The FDA granted emergency use authorisation of the Pfizer mRNA Covid vaccine for use in children aged 12 and over in the USA back on the 10th May 2021. The EMA has recently followed suit, recommending the Pfizer jab should be administered to children aged 12 and over in EU countries.
Because of this there can be no doubt that the MHRA will follow the FDA and EMA’s lead and also grant emergency use authorisation of the Pfizer jab for use in children aged 12 and above.
But are you aware that the clinical trials carried out by Pfizer on children aged 12 – 15 reveal that 86% of children who were given at least one dose of the jab suffered an adverse reaction ranging from mild to serious?
The information is publicly available and contained within an FDA fact sheet which can be viewed here (see page 25, table 5 on-wards).
That fact sheet contains two tables that detail the alarming rate of side effects and damage experienced by 12 – 15- year-old children who were given at least one dose of the Pfizer mRNA “vaccine” (gene therapy).
The tables shows that 1,127 children were given one dose of the mRNA jab, but only 1,097 children received the second dose. This fact in itself raises questions as to why 30 children did not receive a second dose of the Pfizer jab, and we doubt the answer is pretty.
Of the 1,127 children who received a first dose of the jab a shocking 86% experienced an adverse reaction. Of the 1,097 children who received a second dose of the jab a shocking 78.9% experienced an adverse reaction.
Read the full story here: Source: Shocking 86% of Children suffered an Adverse Reaction to the Pfizer Covid Vaccine in Clinical Trial – Daily Expose