In a FDA document titled “Vaccines and Related Biological Products Advisory Committee Meeting October 26, 2021” was prepared for the FDA Advisory Committee meeting who voted in favour for Emergency Use Authorization of Pfizer Covid vaccines for children between ages 5-11 years.

However, in this document we can find on page 14 modified formulation by adding an ingredient called Tromethamine that reduces the acidity of blood and is used to stabilize people who have suffered a heart attack.

The briefing document claims Tromethamine was added to Pfizer’s vaccine for children in order to “provide a vaccine with an improved stability profile.”

On Pfizer’s own website, Tromethamine is given to patients “during cardiac arrest”

https://labeling.pfizer.com/ShowLabeling.aspx?id=4642

Among many side effects caused by Tromethamine are :

·       respiratory depression, local irritation, tissue inflammation, injection site infection, febrile response, chemical phlebitis, venospasm (vein spasms), hypervolemia, IV thrombosis, extravasation (with possible necrosis and sloughing of tissues), transient decreases in blood glucose concentrations, hypoglycemia and hepatic necrosis with infusion via low-lying umbilical venous catheters.

Moderna’s experimental Covid-19 vaccine has been linked to Myocarditis and Pericarditis also includes Tromethamine .

https://dsh.ca.gov/COVID-19/docs/Vaccination/COVID-19_Vaccines_Update_on_Allergic_Reactions_Contraindications_and_Precautions.pdf

The FDA document mentions “serious adverse events and other adverse events of interest” among those who took Moderna’s booster shot, noting specifically “myocarditis, pericarditis, neurologic, neuro-inflammatory and thrombotic events” and “death.” :

https://www.fda.gov/media/152991/download

Even Pfizer did admit that those heart issue have occurred in some people who have received the vaccine.

Kowing all this they should never have authorised the roll out of the Pfizer BioNTech vaccine to children as young as 5 to 11 years old.