Doctors are free to prescribe ivermectin to treat COVID-19, a lawyer representing the U.S. Food and Drug Administration (FDA) said this week.
Hej, nemá vôbec žiaden
FDA schválilo liečbu kovidu s ním. Trvalo to len pár rokov.
Znamená to že odteraz je Food and Drug Administration nejaká dezolé inštitúcia?
Liek vynájdený v 70tych, na svetovom zozname dôležitých liečiv, autor dostal zaň nobelovu cenu. Možno bude ďalšia :
Ivermectin, a potential anticancer drug derived from an antiparasitic drug
A pritom taká blbosť, vylučok bacila z japonskej zeminy...
Od testovania až po schválenie vakcíny môže byť 5-10 rokov. Pharma firmy využili krízovú situáciu na rýchle schválenie vakcíny, akákoľvek alternatívna liečba bola zosmiešnena. Však áno, podľa toho odseku im to reálne mohlo stopnúť biznis, ak by tak neurobili. Bolo zaujímavé sledovať ako sa celosvetovo hejtuje ivermectin.Put simply, an emergency use authorization (EUA) is a tool the Food and Drug Administration (FDA) can use to expedite the availability of medical products, including drugs and vaccines, during a public health emergency. An EUA can only be granted when no adequate, approved, available alternatives exist, and when the known and potential benefits outweigh the potential risks. An EUA also only lasts as long as the public health emergency for which it was declared.
It is the job of the FDA to ensure medical products meet rigorous safety and efficacy standards, a process that can take years for what’s called “full approval.” Though that timeline is condensed when an EUA is granted, the FDA still upholds its strict standards.
