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【Youth Diary】 How the new vaccine against Modena coronavirus infection (Corona 19) was approved for emergency use by the US Food and Drug Administration (FDA) on the 18th (local time) , USA has insured two types of COVID-19 vaccine.
The FDA’s main agency, Health and Human Services Minister Alix Aza, said on the 17th that 5.9 million doses of Modena’s vaccine were assigned to each state.
The United States announced a plan to distribute 2 million doses of Pfizer’s vaccine and distribute 7.9 million doses of the vaccine during the following week to major states, territories and cities across the country.
The US, where the highest number of confirmed and dead corona19 have been recorded so far, is expected to gain momentum with its quarantine strategy through vaccines.
Accelerate Vaccination … Expect to End Pandemic Early
Aza said it could speed up vaccinations for healthcare workers and Americans in long-term care facilities and ultimately bring about a faster end to this pandemic.
Minister Aza assessed that it was the result of public-private partnerships in accordance with the United States government’s vaccine development policy, ‘Operation Warp Speed’.
The US National Institute of Health (NIH) was involved in the development and clinical trials of the Modena vaccine, and the US funded $ 1 billion to develop the Modena vaccine alone.
The United States has even granted immunity to side effects to encourage vaccine development. In accordance with the Public Preparedness and Emergency Preparedness Act (PREP) of 2005, the US guarantees immunity only to products that help control public health crises and applies it to this situation.
Additionally, to avoid unnecessary procedural delays in the vaccine development, manufacturing, and distribution process in the United States, the US ‘high-speed operation’ was conducted by the Ministry of Health and Welfare, the Centers for Disease Control and Prevention (CDC), the National Institute of Health (NIH), the Advanced Biomedical Research and Development Agency (BARDA), several ministries cooperated, including the Ministry of Defense.
Susan Vice, director of the University of Pennsylvania Coronavirus Research Center, told the New York Times (NYT) that “the CDC license, which took several weeks in the past, fell in two days.”
◆ Vaccination denial remains a challenge
FDA approval for emergency use authorizes distribution of the vaccine. Vaccination is recommended by the Advisory Committee on Immunization (ACIP), an advisory body to the Centers for Disease Control and Prevention (CDC), and is only possible with approval from the CDC.
The United States approved the use of the vaccine on the 13th and chose Sandra Lindsay, a black nurse who works in the COVID-19 intensive care unit as the first vaccine.
It aims to encourage vaccination of minorities, such as blacks, who are reluctant to get vaccinated, while demonstrating its willingness to protect medical workers who are at the forefront of Corona 19’s response.
“Many ethnic minorities are hesitant to get vaccinated because of the unfortunate history,” said Nurse Lindsay, who was vaccinated live across the United States. “My first vaccination was to convey a message to people.”
The Vice President of the United States, Mike Pence, was vaccinated against the new coronavirus infection (Corona 19) on the 18th (hereinafter local time).
The vaccination event was broadcast live and the vice president’s wife, Karen, and the director of public health, Jerome Adams, received the vaccine along with Pence.
Adams appealed to the black community to get vaccinated, saying he recognizes the “symbolic importance” of his vaccination as a black man.
“There is no good reason for the lack of faith, especially in the community of people of color.”
Adams said that after 40 years to 1972, following the US government’s “Tusky syphilis test” against blacks in rural Alabama, distrust of the government increased.
At the time, the United States government neglected black people with untreated syphilis to see what would happen if it was not treated.
The trial was started on 600 black men, including 399 men with syphilis and 201 men without syphilis, and the trial participants did not give their consent. Inhumane in vivo experiments are at the heart of the conspiracy theory related to the refusal of vaccination.
Along with this, the side effects of vaccines are also a problem.
After the UK, there have been cases of allergic reactions in the US after receiving a new vaccine against coronavirus infection (COVID-19, Corona 19) from Pfizer, an American pharmaceutical company.
The New York Times reported on the 16th (local time) that a healthcare worker in Alaska, USA, had a severe allergic reaction after receiving the Pfizer vaccine the day before. This patient has no history of allergic reactions to other medications and is currently hospitalized for treatment.
This patient’s allergic reaction is “anaphylaxis.” This reaction is a sudden systemic allergic immune response that occurs in our body. Anaphylaxis is a symptom that causes an acute systemic shock-like reaction as this allergic reaction progresses rapidly.
Two British medical workers who received the Pfizer vaccine earlier this month (local time) also showed anaphylactic reactions.
Consequently, the UK Medicines Regulatory Authority (NHS) and Medicines Health Management Products Regulatory Authority (MHRA) announced that they were conducting an investigation and that those who had allergic reactions to medicines, food and vaccines in the past should not receive the Corona 19 vaccine.
Clinical participants who received the COVID-19 vaccine from Modena experienced both large and small sequelae. On the 16th (local time), the Wall Street Journal (WSJ) reported that clinical participants who received the Corona 19 vaccine from the American biotech company Modena experienced sequelae large and small.
【Youth Daily = Reporter by phone number】
