FDA потребовала у Пфайзера и Модерны провести исследования о связи вакцин с

4. Требуемое исследование безопасности согласно разделу ...
https://www.fda.gov/media/155815/download
We have determined that an analysis of spontaneous postmarketing adverse events
reported under section 505(k)(1) of the FDCA will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis. Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess this serious risk. Therefore, based on appropriate scientific data, we have determined that you are required to conduct the following studies:
4. Required safety study under Section 505(o) (Study mRNA-1273-P903), entitled
“Post-marketing safety of SARS-CoV-2 mRNA-1273 vaccine in the US
Вот так, ковидобесы. Еще вчера у вас это значилось конспирологией, а сегодня это признал FDA. Ваши заказчики вас предали. Сдали как стеклотару.
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