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Sperimentazione genica COVID: richiesta immediata moratoria globale
Vaccini mRNA per il COVID-19: lezioni apprese dalle sperimentazioni di registrazione e dalla campagna di vaccinazione globale
M. Nathaniel Mead • Stephanie Seneff • Russ Wolfinger • Jessica Rose • Kris Denhaerynck • Steve Kirsch • Peter A. McCullough
Fonte: CUREUS
Pubblicato: 24 gennaio 2024
DOI: 10.7759/cureus.52876
( vedi anche: La tossicità dei vaccini a mRNA )
Peer-reviewed
Citare questo articolo come: Mead M, Seneff S, Wolfinger R, et al. (24 gennaio 2024) COVID-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign. Cureus 16(1): e52876. doi:10.7759/cureus.52876
Sommario
La nostra comprensione delle vaccinazioni contro il COVID-19 e del loro impatto sulla salute e sulla mortalità si è evoluta sostanzialmente dalla prima introduzione del vaccino. I rapporti pubblicati dagli studi randomizzati originali di fase 3 hanno concluso che i vaccini mRNA contro il COVID-19 potrebbero ridurre notevolmente i sintomi del COVID-19. Nel frattempo sono emersi problemi con i metodi, l’esecuzione e la rendicontazione di questi studi cruciali. La rianalisi dei dati dello studio Pfizer ha identificato aumenti statisticamente significativi degli eventi avversi gravi (SAE) nel gruppo del vaccino. Numerosi SAE sono stati identificati in seguito all’autorizzazione all’uso di emergenza (EUA), tra cui morte, cancro, eventi cardiaci e vari disturbi autoimmuni, ematologici, riproduttivi e neurologici. Inoltre, questi prodotti non sono mai stati sottoposti ad adeguati test di sicurezza e tossicologici secondo gli standard scientifici precedentemente stabiliti. Tra gli altri argomenti principali affrontati in questa revisione narrativa ci sono le analisi pubblicate sui gravi danni agli esseri umani, i problemi di controllo della qualità e le impurità legate ai processi, i meccanismi alla base degli eventi avversi (EA), la base immunologica per l’inefficacia del vaccino e le tendenze della mortalità basate su i dati della sperimentazione registrativa. Lo squilibrio rischio-beneficio dimostrato dalle prove fino ad oggi controindica ulteriori iniezioni di richiamo e suggerisce che, come minimo, le iniezioni di mRNA dovrebbero essere rimosse dal programma di immunizzazione infantile fino a quando non saranno condotti adeguati studi tossicologici e di sicurezza. L’approvazione da parte dell’agenzia federale dei vaccini mRNA COVID-19 su una base di copertura generale a livello di popolazione non è stata supportata da una valutazione onesta di tutti i dati di registrazione rilevanti e da una considerazione commisurata dei rischi rispetto ai benefici. Considerati gli SAE estesi e ben documentati e il rapporto danno-ricompensa inaccettabilmente elevato, esortiamo i governi a sostenere una moratoria globale sui prodotti a base di mRNA modificato fino a quando non verranno risposte tutte le domande rilevanti relative alla causalità, al DNA residuo e alla produzione aberrante di proteine.
(omissis)
Conclusioni
Una valutazione attenta e obiettiva della sicurezza dei prodotti mRNA di COVID-19 è fondamentale per sostenere gli standard etici e un processo decisionale basato sull’evidenza. La nostra revisione narrativa riguardante le sperimentazioni registrative e le conseguenze dell’EUA offre approfondimenti basati sull’evidenza su come questi vaccini genetici siano stati in grado di entrare nel mercato. Nel contesto dei due studi cardine, la sicurezza non è mai stata valutata in modo commisurato agli standard scientifici precedentemente stabiliti né per i vaccini né per i GTP, la classificazione più accurata di questi prodotti. Molti risultati chiave degli studi clinici sono stati riportati in modo errato o completamente omessi dai rapporti pubblicati. I consueti protocolli di test di sicurezza e requisiti tossicologici sono stati aggirati dalla FDA e dai produttori di vaccini, e la conclusione prematura di entrambi gli studi ha evitato qualsiasi valutazione imparziale dei potenziali SAE a causa di un periodo di tempo insufficiente per una corretta valutazione degli studi. È stato solo dopo l’EUA che le gravi conseguenze biologiche della fretta degli studi sono diventate evidenti, con numerosi SAE cardiovascolari, neurologici, riproduttivi, ematologici, maligni e autoimmuni identificati e pubblicati nella letteratura medica sottoposta a revisione paritaria. Inoltre, i vaccini mRNA per il COVID-19 prodotti tramite il Processo 1 e valutati negli studi non erano gli stessi prodotti poi distribuiti in tutto il mondo; tutti i prodotti mRNA del COVID-19 rilasciati al pubblico sono stati prodotti tramite il Processo 2 e hanno dimostrato di presentare vari gradi di contaminazione del DNA. L’incapacità delle autorità di regolamentazione di divulgare finora le impurità legate al processo (ad esempio, SV40) ha ulteriormente aumentato le preoccupazioni relative alla sicurezza e alla supervisione del controllo di qualità dei processi di produzione del vaccino mRNA.
Dall’inizio del 2021, l’eccesso di morti, eventi cardiaci, ictus e altri SAE sono stati spesso erroneamente attribuiti al COVID-19 piuttosto che alle vaccinazioni contro l’mRNA del COVID-19. L’errata attribuzione degli SAE al COVID-19 spesso può essere dovuta all’amplificazione degli effetti avversi quando le iniezioni di mRNA sono seguite dall’infezione della sottovariante SARS-CoV-2. Le lesioni causate dai prodotti dell’mRNA si sovrappongono sia ai PACS che alla grave malattia acuta da COVID-19, spesso oscurando i contributi eziologici dei vaccini. Iniezioni multiple di richiamo sembrano causare disfunzioni immunitarie, contribuendo così paradossalmente ad una maggiore suscettibilità alle infezioni da COVID-19 con dosi successive. Per la stragrande maggioranza degli adulti di età inferiore ai 50 anni, i benefici percepiti dei potenziatori dell’mRNA sono ampiamente controbilanciati dai loro potenziali danni invalidanti e potenzialmente letali. Anche i danni potenziali per gli anziani sembrano essere eccessivi. Considerati i SAE ben documentati e l’inaccettabile rapporto danno-ricompensa, esortiamo i governi a sostenere e applicare una moratoria globale su questi prodotti di mRNA modificati fino a quando tutte le domande rilevanti relative alla causalità, al DNA residuo e alla produzione aberrante di proteine non avranno risposta.
Riferimenti
Claudio Di maria
Buona sera io spero che dopo questa ennesima disamina i governi si interroghi e cessino l’uso di questi ” veleni” ; ma la storia ci insegna che questo messaggio dovrebbe
arrivare dentro la gente attraverso i media ,giornali televisione e i politici e questo non succederà ,non ammetteranno MAI i loro errori e le colpe di cui si sono macchiati