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Emergency use of vaccine only if "No adequate, approved, and available alternative" (such as vitamin D)- May 2021

What is an Emergency Use Authorization (EUA)? (FDA)

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.

If the FDA admitted that there are indeed proven alternatives (Vitamin D, Ivermetin, etc), it seems that the FDA would have have stop emergency use authorizations for the (profitable) vaccines

Vitamin D

COVID-19 treated by Vitamin D - studies, reports, videos

5 most-recently changed Virus entries

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26 health factors increase the risk of COVID-19 – all are proxies for low vitamin D

83 VitaminDWiki pages with VACCIN in title as of july 2021


Ivermectin and COVID-19 - many studies

Created by admin. Last Modification: Wednesday July 28, 2021 02:59:54 GMT-0000 by admin. (Version 8)