Source: https://banned.video/watch?id=618c7b9111848a41725b16e2
The Food and Drug Administration (FDA) Advisory Committee that voted 17-0 to approve the jabs for children as young as five was notified that the children’s formulation of the drug contains tromethamine (Tris), a chemical that reduces blood acidity and stabilizes people who have suffered a heart attack.
Vaccines and Related Biological Products Advisory Committee Meeting
October 26, 2021
FDA Briefing Document
EUA amendment request for Pfizer-BioNTech COVID-19 Vaccine for use in children 5 through 11 years of age
PDF: https://www.fda.gov/media/153447/download
Page 14, Chapter 5
Vaccine formulation
To provide a vaccine with an improved stability profile, the Pfizer-BioNTech COVID-19 Vaccine for use in children 5-11 years of age uses tromethamine (Tris) buffer instead of the phosphatebuffered saline (PBS) as used in the previous formulation and excludes sodium chloride and potassium chloride. The packaged vials for the new formulation are stored frozen at -90°C to – 60°C. The frozen vials may be thawed and stored at refrigerator at 2°C to 8°C for up to 10 weeks.
https://www.drugs.com/cdi/tromethamine.html
Uses of Tromethamine:
It is used to treat or prevent acid problems in the blood.
What do I need to tell my doctor BEFORE I take Tromethamine?
For all patients taking tromethamine:
If you have an allergy to tromethamine or any other part of tromethamine.
If you are allergic to tromethamine; any part of tromethamine; or any other drugs, foods, or substances. Tell your doctor about the allergy and what signs you had.
If you are not able to pass urine.
Children:
This medicine is not for newborns who have any of these problems: High blood carbon dioxide levels or too much salicylate in the body.
This is not a list of all drugs or health problems that interact with tromethamine.
What are some things I need to know or do while I take Tromethamine?
For all patients taking tromethamine:
Tell all of your health care providers that you take tromethamine. This includes your doctors, nurses, pharmacists, and dentists.
Have blood work checked as you have been told by the doctor. Talk with the doctor.
Check your blood sugar as you have been told by your doctor.
Tell your doctor if you are pregnant or plan on getting pregnant. You will need to talk about the benefits and risks of using tromethamine while you are pregnant.
Tell your doctor if you are breast-feeding. You will need to talk about any risks to your baby.
Children:
Use with care in children. Talk with the doctor.
How is this medicine (Tromethamine) best taken?
Use tromethamine as ordered by your doctor. Read all information given to you. Follow all instructions closely.It is given as an infusion into a vein over a period of time.
https://www.drugs.com/dosage/tromethamine.html
Tromethamine Dosage
Applies to the following strengths: 3.6 g/100 mL
Usual Pediatric Dose for Metabolic Acidosis
Associated with RDS in Neonates and Infants:
1 mL/kg for each pH unit below 7.4
Dose Adjustments
Dosage should be limited to an amount sufficient to increase blood pH to normal limits (7.35 to 7.45) and to correct acid-base derangements
Estimate the IV dosage of tromethamine injection from the buffer base deficit of the extracellular fluid in mEq/liter determined by means of the Siggaard-Andersen nomogram.
Use the following formula as a general guide:
Tromethamine solution (mL of 0.3 M) required =
Body Weight (kg) X
Base Deficit (mEq/liter) X 1.1
Note: Factor of 1.1 accounts for an approximate reduction of 10% in buffering capacity due to the presence of sufficient acetic acid to lower pH of the 0.3 M solution to approximately 8.
https://www.drugs.com/sfx/tromethamine-side-effects.html
Side effects include:
Adverse effects may include respiratory depression, local irritation, tissue inflammation, injection site infection, febrile response, chemical phlebitis, venospasm, hypervolemia, IV thrombosis, extravasation (with possible necrosis and sloughing of tissues), transient decreases in blood glucose concentrations, hypoglycemia, and hepatocellular necrosis with infusion via low-lying umbilical venous catheters. (See Warnings under Cautions.)
Why has Pfizer changed the formulation of its Covid-19 Vaccine for Children to include an ingredient that stabilises people suffering a Heart Attack?
A document prepared for the FDA Advisory Committee meeting, in which members voted seventeen to zero in favour of giving emergency use authorisation for the administration of the Pfizer Covid-19 injection to children aged 5 to 11, confirms that Pfizer have modified the formulation of their injection for children to include an ingredient that reduces the acidity of blood and is used to stabilise people who have suffered a heart attack.
the news network 