In a recent study, CDC stated the data supports the safety of C0V1D-19 v@¢¢ination during pregnancy. (https://www.cdc.gov/mmwr/volumes/71/wr/mm7101e1.htm?s_cid=mm7101e1_w#contribAff) Therefore, CDC now recommends C0V1D-19 genetic v@¢¢ination for women who are pregnant, recently pregnant, who are trying to become pregnant now, or who might become pregnant in the future.
However, there is a marked increase in pregnancy loss for those 1mmun1zed with C0V1D-19 genetic v@¢¢ines in the first 20 weeks of pregnancy. Pregnancy is a precarious time not just for the expectant mother but most importantly the developing fetus.
When expectant mothers are told not to drink coffee, eat deli meats, or take ibuprofen why would it be acceptable to inject them with an experimental genetic v@¢¢ine when the risks are unknown?
#TakeScienceBack
References:
(1) https://bit.ly/3pu64m0
(2) https://bit.ly/31qXWuN
(3) doi.org/10.1056/nejmoa2104983
(4) doi.org/10.1056/NEJMx210016
(5) https://bit.ly/3kxj2On
However, there is a marked increase in pregnancy loss for those 1mmun1zed with C0V1D-19 genetic v@¢¢ines in the first 20 weeks of pregnancy. Pregnancy is a precarious time not just for the expectant mother but most importantly the developing fetus.
When expectant mothers are told not to drink coffee, eat deli meats, or take ibuprofen why would it be acceptable to inject them with an experimental genetic v@¢¢ine when the risks are unknown?
#TakeScienceBack
References:
(1) https://bit.ly/3pu64m0
(2) https://bit.ly/31qXWuN
(3) doi.org/10.1056/nejmoa2104983
(4) doi.org/10.1056/NEJMx210016
(5) https://bit.ly/3kxj2On
For decades, expectant mothers have been considered a vulnerable group to be shielded from potential harms of research for the sake of their fetuses’ health. The first trimester is the riskiest time for the developing fetus.
As of January 23, 2022, a total of 3,692 cases of miscarriage have been reported through the CDC VA3R5 (2).
More safety studies are needed before authorizing these v@cc1nes for use in expectant mothers as it’s premature to recommend them given what preliminary studies have shown when they were administered during the first trimester.
Help us #TakeScienceBack
References:
1- https://bit.ly/3nDykmo crossed referenced with United States Department of Health and Human Services (DHHS), Public Health Service (PHS), Centers for Disease Control (CDC) / Food and Drug Administration (FDA), Va¢¢ine Adverse Event Reporting System (VA3R5) Accessed at https://bit.ly/3FIzhA0
2- https://bit.ly/3nHAzEZ
NOTE: Typos intended. Some original to the report from the source, some to avoid censoring.
As of January 23, 2022, a total of 3,692 cases of miscarriage have been reported through the CDC VA3R5 (2).
More safety studies are needed before authorizing these v@cc1nes for use in expectant mothers as it’s premature to recommend them given what preliminary studies have shown when they were administered during the first trimester.
Help us #TakeScienceBack
References:
1- https://bit.ly/3nDykmo crossed referenced with United States Department of Health and Human Services (DHHS), Public Health Service (PHS), Centers for Disease Control (CDC) / Food and Drug Administration (FDA), Va¢¢ine Adverse Event Reporting System (VA3R5) Accessed at https://bit.ly/3FIzhA0
2- https://bit.ly/3nHAzEZ
NOTE: Typos intended. Some original to the report from the source, some to avoid censoring.
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Phases of Clinical Trials
PRECLINICAL
The drug or treatment is tested first in the laboratory, then in animals. Preclinical studies are important for eliminating potential vaccines that are either toxic or do not induce protective immune responses.
Length of Study: up to 10 years
PHASE 1
The purpose of Phase 1 is to ensure that the treatment is safe in humans and to determine how and where it distributes within the body. This testing takes place with a small group of healthy volunteers, usually 15 to 50.
Length of Study: Several months
PHASE 2
The purpose of a Phase 2 Clinical Trial is to determine the right dosage and effectiveness in treating that particular disease. This testing takes place with a larger number of volunteers who have the disease, up to 100.
Length of Study: Several months to 2 years
Continued in comments
PRECLINICAL
The drug or treatment is tested first in the laboratory, then in animals. Preclinical studies are important for eliminating potential vaccines that are either toxic or do not induce protective immune responses.
Length of Study: up to 10 years
PHASE 1
The purpose of Phase 1 is to ensure that the treatment is safe in humans and to determine how and where it distributes within the body. This testing takes place with a small group of healthy volunteers, usually 15 to 50.
Length of Study: Several months
PHASE 2
The purpose of a Phase 2 Clinical Trial is to determine the right dosage and effectiveness in treating that particular disease. This testing takes place with a larger number of volunteers who have the disease, up to 100.
Length of Study: Several months to 2 years
Continued in comments
A 12-year-old boy dies 5 days after receiving his C0V1D genetic vaccine. He died of septic shock and Meningococcal meningitis.
Genetic vaccines were approved by the FDA for emergency authorization use on children ages 5 and older over, with booster now being recommended.
As of January 28, 2022, the death of 91 children aged 0-18 have been recorded in VA3RS in relation to the C0V1D genetic vaccines (1). Children have higher death rates in car crashes than from C0V1D. (2)
Ask yourself, is this medical treatment necessary for healthy children?
#takescienceback
1 - openvaers.com
2 - https://bit.ly/3qHZ1qM
Genetic vaccines were approved by the FDA for emergency authorization use on children ages 5 and older over, with booster now being recommended.
As of January 28, 2022, the death of 91 children aged 0-18 have been recorded in VA3RS in relation to the C0V1D genetic vaccines (1). Children have higher death rates in car crashes than from C0V1D. (2)
Ask yourself, is this medical treatment necessary for healthy children?
#takescienceback
1 - openvaers.com
2 - https://bit.ly/3qHZ1qM
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