#COVIDIOTS, #Scamdemic, Coronavirus, Genocide, VacGate/Demonjuice

Pfizer’s Official Document! Legalized Crime and Consensual Suicide | toba60

We’ll look back on this in disbelief and say, “what on earth were these people thinking?”. There has never been a situation that’s been this unambiguously malicious in its intent & design from start to finish as this overtly obvious population culling instrument. I have difficulty explaining what I’m seeing. I likely be traumatized.

I’m sticking to my mind control theory. I think they’ve put some kind of frequency out that makes certain already-hypnotized people susceptible to heavy suggestion, at the least. If not full blown loss of mental and physical autonomy. Zombified. This could perhaps be what all the Zombie Apocalypse predictive programming was all about. Or we’re going to have a real one on top of this one.

Translated from Italian….

Source: Ilgiardinodeilibri.tv

Pfizer’s Official Document! Legalized Crime and Consensual Suicide | toba60

What looks like a horror film is a perplexing reality, it is not a file by Josef Mengele drawn up in the privacy of a Nazi concentration camp, but a report that in the light of day has been approved by consensus by every head of world government is hidden from the people who have deliberately accepted their deadly addiction to a social experiment whose purpose has no relation to the health of individuals.

Josef Mengele

Take care to deepen every single word that is transcribed in black and white in the Pfizer report , I have only made a summary, but inside there is the most creepy one can imagine in human memory.

Nothing you read can be denied, just have the foresight to reflect on what at the end of the reading you will have the opportunity to know so that you have the awareness of a reality ‘that has overruled every most ‘ devastating imagination.

Toba60

Stay away from the Vaxxed, it’s official, from the Pfizer Docs

I am so scared of this that my brain is jamming and I am not coding well. Now I am correcting the coding errors.

NEW YORK, NY – NOVEMBER 09: A sign for Pfizer is seen outside the Pfizer headquarters on November 9, 2020 in New York City. Pharmaceutical company Pfizer announced positive early results on its Covid-19 vaccine trial and has proven to be 90% effective in preventing infection of the virus. David Dee Delgado/Getty Images/AFP

Download from the original source type Here and if it is deleted access Here and Here if this third source is removed apply on toba60 and anonymous shipping through onion site DeepWeb

THE ELITE HAS ALREADY GONE IN HIS HIDES, THEY HAVE RELEASED GENOCIDE READ AND CRY , WE’RE FUCKED. PFIZER’S SAME DOCUMENTS STATE THAT BOTH INHALATION AND SKIN CONTACT TRANSMITS EVERYTHING IN VAX FROM VACCINATED TO NON-VACCINATED

Here’s what just this small part of this Pfizer document says:

1) If a man who has not been vaccinated touches a vaccinated woman, or breathes the air she breathes , (in other words, he passes by her in the office) and then has sex with his wife, his wife may have an adverse event and should avoid having children.

2) If a woman who has never been vaccinated is exposed to a woman who has been vaccinated, she can:

A: aborting
B: spontaneous abortion
C: poisoning a baby through its mother’s milk
D: having babies who have conjectural difficulties.

This is universal, and very bad. Here is a small piece of text that I have translated into Italian:

8.3.5.3. Professional exposure

“Occupational exposure occurs when a person receives unscheduled direct contact with a vaccine test subject , which may or may not lead to an adverse event. These people can include health care professionals, family members, and other people who are around the study participant.

When such exposures occur, the investigator should report them to Pfizer saftey within 24 hours of becoming aware of them, whether or not there is an associated secondary adverse event. This should be reported using the Vaccine Secondary Adverse Event Reporting form. BECAUSE THE INFORMATION IS NOT ABOUT A PARTICIPANT INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE STUDY ”.

NEW YORK, NY – NOVEMBER 09: People walk by the Pfizer headquarters on November 9, 2020 in New York City. Pharmaceutical company Pfizer announced positive early results on its COVID-19 vaccine trial and has proven to be 90% effective in preventing infection of the virus. David Dee Delgado/Getty Images/AFP

TO CLARIFY

Participants in vaccine studies become super diffusers of something, “they don’t say what it is,” but it triggers secondary adverse events in people who have never had the vax, when they are exposed to people who have had the vax.

This is so bad that right here, in this little piece of text quoted, it warns that unvaccinated men who have been exposed to a woman who has been vaccinated will pass whatever is in the vax to another woman.

Even the relatively small part of the paper I have placed below says that vax causes miscarriages and reproductive problems when unvaccinated people are exposed to the vaccinated and that a vaccinated mom’s breast milk can harm the baby. And if anyone doesn’t believe it, then click the link here and dive into that huge and deliberately confused document. People get serious, the vax is really the coup de grace.

Don’t let the vaccinated get close to you, it’s official now.

Here is a small part of this huge document, straight from Pfizer:

Terms:

Study Intervention – A vaccine test 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 during pregnancy or lactation and occupational exposure Exposure to the study intervention during pregnancy or lactation and occupational exposure should be reported to Pfizer Safety within 24 hours of the investigator becoming aware.
8.3.5.1. Exposure during pregnancy EDP occurs if:

A female participant was found to be pregnant while receiving or after stopping the study intervention.

A male participant who is receiving or discontinued study intervention exposes a female partner before or around the time of conception.

A woman is found to be pregnant while being exposed or was exposed to study intervention due to environmental exposure. The following are examples of environmental exposure during pregnancy:

A family member or female healthcare provider reports that she is pregnant after being exposed to the study intervention by inhalation or skin contact.

A male family member or healthcare professional who has been exposed to the study intervention by inhalation or skin contact exposes his female partner before or around the time of conception.

If this vaccine does not spread to other people, why should contact between vaccinated and unvaccinated be a noteworthy event? If this vaccine doesn’t spread, then WHY does a man who has been around a vaccinated woman, even if he hasn’t touched her or had sex, have to worry about getting another woman pregnant?

That’s not all, the following is detailed and much worse.

The investigator should report EDP to Pfizer Safety within 24 hours of the investigator becoming aware, regardless of whether an SAE has occurred. Initial information submitted must include the expected date of delivery (see below for information regarding termination of pregnancy).

If a PDE occurs in a participant or partner of a participant, the investigator should report this information to Pfizer Safety on the vaccine SAE reporting form and a supplemental PDE form, regardless of whether an SAE has occurred.

Pregnancy details will be collected after the start of the study intervention and up to 6 months after the last dose of the study intervention.

If EDP occurs within the scope of environmental exposure, the investigator should report the information to Pfizer Safety using the vaccine SAE reporting form and the 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 reporting form is retained in the investigator’s site file.

Follow-up is conducted to obtain general information on pregnancy and its outcome for all reports of EDP with unknown outcome.

epa08940567 A nurse prepares to administer Pfizer-BioNTech COVID-19 vaccine at a hospital in Krakow, southern Poland, 15 January 2021. Poland started a vaccination campaign against the coronavirus disease (COVID-19) on 27 December 2020. EPA/Lukasz Gagulski POLAND OUT

The investigator will follow the pregnancy until completion (or termination of pregnancy) and will inform 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 newborn can be assessed at the time of birth. (??????)

(It is not an interpretation and it is written in black and white on the official Pfizer report)

In the event of termination of pregnancy, 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 the results of preprocedural tests are conclusive of congenital anomaly and the results are reported). Abnormal pregnancy outcomes are considered SAE.

If the pregnancy outcome meets the criteria for an SAE (i.e., ectopic pregnancy, miscarriage, intrauterine fetal death, neonatal death, or congenital anomaly) , the investigator should follow procedures for reporting SAEs. Below is more information on pregnancy outcomes that are reported to Pfizer Safety as an SAE:

Miscarriage, including miscarriage and missed abortion;

Neonatal deaths occurring within 1 month of birth should be reported, regardless of causality, as SAE. In addition, neonatal deaths after 1 month should be reported as SAEs when the investigator evaluates the neonatal death as related or possibly related to exposure to the study intervention.

(As women undergo vaccination trials, they must report every symptom and anomaly (Death or Dysfunction of the unborn child) through a specific form to be delivered to Pfizer)

Further information regarding the EDP can be requested from the sponsor. Further follow-up of birth outcomes will be managed on a case-by-case basis (eg follow-up on preterm infants to identify developmental delays).

In the event of paternal exposure, the investigator will provide the participant with the Pregnant Partner Release of Information form for delivery to their partner.

The investigator must document in the source documents that the participant has received the information release form for the pregnant partner to be given to her partner.

8.3.5.2. Breastfeeding Exposure Breastfeeding exposure occurs if:

It turns out that a female participant is breastfeeding while receiving or after stopping the study intervention.

It turns out that a woman is breastfeeding while she is exposed or has been exposed to study intervention (i.e., environmental exposure).

An example of environmental exposure while breastfeeding is a family member or health care worker who reports breastfeeding after being exposed to the study intervention by inhalation or skin contact. The investigator should report breastfeeding exposure to Pfizer Safety within 24 hours of the investigator becoming aware, regardless of whether an SAE has occurred. The information should be reported using the vaccine’s SAE reporting form.

When exposure during lactation occurs as part of environmental exposure, the exposure information does not concern 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 kept in the investigator’s site file. A breastfeeding exposure report is not created when a Pfizer drug specifically approved for use in breastfeeding women (eg, vitamins) is given in accordance with its licensed use.However, if the infant experiences SAE associated with that drug, SAE is reported along with exposure during breastfeeding. Here is the clear part of this, which everyone can understand: 8.3.5.3. Professional exposure Occupational exposure occurs when a person receives unscheduled direct contact with the study intervention, which may or may not lead to the occurrence of an AE.

Such individuals may include health care professionals, family members, and other roles who are involved in the care of the study participant. The investigator should report occupational exposure to Pfizer Safety within 24 hours of the investigator becoming aware, regardless of whether there is an associated SAE.

The information should be reported using the vaccine’s SAE reporting form.

Since the information does not pertain to a participant enrolled in the study, it is not recorded on a CRF; however, a copy of the completed vaccine SAE reporting form is retained in the investigator’s site file.

Translated into Italian

Occupational exposure occurs when a person receives unscheduled direct contact with a vaccine test subject , which may or may not lead to the occurrence of an adverse event. These people can include health care professionals, family members, and other people who are around the trial participant.

When such exposures occur, the investigator should report them to Pfizer saftey within 24 hours of becoming aware of them, whether or not there is an associated secondary adverse event. This should be reported using the Vaccine Secondary Adverse Event Reporting form.

BECAUSE THE INFORMATION DOES NOT RELATE TO A PARTICIPANT INVOLVED IN THE STUDY, THE INFORMATION WILL BE KEPT SEPARATE FROM THE STUDY. (??????)

Source: Deep Web software Edward Snowden

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