top of page

J&J's Vaccine Removed from US Market Due to Blood Clot Deaths

19 million Americans who took the vaccine could now have a 'ticking time-bomb' in their system.

The Food and Drug Administration (FDA) has revoked authorization of Johnson & Johnson’s Covid-19 vaccines due to deaths and serious injuries becoming impossible to ignore.

The ban was at the request of J&J’s parent company, Janssen. Dr Peter Marks, Director of the FDA’s Center for Biologics Evaluation and Research said: "Because FDA understands that… Janssen Biotech, Inc. has requested that FDA withdraw the EUA for the Janssen COVID-19 Vaccine, FDA has determined that it is appropriate to protect the public health or safety to revoke this authorization.’"

However, industry insiders say that the company feared it was headed for another lawsuit, one it could not withstand, following the payout of $9 Billion in compensation for those it killed with it's cancer-causing baby powder. The FDA, who had previously granted licence for the vaccine only withdrew it when J&J considered the financial risk was too great, showing where their loyalty lies.

Johnson and Johnson's vaccine, used similar technology to AstraZeneca's Covid jab, which has also been banned for killing people in huge numbers. Although AZ's vaccine received massive media attention at launch, it was very quietly withdrawn with little or no coverage by the media.

Now some 19 MILLION million people who received J&J's Covid Vaccine have a potentially deadly substance in their veins, with absolutely no long term risk data for the drug. A biological 'ticking time bomb' with no way of removing the toxin from their system, millions of Americans now face heart attacks, strokes or fatal embolisms after taking the untested vaccine.

Less than a month after the vaccine was granted emergency use authorisation it came under the spotlight as reports began to emerge of people dying or having life changing injuries following the injection. Blood clots were the most common complaint with huge numbers of patients suffering thrombosis with thrombocytopenia syndrome (TTS) many cases were fatal. One US patient reportedly didn't even make it out of the clinic, dying within minutes of receiving the shot, with several others not making it home before succumbing. The FDA refused to acknowledge there was a problem at all, and have now only withdrawn the vaccine due to financial implications and not, as they claim, safety issues.

97 views0 comments


bottom of page