- Liittynyt
- 24.10.2016
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FDA on hyväksynyt parantuneiden veriplasman käyttämisen hoitona.
Stocks rally strongly as US approves COVID-19 treatment
The US Food and Drug Administration (FDA) issued an emergency authorisation for the use of blood plasma to treat COVID-19.
finance.yahoo.com
European stocks rallied strongly at the open on Monday after the US Food and Drug Administration (FDA) issued an emergency use authorisation on Sunday, approving the use of blood plasma from patients who have recovered from COVID-19 to treat the novel coronavirus.
US President Donald Trump said in a press conference the treatment had reduced mortality by 35% in a study of patients by the Mayo Clinic.