<<Define experimental?>>
A treatment that does not need an EUA for starters. My emboldement below btw. I know I am going to have to spell this out for you, so I will. The resistance and incompetence to HCQ, Ivermectine, plus many other treatments by health authorities worldwide is because of the underlined bit. I did the underlining too. They should have left those types of decisions to the medical professionals on the front lines, as is usually the case. That little change in standard procedure raises a big red flag in my view. A bigger red flag than any red flag held in China, Russia, or other communist country. The red flag concern was raised to a higher visual level when the UK Prime Minister (Boris Johnson) went from a Right Wing Tory to a Rabid Ultra Communist almost overnight. There were a number of other strange co incidences during the initial Covid infection period too.
"An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives. Taking into consideration input from the FDA, manufacturers decide whether and when to submit an EUA request to FDA.
Once submitted, FDA will evaluate an EUA request and determine whether the relevant statutory criteria are met, taking into account the totality of the scientific evidence about the vaccine that is available to FDA.
Emergency Use Authorization for Vaccines Explained | FDA |
