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UK Health Watchdog Issues Warning After Two People Suffer Allergic Reaction to Pfizer Vaccine

© AP Photo / Frank AugsteinA nurse prepares to administer the Pfizer-BioNTech COVID-19 vaccine at Guy's Hospital in London, Tuesday, Dec. 8, 2020
A nurse prepares to administer the Pfizer-BioNTech COVID-19 vaccine at Guy's Hospital in London, Tuesday, Dec. 8, 2020 - Sputnik International
Doctors will start giving the Pfizer/BioNTech vaccine next week with more supplies of the jab expected to be shipped into the UK in the coming days. It comes after the first vaccinations were given on Tuesday.

The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has warned people who have a history of "significant" allergic reactions not to take the Pfizer/BioNTech COVID-19 vaccine. 

It comes after NHS England confirmed two workers who had the vaccination on Tuesday, 8 December, suffered allergic reactions, it has emerged.

​The Evening Standard reported that Professor Stephen Powis, national medical director for the NHS in England, said: "As is common with new vaccines the MHRA have advised on a precautionary basis that people with a significant history of allergic reactions do not receive this vaccination after two people with a history of significant allergic reactions responded adversely yesterday. Both are recovering well."

​Britain rolled out a mass coronavirus vaccination program on Tuesday and the first doses will primarily be administered to NHS workers, high-risk groups and people aged over 80.

A video was shared online showing the second person in the UK to receive the vaccine - the splendidly monikered William Shakespeare, 81, from Warwickshire.

​Many social media users in the UK shared concerns about the vaccine and said they were in no rush to take it.

Last month Dr Ruth Blue, secretary of the Thalidomide Society, said talk among anti-vaxxers of comparisons between the vaccine and the thalidomide scandal in the 1960s were a red herring.  

Meanwhile the Food and Drug Administration in the United States will meet on Thursday, 10 December, to decide whether to distribute the Pfizer/BioNTech vaccine. 

June Raine, the chief executive of MHRA, said they would examine all the data from the COVID-19 vaccine trials carried out by Oxford and AstraZeneca.

She said: "Our regulatory review is all encompassing. We will look at all available data."

On the MHRA website Ms Raine lauded the fact that the UK was "the first country in the western hemisphere to issue an approval (of a vaccine)."

​She explained how they managed this: "While the first batch of data from Pfizer was not submitted to the MHRA until early October, we began preparing our safety surveillance systems months before."

Ms Raine said: "Patient safety has always been at the heart of my work. It has been no different for this vaccine, nor will it be for the others to come."

She said the Pfizer vaccine had been independently tested by the National Institute for Biological Standards and Control (NIBSC).

​"Before any batch can reach the public, the NIBSC will conduct a rigorous assessment to check that it is consistent with characteristics derived from results for batches previously shown to be safe and effective in clinical trials, or routine clinical use. This work began in November," said Ms Raine.

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