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  6.  » Pfizer admits in its own mRNA document that NON-vaccinated can be EXPOSED to the vaccine’s spike proteins by INHALATION or SKIN CONTACT –

Blazing Press – Apr 28, 2021

“It’s not a vaccine or anything even remotely related to vaccines. It’s a HUMANICIDE. And it sheds and is highly transmissible by Pfizer’s own gleeful admission.

And the self-extermination of mankind required absolutely nothing more than strangers on television re-naming common seasonal colds and flu, and thus starting a global religion.

Here is the link to the full document…” [Please read page 67]:

Extracts follow:

8.3.5.Exposure During Pregnancy or Breastfeeding, and Occupational Exposure

Exposure to the study interventionunder 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.

PF-07302048 (BNT162 RNA-Based COVID-19 Vaccines)Protocol C4591001

Page 68•

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. The investigator must report EDP to Pfizer Safety within24 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 ReportForm 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.

 

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