No or UNKNOWN RISK
No reports. No current evidence. Click FIELD REPORT to share with us a link or your first-hand account.
EMERGENCY USE AUTHORIZATION ISSUED
Emergency Use Authorizations are a legal means for the Food and Drug Administration (FDA) to approve new drugs, or new indications for previously approved drugs, during a declared emergency.
Background on this indicator will be provided here in the near future.
News relevant to this indicator that emerges from open sources may lead to threatening conditions for the American Nation. The team at FutureDanger will provide a clear explanation of these risks as soon as possible.
Developed by FutureDanger
Indicator Historical Trend
|SHTF||15 Dec 2020||FDA Grants Emergency Use Authorization to First COVID-19 Vaccine||[Targeted Oncology]|
|SEVERE||10 Dec 2020||FDA panel recommends approval of Pfizer's Covid vaccine for emergency use||[Reuters]|
|LOW||01 Dec 2020||Moderna Files for COVID-19 Vaccine Emergency Use Authorization||[TechCrunch]|
|LOW||05 May 2020||Experimental Coronavirus Vaccines Start Emergency Human Testings||[CNBC]|
|SHTF||31 Mar 2020||FDA Grants Anti-Malaria Drugs Emergency Use Authorization||[Daily Signal]|
|LOW||16 Mar 2020||First American Gets Experimental Coronavirus Vaccine||[LiveScience]|
|MOD||11 Mar 2020||FDA to Speed Coronavirus Diagnostics||[Outsourcing-Pharma]|
|LOW||02 Mar 2020||NY State Labs Get FDA Emergency Use Authorization for Coronavirus Test||[GenomeWeb]|