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Please forward this email on to as many people as possible. If you have been forwarded this email, please go to www.healthfreedomsummit.com to sign up for free trainings, resources, (explore two below 👇 by clicking on the images) and future emails. |
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Below are the email addresses of everyone at the FDA/VRBPAC. Share your own story or copy and paste the message below.
Subject line: All reformulated COVID-19 shots MUST go through proper clinical trials
The safety and efficacy of all reformulated COVID-19 shots must be evaluated through:
Large (50,000+ person) double-blind randomized controlled trials with inert saline placebos conducted by an independent third party. The treatment and control groups must be followed for life to monitor adverse events and all-cause mortality (no more wiping out the control group after 6 months to hide bad outcomes). We also demand greater than 90% efficacy against infection with less than 0.1% Grade 3 or higher adverse events; proper monitoring for carcinogenesis, mutagenesis and impairment of fertility; and immediate release to the public of all clinical trial documents submitted to the FDA.
[email protected], commis[email protected], DeanofPubl[email protected], Aux7@cdc.gov, [email protected], [email protected], Richard[email protected], Huilee.[email protected], Leslie.Ball@fda.hhs.gov, Doran.Fink@fda.hhs.gov, [email protected].gov, [email protected], paula.[email protected], adam.[email protected], hbernstein@northwell.edu, [email protected], [email protected], hjanes@fredhutch.org, hgans@stanford.edu, [email protected], asmont[email protected], [email protected], s[email protected], Jportnoy@cmh.edu, [email protected].edu, [email protected], ashane@emory.edu, [email protected].edu, [email protected], Randy[email protected], officeofth[email protected], JYLee@uams.edu, ofer.levy@childrens.harvard.edu, wayne_marasco@dfci.harvard.edu, cmeissner@tuftsmedicalcenter.org, mrn8d@virginia.edu, stanley-perlman@uiowa.edu, [email protected], [email protected], [email protected] |
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