AS REGULAR readers of our regular analyses of the Yellow Card data from the Medicine and Healthcare products Regulatory Agency (MHRA) will know, this quango that’s so energetic when it comes to enabling and authorising inadequately trialled ‘vaccines’ is not nearly so assiduous when it comes to investigating vaccine injuries and death. In fact it is dormant.
The latest set of ‘adverse events’ data, extracted and analysed for us by Jenny Brown, once more makes deeply troubling reading. You will see from the headline breakdown below that now 1 in 149 people injected experienced a serious adverse event and 1 in 181 of these reports were deaths. To date there have been 2,679 (that’s 0.5 per cent of the total events) ‘fatal outcome’ reports. There were 39 additional such fatality reports in the last four-week period. Bear in mind these are acknowledged by the MHRA itself as likely to be but 10 per cent of the true figure (as with all the categories of events).
Shockingly, 445 of the above fatalities are of ‘unknown age’. That’s 16.6 per cent of all fatalities. And 176 or 6.6 per cent are of ‘unknown sex’. I wonder if Mr Sunak or the Health Secretary can be aware of this? Do they ever request such a breakdown from the MHRA?
There is worse to come. For this last report Jenny delved deeper into the AstraZeneca figures. Of the above mentioned 39 new fatalities recorded since the last report four weeks ago, she found that 30 of these are from the AstraZeneca dataset. She says: ‘It appears that these 30 fatalities were filed in the category “injury, poisoning & procedural complications” and sub, sub category “immunisation reactions”. The curious element is that these fatalities were reported under the “patient/carer as the reporter” category, and as an “indirect” report, which the system states as “indirect submission sent to pharmaceutical company and passed on as required in legislation” to MHRA. Also, more odd is that the fatalities appear to be registered as unknown sex and unknown age. Overall AstraZeneca Yellow Card report numbers have increased by 159 (of the total for all vaccines 353 reports filed) in the last 4 weeks . . . and 102 of the AZ reports were categorised as serious excluding the fatalities.’
The implications of this are hugely disturbing given that the government stopped ordering AstraZeneca in 2022 (the NHS announced that it was no longer available for its autumn booster programme of that year). That means no one will have received a AZ vaccine since before then, suggesting that those poor souls who have died recently had a horrible, drawn-out illness and death. I wonder what the two Dames most responsible – Dame Sarah Gilbert and Dame June Raine – feel about that? They should not be able to sleep.
Furthermore the Freedom of Information request to the MHRA requiring all the data that was submitted by AstraZeneca in the application for licence of their Covid-19 vaccine (AZD1222/Vaxzevria), and relied upon in granting a Conditional Marketing Authorisation for its use, has been stonewalled and then categorised by the MHRA as ‘vexatious’.
We know why the MHRA do this. If they answered honestly the entire edifice protecting their lies, recklessness and indeed possible criminality over the authorisation of these vaccines would crumble and collapse.
I will be putting all this information in front of the All-Party Parliamentary Group (APPG) on Pandemic Response and Recovery, who have recently written to the MHRA about their lack of action on covid jabs despite knowing of risks for months before issuing any official warnings, in the hope they will take this forward too.
Here in full is the MHRA Yellow Card reporting summary up to 28th February 2024
Interactive format data
Adult & Child – Primary & Boosters (mono/bivalent)
Government data (archived) up to Sept 2022 showed 53.8million people had received a 1st dose UK-wide
Yellow Card adverse event reports
178,399 (Pfizer-mono) +
6,146 (Pfizer-bivalent) +
249,297 (AZ) +
43,191 (Moderna-mono) +
5,707 (Moderna-bivalent) +
188 (Novavax) +
2,986 (Unknown brand)
TOTAL = 485,914 people impacted (increase of 353 in 4 weeks)
Reports classified as SERIOUS* by MHRA = 74.5 per cent of all reports
126,391 (Pfizer-mono) +
4,747 (Pfizer-bivalent) +
193,209 (AZ) +
31,251 (Moderna-mono) +
4,185 (Moderna-bivalent) +
122 (Novavax) +
2,145 (Unknown)
TOTAL = 362,050 serious reports filed
Over 46,843 of the above serious reports are of ‘Unknown Age’ = 12.9 per cent of all serious reports
Overall 1 in 111 people injected experienced a Yellow Card Adverse Event (assuming one person submits only one report)
1 in 149 people injected experienced an adverse event classified as SERIOUS*
Reports classified as Non-SERIOUS by MHRA = 25 per cent of all reports
51,094 (Pfizer-mono) +
1,336 (Pfizer-bivalent) +
54,634 (AZ) +
11,840 (Moderna-mono) +
1471 (Moderna-bivalent) +
66 (Novavax) +
744 (Unknown)
TOTAL = 121,185 non-serious reports filed
REACTIONS
515,415 (Pfizer-mono) +
16,552 (Pfizer-bivalent) +
884,534 (AZ) +
142,010 (Moderna-mono) +
15,678 (Moderna-bivalent) +
512 (Novavax) +
9,070 (Unknown)
TOTAL = 1,583,771 reaction types
1 in 181 reports are associated with a fatality, which may be less than 10 per cent of actual figures according to MHRA
FATAL
914 (Pfizer-mono) +
63 (Pfizer-bivalent) +
1,454 (AZ) +
100 (Moderna-mono) +
51 (Moderna-bivalent) +
97 (Unknown)
TOTAL = 2679 = 0.5 per cent of all reports (increase of 39 reports with fatal outcome in 4 weeks)
445 of the above fatalities are of ‘unknown age’ = 16.6 per cent of all fatalities, and 176 are of ‘unknown sex’ = 6.6 per cent of all fatalities
* MHRA definition of ‘serious’ – patient died, life threatening, hospitalisation, congenital abnormality, persistent or significant disability or capacity, deemed medically significant by MHRA medical dictionary or reporter
For full reports see here. https://yellowcard.mhra.gov.uk/idaps
