US authorises AstraZeneca COVID-19 treatment in some cases

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WASHINGTON: US health authorities on Wednesday (Dec 9) authorised the use of synthetic antibodies developed by AstraZeneca to prevent COVID-19 infections in people who react badly to vaccines. It was the first time the Food and Drug Administration has given emergency authorisation for such a purely pr

WASHINGTON: US health authorities on Wednesday authorised the use of synthetic antibodies developed by AstraZeneca to prevent COVID-19 infections in people who react badly to vaccines.

The FDA warned the drug Evusheld is"not a substitute for vaccination in individuals for whom COVID-19 vaccination is recommended" and can only be authorised for people who have a weakened immune system or those who cannot be vaccinated for medical reasons, such a strong allergic reaction.Evusheld combines two types of synthetic antibodies , and is given as two intramuscular injections, one straight after the other.

The drug was given to 3,500 people while 1,700 received a placebo. The trial showed that the treatment cut the risk of developing COVID-19 by 77 per cent.

 

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