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Philippines FDA Pharmacovigilance Report from 30 May - 5th June 2022 adds 44 Additional Deaths Following C-19 Vaccination. When Will FDA Recall These EUA Products?
FDA claim No Signal despite their systems allowing Class Drug Recall based on reasonable suspicion of harm. World Council for Health New Report Calls for a Universal C-19 Vaccine Recall due to harm!
New pharmaceutical products usually undergo a 10 (or more) year development process. The covid-19 vaccines, which don’t meet the traditional definition of vaccines because they don't prevent infection or transmission, were brought to market in a mere 10 months, without animal studies or extended safety and efficacy studies. No independent (from manufacturer) studies are available. They are granted EUA use, and recipients are effectively part of the world’s largest clinical trial!
The World Council for Health have conducted an independent review of reported AEFI following covid-19 vaccination using VAERS (US), Vigiaccess (WHO), Yellowcard (UK) and Eudravigilance (European) systems. More than 40,000 deaths are linked as described in this press release, and as detailed in the main report. WCH concluded that there is sufficient evidence of severe harm and that a product recall should be made.
The latest Philippines FDA Pharmacovigilance report for the week ending 5th of June 2022 adds 828 new AEFI (new total of 101,984), including 169 serious reactions (new total serious to date is 8,412) of which 44 are deaths (new total 2,424 deaths to date). Serious reactions comprise 8% of reports; deaths comprise 29% of the serious reactions!
Pharmacovigilance systems are known to grossly underestimate population impacts, this is known as under reporting factor (URF). If my estimated minimal Philippines URF of 126 holds, these reported deaths could be just the tip of the iceberg with the 44 new deaths representing more than 5,500 possible new deaths, and the overall 2,424 deaths reflecting possibly well more than 300,000 AEFI deaths.
Philippines FDA still claim no signal for intervention or changing of the vaccination recommendations.
This is despite the FDA’s own guidelines for Drug recall which only require reasonable suspicion of harm or death! How many AEFI reports, how many deaths will raise that reasonable suspicion? How ironic, the FDA will recall cosmetic products and vitamin supplements, but won’t recall these EUA gene therapy drugs!
Link to the Philippines FDA Pharmacovigilance reporting system for Covid-19 Vaccination here. Anyone experiencing any suspected adverse reaction is encouraged to make a report. This is necessary for the gathering of population effects data.
Readers, please share this information, widely. Please discuss it with your families and friends, and submit it to your heath care professionals and government officials. Please use it for your own due diligence before you accept any (or any more) Covid-19 vaccination.