Covid vaccins


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Parliamentary questions​
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25 August 2021​
P-003960/2021
Priority question for written answer P-003960/2021
to the Commission
Rule 138
Francesca Donato (ID)​
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Subject: Withdrawal of vaccine authorisation​
The EU has granted conditional approval for the emergency use of COVID-19 vaccines, with a six-week review of post-vaccination safety data(1).
To date, EUDRAVIGILANCE has received around 20 000 reports of deaths probably related to the vaccines and some 700 000 adverse reactions, 9% of which severe. These data are, however, underestimated when it comes to the true magnitude of adverse effects, given that there is no active surveillance. The EMA has recently updated the list of adverse reactions to vaccines, adding new diseases(2).
Moreover, the trend in infections among vaccinated people in countries such as Israel and the UK shows that the vaccines themselves are not effective against the variants that are currently predominant.
The possible long-term reactions to mRNA vaccines, which have never before been authorised for humans, remain unknown(3).
In view of this, will the Commission:
1. withdraw or suspend authorisation for the use of those vaccines owing to the lack of safety and efficacy requirements in terms of preventing infection and contagion with the SARS-CoV2 virus;
2. authorise the use of medicines that have proven to be effective in treating COVID-19, such as Ivermectin, and large-scale early home treatment protocols;
3. put in place an active surveillance system for vaccinated people, providing them with support and facilitating the necessary treatment for adverse effects?​
 

Terug naar het Europarl-portaal
arrow_error.gif
Dit document is niet beschikbaar in uw taal, en wordt u aangeboden in een van de andere beschikbare talen in de talenbalk.​
Parliamentary questions​
PDF 43k
spacer.gif
WORD 10k
25 August 2021​

P-003960/2021

Priority question for written answer P-003960/2021
to the Commission
Rule 138
Francesca Donato (ID)​
arrow_title_doc.gif
Subject: Withdrawal of vaccine authorisation​
The EU has granted conditional approval for the emergency use of COVID-19 vaccines, with a six-week review of post-vaccination safety data(1).
To date, EUDRAVIGILANCE has received around 20 000 reports of deaths probably related to the vaccines and some 700 000 adverse reactions, 9% of which severe. These data are, however, underestimated when it comes to the true magnitude of adverse effects, given that there is no active surveillance. The EMA has recently updated the list of adverse reactions to vaccines, adding new diseases(2).
Moreover, the trend in infections among vaccinated people in countries such as Israel and the UK shows that the vaccines themselves are not effective against the variants that are currently predominant.
The possible long-term reactions to mRNA vaccines, which have never before been authorised for humans, remain unknown(3).
In view of this, will the Commission:
1. withdraw or suspend authorisation for the use of those vaccines owing to the lack of safety and efficacy requirements in terms of preventing infection and contagion with the SARS-CoV2 virus;
2. authorise the use of medicines that have proven to be effective in treating COVID-19, such as Ivermectin, and large-scale early home treatment protocols;
3. put in place an active surveillance system for vaccinated people, providing them with support and facilitating the necessary treatment for adverse effects?​
Deze gaat er niet doorkomen, de prikkels moeten erin
 
Houd in gedachten dat de werknemers in kwestie niet alleen verpleegkundigen en directe zorgverleners zijn; het mandaat is van toepassing op iedereen in het gezondheidszorgsysteem, waaronder: administratief personeel, factureringskantoren, codeurs, conciërges, receptionisten, technologie of IT-personeel, communicatiemedewerkers, koks en cafetariawerknemers, in wezen – iedereen in de industrie.
 

Shocking, Urgent News - Share Widely​

Vernon Coleman

 

Shocking, Urgent News - Share Widely​

Vernon Coleman

Ook Vernon gaat nog uit van een levend virus, ... ook nog niet bij de les
 

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