Read it and shudder, Pfizers’s own documents state that both inhalation and skin contact will transmit what is in the vaccine to the unvaccinated.
Here’s what only a small part of this Pfizer document says:
If a man who has not been vaccinated touches a vaccinated woman, or breathes the air she exhales, (in other words, walks past her in the office) and he then has sex with his wife, his wife may have an adverse event and should avoid having children.
If a woman who has never been vaccinated comes into contact with a woman who has been vaccinated, she may:
A: suffer a miscarriage,
B: spontaneously abort,
C: poison a baby through her breast milk,
D: have babies with cognitive problems (memory and concentration problems).
This is universal, and very bad. Here is a small portion of the text translated into plain English:
8.3.5.3. Occupational exposure
“Occupational exposure occurs when a person has unplanned direct contact with a vaccine subject, which may or may not result in the occurrence of an adverse event. These individuals may include health care providers, family members and other people in the subject’s environment.
When such exposures occur, the investigator must report it to Pfizer saftey within 24 hours of being informed of it, whether or not an associated secondary adverse event occurs. This should be reported using the Vaccine Secondary Adverse Event Reporting form. SINCE THE INFORMATION DOES NOT RELATE TO A STUDY PARTICIPANT, THE INFORMATION WILL BE KEPT SEPARATE FROM THE STUDY.”
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Just to make it clear, participants in vaccine studies become super spreaders of something, they don’t say what it is, but it causes secondary adverse events in people who have never had the ‘vaccine’, when exposed to people who have had the ‘vaccine’.
THIS IS SO SLIGHT that here, in this small piece of quoted text, it is warned that unvaccinated men who have been exposed to a woman who did have the vaccine will pass on what is in the vaccine to another woman.
Even in the relatively small section of the document shown below, it says that the vaccine causes spontaneous abortions and reproductive problems when unvaccinated people are exposed to vaccinated people, and that breast milk from a vaccinated mother can be harmful to the infant. And if anyone doesn’t believe that, click on the link above and wade through that huge and intentionally confusing document. It’s really true folks, the vaccine is indeed the killer syringe.
Don’t let the vaccinated near you, it’s now official.
Here is a small portion of this huge document, straight from Pfizer:
Terms
Study intervention – A vaccine trial subject.
AE – Adverse event in someone who received the vaccine.
SAE: An adverse event in someone who has been exposed to someone who has received the vaccine.
EDP: Exposure during pregnancy.
8.3.5. Exposure to the study intervention under study during pregnancy or lactation and occupational exposure must be reported to Pfizer Safety within 24 hours of the investigator becoming aware of it.
8.3.5.1. Exposure during pregnancy – An EDP occurs if:
* A female participant is found to be pregnant while receiving a study intervention or after she has discontinued it.
* A male participant who is undergoing or has discontinued a study intervention is exposed to a female partner before or around the time of conception.
* A woman is found to be pregnant while exposed or has been exposed to a study intervention due to environmental exposure. The following are examples of exposure to the study environment during pregnancy:
* A female family member or caregiver reports that she is pregnant after exposure to the study intervention through inhalation or dermal contact.
* A male family member or caregiver exposed to the study intervention through inhalation or skin contact subsequently exposes his female partner prior to or around the time of conception.
If this vaccination is not transmitted to other people, why would contact between vaccinated and unvaccinated people be a noteworthy event? If this vaccination is not transmitted, WHY should a man who has been around a vaccinated woman, even if he has not touched her or had sex, be concerned if he gets another woman pregnant?
Read also: Got jab? No more fly – why covid-vaccinated are not fit to fly.
That’s not all, the following is detailed, and much worse.
The investigator must report EDP to Pfizer Safety within 24 hours of the investigator becoming aware of it, regardless of whether an SAE has occurred. The first information submitted must include the expected date of delivery (see below for information regarding termination of pregnancy).
* If EDP occurs in the setting of environmental exposure, the investigator must report information to Pfizer Safety using the Vaccine SAE Report Form and the EDP Supplemental Form. Since the exposure information does not relate to the participant participating in the study, the information is not recorded on a CRF; however, a copy of the completed Vaccine SAE Report Form is kept in the investigator’s site file. Follow-up is performed to obtain general information about the pregnancy and its outcome for all EDP reports with an unknown outcome. The investigator follows the pregnancy until it is completed (or until the pregnancy is terminated) and notifies Pfizer Safety of the outcome as a follow-up to the original EDP supplement form. In the case of a live birth, the structural integrity of the neonate may be assessed at the time of birth. In the case of an abortion, the reason(s) for the abortion should be specified and, if clinically possible, the structural integrity of the aborted fetus should be assessed by visual examination (unless the findings of the pre-procedure examination reveal a congenital anomaly and the findings are reported). Abnormal pregnancy outcomes are considered SAEs. If the pregnancy outcome meets the criteria for an SAE (i.e., ectopic pregnancy, spontaneous abortion, fetal death within the uterus, neonatal death, or congenital anomaly), the investigator must follow the procedures for reporting SAEs. The following is additional information on pregnancy outcomes reported as SAEs to Pfizer Safety:
Report of the Israeli People Committee on deaths from vaccination.
* Spontaneous abortion, including miscarriage and missed abortion;
* Neonatal deaths occurring within 1 month of birth, regardless of causality, should be reported as SAEs. In addition, deaths of infants after 1 month should be reported as SAEs when the investigator believes that the infant’s death is related or potentially related to exposure to the study intervention. The sponsor may request additional information on the PBT. Further follow-up of birth outcomes will be handled on a case-by-case basis (e.g., follow-up of preterm infants to determine developmental delays). In the case of paternal exposure, the investigator will provide the participant with the Pregnant Partner Information Release Form to give to their partner. The investigator must document in the source documents that the participant was provided the Pregnant Partner Information Release Form to give to their partner.
8.3.5.2. Exposure during breastfeeding – Exposure during breastfeeding occurs if:
* A female participant is found to be breastfeeding during or after discontinuation of the study intervention.
* A woman is found to be breastfeeding while exposed or exposed to a study intervention (i.e., environmental exposure). An example of environmental exposure during breastfeeding is a female family member or caregiver reporting that she is breastfeeding after being exposed to the study intervention through inhalation or skin contact. The investigator must report exposure during breastfeeding to Pfizer Safety within 24 hours of the investigator becoming aware of it, regardless of whether an SAE occurred. The information must be reported using the Vaccine SAE Report Form. If exposure during breastfeeding occurs in the setting of environmental exposure, the exposure information does not pertain to the participant enrolled in the study and therefore the information is not recorded on a CRF. However, a copy of the completed Vaccine SAE Report Form is kept in the investigator’s file. No breastfeeding exposure report is created when a Pfizer drug specifically approved for use in breastfeeding women (e.g., vitamins) is administered in accordance with the approved use. However, if the infant receives an SAE associated with such a drug, the SAE is reported along with the exposure during breastfeeding.