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Friday, April 8 2022
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Home/GENERAL/BOMB: Stay Away From The Vaccinated!
GENERAL


BOMB: STAY AWAY FROM THE VACCINATED!

Brenda Brown Send an email 4 days ago
00 6 minutes read
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Pfizer’s latest documents shared bombshell data! They stated inhalation and skin
contact with the vaccinated may transfer what’s in the vaccine to the
unvaccinated.

Join Our Telegram channel here: https://t.me/TheTrueReporter

You can read the following disturbing information:

If an unvaccinated man touches a vaccinated woman or inhales the air she exhales
and then has sex with his wife, his wife may have an adverse event and must then
avoid having children.



If a woman who has never been vaccinated comes into contact with a woman who has
been vaccinated, she may:

A: Have a miscarriage,
B: Abort spontaneously,
C. Poison a baby through her breast milk,
D: Have babies with cognitive problems (memory and concentration problems).

Anonymouswire.com reported this was universal!

Monetized by optAd360
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Here’s one segment of the text.

8.3.5.3. Occupational exposure

“Occupational exposure occurs when a person has unplanned direct contact with a
subject for a vaccine, which may or may not lead to the occurrence of an adverse
event. These individuals may include caregivers, relatives, and other people
close to the subject.

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When such exposures occur, the investigator must report this to Pfizer safety
within 24 hours of being notified, whether or not an associated secondary
adverse event occurs. This must be reported using the vaccine secondary adverse
event reporting form. SINCE THE INFORMATION DOES NOT RELATE TO ANY PARTICIPANT
IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE STUDY”.

Don’t let the vaccinated get close to you.

Read a segment of the long document from Pfizer:

Terms

Study Intervention – A Vaccine Subject.
AE – Adverse event in someone who has 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 investigation during pregnancy
or lactation and occupational exposures must be reported to Pfizer Safety within
24 hours of becoming aware of the investigator.

8.3.5.1. Exposure during pregnancy – EDP is present if:

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* A female participant is found to be pregnant while receiving a study
intervention or after she has stopped taking it.
* A male participant undergoing or having 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
research intervention due to environmental exposure. Below are examples of
exposure to the study environment during pregnancy:
* A female relative or caregiver reports that she is pregnant after exposure to
the study intervention through inhalation or skin contact.

* A male relative or caregiver exposed to the study intervention through
inhalation or skin contact then exposes their female partner prior to or around
the time of conception.

†

The worst is yet to come:

”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 the termination of pregnancy).

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* 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 in the study, the information is not recorded on a CRF; however, a
copy of the completed Vaccine SAE Report Form will be kept on file at the
investigator’s site. 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 completion (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 live birth, the structural
integrity of the neonate can be assessed at the time of birth. In the case of
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 examination precede demonstrate a
congenital anomaly to the procedure and the findings are reported). Abnormal
pregnancy outcomes are considered SAEs. If the outcome of the pregnancy meets
the criteria for an SAE (ie, ectopic pregnancy, spontaneous abortion,
intrauterine fetal death, neonatal death, or congenital malformation), the
investigator should follow the procedures for reporting SAEs.

* 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, infant mortality at 1 month should be
reported as SAE when the investigator believes that infant death is or may be
related to exposure to the study intervention. The client may request additional
information about the PBT. Further follow-up of birth outcomes will be addressed
on a case-by-case basis (eg follow-up of preterm infants to identify
developmental delays). In the case of father exposure, the researcher will
provide the participant with the Pregnant Partner Information Disclosure Form to
give to his partner.

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8.3.5.2. Exposure During Breastfeeding – Exposure during breastfeeding occurs
if:

* A female participant was found to be breastfeeding during or after
discontinuation of the study intervention.

* A woman has been found to be breastfeeding while exposed or exposed to a
research intervention (ie exposure to the environment). An example of
environmental exposure during breastfeeding is a female relative 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 lactation to Pfizer Safety within 24 hours of becoming aware of
it, whether or not an SAE has 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 relate to
the participant enrolled in the study and thus the information is not recorded
on a CRF. However, a copy of the completed Vaccine SAE Report Form will be kept
in the investigator’s file. No report of exposure during breastfeeding is
created when a Pfizer drug specifically approved for use in breastfeeding women
(eg, vitamins) is administered in accordance with its approved use. However, if
the infant develops an SAE associated with such a drug, the SAE will be reported
along with the exposure during lactation. However, a copy of the completed
Vaccine SAE Report Form will be kept in the investigator’s file. No report of
exposure during breastfeeding is created when a Pfizer drug specifically
approved for use in breastfeeding women (eg, vitamins) is administered in
accordance with its approved use. However, if the infant develops an SAE
associated with such a drug, the SAE will be reported along with the exposure
during lactation. However, a copy of the completed Vaccine SAE Report Form will
be kept in the investigator’s file. No report of exposure during breastfeeding
is created when a Pfizer drug specifically approved for use in breastfeeding
women (eg, vitamins) is administered in accordance with its approved use.
However, if the infant develops an SAE associated with such a drug, the SAE will
be reported along with the exposure during lactation.”

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Here’s something that everyone would understand.

8.3.5.3. Occupational exposure – Occupational exposure occurs when a person
comes into unplanned direct contact with the study intervention, which may or
may not lead to the occurrence of an AE. Such individuals may include
caregivers, relatives, or other individuals involved in the care of the study
participant. The investigator must report occupational exposures to Pfizer
Safety within 24 hours of the investigator’s knowledge, regardless of whether an
associated SAE occurs. The information must be reported using the Vaccine SAE
Report Form. Since the information does not relate to a participant
participating in the study, the information is not recorded in a CRF;

Occupational exposure occurs when a person has unplanned direct contact with a
vaccine subject, which may or may not lead to the occurrence of an adverse
event. These people may be caregivers, family members, and other people close to
the subject.

When such exposures occur, the investigator must report this to Pfizer Saftey
within 24 hours of being notified, whether or not an associated secondary
adverse event occurs. This must be reported using the vaccine secondary adverse
event reporting form. SINCE THE INFORMATION DOES NOT RELATE TO ANY PARTICIPANT
INVOLVED IN THE STUDY, THE INFORMATION WILL BE KINDED SEPARATELY FROM THE STUDY.

COVID ‘Vaccine Shedding’, Evidence SARS-CoV-2 Spike Protein Can ‘Alter Human
Genes’ & VAERS Truth:

 

Join Our Telegram channel here: https://t.me/TheTrueReporter

Source: thetruedefender.com



Brenda Brown Send an email 4 days ago
0 4,534 6 minutes read
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BRENDA BROWN





COVID ORIGIN MAY BE FROM AN EVIL SYMBOL! ‘’WATCH THE WATER’’ [WATCH]


FALSE FLAG: BUCHA MASSACRE: DEAD BODIES MOVING AROUND!


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