On March 13, 2021, a healthcare professional fills a syringe with AstraZeneca vaccine at Santa Caterina Da Siena, Salerno’s Amendra Junior High School in Salerno, Italy.
Francesco Pecoraro | Getty Images News | Getty Images
The Dutch government said on Sunday that the Oxford-AstraZeneca vaccine would not be used until at least March 29, but Ireland said it had temporarily suspended shots as a precautionary measure earlier that day.
The World Health Organization has sought to downplay ongoing safety concerns, saying last week there was no link between firing and an increased risk of developing blood clots. The United Nations Health Organization has urged countries to continue using the Oxford-AstraZeneca vaccine.
Nevertheless, many European countries Already paused Oxford-Use of AstraZeneca vaccine.It was added to the local worries Affected vaccination campaign When the German public health agency warns: Third wave of coronavirus infection It has already started.
Thailand has also stopped the planned deployment of the vaccine.
A move by Dutch and Irish authorities to suspend its use took place shortly after the Norwegian pharmaceutical institution. Said After receiving the Oxford-AstraZeneca vaccine, three health care workers were informed that they were being treated in the hospital for bleeding, thrombocytosis, and decreased thrombocytopenia. Norway has put the Oxford-AstraZeneca vaccine program on hold.
“We will track these suspicious side effects and take the necessary steps in this serious situation,” said Geir Bukholm, director of infection control and environmental hygiene at the Norwegian Institute for Public Health.
The photo, taken on November 27, 2020, shows “Nikki” Anikenhaas treating a Covid-19 patient in the intensive care unit of the Rikshospitalet, Oslo University Hospital in Oslo, Norway.
JIL YNGLAND | AFP | Getty Images
The European Medicines Agency, the European drug regulator, also said there were no signs that the Oxford-AstraZeneca vaccine was causing blood clots, adding that it believed that the benefits of the vaccine “continue to outweigh the risks.”
The EMA has confirmed that some European countries have suspended the use of Oxford-AstraZeneca shots, but said vaccinations could continue while investigations of cases of blood clots were ongoing. It was.
“A careful review of all available safety data for more than 17 million people vaccinated with the COVID-19 vaccine AstraZeneca in the European Union (EU) and the United Kingdom revealed pulmonary embolism, deep vein thrombosis (DVT) or Defined age group, gender, batch, or thrombocytopenia in a particular country, AstraZeneca Said In a statement on Sunday.
The most common side effects of the Oxford-AstraZeneca vaccine are virus-free and cannot cause Covid, but are usually mild or moderate and improve within a few days of vaccination.
At the Bamuras Naradura Infectious Diseases Research Institute in Nonthaburi, a suburb of Bangkok, healthcare professionals have a box of AstraZeneca vaccines.
Chai Watt Subprime | SOPA Images | Light Rocket via Getty Images
Pharmaceutical giants said 15 events of deep vein thrombosis and 22 events of pulmonary embolism were reported among vaccinated people throughout the EU and the UK.
“This is much lower than expected to occur naturally in the general population of this size and is similar across all other licensed COVID-19 vaccines,” said AstraZeneca.
Stephen Evans, a professor of pharmacoepidemiology at the London School of Economics and Tropical Medicine, said:
“Therefore, it is very likely that the benefits of the vaccine will significantly outweigh the risk of coagulopathy, and the vaccine will prevent other Covid outcomes, including death from other causes.”
Evans said researching vaccines and coagulopathy is “fully rational,” but “one step to take precautions to prevent people from getting vaccines to prevent the disease. It seems too far away, “he added.
Many high-income countries, such as the United Kingdom, France, Australia and Canada, have opted to continue deploying their respective Oxford-AstraZeneca vaccines.
“If there is clear evidence of serious or life-threatening side effects, it will have important consequences,” Adam Finn, a professor of pediatrics at the University of Bristol, said in a statement.
“But so far, it is highly undesirable to interrupt a complex and urgent program every time a person develops a disease after vaccination that may be accidental and non-causal. Making the right phone call in a situation is not easy, but holding the tiller firmly is probably the most necessary thing. “
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