Electronic Submission of Adverse Event Reports to FDA FAERS
fda.gov
Electronic Submission of Adverse Event Reports to FDA FAERS
The purpose of these public meetings is to provide the pharmaceutical industry and other interested parties with information on the plans, progress, and technical specifications to upgrade electronic submission standards for the premarket and postmarket safety surveillance programs managed by CDER and CBER
Apr 28, 2019
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regdesk.co5 months ago
“THE SLIDE THEY TRIED TO HIDE” You can watch when your FDA approved these toxic shots. THEY SHOWED THE SLIDE WITH KNOWN SIDE EFFECTS so fast they tried to hide it!! ALERT everyone! If you or family haven taken one or more covid vaccines, I recommend those who received a covid 'vaccine' (mRNA gene therapy) take time to report your side effects or deaths of your child or spouse since 2021 using CDC VAERS Vaccine Adverse Event Reporting System here: https://vaers.hhs.gov/ ask Julie Threet she’s cer
“THE SLIDE THEY TRIED TO HIDE” You can watch when your FDA approved these toxic shots. THEY SHOWED THE SLIDE WITH KNOWN SIDE EFFECTS so fast they tried to hide it!! ALERT everyone! If you or family haven taken one or more covid vaccines, I recommend those who received a covid 'vaccine' (mRNA gene therapy) take time to report your side effects or deaths of your child or spouse since 2021 using CDC VAERS Vaccine Adverse Event Reporting System here: https://vaers.hhs.gov/ ask Julie Threet she’s cer
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