The J&J Shot has Been Restricted by the FDA
Is This Just Political Ass Covering? Or a Sign of Things to Come?
The Johnson&Johnson (AKA Jahnssen) Covid “vaccine,” marketed widely as a one and done, non mRNA deal before the obvious and never ending need for boosters was brought up, has been severely restricted in use by the FDA. This is the article that popped onto my email from MedPage regarding this.
“Due to an updated analysis of the rare cases of thrombosis with thrombocytopenia syndrome (TTS), which typically occur 1 to 2 weeks after vaccination, use of the J&J vaccine should be restricted to those for whom mRNA vaccines are "not accessible or clinically appropriate," or who would not get vaccinated if not for the J&J vaccine, the agency said.”
"The reporting rate of TTS is 3.23 per million doses of vaccine administered and the reporting rate of TTS deaths is 0.48 per million doses of vaccine administered," the FDA said in its announcement. The greatest risk is among women ages 30 to 49 years (about 8 cases per million doses).”
“Additional reasons for this action included that the risk factors for TTS were "unknown," that an individual with TTS may deteriorate rapidly "despite prompt diagnosis and treatment," and that TTS may have "long-term and debilitating" health consequences.”
So I’m going of dive into this a bit. Of course the FDA used the obligatory term “rare,” regarding the one specific side effect of TTS after the J&J jab. This shows progress from “extremely rare,” which is the most common quote used for adverse reactions, but I guess they can downgrade that since they’re not pushing this shot anymore.
They proceed to give very low numbers of deaths from this condition (less than 1 TTS death in 2 million jabs given), but say risk factors are “unknown,” after saying these blood clot issues arise most commonly in women in their 30’s and 40’s. Some of this seems contradictory.
Of course the FDA is extremely lowballing the numbers. The easies way to do this is through classification segmenting. How many thousands of symptoms might arise from a blood clot somewhere in the body? It could manifest as what is labelled as a stroke, a pulmonary embolism, a heart attack, or a brain aneurysm. By attaching one specific very narrow label and only allowing people with that label to be considered a “vaccine injury,” the field substantially narrows. That’s even before underreporting is taken into account.
The FDA’s numbers seem low to restrict the jab in this way. They didn’t suspend it, just walked it back. This strikes me as a type of ass covering. J&J wants out of the game.
I hope this is a sign of things to come for the other “safe and effective” jabs. What do you all think?
I think the FDA is a wholly corrupt entity and for them to even make this lukewarm half measures statement is a pretty good indication that the data is overwhelming.
They paused if for a year per the medpage link.
"Use of Johnson and Johnson's (J&J) COVID-19 vaccine should only be limited to certain adults, the FDA said on Thursday.
Due to an updated analysis of the rare cases of thrombosis with thrombocytopenia syndrome (TTS), which typically occur 1 to 2 weeks after vaccination, use of the J&J vaccine should be restricted to those for whom mRNA vaccines are "not accessible or clinically appropriate," or who would not get vaccinated if not for the J&J vaccine, the agency said."
Let's remember that the period within 1 to 2 weeks post "vaccination" has been dumped into the "unvaccinated" pile in the public health record keeping needed to continue the narrative of pandemic of the unvaccinated.
Even the best that they can finesse it, they see that this deal is going to come unraveled.
Isn’t this the one Alex Berenson said he’d take? 😂