Publications questioning the acceptance of the vaccine Coronavac Against one COVID-19 In Europe it has been shared more than 9,500,000 times on social media since June 20. However, the accusation spreads without context, except that the immunization agent already has its emergency use approved by the World Health Organization (WHO) And it is analyzed by the European Pharmaceutical Institute (EMA).
“There is so much sacrifice in line to get the Chinese vaccine. When I come here to Europe and show the vaccination certificate, they tell me I am ‘someone in the valley’ everywhere.”, Says the text of the shared publication Twitter, No Facebook (1, 2, 3) And on Instagram (1, 2, 3).
Approved National Institute of Health Monitoring (Anvisa) On January 17 this year, Coronavac was developed by Sinovac Biotech, a Chinese pharmaceutical company, and co-created in Brazil. Button Company, Is under continuous analysis European Pharmaceuticals Company (EMA, abbreviated in English) May 4, 2021 onwards.
According to the EMA, continuous review is a regulatory tool used to expedite the evaluation of a promising drug during a public health emergency.
In this case, an EMA team reviews data on vaccine safety, efficacy and quality. Once the EMA has determined that there is sufficient data the manufacturer can file a formal application for accreditation.
About a month after the EMA announcement, on June 1, 2021, Sinovac was vaccinated Verified by WHO For emergency use. The organization’s emergency utility list evaluates the suitability of new health products for public health emergencies.
According to Who, “The goal is to make medicines, vaccines and diagnoses available as soon as possible to meet emergencies while respecting strict safety, efficacy and quality standards.”.
Entering the European Union
To control the spread of COVID-19, in March 16, 2020, EU leaders have established integrated control over travelers, a type of activity that excludes or deeming European citizens and their families, longtime residents of the EU and their families. , Diplomats, military and humanitarian workers.
In June 2020, the EU Council adopted a recommendation Possible suspensions S input recovery is not blocked.
In addition, camp states can lift the ban on non-essential travel to arriving states, at least 14 days prior to arrival, with the last recommended dose Vaccines Listed for WHO emergency use.
So this recommendation opens the door for Brazilians to be vaccinated as Coronavac enters the EU.
However, the text of the Board insists that the recommendation “Not a legal binding tool” Is responsible for using these guidelines “Member State Officials” Of the European Union. In other words, the countries of the camp are not obliged to accept the recommendations.
The EU still maintains one Ready, Will be updated every two weeks from countries where travel restrictions can be phased out. Country selection takes into account measures of epidemiological status and social distance, in addition to economic and social factors.
Ann Last listReviewed on June 18, 2021, there were 13 countries, including China and the United States. Not among the beneficiaries in Brazil.
Faces new dangers Types Can represent, the Council also refers to an emergency mechanism, which is a “Emergency and temporary restrictions on all travel to the EU” This does not apply only to European citizens and their families, longtime residents of the EU and their family members or to those who perform activities that are considered essential.
Finally, all people traveling from any country are recommended to have a PCR test for a compelling reason or with a negative result within 72 hours of travel.
In addition, European countries will have to isolate and reconsider for a maximum of 14 days.