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<blockquote data-quote="D2Cat" data-source="post: 1700657" data-attributes="member: 19322"><p>This entire covid treatment is catching people off guard, Drs included. We hear a lot of negative about ivermectin and hydroxoclorouine. It's not approved by the FDA for human use. It probably never will be approved because it takes millions of dollars to go through the testing to get approval. It's currently being sold for $6 a tube to treat a 1200# horse. There's not enough income potential to ever proceed with testing for approval.</p><p></p><p>What about the vaccines available? They are EUA (emergency use authorization). What does that mean?</p><p></p><p>Here's what it means: Here's the link to the publication. <a href="https://www.phe.gov/Preparedness/planning/authority/Pages/eua.aspx" target="_blank">https://www.phe.gov/Preparedness/planning/authority/Pages/eua.aspx</a></p><p></p><p>Here's the second half describing what can happen that they don't know about.</p><p></p><p>FDA may then issue an EUA for a product if FDA finds that:</p><p></p><p></p><ul> <li data-xf-list-type="ul">the agent specified in the declaration of emergency can cause a serious or life-threatening disease or condition;</li> <li data-xf-list-type="ul"><br /> </li> <li data-xf-list-type="ul">based on the totality of scientific evidence available, it is reasonable to believe that the product may be effective in diagnosing, treating, or preventing the serious or life-threatening disease or condition, or a serious or life-threatening disease or condition caused by a product authorized approved, cleared, or licensed by FDA for diagnosing, treating, or preventing the disease or condition;</li> <li data-xf-list-type="ul"><br /> </li> <li data-xf-list-type="ul">the known and potential benefits of the product outweigh the known and potential risks of the product when used to diagnose, prevent, or treat the serious or life-threatening disease or condition, taking into consideration the material threat posed by the agent or agents identified in a declaration by the DHS Secretary, if applicable;</li> <li data-xf-list-type="ul"><br /> </li> <li data-xf-list-type="ul"><span style="color: rgb(184, 49, 47)">there is no adequate, approved, and available alternative to the product for diagnosing, preventing, or treating such serious or life-threatening disease or condition</span>; and</li> <li data-xf-list-type="ul"><br /> </li> <li data-xf-list-type="ul">in the case of a determination by the Secretary of Defense regarding risk to U.S. military forces from agents other than chemical, biological, radiological and nuclear agents, that the request for emergency use is made by the Secretary of Defense.</li> </ul><p></p><p>FDA will, in issuing the EUA, impose conditions on the emergency use that is authorized. For more information on the emergency use authority, please see <a href="http://www.fda.gov/EmergencyPreparedness/Counterterrorism/ucm182568.htm" target="_blank">Emergency Preparedness and Response: Emergency Use Authorization</a>.</p><p></p><p>The sentence I highlighted in red tells you why nothing will be approved in the near future. Because if there was an alternative the vaccines they are using would not meet the criteria.</p></blockquote><p></p>
[QUOTE="D2Cat, post: 1700657, member: 19322"] This entire covid treatment is catching people off guard, Drs included. We hear a lot of negative about ivermectin and hydroxoclorouine. It's not approved by the FDA for human use. It probably never will be approved because it takes millions of dollars to go through the testing to get approval. It's currently being sold for $6 a tube to treat a 1200# horse. There's not enough income potential to ever proceed with testing for approval. What about the vaccines available? They are EUA (emergency use authorization). What does that mean? Here's what it means: Here's the link to the publication. [URL]https://www.phe.gov/Preparedness/planning/authority/Pages/eua.aspx[/URL] Here's the second half describing what can happen that they don't know about. FDA may then issue an EUA for a product if FDA finds that: [LIST] [*]the agent specified in the declaration of emergency can cause a serious or life-threatening disease or condition; [*] [*]based on the totality of scientific evidence available, it is reasonable to believe that the product may be effective in diagnosing, treating, or preventing the serious or life-threatening disease or condition, or a serious or life-threatening disease or condition caused by a product authorized approved, cleared, or licensed by FDA for diagnosing, treating, or preventing the disease or condition; [*] [*]the known and potential benefits of the product outweigh the known and potential risks of the product when used to diagnose, prevent, or treat the serious or life-threatening disease or condition, taking into consideration the material threat posed by the agent or agents identified in a declaration by the DHS Secretary, if applicable; [*] [*][COLOR=rgb(184, 49, 47)]there is no adequate, approved, and available alternative to the product for diagnosing, preventing, or treating such serious or life-threatening disease or condition[/COLOR]; and [*] [*]in the case of a determination by the Secretary of Defense regarding risk to U.S. military forces from agents other than chemical, biological, radiological and nuclear agents, that the request for emergency use is made by the Secretary of Defense. [/LIST] FDA will, in issuing the EUA, impose conditions on the emergency use that is authorized. For more information on the emergency use authority, please see [URL='http://www.fda.gov/EmergencyPreparedness/Counterterrorism/ucm182568.htm']Emergency Preparedness and Response: Emergency Use Authorization[/URL]. The sentence I highlighted in red tells you why nothing will be approved in the near future. Because if there was an alternative the vaccines they are using would not meet the criteria. [/QUOTE]
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