INFORMED CONSENT
VAERS NUMBERS (As of 11/12/21)
Practice Informed Consent! Did you know that Harvard medical did a study on our VAERS system? The results were that less than 0.3% of all adverse drug events and 1-13% serious events are reported to the FDA. Likewise, fewer than 1% of vaccine adverse events are reported...
Deaths- 18,853
Heart Attacks- 9,332
Hospitalizations-94,537
Myocarditis- 13,237
Urgent Care-99,470
Permanently Disabled- 30,010
Doctor Office Visits-139,952 T
Thrombocytopenia/Low Platelet- 4,387
Anaphylaxis-8,082
Life Threatening- 21,089
Bell’s Palsy-11,229
Severe Allergic Reactions- 33,660
Miscarriages-2,996
Shingles- 10,455
MYOCARDITIS:
Here’s a look at the CDC’s risk of myocarditis by age
* Did you know The ACIP requested an ingredient change on the pediatric dose?
“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 phosphate-buffered saline (PBS) as used in the previous formulation and excludes sodium chloride and potassium chloride. The packaged vials for the new formulation.”
Side Effects of tromethamine
(A blood acid that helps treat and prevent heart attacks.)
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.
*Here’s the FDA’s working list of possible adverse event outcomes.
Why weren’t we warned of this?
