FDA Refuses To Provide Key COVID-19 Vaccine Safety Analyses
In accordance with the operating procedure records, the CDC intended to carry out a different kind of data mining analysis known as Proportional Reporting Ratio (PRR) mining. Now, the FDA is refusing to provide the key COVID-19 vaccine safety analyses.
FDA Warns Puberty Blockers May Cause Vision Loss In Children
The use of puberty blockers may result in vision loss. The FDA issues a warning about idiopathic intracranial hypertension, also known as pseudotumor cerebri in children.
There May Be No Clinical Trials For Future Covid Vaccines
So Pfizer and Moderna have figured out a way to use regulatory capture to get their reformulated Covid-19 shots approved WITHOUT further clinical trials. Their scheme is called the “Future Framework” and it will be voted on by the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) on June 28.
FDA Sued Over Hiding Records From Moderna COVID-19 Vaccine Approval
A Freedom of Information Act lawsuit has been filed against the FDA over hiding records from the approval of a Moderna COVID-19 vaccine named Spikevax by Defending the Republic.
Doctors Suing FDA Over Ivermectin
The doctors want the Food and Drug Administration to stop meddling with the prescription of Ivermectin for the treatment of COVID-19. Towards this goal, doctors are suing the FDA over Ivermectin and its usage.
Pfizer Asks To Dismiss Lawsuit Revealing Problems At COVID-19 Vaccine Trial Sites
The regulators have not revoked approval of Pfizer’s vaccine, which was approved by the FDA in late 2020, even after Brook Jackson disclosed problems at sites managed by Ventavia Research Group. Now, Pfizer is asking to dismiss the lawsuit revealing problems at COVID-19 vaccine trial sites entirely.
FDA Says CRISPR Gene Edited Cattle Safe For Human Consumption
Cattle created using CRISPR Gene Editing produced by Acciligen, have been declared safe for human consumption by the FDA.
FDA Investigating Reports Of COVID Relapses Following Use Of Pfizer’s Pill
The US FDA has launched an investigation after reports of COVID relapses in patients within 5 to 9 days following the use of Pfizer’s pill known as nirmatrelvir.
The FDA Finally Admits We Should Treat COVID-19 Like The Flu
A report in the Journal of the American Medical Association, written by the top vaccine official in the FDA, has admitted that we should treat COVID-19 just like the flu.
FDA Authorizes First 3 Minute COVID Breath Test
The US Food and Drug Administration (FDA) has authorized the first 3 minute COVID breath test publishing an emergency usage permission on Thursday for the very first equipment that can identify COVID-19 in breathing samples, according to the agency.