The WHO has once again modified its recommendations regarding the
coronavirus
.
The advisory group of experts on
vaccines
of the
World Health Organization
(WHO) has recommended that patients in certain groups at risk receive a third additional dose of
anticovid
vaccine
, despite the fact that the agency had asked in August for a moratorium on these inoculations of reinforcement.
The data of the coronavirus in Spain
Total figures
: 4,977,448 confirmed coronavirus cases with a diagnostic test for active infection;
There have been 86,827 deaths with a positive test as of October 10.
803,876 in Andalusia (11,200 dead)
161,616 in Aragon (3,853 dead)
71,003 in Asturias (2,070 dead)
99,803 in the Balearic Islands (965 dead)
95,830 in the Canary Islands (1,001 dead)
46,453 in Cantabria (608 dead)
238,933 in Castilla-La Mancha (6,475 dead)
299,890 in Castilla y León (7,321 dead)
921,841 in Catalonia (15,758 dead)
7,570 in Ceuta (128 dead)
511,551 in the Valencian Community (7,784 dead)
102,763 in Extremadura (1,993 dead)
186,863 in Galicia (2,639 dead)
893,471 in Madrid (16,145 dead)
11,038 in Melilla (108 dead)
141,310 in Murcia (1,739 dead)
82,742 in Navarra (1,248 dead)
261,353 in the Basque Country (4,969 dead)
39,542 in La Rioja (823 dead)
07.00.
EMA studies authorizing Ronapreve monoclonal antibodies against coronavirus
The European Medicines Agency (EMA) has received a request to study the possible authorization in the European Union (EU) of
Ronapreve
, a cocktail of monoclonal antibodies developed by the firms
Regeneron
and
Roche
for the treatment and prevention of
Covid-19
.
The agency is evaluating the marketing license requested by
Roche Registration GmbH
for the approval of the drug that combines the monoclonal antibodies
casirivimab
and
imdevimab
, to treat adults and adolescents over 12 years of age who do not require supplemental oxygen and are at increased risk of developing
Covid -19
serious.
This cocktail could also be used for the prevention of
Covid-19
in adults and adolescents older than 12 years, according to data in the hands of the Committee for Human Medicines (CHMP).
The EMA estimates that it will be able to complete its evaluation of the benefits and risks of the drug in a "reduced" period of two months, depending on the strength of the data presented by the pharmacist, and provided that no additional information is required to support the analysis.
The agency began in February a real-time review of the data of this treatment that combines monoclonal antibodies, after seeing that the "preliminary results of a study indicate a beneficial effect of the drug in reducing the amount of virus in the blood (viral load) in non-hospitalized patients "who contracted it.
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