21 Comments
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Jenna McCarthy's avatar

Funny, that’s not how the “media” spun it. 🤦‍♀️ https://open.substack.com/pub/jennamccarthy/p/breaking-fda-approves-new-covid-vaccines?

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Bonnie Lester's avatar

I am sooo happy! Ty RFK jr. ❤️.

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Craig g USMC's avatar

Great job Bobby, now let the lawsuits stack up and throw the pharma CEO'S in fuckin prison!!!

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Closed VAERS's avatar

FDA if they want to radically transparent should all full downloadable FAERS files just like VAERS!

https://welcometheeagle.substack.com/p/fda-faers-nefariously-hides-death

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Rob Landeros's avatar

The announcement should have included a statement that there should never have been any medical intervention mandates issued in the first place!

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Pony Wisdom's avatar

Finally reality is catching up with real science!

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Craig g USMC's avatar

BTW the only ones jabbing are the libtards lolol KEEP BOOSTING, Y'ALL WON'T BE MISSED

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Ray Flores's avatar

"Controversially, vaccines and other medicines taken under EUA are given a liability shield thanks to the 2005 Public Readiness and Emergency Preparedness (PREP) Act," is not accurate. Licensed CV VX is still protected by PREP currently through 12.31.29.

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Craig g USMC's avatar

WE TRUST THE SCIENCE NOT THE POLITICAL SCIENCE!! TIME TO TAKE DOWN FAUCI!!!

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Shanna L's avatar

RFKJ is the BEST! POTUS has the BEST administration Ever! 🇺🇸🇺🇸🇺🇸🇺🇸

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VictorDianne Watson's avatar

Thank you, Bobby!!

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John T's avatar

The FDA isn't following his goals. Take a look at this drug Lenacapavir. Approved on June 18, 2025.

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=220018

You can view what Gilead did from their website.

Per trial protocol, because PURPOSE 1 met its key efficacy endpoints of superiority of twice-yearly lenacapavir to bHIV and once-daily oral Truvada at interim analysis, the independent Data Monitoring Committee recommended that Gilead stop the blinded phase of the trial and offer open-label lenacapavir to all participants. As of July 23, more than 840 trial participants have already opted to switch to lenacapavir.

There is strike on to double blind.

Because effective PrEP options already exist, there is broad consensus in the PrEP field that a placebo group would be unethical; thus, the trial used bHIV as the primary comparator and Truvada as a secondary comparator.

There is strike two to double blind. FDA did approve it anyway. I am not a drug regulator, but I can find these things. People getting paid to look for our safety can't or don't care. Actions always speak louder than words.

https://www.gilead.com/news/news-details/2024/full-efficacy-and-safety-results-for-gilead-investigational-twice-yearly-lenacapavir-for-hiv-prevention-presented-at-aids-2024?utm_source=substack&utm_medium=email

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Edward Flynn's avatar

👍

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Messenger17's avatar

Excellent, more progress. I can only help but wonder what kind of spin the pharma propagaindists in the legacy media are putting on it. We're sure to have lots of misleading "news" on the way, that I would bet on, and I'm very averse to gambling.

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RandyDelivers's avatar

You are being taken for a ride folks.

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Alio McDavis's avatar

I feel like Alio in Wonderland. I certainly did overestimate the intelligence on this ridiculous planet when I bought my ticket. It's going to get more interesting when more people learn about the extraterrestrial persuasions and directives that are driving humanity into a digital corral via their hybrids and human operatives at Davos. I'm dead serious and almost sober. Anyone interested in the ET presence and whatever that might have to do with what we are witnessing ought to scan "The Briefings"

Here, if you want them, www.alliesofhumanity.org/the-briefings

I've been on the ET thing for 50 years and I think you can take my word, the briefings are important. BTW Who blew up The Georgia Guidestones?

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