The FDA approved the Pfizer-BioNTech vaccine on Aug. 23, 2021. The new version of the popular inoculation will be rebranded as “COMIRNATY”, however, will feature the same “formula” as the original Pfizer-BioNTech, allowing the concoction to legally be marketed to the general public.
What are the differences between Pfizer’s versions of the coronavirus vaccine? The FDA’s website states, “The FDA-approved Comirnaty (COVID-19 Vaccine, mRNA), made by Pfizer for BioNTech and the FDA-authorized Pfizer-BioNTech COVID-19 Vaccine under EUA have the same formulation and can be used interchangeably to provide the COVID-19 vaccination series without presenting any safety or effectiveness concerns.”
A Deeper Insight Into the New Pfizer Approved Drug
Although both vaccines have similar formulas, COMIRNATY is treated as a separate product under U.S. law.
Many people around the world, however, are hesitant to be injected with either of these newly developed products. This comes from a variety of reasons ranging from the belief that one simply “doesn’t need it”, to much more elaborate reasoning. What are the potential long term dangers of this FDA approved substance? Where is the data to support these claims?
Unlike the emergency use authorization version of the [same] Pfizer drug, the newer [legally approved] version includes a package insert—providing disclaimers and potential side effects of these concoctions, from Pfizer themselves.
Potential Long-term Dangers of COMIRNATY
The package insert states that COMIRNATY “has not been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility.” However it states that “[i]n a developmental toxicity study in rats” there were “no vaccine-related effects on female [rat] fertility”
Typical rats live 2-3 years. Are rats a proper subject to determine potential long term health issues that may develop as a result of these injections?
FDA propaganda now suggests all pregnant women should get vaccinated with a coronavirus vaccine. The package insert for the COMIRNATY drug also states that “All pregnancies have a risk of birth defect, loss, or other adverse outcomes.”
“It is not known whether COMIRNATY is excreted in human milk.”
“The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for COMIRNATY”—“from the underlying maternal condition. For preventive vaccines, the underlying maternal condition is susceptibility to disease prevented by the vaccine.”
Animal Data –
Where does the data to support suggestions for pregnancy come from? Injecting a single dose into rats, on four occasions. (two prior to mating, two while pregnant) The pamphlet reads, “No vaccine-related adverse effects on female fertility, fetal development, or postnatal development were reported in the study.”
Pfizer has already begun the mass testing of these injections on children ages 5-11, however the package insert states “The safety and effectiveness of COMIRNATY in individuals younger than 16 years of age have not been established.”
Despite this disclaimer, COMIRNATY has already begun marketing their product to ages 12-16 years, under emergency use authorization. Comirnaty’s public website states “the vaccine is authorized for ages 12 years & up”. The company continues to experiment on children ages 5-11 years old to test side effects in Clinical Trials.
The insert also shows lipid nanoparticles are used to deliver mRNA into the cells.
Nanoparticles are an ingredient used in coronavirus concoctions. A drawback of using mRNA-lipid nanoparticles (LNP) COVID-19 “vaccines” is that they must be stored at cold temperatures.
How mRNA Vaccines Work –
mRNA is negatively charged, and repelled by the same negatively charged cell membrane. Therefore, the researchers used positively charged lipid molecules to help LNP enter the cell. This combination is called an mRNA-lipid nanoparticle.
Dangers of Nanoparticles –
The National Institutes of Health (NIH), states in their International Journal of Nanomedicine that “nanoparticles could also cause new types of effects not previously seen with larger particles (eg, mitochondrial damage, uptake through olfactory epithelium, platelet aggregation, cardiovascular effects).”
Each vial must be diluted with 1.8 mL of sterile 0.9% Sodium Chloride Injection, USP prior to use to form the vaccine.
Ingredients in Comirnaty
Each 0.3 mL dose of the COMIRNATY includes the following ingredients:
- 30 mcg of a nucleoside-modified messenger RNA (mRNA) encoding the viral spike (S) glycoprotein of SARS-CoV-2.
- 0.43 mg ((4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate),
- 0.05 mg 2-(polyethylene glycol 2000)-N,N-ditetradecylacetamide
- 0.09 mg 1,2-distearoyl-sn-glycero-3-phosphocholine
- 0.2 mg cholesterol)
- 0.01 mg potassium chloride,
- 0.01 mg monobasic potassium phosphate
- 0.36 mg sodium chloride,
- 0.07 mg dibasic sodium phosphate dihydrate
- 6 mg sucrose.
- The diluent (0.9% Sodium Chloride Injection, USP) contributes an additional 2.16 mg sodium chloride per dose.
- COMIRNATY does not contain preservative.
- The vial stoppers are not made with natural rubber latex.
Should potential health effects of these vaccinations be considered? Should pregnant women be given more awareness of the risks involved with these experimental inoculations?
Is this pandemic about the data driven safety of the American population, or is something more nefarious afoot? Are major pharmaceutical companies overlooking opportunities to gain deeper insight into their concoctions before deeming this modern technology completely safe for public use?