VAERS Batches with Deaths & Adverse Reactions Identified - How Bad Is My Batch
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VAERS Batches with Deaths & Adverse Reactions Identified - How Bad Is My Batch
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Welcome to CVAR, a #Covid-Vaccine-Adverse-Reactions podcast. Today, we talk to pharmaceutical researcher and scientist, Mr. Craig Paardekooper about his discoveries organizing the CDC’s VAERS website to see which batch lot numbers had deaths and adverse reactions.
Watch the video presentation here:
https://rumble.com/covidvaccineadversereactions
https://www.bitchute.com/covidvaccineadversereactions/
https://www.brighteon.com/channels/covidvaccineadversereactions
https://odysee.com/@covidvaccineadversereactions:9
Podcast audio version: https://anchor.fm/covidvaxadversereactions
Donate to Mr. Craig Paardekooper’s research here: https://howbadismybatch.com/donatecreditcard.html
Look up your batch number here: https://howbadismybatch.com/
VAERS Lot# Look-up tool: https://wonder.cdc.gov/vaers.html
MedAlerts: https://medalerts.org/vaersdb/index.php
Do not despair. For more information about the #Defeat-the-Mandates march on Jan. 23, 2022 at Washington DC, USA: https://defeatthemandatesdc.com/
The United States Federal Food, Drug, and Cosmetic Act is a set of laws passed by Congress in 1938 giving authority to the U.S. Food and Drug Administration to oversee the safety.
https://www.fda.gov/regulatory-information/laws-enforced-fda/federal-food-drug-and-cosmetic-act-fdc-act
US Code Title 21, Sections 351 (Adulterated Penalties) & Sections 352 (Misbranded Penalties)
https://uscode.house.gov/view.xhtml?req=(title:21%20section:351%20edition:prelim)%20OR%20(granuleid:USC-prelim-title21-section351)&f=treesort&edition=prelim&num=0&jumpTo=true
https://uscode.house.gov/view.xhtml?req=(title:21%20section:352%20edition:prelim)%20OR%20(granuleid:USC-prelim-title21-section352)&f=treesort&edition=prelim&num=0&jumpTo=true
2020 Prep Act authorizes the Secretary of the Department of Health and Human Services to give vaccine administrators immunity except for “willful misconduct”:
https://www.phe.gov/Preparedness/legal/prepact/Pages/prepqa.aspx#q3
Under Title 21 of the FDA’s Code of Regulations section 50.20 regarding Informed Consent of Human Subjects:
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=50.20
For more information about CICP, contact 1-855-266-2427 (CICP) or cicp@hrsa.gov
#Covid-Vaccine-Adverse-Reactions,#How-Bad-Is-My-Batch, #VAERS, #Craig-Paardekooper, #Defeat-the-Mandates-DC