The EU Commission has admitted that the Covid vaccinations were rolled out across the population without complete safety data. The EU population became lab rats.
Originally published: TKP.at; editorial office; 15 September 2025
The EU Commission submitted an explosive response to an answer from MEP Gerald Hauser (FPÖ) at the end of August. The Commission had to comment on the fact that a contract was signed which states: “Member States accept that the long-term effects and efficacy of the vaccine are not known and that unknown side effects may occur.” Brussels has now admitted that data is indeed missing.
Hauser asked the Commission: “Why did the Commission not inform the citizens that the effectiveness and safety of the gene vaccination – as stipulated in the contract – were not guaranteed?”
In their response, those responsible tried to evade the question, but confirmed the uncertain risk of the vaccinations. The Commission argues with the “emergency authorisation”. One writes:
“The first COVID-19 vaccines have been granted a conditional marketing authorisation, a special type of authorisation that facilitates access to medicines that need to fill a medical supply gap in emergency situations such as the COVID-19 pandemic, for example, while a comprehensive data dossier is not yet available. Regulatory authorities can use this option to authorise such medicines as soon as sufficient data demonstrates that the benefits of the medicine outweigh the risks, with strict safeguards and controls required after authorisation.”
Hauser sees this as the first confirmation of his criticism. A press release states:
“For the first time, it has been officially confirmed that all those vaccinated were guinea pigs,” said Gerald Hauser, MEP for the Freedom Party, explaining his statement: “Following a parliamentary question from me, the EU Commission admits that no complete data was available for the COVID-19 vaccines approved on 21 December 2020 and therefore only conditional approval was granted. Hundreds of millions of Europeans were thus treated with insufficiently tested vaccines – even though it had long been known that COVID-19 is less dangerous than the flu.”
Hauser reported on a new working group in the US Advisory Committee on Immunisation Practices (ACIP) , which is now reviewing all available and previously unpublished data on the vaccines. “The focus is on the risk-benefit analysis, recording side effects, possible impurities and the fate of mRNA and spike proteins in the body.” Five years too late, as Hauser emphasised.
The Freedom Party MEP was impressed by the stance taken by Health Secretary Robert Kennedy Jr. in the USA: “On 27 August 2025, emergency approvals for COVID vaccines were revoked there. Healthy adults under 65 and children without pre-existing conditions effectively no longer have access to them, and each vaccination requires a detailed medical explanation of the risks. In the EU, on the other hand, these vaccines are still freely available – including for pregnant women, babies, children and healthy people.”
“That is why I have asked the EU Commission whether the authorisations for Covid-19 vaccinations for babies, children, pregnant women and healthy people will now also be revoked. I also want to know who is responsible for possible vaccine damage in the Commission and what the Commission’s position is on the continuing lack of data on safety and efficacy – the FDA recently confirmed these shortcomings,” says Hauser.
MEP Hauser is calling for a rapid reassessment of vaccination policy in Europe due to the current developments regarding mRNA vaccines in the USA: “It is time for the EU to rethink the authorisation of Covid-19 vaccines and withdraw these corona vaccines from the market to protect the population!”
