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 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.
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.
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.
Clinical trials using Omicron-specific vaccinations are now underway, but no data on human participants has been released. Meanwhile, the FDA wants to move COVID vaccines to a flu like model.
BA.2 (a subvariant of omicron) was liable for 12.6 percent of COVID-19 infections in the United States in the week ending March 5. As such, the FDA has told doctors in 8 states to stop using COVID treatment.
Laboratory mice who were administered the compound labelled as GPHR-529 witnessed dramatic decline in semen. With this result in view, FDA is set to start trials for birth control pill for men soon.
According to an FDA official Biden administration has plans for annual covid vaccines for toddlers. “It’ll be a recurring fountain of revenue. It might not be that much initially, but it’ll be recurring… if they can get every person required at an annual vaccine, that is a recurring return of
The US FDA used a ‘critically flawed’ risk-benefit analysis to ‘justify’ COVID vaccines for children. The hazards of COVID-19 vaccination exceed the advantages for millions of children.
As explained in prior posts, in a lawsuit seeking all of the documents the FDA relied upon to license Pfizer’s COVID-19 vaccine, a federal judge shot down the FDA’s requested rate of 500 pages per month and instead ordered the FDA to produce at the rate of 55,000 pages per
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