Pfizer CEO Albert Bourla on Sunday said the vaccine maker plans to submit data on a fourth dose of its COVID-19 vaccine to the U.S. Food and Drug Administration because protection after three doses is “not that good against infections” and “doesn’t last very long” when faced with a variant like Omicron.
Pfizer will "no longer initiate new clinical trials in Russia, and we will stop recruiting new patients in our ongoing clinical trials in the country."
Cardiologist, professor and frontline doctor Peter McCullough asserts that early COVID-19 testing data indicates the genetic materials in the vaccine could be incorporated into the human genome.
Only "researchers, trial participants, regulators, and others" who act in what Pfizer deems to be "the best interest" of patients have access to the pharmaceutical company's clinical trial documents that reveal injuries and deaths from their Covid-19 mRNA drug.
Repurposed drugs that have been shown to prevent or treat COVID-19 may be prescribed by physicians, the Florida Department of Health said in its new COVID-19 guidance for health care practitioners.