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Pfizer and FDA Knew in Early 2021 That Pfizer mRNA COVID “Vaccine” Caused Dire Fetal and Infant Risks, Including Death.

They Began an Aggressive Campaign to Vaccinate Pregnant Women Anyway.


 
by Amy Kelly, Program Director of the War Room/DailyClout Pfizer Documents Analysis Project

The April 2023 batch of Pfizer clinical trial documents released under court order by the Food and Drug Administration (FDA) contains a shocking, eight-page document titled, “Pregnancy and Lactation Cumulative Review.” The data in the Cumulative Review are “…from the time of drug product development to 28-FEB-2021,” and Robert T. Maroko of the FDA approved the Review on April 20, 2021 (p. 8). It reveals that Pfizer and the FDA knew in early 2021 that Pfizer’s mRNA COVID vaccine, BNT162b2, resulted in:

  • Adverse events in over 54% (248 out of 458) of “maternal exposure” to vaccine cases (defined on pp. 1-2 as, “PTs Maternal exposure timing unspecified, Maternal exposure during pregnancy, Maternal exposure before pregnancy, Exposure during pregnancy”) including:
    • Fetal deaths (spontaneous abortion, pp. 2 and 4).
    • Fetal tachycardia requiring early delivery and hospitalization of the affected neonate for five days (outcome “unknown”). (p. 2)
    • Premature labor and delivery (p. 3) resulting in:
      • Neonatal deaths.
      • Neonatal severe respiratory distress.
      • Neonatal pneumothorax, which is a collection of air between the lung and the chest wall that develops when air leaks out of the lung.

Moreover, in the Cumulative Review, nineteen percent of babies exposed to Pfizer’s COVID mRNA vaccine via lactation (breast milk) were reported to be suffering from 48 different adverse events* (pp. 6-7) such as:

Preferred Term Explanation # of Events
Pyrexia   9
Off label use   8
Product use issue   7
Infant irritability   5
Headache   5
Rash   5
Diarrhoea   3
Illness   3
Insomnia   3
Suppressed lactation   3
Breast milk discolouration   2
Infantile vomiting   2
Lethargy   2
Pain   2
Peripheral coldness   2
Urticaria Hives 2
Vomiting   2
Abdominal discomfort   1
Agitation   1
Allergy to vaccine   1
Angioedema An area of swelling of the lower layer of skin and tissue just under the skin or mucous membranes. The swelling may occur in the face, tongue, larynx, abdomen, or arms and legs. Often it is associated with hives, which are swelling within the upper skin. 1
Anxiety   1
Axillary pain   1
Breast pain   1
Breast swelling   1
Chills   1
Cough   1
Crying   1
Dysgeusia Also known as parageusia. A distortion of the sense of taste. 1
Dysphonia Hoarseness, most frequently caused by a problem with a person’s vocal cords or larynx. 1
Eructation Belching. 1
Epistaxis Nosebleeds. 1
Eyelid ptosis Droopy eyelid. 1
Facial paralysis   1
Fatigue   1
Increased appetite   1
Lymphadenopathy Swollen lymph nodes. 1
Myalgia   1
Nausea   1
Paresis   1
Poor feeding infant   1
Poor quality sleep   1

Pruritis

Itchy skin. 1
Restlessness   1
Rhinorrhoea Runny nose. 1
Roseola An infection that can cause a high fever followed by a rash. 1
Skin exfoliation   1
Vision blurred   1
*From Table 2 - Number of Adverse Events Reported in Infants with ‘Exposure via Lactation’ (pp. 6-7)

There were 10 Serious Adverse Events (SAEs) from “Exposure via Lactation,” and the Review outlines six of them (p. 7):

  1. “A 15-month old infant with medical history of vomiting experienced skin exfoliation and infant irritability while being breastfed (latency <7 days). The outcome of the event ‘skin exfoliation’ was not recovered and outcome of event ‘infant irritability’ was unknown. No causality was reported by the physician.”

  2. “A 9-month old infant with a medical history of meningococcal vaccine and no history of allergies, asthma, eczema or anaphylaxis experienced rash and urticaria a day after exposure via lactation. The outcome of the events was ‘resolved’ and event did not happen after the second day. No causality assessment was provided.”
  3. “A day after the mother received vaccination, a baby developed a rash after breastfeeding. At the time of the report, the event was ‘not recovered. A causality assessment was not provided.”

  4. “An 8-month old infant experienced angioedema one day after his mother received vaccination. The event was considered non-serious by health authority and the outcome at the time of the report was unknown. No causality was provided.”
  5. “There were 2 cases reporting ‘illness’ after exposure via breast milk’. In the first case, a 6-month old infant developed an unspecified sickness 2 days post mother’s vaccination. The outcome of the event sickness was recovered, and no causality assessment was provided. The second case, a 3-month old infant developed an unspecified illness and required hospitalization for 6 days post exposure via breast milk (>7 days latency). The event outcome was reported as ‘recovering’ and no causality assessment was provided.”

 

Pfizer’s Summary and Conclusion section (p. 7) of the Cumulative Review states, “The cases reviewed above are indicative of what is in the Pfizer safety database as of 28 February 2021. The sponsor (Pfizer/BioNTech) will continue to monitor and report on all pregnancy exposure and lactation cases. It is important to note that the spontaneous safety database is intended for hypothesis generation and not hypothesis testing.”

Despite knowing the deaths and harms enumerated above, on April 23, 2021, the Centers for Disease Control and Prevention (CDC) began recommending COVID-19 vaccines for pregnant women. (https://www.verywellhealth.com/pregnant-women-covid-vaccine-5092509)

Please read this damning “Pregnancy and Lactation Cumulative Review” below.

 

Pre-Order Your Copy of the Pfizer Reports Paperback Book.
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