A landmark decision by a Greek court recognizes that Covid-19 vaccines lead to death.
The damning decision for the politicians who imposed mandatory vaccination with vaccines minimally tested under normal circumstances was issued by a Piraeus court, which was called to rule on the death of a 60-year-old healthy woman after her vaccination with the AstraZeneca vaccine, opening the way for compensation to her relatives, as well as many other citizens whose lives were overturned by the side effects.
The case of the 60-year-old
As became known during the trial, the 60-year-old was vaccinated at the Piraeus Health Center with the Vaxzevria vaccine of AstraZeneca against Covid-19 on 22 February 2021 (1st dose).
Within the next 24 hours, the patient developed fever, which soon subsided.
On 2 March 2021, she presented severe symptoms such as headache, blurred vision, and muscle weakness, which led her to seek medical care.
On 4 March 2021, she was admitted to the Increased Care Unit of the Neurology Clinic of G.N.A. “G. Gennimatas”, with symptoms of dysarthria and weakness of the left lower limb.
Laboratory tests showed she was suffering from thrombocytopenia, one of the vaccine’s adverse reactions.
“The thrombocytopenia caused inhibition of thrombolysis and required daily platelet transfusions to stabilize her condition.
Two weeks after receiving the vaccine, the patient developed clotting in the carotid arteries and the femoral artery, leading to an ischemic stroke.
Furthermore, due to clotting of the femoral artery of the left lower limb, the patient underwent a forced amputation of the limb on 14 March 2021.
She eventually passed away on 21 March 2021,”
described lawyer Nikolaos Ath. Dialynas, PhD, University of Munich.
Recording of the incident
The incident was recorded in the Yellow Card database of the National Organization for Medicines (EOF), the system monitoring adverse vaccine reactions in Greece.
The Yellow Card entry was classified as “probable”, indicating the case was considered potentially linked to the Vaxzevria vaccine, based on available clinical data, considering:
1) The short interval between vaccination and first symptoms (10 days)
2) The appearance of unusual thromboses in two different areas
3) The presence of severe thrombocytopenia concurrent with thromboses
4) The absence of underlying conditions explaining the clinical picture
No other underlying diseases
The Three-Member Administrative Court of First Instance, before which a compensation claim was filed by the deceased’s husband and two children against the Greek State, ruled that the cause of death was thrombosis with thrombocytopenia syndrome, a dangerous adverse reaction of the Vaxzevria vaccine.
This link was reinforced by the fact that the woman had no underlying conditions that could explain the symptoms and rapid deterioration.
The temporal proximity of symptoms to the vaccination makes the connection between the vaccine and the side effects clear, the court ruled.
As Dialynas stated:
“The decision was based on the short interval between vaccination and symptoms, the appearance of thromboses in two different organs, the occurrence of thrombocytopenia, and the fact that the woman had no other underlying disease.”
The responsibility of the Greek state
The Court’s decision recognized the responsibility of the Greek State for circulating the vaccine and confirmed that authorities failed to sufficiently warn about its rare but potentially fatal side effects.
By its ruling No. A11407/2025, which is a landmark because it recognizes the link between the Vaxzevria (AstraZeneca) vaccine and the woman’s death, as well as the dangerous consequences of the vaccine, which, despite approval by the authorities, carries serious and potentially fatal side effects, the Court awarded compensation to the relatives for mental anguish, acknowledging the severity of the suffering caused by the loss of their loved one.
It is noted that three more lawsuits have been filed involving other individuals who suffered thromboses after different vaccines, resulting in significant disabilities.
Νεκρή 60χρονη από τον Πειραιά, από το εμβόλιο της #AstraZeneca Σύμφωνα με απόφαση δικαστηρίου το ελληνικό δημόσιο θα πληρώσει αποζημίωση. Δεκάδες οι αγωγές για αναπηρίες και θανάτους από τις ενέσεις #mRNA
— Chris Freeman (@PanagiotisMylo6) November 14, 2025
Η απόφαση του Δικαστηρίου αναγνώρισε την ευθύνη του Ελληνικού Δημοσίου… pic.twitter.com/FZ28DLPSlG
Shocking admission by Von der Leyen: Mandatory vaccination imposed without knowing what would happen to citizens
The European Commission now admits that it had no knowledge of what would happen to EU citizens after mandatory and coercive Covid-19 vaccinations, imposed despite lacking safety data.
Vaccines were administered without sufficient safety data, leaving millions exposed to unknown consequences.
Austrian MEP Gerald Hauser (FPÖ) stated:
“Why did the Commission not inform citizens that the effectiveness and safety of genetic vaccines, as defined in the treaty, were not guaranteed?”
The European Commission had signed the Advance Purchase Agreement for the BioNTech/Pfizer COVID-19 vaccine on 20 November 2020.
On pages 48-49, it states:
“Member States acknowledge that the long-term effects and efficacy of the vaccine are unknown and that unknown side effects may appear.”
Despite these warnings, the Commission proceeded with approval.
In late August, the Commission stated that vaccines received conditional marketing authorization, which facilitates access to medicines that must fill an urgent medical need, such as a pandemic, even when a complete data package is not yet available.
The Commission added that regulators may approve medicines under certain conditions if there are sufficient data showing that a drug’s benefits outweigh its risks.
Hauser continued: “This downgrades all vaccinated persons in the EU to experimental subjects.”
He posed three questions:
1) Will the Commission now revoke authorization of COVID-19 vaccines for the entire population?
2) Who within the Commission is responsible for vaccine side effects, especially in healthy individuals without pre-existing conditions?
3) What does the Commission say about the continued lack of essential safety and efficacy data for COVID-19 vaccines, as confirmed by the FDA?
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