They know EVERYTHING, even the EMA!

… Pfizer’s pharmacovigilance documents requested by the European Union’s drug regulator, EMA    [ Periodic Safety Update Report, PSUR #3 ]

… Pfizer knew about a sickening level of injury early on

… 508,351 individual case reports of adverse events containing 1,597,673 events

… One-third of the AEs were classified as serious

… Women reported AEs at three times the rate of men

… 60% of cases were reported with either “outcome unknown” or “not recovered,”

… so many of the injuries were not transient

… Highest number of cases occurred in the 31-50 year age group

… 92% did not have any comorbidities

… which makes it very likely it was the vaccine causing such widespread, sudden injury

… Pfizer observed over 10,000 categories of diagnosis, many of them very severe and very rare

… hundreds of categories of nervous system disorders, totaling 696,508 cases

… over 100 categories of eye disorders, which is unusual for a vaccine injury

… over 47,000 ear disorders

… 225,000 cases of skin and tissue disorders

… 190,000 cases of respiratory disorders

… 178,000 cases of reproductive or breast disorders

… 506 cases of erectile dysfunction in men

… over 77,000 psychiatric disorders

… 3,711 cases of tumors – benign and malignant

… 127,000 cardiac disorders, running the gamut of about 270 categories of heart damage, including many rare disorders, in addition to myocarditis

… over 100,000 blood and lymphatic disorders

… it’s clear that nobody could have mistaken most of these AEs for mere incidental ailments

… The broad scope of injuries affecting every single organ system is simply extraordinary

… So far, there has been no reckoning for their false marketing and the devastating human toll it has cost. Oh, and that is just the short-term human toll

 

                Periodic Safety Update Report, PSUR #3

 

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