1 in 100,000 had extreme reactions to Pfizer vaccine: US study

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1 in 100,000 had extreme reactions to Pfizer vaccine: US study
Roughly one in a hundred thousand persons who received the Pfizer-BioNTech Covid-19 vaccine have had severe allergies, US health officials said Wednesday while stressing that the advantages of immunization greatly outweigh the best-known risks.

The data originates from the Centers for Disease Control and Prevention, which documented 21 cases of anaphylaxis after administration of a reported 1,893,360 pictures from December 14 to December 23.

"This averages away to a rate of 11.1 anaphylaxis situations per one million dosages administered," senior CDC official Nancy Messonnier told reporters.

In comparison, flu vaccines cause about 1.3 anaphylaxis conditions per million doses administered, and so the amount of anaphylaxis for the Pfizer vaccine is roughly ten circumstances greater.

Messonnier added that anaphylaxis circumstances were still "exceedingly rare" and it remains to be in people's best fascination to take the vaccine, particularly found in the context of the Covid-19 pandemic that is clearly a far greater danger to their health.

"An excellent value proposition for you to definitely get vaccinated is their risk from Covid and poor outcomes from Covid continues to be more than the chance of a severe end result from the vaccine," she said.

"Fortunately, we find out how to deal with anaphylaxis, and we've put provisions in place to ensure that at immunization sites, the people administering the vaccine are ready to treat anaphylaxis."

The 21 cases ranged in age from 27 to 60 years old, with a median age of 40, and all but two were treated with epinephrine.

Nineteen of the conditions (90 percent) occurred found in females, and the median starting point time of symptoms was 13 minutes, but ranged from two to 150 minutes.

Four (19 percent) of individuals were hospitalized, including three in intensive health care, and 17 (81 percent) were treated within an emergency department. All except one was regarded to have been discharged residence or recovered at the time of the research, and there have been no deaths.

Symptoms included rash, sensation of throat closure, swollen tongue, hives, problems breathing, hoarseness, swollen lips, nausea and persistent dry out cough.

The US has so far authorized two vaccines for emergency use -- one produced by Pfizer and the other by Moderna.

Both are based on cutting-border mRNA (messenger ribonucleic acid) technology and authorities have attached comparable warning labels to both, which advise that persons who have a known record of allergies to the vaccines' ingredients avoid taking them.

Those who have a severe reaction to the primary dose are also asked never to take a second dose.

Messonnier said that investigations were underway to know what may come to be the cause of the allergies.

There is not enough data but to know very well what the rate of anaphylaxis is for the Moderna vaccine, that was authorized in the US weekly following the Pfizer shot, or whether a big change between your two vaccines will emerge.

One preliminary hypothesis for the reactions may be the presence of the substance polyethylene glycol (PEG), which has never before been found in an approved vaccine, but is situated in everyday products including laxatives, shampoos and toothpastes.

Both the Pfizer and Moderna vaccines use PEG molecules as part of the shielding casing around their key ingredient, the mRNA that carries genetic instructions to cells. -- AFP
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