recent first, with year and reason):

1. Oxbryta (2024) - Increased deaths/complications in sickle cell patients.

2. Makena (2023) - Lack of effectiveness.

3. Ranitidine (Zantac, 2020) - Carcinogen contamination.

4. Lorcaserin (Belviq, 2020) - Cancer risk.

5. Ingenol mebutate (2020) - Skin cancer risk.

6. Flupirtine (2018) - Liver toxicity.

7. Tetrazepam (2013) - Skin reactions.

8. Drotrecogin alfa (2011) - No efficacy.

9. Gemtuzumab ozogamicin (2010) - Death risk.

10. Propoxyphene (2010) - Heart risks.

11. Rosiglitazone (2010) - Heart attacks.

12. Sibutramine (2010) - Heart attack/stroke.

13. Sitaxentan (2010) - Liver damage.

14. Lumiracoxib (2008) - Liver damage.

15. Rimonabant (2008) - Depression/suicide.

16. Aprotinin (2008) - Death risk.

17. Pergolide (2007) - Heart valve damage.

18. Tegaserod (2007) - Heart attack/stroke.

19. Clobutinol (2007) - Arrhythmias.

20. Alatrofloxacin (2006) - Liver toxicity.

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