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That’s why I asked to the EMA’s general director to explain why EMA demanded to US VAERS to remove the batch codes of vials reported for adverse effects. She answered it was “to comply with EU GDPR” (data protection regulation), to protect the PRIVACY of reporters…
RT @P_McCulloughMD: BREAKING--Danish study shows 4.2% lots loaded with side effects! Confirms suspicions not all lots are equally safe--must have differing amounts of mRNA or contaminants makin…

🐦🔗: n.respublicae.eu/ladyonorato/s

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