Eudravigilance, a body belonging to the European Medicines Agency, publishes on the adverse effects of vaccines. The data comes from national drug regulatory authorities and pharmaceutical companies.
Inmaculada Fernández
23.04.21
The European body Eudravigilance, a part of the European Medicines Agency, is in charge of collecting reports of fatalities and serious adverse events, suspected of being the result of medications. These cases come to them through the different national drug agencies. The numbers do not take into account the data of all European countries, only those of the European Economic Area (those of the EU plus Iceland, Liechtenstein and Norway). Thus, countries like the United Kingdom have their own drug surveillance system and case registration.
As of April 17th, reports on individual cases of adverse reactions reported to Eudravigilance (on the four experimental vaccines used in Europe against Covid19) have been 330,218, of which 7,766 were fatal.
Specifically, for the Moderna vaccine, 15,979 adverse cases have been identified and 2,094 have resulted in death.
The Pfizer-BiOnTech vaccine: 144,607 cases of adverse reactions, resulting in the deaths of 4,293.
For the Astrazeneca vaccine: 169,386 cases, of which 1,360 have been recorded as fatal.
And for the new Janssen vaccine (introduced very recently): 246 registered cases, of which 19 are deaths.
In the following links, any citizen has access to, and can count, the published data by himself:
- Moderna, vacuna de ARNm COVID-19 (CX-024414).
- Pfizer-BionTech vacuna de ARNm COVID19 (Tozinameran).
- Vacuna de Astrazeneca (CHADOX1 NCOV-19).
- Vacuna COVID-19 JANSSEN (AD26.COV2.S).
To access the data on total deaths for each vaccine, the individual deaths from each of the groups of adverse reactions must be added, and these are found in the section (upper tab) entitled 'Number of Individual Cases for a selected Reaction' (Number of Individual Cases for a selected Reaction).
In a higher up section (upper tabs) you can obtain general graphs according to the type of serious adverse reactions reported by each vaccine. For example, these two, from Moderna and Pfizer:
The Eudravigilance website was launched by the European Medicines Agency in 2012 to provide public access to reports of suspected side effects (also known as suspected adverse drug reactions). These reports are sent to Eudravigilance by the national drug regulatory authorities and by the pharmaceutical companies that hold marketing authorisation (licenses) for the drugs.
Eudravigilance is a system designed to collect reports of suspected side effects. The reports are used to assess the benefits and risks of medicines during their development and to monitor their safety after authorisation in the European Economic Area (EEA). It has been in use since December 2001.
Reports on suspected side effects are processed by national drug regulatory authorities and marketing authorisation-holders and sent to EudraVigilance in accordance with applicable data protection rules as set out in the General Data Protection Regulation (GDPR) (Regulation (EU) 2016/679).
How to report side effects
The European Medicines Agency and Eudravigilance specify that “health professionals are the ones who usually report side effects and therefore it is recommended to consult with a health professional, such as your doctor or pharmacist. With increasing ease, patients can report suspected side effects directly through a variety of avenues, such as online, using patient report forms offered by national drug regulatory authorities, or by phone. For information on how to report a side effect, see the relevant authority on the list of national drug regulatory authorities in the EEA '.
They add: “If you are experiencing a side effect or think you may be experiencing it, you should consult a healthcare professional. The European Medicines Agency cannot accept reports of side effects coming directly from patients or consumers. Furthermore, the Agency is not in a position to provide individual medical advice or to confirm whether your symptoms are due to the drug.”
The way to report adverse events to the Ministry of Health is through the doctor who will study the case and report on it; In Spain, patients can also report cases of adverse reactions to drugs, through a long form from the Ministry of Health (Spanish Agency for Medicines and Health Products) that consists of 5 steps. Notification of Suspected Adverse Drug Reactions in Spain: www.notificaRAM.es
Why don't the mainstream media mention these figures?
Whenever before the deaths occur after transgenic experimental vaccines, there is the immense silence, if not contempt, for these serious cases of collateral effects.
Deaths and serious incidents after vaccination are minimised to such a degree that they have lied and denied all death from the Covid-19 vaccine. Meanwhile, most other media continue to fervently encourage vaccination of the entire population, without reporting these figures.
Health Impact News and some specialised and committed blogs have been the first and only media to sound the alarm and publicise these dramatic numbers, occurring as they do, in often completely healthy people. From here, I thank these real journalists and researchers. They are wonderful.
The other media (the "correct-thinking" media) only dedicate themselves to following the inertia of (dis)information and to repeating, like good parrots, the dizzying daily contagion figures, which refers above all to controversial PCRs. Due to ignorance or negligence they refuse to consult other official sources, see for example the FDA (US Food & Drug Administration) and they do not want to report whatever is off-script. Or perhaps, more suspiciously, it is because many media receive millionaire subsidies or have advertising contracts with political organisations that encourage experimental vaccination of the entire population.
This negligent media refuses to listen to any dissenting voice that contradicts the official version, and they refuse scientific debate. They refuse to report, for example, that a group of Spainish doctors and biologists, many of them quite renowned, have signed a document calling for the immediate halting of experimental Covid-19 vaccination: "We firmly believe that the risks are not acceptable, not a single adverse effect or death should be tolerated."
How many suspicious deaths must a drug or vaccine attain to be treated as more than just "isolated cases" by the media and the European Medicines Agency ?
Are 7,766 deaths and more than 330,000 reported adverse reactions after Covid vaccination in the European Economic Area not enough?
And these figures of injuries in Europe only refer to suspected cases that occurred in the short term after vaccination. What await us in the medium and long term with experimental vaccines that have not met the minimum requirements or the minimum terms that any other medicine or vaccine is required?
These are experimental vaccines, in which the pharmaceutical companies themselves showed little or no faith when they demanded that the governments exempt them from financial compensation for these adverse effects.
These are vaccines whose own safety data sheets detail that there are no interaction studies of the vaccine with other drugs that a citizen may be taking. The data sheets also acknowledge that they do not know how long immunity lasts: "The duration of protection provided by the vaccine is unknown, as it is still being determined in ongoing clinical trials."
Here you can consult the safety data sheets of:
The Prime Minister of Israel, Benjamin Netanyahu, already announced that it may be necessary to vaccinate again every six months.
It is all a lucrative business for them: no losses and large sums from annual sales, over a prolonged period of time. Or perhaps forever? That's what we're given to understand.
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Original version: https://www.actuall.com/economia/reportan-7-766-muertes-y-mas-de-330-000-reacciones-adversas-a-las-vacunas-contra-el-covid/
Translation: David Montoute
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