https://healthimpactnews.com/2021/f...on-for-another-experimental-covid-19-vaccine/
The FDA today issued an emergency use authorization (EUA) for Janssen Biotech’s adenovirus experimental COVID-19 vaccine.
Janssen Biotech, Inc., is a subsidiary of the Johnson and Johnson multi-national corporation, which has paid out BILLIONS in criminal settlements, which is ongoing due to the opioid crisis. You can read their criminal rap sheet here.
The Johnson and Johnson experimental COVID vaccine is not an mRNA vaccine, it is an “adenovirus” vaccine, but like mRNA vaccines, there are currently no approved adenovirus vaccines in the market, although the military has used experimental adenovirus vaccines that are not FDA approved.
So by getting the FDA to issue an EUA, Johnson and Johnson can now test their experimental vaccine on the public as part of their Phase 3 trials.
The vaccine is being produced in Belgium, by the same company that in the past produced the anthrax vaccine that destroyed the lives of so many military personnel. See:
35,000 Soldiers Died from the Experimental Anthrax Vaccine – More Than Those Who Died in Combat in Afghanistan and Iraq Combined
The FDA’s vaccine advisory committee met yesterday, Friday, February 26th, and gave their endorsement to the FDA to issue the EUA.
Dr. Meryl Nass, MD, a leading national expert on the failures of the military anthrax vaccine listened to the meeting yesterday, and today she published what she learned from the vaccine committee meeting.
The FDA today issued an emergency use authorization (EUA) for Janssen Biotech’s adenovirus experimental COVID-19 vaccine.
Janssen Biotech, Inc., is a subsidiary of the Johnson and Johnson multi-national corporation, which has paid out BILLIONS in criminal settlements, which is ongoing due to the opioid crisis. You can read their criminal rap sheet here.
The Johnson and Johnson experimental COVID vaccine is not an mRNA vaccine, it is an “adenovirus” vaccine, but like mRNA vaccines, there are currently no approved adenovirus vaccines in the market, although the military has used experimental adenovirus vaccines that are not FDA approved.
So by getting the FDA to issue an EUA, Johnson and Johnson can now test their experimental vaccine on the public as part of their Phase 3 trials.
The vaccine is being produced in Belgium, by the same company that in the past produced the anthrax vaccine that destroyed the lives of so many military personnel. See:
35,000 Soldiers Died from the Experimental Anthrax Vaccine – More Than Those Who Died in Combat in Afghanistan and Iraq Combined
The FDA’s vaccine advisory committee met yesterday, Friday, February 26th, and gave their endorsement to the FDA to issue the EUA.
Dr. Meryl Nass, MD, a leading national expert on the failures of the military anthrax vaccine listened to the meeting yesterday, and today she published what she learned from the vaccine committee meeting.
