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Kraken
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OP in raypeat forum : https://raypeatforum.com/community/...om-the-vaccinated-to-the-un-vaccinated.40111/
inb4 dn , i highlighted the important parts
PFIZER’S OWN DOCUMENTS
STATE BOTH INHALATION AND SKIN CONTACT WILL TRANSMIT WHATEVER IS IN THE
VAX FROM THE VACCINATED TO THE UN-VACCINATED
Here is what just this
small portion of this Pfizer document is saying:
1. If a man who was not vaccinated touches a vaccinated woman, or
breathes any of the air she breathes, (in other words, walks by her in
the office) and he then has sex with his wife, his wife can have an
adverse event and she should avoid having children.
2. If a woman who was never vaccinated gets exposed to a woman who was
vaccinated, she can:
A: miscarry,
B: spontaneously abort,
C. poison a baby via her breast milk
D: Have babies that have congitive difficulties.
This is universal, and very bad. Here is a small section of text I
translated to English:
8.3.5.3. Occupational Exposure
“An occupational exposure occurs when a person receives unplanned
direct contact with a vaccine test subject, which may or may not lead to
the occurrence of an adverse event. These people may include health care
providers, family members, and other people who are around the trial
participant.
When such exposures happen, the investigator must report them to Pfizer
saftey within 24 hours of becoming aware of when they happened,
regardless of whether or not there is an associated secondary adverse
event. This must be reported using the vaccine secondary adverse event
report form. SINCE THE INFORMATION DOES NOT PERTAIN TO A PARTICIPANT
INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE
STUDY.”
TO CLARIFY: Vaccine study participants become super spreaders of
something, they don’t say what it is, but it triggers secondary
adverse events in people that never had the vax, when they are exposed
to people who did have the vax.
THIS IS SO BAD that right here, in this little bit of quoted text, it
warns that un-vaccinated men who have been exposed to a woman who was
vaxxed will then pass whatever is in the vax to another woman.
Even the relatively small portion of the document I have put below here
says the vax triggers spontaneous abortions and reproductive problems
when un-vaccinated people are exposed to the vaccinated and that breast
milk from a vaccinated mom can harm the infant. And if anyone does not
believe it, then click the link above and wade through that enormous and
intentionally confusing document. It’s for real folks, the vax is
indeed the kill shot.
Do not permit the vaccinated to come anywhere near you, it is now
official.
Here is a small portion of this huge document, straight from pfizer:
Terms:
Study intervention – A vaccine test subject.
AE – Adverse event in someone who got the vax.
SAE: An adverse event in someone who was exposed to someone who got the
vax.
EDP: Exposure during pregnancy
8.3.5. Exposure During Pregnancy or Breastfeeding, and Occupational
Exposure Exposure to the study intervention under study during pregnancy
or breastfeeding and occupational exposure are reportable to Pfizer
Safety within 24 hours of investigator awareness.
8.3.5.1. Exposure During Pregnancy An EDP occurs if:
* A female participant is found to be pregnant while receiving or after
discontinuing study intervention.
* A male participant who is receiving or has discontinued study
intervention exposes a female partner prior to or around the time of
conception.
* A female is found to be pregnant while being exposed or having been
exposed to study intervention due to environmental exposure. Below are
examples of environmental exposure during pregnancy:
* A female family member or healthcare provider reports that she is
pregnant after having been exposed to the study intervention by
inhalation or skin contact.
* A male family member or healthcare provider who has been exposed to
the study intervention by inhalation or skin contact then exposes his
female partner prior to or around the time of conception.
____
If this vax is not shedding into other people, why would contact between
vaccinated and un-vaccinated be an event worth noting? If this vax is
not shedding, then WHY does a guy who has been around a vaccinated
woman, even if he did not touch her or have sex, need to worry about
getting a different woman pregnant?
That’s not all, the following is detailed, and far worse.
The investigator must report EDP to Pfizer Safety within 24 hours of the
investigator’s awareness, irrespective of whether an SAE has occurred.
The initial information submitted should include the anticipated date of
delivery (see below for information related to termination of
pregnancy).
* If EDP occurs in a participant or a participant’s partner, the
investigator must report this information to Pfizer Safety on the
Vaccine SAE Report Form and an EDP Supplemental Form, regardless of
whether an SAE has occurred. Details of the pregnancy will be collected
after the start of study intervention and until 6 months after the last
dose of study intervention.
* If EDP occurs in the setting of environmental exposure, the
investigator must report information to Pfizer Safety using the Vaccine
SAE Report Form and EDP Supplemental Form. Since the exposure
information does not pertain to the participant enrolled in the study,
the information is not recorded on a CRF; however, a copy of the
completed Vaccine SAE Report Form is maintained in the investigator site
file. Follow-up is conducted to obtain general information on the
pregnancy and its outcome for all EDP reports with an unknown outcome.
The investigator will follow the pregnancy until completion (or until
pregnancy termination) and notify Pfizer Safety of the outcome as a
follow-up to the initial EDP Supplemental Form. In the case of a live
birth, the structural integrity of the neonate can be assessed at the
time of birth. In the event of a termination, the reason(s) for
termination should be specified and, if clinically possible, the
structural integrity of the terminated fetus should be assessed by gross
visual inspection (unless preprocedure test findings are conclusive for
a congenital anomaly 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 demise, neonatal death, or congenital anomaly), the
investigator should follow the procedures for reporting SAEs. Additional
information about pregnancy outcomes that are reported to Pfizer Safety
as SAEs follows:
* Spontaneous abortion including miscarriage and missed abortion;
* Neonatal deaths that occur within 1 month of birth should be reported,
without regard to causality, as SAEs. In addition, infant deaths after 1
month should be reported as SAEs when the investigator assesses the
infant death as related or possibly related to exposure to the study
intervention. Additional information regarding the EDP may be requested
by the sponsor. Further follow-up of birth outcomes will be handled on a
case-by-case basis (eg, follow-up on preterm infants to identify
developmental delays). In the case of paternal exposure, the
investigator will provide the participant with the Pregnant Partner
Release of Information Form to deliver to his partner. The investigator
must document in the source documents that the participant was given the
Pregnant Partner Release of Information Form to provide to his partner.
8.3.5.2. Exposure During Breastfeeding An exposure during breastfeeding
occurs if:
* A female participant is found to be breastfeeding while receiving or
after discontinuing study intervention.
* A female is found to be breastfeeding while being exposed or having
been exposed to study intervention (ie, environmental exposure). An
example of environmental exposure during breastfeeding is a female
family member or healthcare provider who reports that she is
breastfeeding after having been exposed to the study intervention by
inhalation or skin contact. The investigator must report exposure during
breastfeeding to Pfizer Safety within 24 hours of the investigator’s
awareness, irrespective of whether an SAE has occurred. The information
must be reported using the Vaccine SAE Report Form. When exposure during
breastfeeding occurs in the setting of environmental exposure, the
exposure information does not pertain to the participant enrolled in the
study, so the information is not recorded on a CRF. However, a copy of
the completed Vaccine SAE Report Form is maintained in the investigator
site file. An exposure during breastfeeding report is not created when a
Pfizer drug specifically approved for use in breastfeeding women (eg,
vitamins) is administered in accord with authorized use. However, if the
infant experiences an SAE associated with such a drug, the SAE is
reported together with the exposure during breastfeeding.
Here’s the clear part of this, that everyone can understand:
8.3.5.3. Occupational Exposure An occupational exposure occurs when a
person receives unplanned direct contact with the study intervention,
which may or may not lead to the occurrence of an AE. Such persons may
include healthcare providers, family members, and other roles that are
involved in the trial participant’s care. The investigator must report
occupational exposure to Pfizer Safety within 24 hours of the
investigator’s awareness, regardless of whether there is an associated
SAE. The information must be reported using the Vaccine SAE Report Form.
Since the information does not pertain to a participant enrolled in the
study, the information is not recorded on a CRF; however, a copy of the
completed Vaccine SAE Report Form is maintained in the investigator site
file.
I WILL TRANSLATE THAT TO ENGLISH:
An occupational exposure occurs when a person receives unplanned direct
contact with a vaccine test subject, which may or may not lead to the
occurrence of an adverse event. These people may include health care
providers, family members, and other people who are around the trial
participant.
When such exposures happen, the investigator must report them to Pfizer
saftey within 24 hours of becoming aware of when they happened,
regardless of whether or not there is an associated secondary adverse
event. This must be reported using the vaccine secondary adverse event
report form. SINCE THE INFORMATION DOES NOT PERTAIN TO A PARTICIPANT
INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE
STUDY.
My comment:
India is having their disaster happen now because they started with the
vaxxes first, and have more people vaxxed than any other country.
https://media.tghn.org/medialibrary/2020/11/C4591001_Clinical_Protocol_Nov2020_Pfizer_BioNTech.pdf
@Chadlite Rutherford thoughts?
inb4 dn , i highlighted the important parts
PFIZER’S OWN DOCUMENTS
STATE BOTH INHALATION AND SKIN CONTACT WILL TRANSMIT WHATEVER IS IN THE
VAX FROM THE VACCINATED TO THE UN-VACCINATED
Here is what just this
small portion of this Pfizer document is saying:
1. If a man who was not vaccinated touches a vaccinated woman, or
breathes any of the air she breathes, (in other words, walks by her in
the office) and he then has sex with his wife, his wife can have an
adverse event and she should avoid having children.
2. If a woman who was never vaccinated gets exposed to a woman who was
vaccinated, she can:
A: miscarry,
B: spontaneously abort,
C. poison a baby via her breast milk
D: Have babies that have congitive difficulties.
This is universal, and very bad. Here is a small section of text I
translated to English:
8.3.5.3. Occupational Exposure
“An occupational exposure occurs when a person receives unplanned
direct contact with a vaccine test subject, which may or may not lead to
the occurrence of an adverse event. These people may include health care
providers, family members, and other people who are around the trial
participant.
When such exposures happen, the investigator must report them to Pfizer
saftey within 24 hours of becoming aware of when they happened,
regardless of whether or not there is an associated secondary adverse
event. This must be reported using the vaccine secondary adverse event
report form. SINCE THE INFORMATION DOES NOT PERTAIN TO A PARTICIPANT
INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE
STUDY.”
TO CLARIFY: Vaccine study participants become super spreaders of
something, they don’t say what it is, but it triggers secondary
adverse events in people that never had the vax, when they are exposed
to people who did have the vax.
THIS IS SO BAD that right here, in this little bit of quoted text, it
warns that un-vaccinated men who have been exposed to a woman who was
vaxxed will then pass whatever is in the vax to another woman.
Even the relatively small portion of the document I have put below here
says the vax triggers spontaneous abortions and reproductive problems
when un-vaccinated people are exposed to the vaccinated and that breast
milk from a vaccinated mom can harm the infant. And if anyone does not
believe it, then click the link above and wade through that enormous and
intentionally confusing document. It’s for real folks, the vax is
indeed the kill shot.
Do not permit the vaccinated to come anywhere near you, it is now
official.
Here is a small portion of this huge document, straight from pfizer:
Terms:
Study intervention – A vaccine test subject.
AE – Adverse event in someone who got the vax.
SAE: An adverse event in someone who was exposed to someone who got the
vax.
EDP: Exposure during pregnancy
8.3.5. Exposure During Pregnancy or Breastfeeding, and Occupational
Exposure Exposure to the study intervention under study during pregnancy
or breastfeeding and occupational exposure are reportable to Pfizer
Safety within 24 hours of investigator awareness.
8.3.5.1. Exposure During Pregnancy An EDP occurs if:
* A female participant is found to be pregnant while receiving or after
discontinuing study intervention.
* A male participant who is receiving or has discontinued study
intervention exposes a female partner prior to or around the time of
conception.
* A female is found to be pregnant while being exposed or having been
exposed to study intervention due to environmental exposure. Below are
examples of environmental exposure during pregnancy:
* A female family member or healthcare provider reports that she is
pregnant after having been exposed to the study intervention by
inhalation or skin contact.
* A male family member or healthcare provider who has been exposed to
the study intervention by inhalation or skin contact then exposes his
female partner prior to or around the time of conception.
____
If this vax is not shedding into other people, why would contact between
vaccinated and un-vaccinated be an event worth noting? If this vax is
not shedding, then WHY does a guy who has been around a vaccinated
woman, even if he did not touch her or have sex, need to worry about
getting a different woman pregnant?
That’s not all, the following is detailed, and far worse.
The investigator must report EDP to Pfizer Safety within 24 hours of the
investigator’s awareness, irrespective of whether an SAE has occurred.
The initial information submitted should include the anticipated date of
delivery (see below for information related to termination of
pregnancy).
* If EDP occurs in a participant or a participant’s partner, the
investigator must report this information to Pfizer Safety on the
Vaccine SAE Report Form and an EDP Supplemental Form, regardless of
whether an SAE has occurred. Details of the pregnancy will be collected
after the start of study intervention and until 6 months after the last
dose of study intervention.
* If EDP occurs in the setting of environmental exposure, the
investigator must report information to Pfizer Safety using the Vaccine
SAE Report Form and EDP Supplemental Form. Since the exposure
information does not pertain to the participant enrolled in the study,
the information is not recorded on a CRF; however, a copy of the
completed Vaccine SAE Report Form is maintained in the investigator site
file. Follow-up is conducted to obtain general information on the
pregnancy and its outcome for all EDP reports with an unknown outcome.
The investigator will follow the pregnancy until completion (or until
pregnancy termination) and notify Pfizer Safety of the outcome as a
follow-up to the initial EDP Supplemental Form. In the case of a live
birth, the structural integrity of the neonate can be assessed at the
time of birth. In the event of a termination, the reason(s) for
termination should be specified and, if clinically possible, the
structural integrity of the terminated fetus should be assessed by gross
visual inspection (unless preprocedure test findings are conclusive for
a congenital anomaly 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 demise, neonatal death, or congenital anomaly), the
investigator should follow the procedures for reporting SAEs. Additional
information about pregnancy outcomes that are reported to Pfizer Safety
as SAEs follows:
* Spontaneous abortion including miscarriage and missed abortion;
* Neonatal deaths that occur within 1 month of birth should be reported,
without regard to causality, as SAEs. In addition, infant deaths after 1
month should be reported as SAEs when the investigator assesses the
infant death as related or possibly related to exposure to the study
intervention. Additional information regarding the EDP may be requested
by the sponsor. Further follow-up of birth outcomes will be handled on a
case-by-case basis (eg, follow-up on preterm infants to identify
developmental delays). In the case of paternal exposure, the
investigator will provide the participant with the Pregnant Partner
Release of Information Form to deliver to his partner. The investigator
must document in the source documents that the participant was given the
Pregnant Partner Release of Information Form to provide to his partner.
8.3.5.2. Exposure During Breastfeeding An exposure during breastfeeding
occurs if:
* A female participant is found to be breastfeeding while receiving or
after discontinuing study intervention.
* A female is found to be breastfeeding while being exposed or having
been exposed to study intervention (ie, environmental exposure). An
example of environmental exposure during breastfeeding is a female
family member or healthcare provider who reports that she is
breastfeeding after having been exposed to the study intervention by
inhalation or skin contact. The investigator must report exposure during
breastfeeding to Pfizer Safety within 24 hours of the investigator’s
awareness, irrespective of whether an SAE has occurred. The information
must be reported using the Vaccine SAE Report Form. When exposure during
breastfeeding occurs in the setting of environmental exposure, the
exposure information does not pertain to the participant enrolled in the
study, so the information is not recorded on a CRF. However, a copy of
the completed Vaccine SAE Report Form is maintained in the investigator
site file. An exposure during breastfeeding report is not created when a
Pfizer drug specifically approved for use in breastfeeding women (eg,
vitamins) is administered in accord with authorized use. However, if the
infant experiences an SAE associated with such a drug, the SAE is
reported together with the exposure during breastfeeding.
Here’s the clear part of this, that everyone can understand:
8.3.5.3. Occupational Exposure An occupational exposure occurs when a
person receives unplanned direct contact with the study intervention,
which may or may not lead to the occurrence of an AE. Such persons may
include healthcare providers, family members, and other roles that are
involved in the trial participant’s care. The investigator must report
occupational exposure to Pfizer Safety within 24 hours of the
investigator’s awareness, regardless of whether there is an associated
SAE. The information must be reported using the Vaccine SAE Report Form.
Since the information does not pertain to a participant enrolled in the
study, the information is not recorded on a CRF; however, a copy of the
completed Vaccine SAE Report Form is maintained in the investigator site
file.
I WILL TRANSLATE THAT TO ENGLISH:
An occupational exposure occurs when a person receives unplanned direct
contact with a vaccine test subject, which may or may not lead to the
occurrence of an adverse event. These people may include health care
providers, family members, and other people who are around the trial
participant.
When such exposures happen, the investigator must report them to Pfizer
saftey within 24 hours of becoming aware of when they happened,
regardless of whether or not there is an associated secondary adverse
event. This must be reported using the vaccine secondary adverse event
report form. SINCE THE INFORMATION DOES NOT PERTAIN TO A PARTICIPANT
INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE
STUDY.
My comment:
India is having their disaster happen now because they started with the
vaxxes first, and have more people vaxxed than any other country.
https://media.tghn.org/medialibrary/2020/11/C4591001_Clinical_Protocol_Nov2020_Pfizer_BioNTech.pdf
@Chadlite Rutherford thoughts?
So it's over ?
