THE DATA FROM THE LAST 6 YEARS IS ALARMING AND MOST PEOPLE HAVE NEVER SEEN PFIZER’S FIRST COVID VACCINE SAFETY REPORT IN THE FIRST MONTHS.
I have. And I’m appalled. And after reading the actual document, I think everyone should know what was being reported in the FIRST months of the rollout. Not rumors. Not memes. Not someone’s interpretation. The actual numbers.
Pfizer’s first major cumulative post-authorization safety analysis covered reports received from the beginning of the worldwide rollout through February 28, 2021. Approximately three months. By that point, Pfizer’s worldwide safety database contained: 42,086 adverse-event cases representing 158,893 individual adverse events.
And among those 42,086 cases: 1,223 had fatal outcomes. 11,361 had NOT recovered at the time the report was recorded.
Stop there for a minute. This was February 2021. We were barely into the worldwide rollout. And these weren’t simply sore arms, headaches and fevers. Look at what was already being reported and evaluated.
CARDIOVASCULAR
1,403 cardiovascular cases
1,098 tachycardia
102 arrhythmia
89 myocardial infarction
80 cardiac failure
41 acute myocardial infarction
7 cardiogenic shock
136 fatal outcomes were reported within the cardiovascular category.
NEUROLOGICAL
501 neurological cases
204 seizures
83 epilepsy
33 generalized tonic-clonic seizures
24 Guillain-Barré syndrome
17 trigeminal neuralgia
11 transverse myelitis
10 multiple-sclerosis relapses
10 optic neuritis
There were also reports involving encephalopathy, demyelination, meningitis, narcolepsy, ataxia and other neurological conditions.
16 fatal outcomes were reported within the neurological category.
STROKE
275 stroke cases
160 cerebrovascular accidents
41 ischemic strokes
26 cerebral hemorrhages
15 cerebral infarctions
11 hemorrhagic strokes
There were also reports involving cerebral thrombosis, cerebral venous sinus thrombosis, lacunar infarction and thrombotic stroke.
61 fatal outcomes were reported within the stroke category.
BLOOD CLOTS
151 thromboembolic cases
60 pulmonary embolisms
39 thromboses
35 deep-vein thromboses
Of 168 thromboembolic events reported, 165 were classified as serious.
18 fatal outcomes were reported within this category.
IMMUNE AND AUTOIMMUNE
1,050 immune-mediated/autoimmune cases
49 peripheral neuropathy
32 pericarditis
25 myocarditis
16 diabetes mellitus
16 encephalitis
14 psoriasis
11 autoimmune disorders
FACIAL PARALYSIS
449 cases.
Of 453 events, 399 were classified as serious.
At the time of reporting, 183 had not resolved.
KIDNEY INJURY
69 renal cases
40 acute kidney injuries
30 renal-failure events
All 70 renal events were classified as serious.
23 fatal outcomes were reported within this category.
HERPES VIRUS EVENTS
The database also contained:
259 herpes zoster events
80 oral herpes events
17 herpes-virus infections
13 herpes simplex events
10 ophthalmic herpes zoster events
PREGNANCY
Pfizer had information involving 270 unique pregnancies.
Among the reported outcomes were:
23 spontaneous abortions
2 premature births with neonatal death
But this is extremely important:
Pregnancy outcomes were unavailable for 238 of the 270 pregnancies.
AND THEN I FOUND THIS.
Pfizer said the volume of adverse-event reports was so large that approximately 600 additional full-time employees had already been brought in to process them. And Pfizer anticipated bringing in more than 1,800 additional resources by the end of June 2021.
Again: This was happening within MONTHS of rollout. These databases contain events reported after vaccination. They are surveillance systems.
But that is precisely why this information matters. Because pharmacovigilance exists to find signals before causation has necessarily been established. You collect the reports. You look for patterns. You investigate. You compare what you’re seeing against what would normally be expected. And when a signal becomes strong enough, you act. YOU PULL THE DRUG before any more people are harmed or killed.
So what happened next?
2021: THE REPORTS KEPT COMING
The U.S. Vaccine Adverse Event Reporting System, VAERS, was receiving hundreds of thousands of reports following COVID vaccination. And something particularly important happened. Myocarditis began emerging as a recognizable signal.
Remember: Pfizer’s February 2021 report already contained: 25 myocarditis reports and 32 pericarditis reports. By April 2021, cases of myocarditis following COVID vaccination, particularly among young males, were being reported to VAERS. Eventually the evidence became strong enough that myocarditis and pericarditis became OFFICIALLY recognized risks of mRNA COVID vaccination.
Think about that. Something visible in those early safety reports eventually became an acknowledged vaccine adverse effect.
2022. VAERS continued accumulating reports following COVID vaccination.
In the current public VAERS dataset, records associated with COVID vaccines and received during 2022 include approximately:
221,580 adverse-event reports
8,133 records mentioning death
38,360 involving hospitalization
Again, these are reports following vaccination.
BY MARCH 2023 CDC itself reported something that I think everyone deserves to know. By March 1, 2023, VAERS had received:
19,476 preliminary reports of death following COVID vaccination in the United States. CDC did NOT say that the vaccines caused 19,476 deaths. Why would they admit to this genocide?
2023
The current VAERS data contain approximately:
54,720 COVID-vaccine reports
2,087 records mentioning death
13,999 hospitalizations
received during 2023.
2024
Approximately:
20,246 reports
824 records mentioning death
2,117 hospitalizations
2025
Approximately:
10,644 reports
540 records mentioning death
1,211 hospitalizations
And something changed in 2025 that you need to know.
CDC and FDA expanded the public VAERS database to include certain secondary reports submitted by additional sources about the same patient, vaccine and dose. That means some records appearing in today’s database are different reports concerning the same underlying event.
2026
The federal VAERS files are currently processed through July 31, 2026.
The current data contain approximately:
500 COVID-vaccine reports received in 2026
20 records mentioning death
72 hospitalizations
And remember that reports can arrive long after the event itself, so the year a report was received is not necessarily the year the medical event occurred.
WHAT DOES THE CURRENT DATABASE SHOW?
Across the current public VAERS COVID-vaccine records from the beginning of the rollout through the available 2026 data, there are approximately:
1.076 MILLION adverse-event report records (read that again)
and
24,575 records mentioning death.
VAERS exists for a reason but also know that many deaths and adverse reactions are not reported. When someone gets diagnosed with turbo cancer or an athlete dies on the field from a heart attack, the dots do not always get connected. People are NOT reporting these heinous crimes against humanity. They just don’t know any better.
CDC itself says VAERS is designed to rapidly detect unusual or unexpected patterns of adverse events called SAFETY SIGNALS. And here is the part I cannot get past. Go back to February 2021. Within approximately three months, Pfizer already had:
42,086 cases.
158,893 adverse events.
1,223 cases with fatal outcomes.
11,361 people not recovered.
Cardiovascular events.
Neurological events.
Strokes.
Blood clots.
Seizures.
Guillain-Barré syndrome.
Transverse myelitis.
Facial paralysis.
Autoimmune events.
Kidney injuries.
Pregnancy events.
Myocarditis.
Pericarditis.
And such a volume of reports that Pfizer was dramatically expanding its pharmacovigilance workforce.
Those were SIGNALS.
And one of those signals, myocarditis and pericarditis, was subsequently recognized as causally associated with mRNA COVID vaccination.
Yet the rollout continued.
Eligibility expanded.
Younger populations were added.
Boosters followed.
Mandates followed.
So no, I don’t need to claim that every illness or every death reported after vaccination was caused by the vaccine. But I will lean very heavily on that data and connect the dots to determine that it is more than probable. What I DO know is what the documents show. And I believe these numbers should have generated enormous scrutiny, transparency and public discussion from the very beginning.
The question isn’t: “Can you prove every one of these events was caused by the vaccine?” That’s not how an early-warning system works.
The question is: HOW MANY SAFETY SIGNALS DOES IT TAKE BEFORE YOU HIT THE BRAKES?
Because informed consent isn’t simply telling people what has already been proven. It’s telling them what is being observed. What is being investigated. What is unknown. And what risks may be emerging. People deserved to know that. They deserved the numbers. They deserved the uncertainty. THEY DESERVED THE CHOICE. The documents exist. The reports exist. The numbers exist. Read them. Ask questions. And connect your own dots. It’s time people wake up to the aftermath of this long-planned genocide.
- Lindy Werwa