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Infants and Children Under 12 Given the Pfizer mRNA COVID “Vaccine” Seven Months BEFORE Pediatric Approval.

71% of Adverse Event Cases Classified As Been Serious: 132 adverse events were reported in the 34 children – i.e., an average of 3.88 AEs per child.
Report 54: Infants and Children Under 12 Given the Pfizer mRNA COVID “Vaccine” Seven Months BEFORE Pediatric Approval. 71% of Adverse Event Cases Classified As Been Serious: 132 adverse events were reported in the 34 children – i.e., an average of 3.88 AEs per child.
Important points from this report include:
-A seven-year-old experienced a stroke.
-One child and one infant suffered facial paralysis.
-One infant had a kidney adverse event, either kidney injury or failure.
Of the 34 adverse event cases, 24 (71%) were classified as serious.
-Predominantly female patients were affected — at least 25 of 34 (73.5%) patients.
-Table 6 reports 34 cases of use in pediatric individuals. However, 28 additional cases were excluded because details such as height and weight were “not consistent with pediatric subjects.”
-Ages ranged from two months to nine years, with median 4.0 years, which means half the children were under four years of age.
Report

Replies, comments and Discussions:

  • 枫下家园 / 医药保健 / Infants and Children Under 12 Given the Pfizer mRNA COVID “Vaccine” Seven Months BEFORE Pediatric Approval. +1
    71% of Adverse Event Cases Classified As Been Serious: 132 adverse events were reported in the 34 children – i.e., an average of 3.88 AEs per child.
    Report 54: Infants and Children Under 12 Given the Pfizer mRNA COVID “Vaccine” Seven Months BEFORE Pediatric Approval. 71% of Adverse Event Cases Classified As Been Serious: 132 adverse events were reported in the 34 children – i.e., an average of 3.88 AEs per child.
    Important points from this report include:
    -A seven-year-old experienced a stroke.
    -One child and one infant suffered facial paralysis.
    -One infant had a kidney adverse event, either kidney injury or failure.
    Of the 34 adverse event cases, 24 (71%) were classified as serious.
    -Predominantly female patients were affected — at least 25 of 34 (73.5%) patients.
    -Table 6 reports 34 cases of use in pediatric individuals. However, 28 additional cases were excluded because details such as height and weight were “not consistent with pediatric subjects.”
    -Ages ranged from two months to nine years, with median 4.0 years, which means half the children were under four years of age.
    • 视频中所说内容在辉瑞官方报告第13页,截止到2021年2月底(那时还根本没批准儿童疫苗),辉瑞收到34个12岁以下儿童副作用报告,其中24个为严重副作用。 +2