According to an argument made by government lawyers during a recent hearing, the US Food and Drug Administration (FDA), which made fun of Americans for using Ivermectin to treat Covid-19, now claims that its campaign encouraging people to "stop" taking it was informal and merely an recommendation.
The FDA have announced a new definition of what they consider healthy. Recent dietary recommendations emphasize a plant-based diet rich in vegetables, fruits, whole grains, legumes, nuts, and seeds.
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.
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.
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.
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.
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.
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.
Cattle created using CRISPR Gene Editing produced by Acciligen, have been declared safe for human consumption by the FDA.
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.