Philippines and the VAERS System: Serious Adverse Events / Deaths Following Receipt of US Manufactured Vaccines are Reported By Philippines FDA to VAERS.
These reports can be searched using various search engines developed by concerned citizens and aided by FOI data releases forced by Aaron Siri's / the ICAN team.
The VAERS systems is the US system for reporting of adverse events following immunization.
While this system mostly contains US reports, it does contain some international reports, including reports for the Philippines.
The reporting of Philippines foreign lot AEFIs was brought to my attention by Welcome the Eagle in this article.
Eagle runs the VAERS Aware site which has interactive dashboards, and also has an excellent substack discussing his findings and the VAERS data. I am only just beginning to learn how to get around his site.
Philippines and VAERS
Filipinos cannot report adverse events following vaccination to VAERS. The only way for a Filipino AEFI to enter the system is if that event was reported to the Philippines FDA, if FDA then transmitted the event report to the US registered vaccine manufacturer, and if that manufacturer then filed a VAERS report. US manufacturers are required under US law to report offshore serious adverse events and deaths to VAERS.
To summarize, this means that:
Only serious foreign events or deaths could be expected to be included in the VAERS reports, and
Only US manufacturer reports are included. I.e. no VAERS reports will be found for the other vaccines used in the Philippines including Coronavac or Sinopharm (Chinese), Sputnik (Russian), or AstraZeneca (UK).
As discussed by Welcome the Eagle, the underreporting factor for VAERS for international data could be massive, certainly well higher than the internationally accepted level of 41, because there are 3 layers where reports can be lost before they are actually entered into VAERs.
The 1st layer is victims / doctors / medical team knowing about and being able to make their report to the Philippines FDA. In the Philippines there is very poor knowledge about the reporting system, access to make a report is even lower. Then, even when informed and offered assistance to report an adverse outcome, many still refuse, perhaps scared to draw any attention to themselves.
The 2nd layer is the Philippines FDA, assessing an event to be serious, and submitting the report to the manufacturer.
I assisted in filing a report for a close friends 46-year-old relative who had no known underlying conditions, but immediately became ill and died within 48 hours after a second dose of Moderna in early 2022. I have searched by his batch number but cannot find any VAERs report matching the details that I filed and which was acknowledged as received by the FDA Pharmacovigilance team.
The 3rd layer is the manufacturer submitting to VAERS with adequate enough (and without errors) information for the event to be searched and found by enquirers.
It then follows that the numbers of Philippines AEFI, reactions, and deaths in VAERS are far lower than those in the Philippines Pharmacovigilance report (which does not give death count by vaccine type), which are in turn far lower than the actual cases and deaths which happened to recipients.
VAERS « Philippines FDA System « ACTUAL PEOPLE SUFFERING, SICK, AND DYING
Other search engines for exploring VAERS Philippines include: -
Open VAERS, which summarizes VAERS data for easy public access. Searching this database, I can find 7,784 AEFI reports received for the Philippines, which includes 1,157 reported deaths. Of these deaths, 531 were attributed to Pfizer, 459 to Janssen, and 190 to Moderna. Note that the breakdown of deaths by vaccine type adds up to 1,190 (not the initial 1,157 when I searched Philippines without vaccine type specified), so there are clearly some discrepancies in the system.
You can sort by vaccine type and click on any report and see what happened. For example, ID1730687 was a 29-year-old (Filipino) male who died on 4th of September, the same day that he received a dose of Moderna with the events of vaccination site pain, headache and dizziness. No cause of death is specified, and the company report says the “risk-benefit relationship is not affected by this report”. Since when do 29 yo men die suddenly without cause? The vaccine as cause is dismissed! Clearly, Janssen don’t consider DEATH a risk that would affect their safety calculations! My head is exploding with the ignorance, deceit and cruelty!
How Bad is My Batch - Use this to search just by Batch Number and adverse events.
Japanese Data Base. This seems to have more complete batch and reports compared to VAERS. Select “world” then enter vaccine batch number to search. The reports come up and you can select either all, or deaths only. When you read the reports, you will see that they were submitted by the Philippines FDA. You can then review the cases and see the ASTOUNDING QUALITY of investigation that was done! I am dripping sarcasm; in case you didn’t realize!
The cases are shocking. Even in cases with death of a young person soon after injection, it typically says “event is unassessable”. The following report was for a 32-yo woman who died less than a week after dosing. Her deaths is considered as having unknown scientific plausibility and is unassessable.
The same goes for a 19-year-old man. His cause of death is numbness, pain at left thigh and leg, and vomiting. WHAT? He was injected on 18 Jan 2022 and died on or shortly after 25th Jan 2022. His death is temporally linked but again is listed as unassessable!
GASLIGHTING MUCH! Every single report is more of the same tragedy. I am so upset and angry reading these reports. Everyone should be angry at this genocide which has been so openly covered up! When will there be accountability?
COVID-19 Vaccination in the Philippines by Vaccine Type
Philippines weekly vaccine doses are color coded. The dosing reported is weekly dosing from the Philippines FDA Pharmacovigilance reports. Ignore the big spike in March 2023, it is a correction by DOH just before they stopped reporting dosing, even though there was still dosing of bivalent and left over products up to at least 3rd quarter 2023.
Initially the main vaccine used in the Philippines was Coronavax (26.8% of doses). This was ceded over time to Comirnaty / Pfizer which ended up the most used product (42.4% of doses). AstraZeneca was the 3rd most used (13.2%), followed by Moderna (11.9%), and with Janssen lagging at only 4.2% of total doses.
Deaths Reported to VAERS vs. Doses of Vaccines
I compared VAERS reports of adverse reactions and deaths with the Philippines known total doses of Vaccines and FDA Serious Adverse Events (SAE) reported. Note that the VAERS SAE reports (recall FDA is only required to report serious reactions to vaccine manufacturers) are higher than the Philippines FDA reports classified as serious. I thought the Philippines FDA was only required to report SAE to the drug manufacturers - or was internal coding of “serious” different from that reported in their Pharmacovigilance reports?
Please note that based on doses administered Janssen has 4x more reports of SAE compared to both Pfizer and Moderna. Further, 25.2% of the VAERS Reports to VAERS for Janssen are deaths (1 in 4 reports), higher than both Moderna (18.3% or 1 in 5.5 of reports are deaths), and Pfizer (10.6% or about 1 in 10 reports are deaths).
Given that Janssen was the outstandingly least safe product based on reports, I discuss further.
Janssen Batches in Philippines
3.2 million doses of Janssen were first delivered on 16 and 17 July, 2021. Dosing started on 20th July 2021 and were completed within less than 1 month (until doses were consumed). Further deliveries of Janssen arrived by late 4th quarter 2021 and were mostly administered from December 2021 through to March 2022.
Given the standout signal from Janssen, I looked further at the Janssen reports using the Japanese data-base and I checked batches that were identified by Eagle to have been used (apparently exclusively) in the Philippines, plus one other batch (ACB1894) that I found from local searching / reports crowd-sourced local vaccine card data.
Some of the worst outcome batch numbers, cases, deaths are set out below, along with administration periods extracted from the reports.
From my current limited crowd data sourcing, so far I have only found on-the ground (via vaccine-cards) evidence of distribution for batches 212C21A, 213C21A, ACB6894 and ACB3221, which may have been substantially sized batches (I still need to find batch size data).
212C21A- 134 Case Reports / 67 deaths (50% deaths) - July to Sept 2021
213C21A - 539 Case Reports / 114 Deaths (21.2% deaths) - July to Sept 2021
205C21A - 36 Case Reports / 14 Deaths (39% deaths) - July to Sept 2021
231C21A - 7 Case Reports / 1 Death (14% deaths) - July to early August 2021
218C21A - 1 Case Report / 1 Death (100% deaths) - administered in July 2021
209C21A - 14 Case Reports / 7 Death (50% deaths) - some administered July-August 2021, some in early 2022 reports)
ACB6894 - 18 Case Reports / 3 Deaths (16.7% deaths) - 31 Dec 21 to Feb 2022.
ACB3221 - 81 Case Reports / 17 Deaths (21% deaths) - early 2022
Conclusion
Sorry, this is all quite complicated (and very shocking) and I am still trying to wrap my head around it all. In short initial provisional summary:-
Philippines SAE for Pfizer, Moderna, and Janssen can be found in the US VAERS system, and using international trackers developed by concerned world citizens.
There are considerable reports of Philippines severe injuries and deaths in VAERS (filed by the Philippines FDA, to manufacturers, who entered data into VAERS.
Despite temporally related deaths, the Philippines FDA and the Manufacturers appear to have concluded either no scientific plausibility or insufficient information to determine causality for most reported events.
Janssen outcomes were 4x worse than Moderna, which was worse than Pfizer / Comirnaty for at least short-term fatal outcomes based on number of doses administered. I expect that likelihood of reporting decreases with time since injection as people are less likely to link delayed outcomes with the long-ago received dose.
Real outcomes may be far worse (» 41x) than apparent from the Philippines FDA and VAERS reporting systems.
Cases are shocking and heart-breaking! A great disservice has been done in the official cold dismissal of so much devastating harm and so many deaths by the agencies that should have been the safety gate-keepers, but which dismally failed!
This discussion is not over!!!
The whole system is rigged globally! We need to tear it down bit by bit!
be sure to check out and reshare widely a post on rumble and on my gestapo book page......interview with steve kirsch the miligram experiment that was covid