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According to him, it is already impossible to accumulate the vaccine liquid, which, according to the doctors, remains in the vials after 5 people have been vaccinated according to the prescribed procedure, because if the vial is damaged, the vaccine should be used within the 5 hours. Therefore, Š continues. Machinsk, the decisions on the so-called “sixth dose” are very well received.
“For the sixth dose, we are eager to make decisions about how to handle the sixth dose, because when the vaccine is diluted and ready to use, the shelf life is very short – it should be used within 5 hours.” This means that it is no longer possible to use them in the future. Therefore, at the end of the term, they are destroyed according to the established procedure, ”said the head of the Outpatient Services Coordination Service of the Kaunas Clinics at a press conference on Thursday.
“It is established that the organism that organizes the vaccination is responsible for the correct elimination of residual products, that is to say, remaining ampoules and liquids, in accordance with the requirements,” he added, noting that the vaccine residues are effectively destroyed and not used by anyone.
“All established procedures are followed, so there is no possibility that they (vaccine residues – ELTA) will go anywhere,” assured Š. Machinsk.
This week, Health Minister Arūnas Dulkys stated that a proposal from the European Medicines Agency is expected in the near future to extract more doses of the COVID-19 vaccine from a package. According to the minister, this would be positive news and would bring clarity to the vaccination of the population.
There are 5 doses in the COVID-19 vaccine package, but doctors note that more patients have enough vaccine in a frequent vial.
“Of course, a coordinated agreement between the European Commission and the manufacturers is important to us. (…) The European Medicines Agency discussed this yesterday, but has not yet made a decision, and we really hope that they will adopt it in a near future and that we all have clarity. Because the contracts are concluded in a coordinated manner between the European Commission and the manufacturers, and we adhere to the common rules very strictly “, said A. Dulkys in a press conference held at the Ministry of Health (SAM).
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