by Brian Shilhavy
Originally published by Health Impact News
The European Medicines Agency (EMA) database of adverse drug reactions is now reporting 46,618 deaths and 4,682,268 injuries following COVID-19 vaccines (details below).
In the United States, the Vaccine Adverse Events Recording System (VAERS) is now reporting 29,635 deaths and 1,350,950 injuries following COVID-19 vaccines. (Source.)
A 2011 report by Harvard Pilgrim Health Care, Inc. for the U.S. Department of Health and Human Services (HHS) stated that less than 1% of all adverse events following vaccines are ever reported to VAERS.
Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA).
Likewise, fewer than 1% of vaccine adverse events are reported. Low reporting rates preclude or slow the identification of “problem” drugs and vaccines that endanger public health. New surveillance methods for drug and vaccine adverse effects are needed. (Source.)
There have now been more deaths and vaccine side effects reported during the past 20 months to VAERS following COVID-19 vaccines than there has been for the entire previous 30 years for all FDA-approved vaccines before the Emergency Use Authorization of the COVID-19 shots in December of 2020. (833,968 cases, 9,279 deaths – source.)
The European (EEA and non-EEA countries) database of suspected drug reaction reports is EudraVigilance, verified by the European Medicines Agency (EMA), and they are now reporting 46,618 fatalities, and 4,682,268 injuries following injections of five experimental COVID-19 shots:
From the total of injuries recorded, almost half of them (2,126,925) are serious injuries.
“Seriousness provides information on the suspected undesirable effect; it can be classified as ‘serious’ if it corresponds to a medical occurrence that results in death, is life-threatening, requires inpatient hospitalisation, results in another medically important condition, or prolongation of existing hospitalisation, results in persistent or significant disability or incapacity, or is a congenital anomaly/birth defect.”
A Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. It is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.
Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals. Here is the summary data through July 16, 2022.
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Total reactions for the mRNA vaccine Tozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer: 21,999 deaths and 2,418,846 injuries to 16/07/2022
Total reactions for the mRNA vaccine SPIKEVAX/mRNA-1273 (CX-024414) from Moderna: 12,225 deaths and 773,142 injuries to 16/07/2022
Total reactions for the vaccine AZD1222/VAXZEVRIA (CHADOX1 NCOV-19) from Oxford/ AstraZeneca: 9,318 deaths and 1,318,927 injuries to 16/07/2022
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Total reactions for the COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson: 3,076 deaths and 168,267 injuries to 16/07/2022
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The latest update in VAERS shows 4,358 fetal deaths following COVID-19 vaccines injected into pregnant and child-bearing aged women. (Source.)
This has to be the saddest, most criminal activity of Big Pharma and the FDA by allowing these COVID-19 shots to be injected into pregnant and young women.
Pfizer had data showing how dangerous these shots were for pregnant women, but the FDA gave authorization anyway.
Dr. Byram W. Bridle addressed this human tragedy on his blog earlier this week:
I Am In Shock.
The United States Food and Drug Administration (US-FDA) had requested 75 years to release the documents that they reviewed from Pfizer prior to issuing emergency use authorization for the Pfizer-BioNTech BNT162b mRNA ‘vaccine’ (Comirnaty) against SARS-CoV-2, which can cause COVID-19. However, a judge over-ruled this and issued a court order that the documents be released in large monthly installments. Today, an absolutely shocking set of data were brought to my attention.
They are not new. They are from a document that was in the data dump released back in May of this year. However, I want to help my fellow scientists in making sure that this science gets widely distributed throughout the world. This is for the sake of ‘fully informed consent’, something that regulatory agencies, public health officials and too many physicians seem to have abandoned over the past couple of years.
For a long time I have been arguing that our children need to be left out of the massive conflicts over the science underpinning COVID-19. In my opinion, adults can conduct their own risk-benefit analyses regarding whether they want to receive one of the current COVID-19 inoculations.
However, far too many adults are making these decisions based on pseudo-science, data from flawed studies, misinformation, and outright disinformation being propagated by physicians and public health officials, many of whom are unqualified to opine on anything in the field of vaccinology. I have never felt comfortable about these injections being used in ‘children, adolescents and young-adults of child-bearing age’. This was the precise terminology I used in a parent’s guide to COVID-19 vaccines that I wrote more than one year ago.
The highest quality data for assessing a novel medical product are derived from clinical studies. This is because these types of experiments in people are typically well-controlled and include what is known as ‘active monitoring’; there is follow-up to assess safety and efficacy. This is why the clinical testing phases should never be compromised. With this in mind, let’s explore a stunning set of data that Pfizer provided to the US-FDA.
«The data in this document were accumulated up until February 28, 2021. Notably, on page 9, safety concerns based on the US Pharmacovigilance Plan included “missing information” on “Use in Pregnancy and lactation”. The data that had accumulated up to the end of February, 2021 were from too small of a sample size (i.e., # of pregnant or lactating women) to justify its use in these populations. However, here are the data that were available at that time regarding outcomes in pregnant women that had received Pfizer’s COVID-19 inoculation; this is quoted from the top of table 6 (I have italicized and/or bolded the most important points)» Dr. Byram W. Bridle pointed out.
Pregnancy cases: 274 cases including:
• 270 mother cases and 4 foetus/baby cases representing 270 unique pregnancies (the 4 foetus/baby cases were linked to 3 mother cases; 1 mother case involved twins).
• Pregnancy outcomes for the 270 pregnancies were reported as spontaneous abortion (23), outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each). No outcome was provided for 238 pregnancies (note that 2 different outcomes were reported for each twin, and both were counted).
Apparently, outcomes will never be known for 88% (238/270) of the pregnancies. Why was the follow-up rate on these cases so abysmal?
NutriTruth has a great graph on their website that summarizes the results from cases for which follow-up data were available…
by Brian Shilhavy
Originally published by Health Impact News
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