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According to one study, adolescents aged 12 to 15 who received the Pfizer vaccine experienced mild to moderate side effects that wore off quickly.
The jab has been administered to adolescents in the age group who are at high risk of complications from coronavirus due to certain conditions of coexistence.
The authors said the results should reassure parents as reports revealed the NHS made plans to start immunizing all children ages 12 to 15 from the first week back to school.
The NHS Trusts were asked on Wednesday to prepare for the possible roll-out of the vaccination program to all schoolchildren in the age range, The Telegraph reported.
Emails seen by the newspaper, sent from NHS England regional offices, say trusts must have plans ready by 4 p.m. Friday.
Health officials have reportedly said children will not need parental consent to receive the vaccine.
The study that looked at the use of the Pfizer vaccine in 12 to 15 year olds asked parents of 27 children who received the vaccine to record all side effects.
The authors of the study, which is published in the Archives of Disease in Childhood, said: “The numbers were low, but this data is particularly important because it is representative of the children most likely to benefit from immunization, as well as parents and clinicians. may have concerns about an increased risk of unexpected events. “
Of the 27 children, three were hospitalized, 16 were boys and most, 21, were Caucasian.
They suffered from various neurological conditions including muscular dystrophy and cerebral palsy, as well as a range of coexisting medical conditions, such as epilepsy, congenital heart defects and immune deficiency, for which they received drug treatment from various types.
The reported side effects were all mild to moderate, with the exception of one child who experienced severe fatigue and discomfort, combined with increased restlessness. One family also reported that the type of seizure changed in clusters, although this resolved a week later.
In total, there were eight “events” in six children after the first dose, all of which resolved within 72 hours: mild rash; headache; diarrhea; suspected sore throat; neck pain; Difficulty sleeping; and low blood sugar.
After the second dose, eight more events occurred in five children: diarrhea; vomiting; swelling of the armpits; and blisters around the mouth.
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The use of paracetamol after the first dose was high and fever was more common than that reported in studies in adults (13% vs. 4% in 16-55 year olds).
But all the recorded side effects disappeared within a week.
Children deemed at high risk for coronavirus were protected during the pandemic because of their risk of infection and would not have been included in early vaccine safety studies, the study’s authors said.
Healthy children who contracted the coronavirus usually suffered from mild illness.
However, the Joint Committee on Vaccination and Immunization (JCVI), the UK vaccine advisory group, has advised that children aged 12 and over with severe neurological conditions, who tend to have recurrent respiratory infections and have complex care needs, should be offered the COVID-19[female[feminine cut.
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