Johnson & Johnson – What’s The End Game?
So much more is at stake here and its aimed at the most vulnerable of our population. Our children. On Feb. 26, the FDA announced that the agency granted another Emergency Use Authorization ; this time for for Johnson & Johnson’s COVID vaccine. Claiming that “we’re in a hurry” because there’s not enough supply of the two COVID-19 vaccines already authorized for emergency use — Pfizer’s and Moderna’s — members of FDA’s committee agreed without dissent to allow a third COVID injection.
Well, the mainstream media is applauding the emergency approval of J&J’s COVID vaccine and the company’s plans to team up with Merck on productions. As if to imply they are forgoing profits for an altruistic humanity driven purpose. Not a chance!
The Washington Post on March 2 offered the write up of an “historic” production partnership between J&J and Merck, Normally intense competitors.” Many say J&J’s one-dose injections, which are storable for several months at refrigerator temperatures, as the ideal solution for vaccination as today health care is challenged by the difficult storage of the two-dose Pfizer and Moderna shots. The press is all about positivity. Let’s not focus on the rush to market. Or lack of long-term safety and efficacy information. Okay… And, in all the fanfare, I have yet to see any coverage of the safety data, known safety concerns or theses two big pharma companies criminal track records. Nothing sinister going on that pushed this from end of year to March release. Or is there?
Pfizer and Moderna injections are using a new mRNA technology but this one is using a genetically engineered “viral vector” design reliant on a weakened common-cold virus called adenovirus 26. A microbiologist shared this approach is immunologically powerful, saying that the modified adenovirus vector is “about as subtle as a wrecking ball” and “very visible to the immune system.” The vectors’ has the ability to generate damaging and even fatal inflammatory effects, vaccine researchers embraced the strategy anyway and following discovered that booster shots might “unleash an antibody attack on the vaccine itself.” And then yet another problem when it conducted clinical trials for an adenoviral-vectored HIV vaccine that appeared increased the risk of HIV infection in some and they stopped all developments. Until now.
Now we move to Ethical problems. Catholic Bishops, which expressed concern about the development of COVID-19 vaccines reliant on cell lines. Yep, you got it aborted fetal cells. The cell line in which Janssen grows its adenovirus vector is a human embryonic cell line called PER.C6. The retinal tissue that launched the cell line was obtained following the elective abortion of a healthy, 18-week-old fetus. The AstraZeneca-Oxford COVID vaccine uses a different human embryonic cell line called HEK293T to propagate its adenovirus. My understanding both were from the Netherlands…
To produce a continuous cell line of this type — what is called an “immortalized” cell line — scientists must artificially manipulate the original cells, which otherwise would have finite lifespans. This is accomplished by introducing chemical exposures or rendering them cancerous. Because this manipulation introduces genetic changes into the cells, “cell populations and cellular mechanisms are altered.” A senior FDA official warned over two decades ago about the inherent risks of using continuous cell lines for vaccine development, noting that such cell lines, “by definition” have abnormalities, and worriedly acknowledging their “potential for growing tumors in laboratory animals.” An FDA document published in late 2020 shows that these issues are far from resolved; explicitly referring to cell lines such as PER.C6 and HEK293T, the FDA author states: “The use of tumorigenic and tumor-derived cells is a major safety concern” and observes that the cell lines contain “latent” or “quiet” threats that “might become active under vaccine manufacturing conditions.” The fact sheet for healthcare providers administering the J&J COVID vaccine specifies that each dose of vaccine “may … contain residual amounts of host cell proteins … and/or host cell DNA,” but the simplified fact sheet intended for vaccine recipients and their caregivers does not.
That means that unless vaccine recipients seek out the healthcare provider fact sheet, they’ll be unaware of this potentially crucial piece of information.
The Italian vaccine research and advocacy organization, Corvelva, which has conducted detailed studies of DNA from aborted fetal cell lines in vaccines, warns that such DNA is abnormal and potentially tumor-causing. Corvelva concludes that vaccines of this type “should be considered defective and potentially dangerous to human health.”
Along with a variety of other inactive ingredients, the J&J COVID vaccine also includes polysorbate-80, a stabilizer that studies have shown capable of transporting other substances across the blood-brain barrier.
Consider the fact that they are a serial felon! When evaluating the potential safety of the J&J-plus-Merck experimental COVID vaccine, it would be prudent to take note of the corporate behemoths’ less-than-flattering track records as serial felons. Merck, for example, paid out $4.85 billion in 2007 after pleading guilty to criminal charges over illegal marketing of its lethal drug Vioxx. The company has gone on to face numerous other allegations of fraud, deceit and negligence, including for its measles, mumps and rubella (MMR) and human papillomavirus (HPV) vaccines.
For its part, J&J’s recent criminal history includes:
A 2013 order by the U.S. Department of Justice to pay $2.2 billion in civil and criminal fines related to the antipsychotic drug Risperdal and two other drugs, following aggressive off-label marketing and other dubious practices such as fraud and kickbacks.
A 2019 award by a Philadelphia jury of $8 billion in punitive damages to a man alleging that J&J failed to warn that Risperdal could lead to breast growth in boys. Thousands of other lawsuits against J&J feature the same allegation.
A $572 million judgment against J&J by the state of Oklahoma in 2019 for the company’s role in the opioid epidemic. Nearly 4 billion also set aside for lawsuits related to J&J’s cancer causing asbestos-tainted baby powder. Known as one of the largest punitive-damages awards in U.S. legal history, after internal documents showed that the company had been aware of the baby powder contamination since the 1970s.
Just this year they had to shut down the Vaccine because of distribution errors in the dilution of the vaccine. Add in, yet another Johnson and Johnson recall for its Sunscreen as it has now been linked to cancer. It’s a reoccurring theme and yet, the FDA, CDC and Federal Administration refuses to acknowledge that they are known felons.
With the advent of J&J’s COVID vaccine (an injection already being hawked as a “vaccine for the world” and the potential “end of the pandemic”), forgetting J&J’s paused clinical trial last October) or their recent association to blood clots from their COVID vaccine, it’s a shame that a great number of COVID-frightened Americans will line up for J&J’s experimental inoculation that, in the FDA’s words, is “not licensed for any indication.” Sadly, many of these individuals will be unaware that they cannot sue indemnified COVID vaccine manufacturers should anything go wrong under this emergency use.
But, is that all OR is there something more going on, something not being considered… and intentional and sinister in nature… I’d even suggest much more sinister.
Right now, under emergency use everyone takes a known risk that they could have adverse reactions.
Anticipating a big pay day, Johnson & Johnson now announced is preparing to initiate expanded clinical trials that will now in children (including newborns and infants) and pregnant women.
What happens when the Vaccines become FDA approved for Children…? It then goes before the ACIP and they add it to the childhood vaccination schedule. Mandating it be taken for school… It also means you cannot sue the manufacturer for death and injury… They become protected from all lawsuits… Summer is here and now is the time to demand that the CDC and ACIP stop experimenting on our children. Stand your ground.
Join us by becoming a part of the CHD Florida today to stop the onslaught of corruption and collusion.
