By Nicanor Perlas

09 December 2021

Pfizer’s “vaccine” is not a vaccine. It is a medical device meant to turn your entire body into a permanent facility for manufacturing spike proteins, as Bill Gates once blogged with glee[2] Unfortunately, in itself, these spike proteins are toxic and can also harm and cause deaths on their own[3], irrespective of whether there is a virus or not.

Beware! The Pfizer vaccine is the perfect assassin. It is a perfect tool for destroying your future and even your life. It can quietly give you any of the hundreds of different kinds of adverse effects. Pfizer’s own internal confidential study has revealed this stark reality.

This article is dedicated to exposing the dangers of the so-called Pfizer vaccine, which, in reality, is a bioweapons[4]


Recently, we wrote about the onerous and totally coercive secret contract that Pfizer extracted from at least 110 countries[5]  In that article we referred to section “5.5 Purchaser Acknowledgement” and quoted the Pfizer secret contract as claiming:

 “Purchaser [Brazil in this case] … acknowledges that the long-term effects and efficacy of the Vaccine are not currently known and that there may be adverse effects of the Vaccine that are not currently known.”   (Emphasis added.)

We then went on to demonstrate that Pfizer knew their “vaccine” had thousands of adverse events stemming from hundreds of different kinds of negative restructuring of human metabolic pathways, cells, tissues, and organs. Yet Pfizer made false representations to their Purchaser countries that it was not “currently” aware of such serious side effects.

We promised our readers that we would devote an entire article to the confidential report that Pfizer submitted to the US Food and Drug Administration (FDA) on this issue.

Secret Pfizer Report Detailing Hundreds of Different Kinds of Vaccine-Induced Illnesses Producing Tens of Thousands of Negative Impacts

As we already reported, the Public Health and Medical Professionals for Transparency (PHMPT) did a Freedom of Information request from the FDA. PHMPT is a group of dozens of prestigious scientists whose sole objective is to enable the scientific community to get the necessary regulatory information on the various Covid vaccines that are now used for mass, often coercive vaccination programs. Based on this FOI-released information, any group can do their own independent analysis of the data[6]

FDA initially did not give the documents. So PHMPT sued FDA and won the case. However, the judge in the case allowed only a very slow release of the Pfizer documents, 55 YEARS to be exact[7] Nonetheless, the first batch of documents released showed that Pfizer knew that their “vaccines” had hundreds of different kinds of serious side effects and/or adverse events of special interest.

We have to distinguish between these different kinds of adverse side effects from the actual number of “adverse events”.  In this case, the total number of adverse events is not caused by just a few kinds of side effects; say from a damaged heart or a deteriorating kidney. Pfizer’s report reports hundreds of different kinds of illnesses that are producing negative side effects, including deaths.

The Pfizer document is entitled, “5.3.6. CUMULATIVE ANALYSIS OF POST AUTHORIZATION ADVERSE EVENTS REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021”[8] (Caps in the original.) All quotes about Pfizer’s product are from this confidential study.

Pfizer’s “Worldwide Safety Group” prepared the report that Pfizer submitted to the FDA. It covered a period of three months, from 01 December 2020 to 28 February 2021.

Pfizer gives a general overview of its report. The report covers 42,086 case reports covering 158,893 “events” or adverse events. Pfizer makes a huge admission in this Report. Of the total case reports, Pfizer admits that 25,739 cases were medically confirmed. This admission totally blows the cover of any health agency that says that the adverse events from the Pfizer vaccine are not real. They can be medically confirmed.

Here, Pfizer clearly states that more than 25,000 cases were medically confirmed as real. Despite the usual disclaimer on causality, we will show below from Pfizer’s own data and outside expert analysis that the causality link can clearly be established with a strong possibility of likelihood. That is, the massive number of diseases recorded most likely indicates that the Pfizer “vaccine” is the culprit, as can be gleaned from the whole context of their confidential report to FDA and outside independent analysis of the VAERS data.

Table 1 of the report shows that 1,223 died from the vaccines. Another 520 recovered but with “sequalae”, that is, continuing, most likely, permanent injuries.

Figure 1 of the Report that follows Table 1 is important for two reasons. First, it demonstrates that thousands of these adverse events are serious. (See purplish color in the bar chart of Figure 1.) Pfizer makes it difficult for the analyst to come up with the exact number of serious adverse events. Nonetheless, one can extract this information in Figure 1 and the subsequent Tables that follow where the serious adverse events are indicated, albeit scattered.

Second, Pfizer identifies the “System Organ Classes (SOCs) that contained the greatest number (≥2%) of events, in the overall dataset”.  Note again, Pfizer’s reporting is not

Table 1. General Overview:

Selected Characteristics of All Cases Received During the Reporting Interval

a. in 46 cases reported age was <16-year-old and in 34 cases <12-year-old.

Very helpful because it sets the range at greater than or equal to 2%, making the reader focus at the lower value of 2%. Yet, when one does an independent calculation of the side effects, we can see that there were 25,957 Nervous System Disorders (NSDs) out of the total 158,893 adverse events. If we take the 25,957 NSDs and divide it by the 158,893 adverse events, we get 25,957/158,893 or 16.33%, which is a more meaningful, albeit alarming number. This shows that 1 out of 6 of the adverse events were connected with the nervous system, which is very concerning.

With these caveats, we can now show the other organ “classes” being damaged by the Pfizer vaccine:

“General disorders and administration site conditions (51,335 AEs), Nervous system disorders (25,957), Musculoskeletal and connective tissue disorders (17,283), Gastrointestinal disorders (14,096), Skin and subcutaneous tissue disorders (8,476), Respiratory, thoracic and mediastinal disorders (8,848), Infections and infestations (4,610), Injury, poisoning and procedural complications (5,590), and Investigations (3,693).” [Emphasis added.]

Figure 1. Total Number of BNT162b2 AEs

By System Organ Classes and Event Seriousness

Even from just this unhelpful summary presentation of the facts by Pfizer, one immediately sees that the Pfizer vaccine adversely impacts many of our organs in the body. This confirms what a number of scientists have pointed out. The “vaccines” contain spike proteins that are toxic in their own right and that spread throughout the body[9] and … Continue reading. Not surprisingly, Pfizer’s own secret studies in Japan on the dynamics of the distribution of its “vaccine” revealed that the toxic spike proteins in the vaccine spread throughout the body[10] In addition, autopsies revealed this is a fact[11]

This overview account will show its significance once we take a detailed look below at what kinds of adverse events are contained in these various “organ classes”.

Pfizer identifies the “important identified risk” associated with its vaccine. See Pfizer’s Table 4 immediately below.

Table 2. Important Identified Risk

(Table 4 in the Original Pfizer Document)

“a  Different clinical outcome may be reported for an event that occurred more than once to the same individual.

b  There were 4 individuals in the anaphylaxis evaluation who died on the same day they were vaccinated. … Although these patients experienced adverse events (9) that are potential symptoms of anaphylaxis, they all had serious underlying medical conditions, and one individual appeared to also have COVID-19 pneumonia, that likely contributed to their deaths.“

There are numbers of important points to learn from Table 4.  First, anaphylaxis is a serious negative adverse impact of the Pfizer “vaccines” as can be seen from the discussion above. Note the Brighton Collaboration Levels above. Even Pfizer named its Table 4 as “Important Identified Risk”.

Second, note this language that you will find throughout the Pfizer Tables in this document. After every category of adverse effects, Pfizer has this conclusion: “Evaluation … did not reveal any significant new safety information.” 

In other words, while Pfizer was denying to the world that its vaccines caused anaphylaxis, its internal documents showed that Pfizer was well aware of this problem and even told the FDA that “Anaphylaxis is appropriately described in the product labeling”. In other words, Pfizer’s product label admits and warns of the anaphylaxis danger.

But does the product label actually say this?  This is definitely not the case in the Philippines where many of those who report their forced vaccination to us say they never had such information.

Third, by repeatedly saying in its entire document that the data did not show any new safety problems, Pfizer is exactly admitting that it knows of ALL the hundreds of disease problems that it mentions in this report. Pfizer’s language is classic doublespeak.

It uses manipulative language to make people think in a certain way that Pfizer wants them to think. In reality, the stinking problem is right under the nose of Pfizer. By saying the data shows no significant new problem, Pfizer is actually saying: a) yes, there is a problem; b) we already know this from before; c) now that it is showing up in the data again, this danger signal is not new; and, d) since it is not new, there is nothing to be concerned about. DISGUSTING!

In fact, there should be a deep concern because the “vaccines” are responsible for these problems, which should not be there in the first place. So what if the problem is already known from before? It does not make the problem go away. It remains a safety problem. Period!

Fourth and most important, Pfizer’s discussion of its Table 4 is as near as it gets to admitting their vaccines can result in the death of the Pfizer-vaccinated: a) Pfizer knows that anaphylaxis is an “important identified risk”; b) it has a significant number of cases that show the “highest level of diagnostic certainty of anaphylaxis”; c) four people actually died of anaphylaxis “on the same day” after taking the Pfizer vaccine; and d) Pfizer uses the convenient excuse that the 9 people who died from their vaccines had other co-morbidities.

The latter reasoning is specious. The “vaccine” is the straw that broke the camel’s back. It triggered the death of people who had other illnesses but who would not have died necessarily if they had not taken the vaccine.

For example, one may have hypertension. Without the vaccine, that person could have lived longer with hypertension given the proper medical attention and proper lifestyle changes[12]Caldwell Esselstyn, M.D., Prevent and Reverse Heart Disease by  New York: Avery (Penguin Books).. Yet, the Pfizer “vaccine”, by Pfizer’s own admission, as will be seen below, worsens heart problems and can cause death. Clearly, the vaccine is the cause of death.

Here is another lie to demolish. In 2020, when the government wanted to inflate the Covid death figures to scare people to submission and vaccination, they had a mantra. All deaths had to be counted as Covid deaths even if the deaths are from co-morbidities. Plus, even other deaths, including motorcycle deaths, will be counted as Covid deaths if the latter tested positive in a notoriously inaccurate RT-PCR test[13]Conversation with Governor Gwen Garcia of Cebu Province, around 22 February 2021..

Now that there is a pandemic of vaccine deaths, blame these deaths on co-morbidities. This is all very convenient, right?

Plus government wanted to give priority vaccination to those with co-morbidities. Again, this is all too convenient. So when these people with co-morbidities die, the vaccine toxic spike proteins will not be blamed for their deaths. Instead, the government will focus on co-morbidities as the primary cause. Yes, all too convenient. They will do anything to perpetuate a lie; anything to get people vaccinated.

I will now discuss another Table to demonstrate that Table 4 is not a fluke. Please take a look at the document itself to satisfy one that this entire vaccine thing is as dangerous as it is a disgusting scam.

Table 5 in the Pfizer document is the other example. It discusses another kind of  “Potential Important Risk”.  These risks are very interestingly described as “Vaccine- Associated Enhanced Disease (VAED), including Vaccine- Associated Enhanced Respiratory Disease (VAERD)”.

This is brutally frank. Maybe Pfizer thought that their document would not see the light of day. They admit that there are diseases enhanced by their vaccines including respiratory diseases. However, Pfizer still has tricks up its sleeve as we shall see.

Table 5 reveals this conclusion. “VAED may present as severe or unusual clinical manifestations of COVID-19.” Note the emphasized work “may present”. The severe event, Pfizer claims, is most likely from COVID-19, and not from VAED, the symptoms of which are similar to severe or unusual symptoms of COVID-19.

“Overall, there were 37 subjects with suspected COVID-19 and 101 subjects with confirmed COVID-19 following one or both doses of the vaccine; 75 of the 101 cases were severe, resulting in hospitalisation, disability, life-threatening consequences or death. None of the 75 cases could be definitively considered as VAED/VAERD.”

“In this review of subjects with COVID-19 following vaccination, based on the current evidence, VAED/VAERD remains a theoretical risk for the vaccine. Surveillance will continue.” (Emphasis added.)

The cognitive blindness of Pfizer is incredible. Scientific data after scientific data is showing exactly that the “vaccines” do not work. They do not prevent infection and transmission. The vaccinated get hospitalized. The most vaccinated countries are also the places where many people are dying after mass vaccination[14] In addition, the respiratory system is one of the main targets of toxic spike proteins in the vaccines, as well as the auto-produced spike proteins of our mRNA-infested genetic system[15]See references #8 and 1 above..

Yet here they are claiming that VAED and VAERD do not exist and that these are only theoretical risks. Yet their own data is showing that the Pfizer-vaccinated have severe Covid cases, are hospitalized and 75 out 101 cases died just like real-world data sets are showing.

The Pfizer report also has a very long Table 7 where it lists the hundreds of adverse events of special interest or AESI. To get a feel of Table 7 here is just a small portion of details supporting Table 7. There are a total of 10 pages of these kinds of AESI. It can be found in Appendix 1.


1p36 deletion syndrome;2-Hydroxyglutaric aciduria;5’nucleotidase increased;Acoustic neuritis;Acquired C1 inhibitor deficiency;Acquired epidermolysis bullosa;Acquired epileptic aphasia;Acute cutaneous lupus erythematosus;Acute disseminated encephalomyelitis;Acute encephalitis with refractory, repetitive partial seizures;Acute febrile neutrophilic dermatosis;Acute flaccid myelitis;Acute haemorrhagic leukoencephalitis;Acute haemorrhagic oedema of infancy;Acute kidney injury;Acute macular outer retinopathy;Acute motor axonal neuropathy;Acute motor-sensory axonal neuropathy;Acute myocardial infarction;Acute respiratory distress syndrome;Acute respiratory failure;Addison’s disease;Administration site thrombosis;Administration site vasculitis;Adrenal thrombosis;Adverse event following immunisation;Ageusia;Agranulocytosis;Air embolism;Alanine aminotransferase abnormal;Alanine aminotransferase increased;Alcoholic seizure;Allergic bronchopulmonary mycosis;Allergic oedema;Alloimmune hepatitis;Alopecia areata;Alpers disease;Alveolar proteinosis;Ammonia abnormal;Ammonia increased;Amniotic cavity infection;Amygdalohippocampectomy;Amyloid arthropathy;Amyloidosis;Amyloidosis senile;Anaphylactic reaction;Anaphylactic shock;Anaphylactic transfusion reaction;Anaphylactoid reaction;Anaphylactoid shock;Anaphylactoid syndrome of pregnancy;Angioedema;Angiopathic neuropathy;Ankylosing spondylitis;Anosmia;Antiacetylcholine receptor antibody positive;Anti-actin antibody positive;Anti-aquaporin-4 antibody positive;Anti-basal ganglia antibody positive;Anti-cyclic citrullinated peptide antibody positive;Anti-epithelial antibody positive;Anti-erythrocyte antibody positive;Anti-exosome complex antibody positive;Anti- GAD antibody negative;Anti-GAD antibody positive;Anti-ganglioside antibody positive;Antigliadin antibody positive;Anti-glomerular basement membrane antibody positive;Anti-glomerular basement membrane disease;Anti-glycyl-tRNA synthetase antibody positive;Anti-HLA antibody test positive;Anti-IA2 antibody positive;Anti-insulin antibody increased;Anti-insulin antibody positive;Anti-insulin receptor antibody increased;Anti- insulin receptor antibody positive;Anti-interferon antibody negative;Anti-interferon antibody positive;Anti-islet cell antibody positive;Antimitochondrial antibody positive;Anti-muscle specific kinase antibody positive;Anti-myelin-associated glycoprotein antibodies positive;Anti-myelin-associated glycoprotein associated polyneuropathy;Antimyocardial antibody positive;Anti-neuronal antibody positive;Antineutrophil cytoplasmic antibody increased;Antineutrophil cytoplasmic antibody positive;Anti-neutrophil cytoplasmic antibody positive vasculitis;Anti-NMDA antibody positive;Antinuclear antibody increased;Antinuclear antibody positive;Antiphospholipid antibodies positive;Antiphospholipid syndrome;Anti-platelet antibody positive;Anti-prothrombin antibody positive;Antiribosomal P antibody positive;Anti-RNA polymerase III antibody positive;Anti-saccharomyces cerevisiae antibody test positive;Anti-sperm antibody positive;Anti-SRP antibody positive;Antisynthetase syndrome;Anti-thyroid antibody positive;Anti-transglutaminase antibody increased;Anti-VGCC antibody positive;Anti- VGKC antibody positive;Anti-vimentin antibody positive;Antiviral prophylaxis;Antiviral treatment;Anti-zinc transporter 8 antibody positive;Aortic embolus;Aortic thrombosis;Aortitis;Aplasia pure red cell;Aplastic anaemia;Application site thrombosis;Application site vasculitis;Arrhythmia;Arterial bypass occlusion;Arterial bypass thrombosis;Arterial thrombosis;Arteriovenous fistula thrombosis;Arteriovenous graft site stenosis;Arteriovenous graft thrombosis;Arteritis;Arteritis

coronary;Arthralgia;Arthritis;Arthritis enteropathic;Ascites;Aseptic cavernous sinus thrombosis;Aspartate aminotransferase abnormal;Aspartate aminotransferase increased;Aspartate-glutamate-transporter deficiency;AST to platelet ratio index increased;AST/ALT ratio abnormal;Asthma;Asymptomatic COVID- 19;Ataxia;Atheroembolism;Atonic seizures;Atrial thrombosis;Atrophic thyroiditis;Atypical benign partial epilepsy;Atypical pneumonia;Aura;Autoantibody positive;Autoimmune anaemia;Autoimmune aplastic anaemia;Autoimmune arthritis;Autoimmune blistering disease;Autoimmune cholangitis;Autoimmune colitis;Autoimmune demyelinating disease;Autoimmune dermatitis;Autoimmune disorder;Autoimmune encephalopathy;Autoimmune endocrine disorder;Autoimmune enteropathy;Autoimmune eye disorder;Autoimmune haemolytic anaemia;Autoimmune heparin-induced thrombocytopenia;Autoimmune hepatitis;Autoimmune hyperlipidaemia;Autoimmune hypothyroidism;Autoimmune inner ear disease;Autoimmune lung disease;Autoimmune lymphoproliferative syndrome;Autoimmune myocarditis;Autoimmune myositis;Autoimmune nephritis;Autoimmune neuropathy;Autoimmune neutropenia;Autoimmune pancreatitis;Autoimmune pancytopenia;Autoimmune pericarditis;Autoimmune retinopathy;Autoimmune thyroid disorder;Autoimmune thyroiditis;Autoimmune uveitis;Autoinflammation with infantile enterocolitis;Autoinflammatory disease;Automatism epileptic;Autonomic nervous system imbalance;Autonomic seizure;Axial spondyloarthritis;Axillary vein thrombosis;Axonal and demyelinating polyneuropathy;Axonal neuropathy;Bacterascites;Baltic myoclonic epilepsy;Band sensation;Basedow’s disease;Basilar artery thrombosis;Basophilopenia;B-cell aplasia;Behcet’s syndrome;Benign ethnic neutropenia;Benign familial neonatal convulsions;Benign familial pemphigus;Benign rolandic epilepsy;Beta-2 glycoprotein antibody positive;Bickerstaff’s encephalitis;Bile output abnormal;Bile output decreased;Biliary ascites;Bilirubin conjugated abnormal;Bilirubin conjugated increased;Bilirubin urine present;Biopsy liver abnormal;Biotinidase deficiency;Birdshot chorioretinopathy;Blood alkaline phosphatase abnormal;Blood alkaline phosphatase increased;Blood bilirubin abnormal;Blood bilirubin increased;Blood bilirubin unconjugated increased;Blood cholinesterase abnormal;Blood cholinesterase decreased;Blood pressure decreased;Blood pressure diastolic decreased;Blood pressure systolic decreased;Blue toe syndrome;Brachiocephalic vein thrombosis;Brain stem embolism;Brain stem thrombosis;Bromosulphthalein test abnormal;Bronchial oedema;Bronchitis;Bronchitis mycoplasmal;Bronchitis viral;Bronchopulmonary aspergillosis allergic;Bronchospasm;Budd- Chiari syndrome;Bulbar palsy;Butterfly rash;C1q nephropathy;Caesarean section;Calcium embolism;Capillaritis;Caplan’s syndrome;Cardiac amyloidosis;Cardiac arrest;Cardiac failure;Cardiac failure acute;Cardiac sarcoidosis;Cardiac ventricular thrombosis;Cardiogenic shock;Cardiolipin antibody positive;Cardiopulmonary failure;Cardio-respiratory arrest;Cardio-respiratory distress;Cardiovascular insufficiency;Carotid arterial embolus;Carotid artery thrombosis;Cataplexy;Catheter site thrombosis;Catheter site vasculitis;Cavernous sinus thrombosis;CDKL5 deficiency disorder;CEC syndrome;Cement embolism;Central nervous system lupus;Central nervous system vasculitis;Cerebellar artery thrombosis;Cerebellar embolism;Cerebral amyloid angiopathy;Cerebral arteritis;Cerebral artery embolism;Cerebral artery thrombosis;Cerebral gas embolism;Cerebral microembolism;Cerebral septic infarct;Cerebral thrombosis;Cerebral venous sinus thrombosis;Cerebral venous thrombosis;Cerebrospinal thrombotic.

There are 8 more such pages. But I think readers get the idea. There are hundreds of these side effects, literally.  DOH, I challenged you to now continue claiming that the vaccines are safe and effective!

The question that naturally surfaces is this. How on earth can such a dangerous product not only get used in over a hundred countries, which, oblivious to the danger, are giving Pfizer a red carpet rollout?

The short answer is this. Please read our article on how Pfizer got to control 110 countries through secret one-sided and coercive contracts[16]

Independent Scientific Analysis Supports this CCH Analysis

The secret Pfizer document above reveals hundreds of possible pathways to produce adverse events, whether “important” or of  “special interest”. Independent scientists and savvy researchers are demonstrating decisively that these hundreds of kinds of adverse effects DO EXIST in the real world. They are found in the already under-reported Vaccine Adverse Events Reporting System (VAERS) of the CDC.

Table 3 below shows this very clearly. Table 3 is taken, with some minor modifications from the work of Steve Kirsch who has become an effective independent analyst of FDA, CDA, NAIAD, and NIH fake news[17] He has also convened a team of top scientists with whom the FDA refuses to have a debate with.

Table 3. Multiplier Factor (X):

VAERS Reported Adverse Events for Covid Vaccines Versus VAERS Reported Adverse Events for All Vaccines (Average) from 2015-2019[18]To get the Multiplier Factor X, divide the number of AEs from the Covid vaccines by the number of AEs from ALL vaccines from 2015-2019.

SymptomMultiplier Factor (X)
Pulmonary embolism473.0
Deep vein thrombosis264.3
Fibrin D dimer increased220.8
Tinnitus 97.3
Cardiac arrest 75.0
Death 58.1
Parkinson’s disease 55.0
Slow speech 54.3
Aphasia (inability to talk) 52.3
Pericardial effusion 50.5
Deafness 44.7
Myocarditis 43.2
Hemorrhage intracranial 42.5
Abortion Spontaneous 41.3
Bell’s Palsy 36.6
Paraesthesia   29.5
Blindness   29.1
Dyspnea (difficulty breathing) 28.4
Seizure   27.0
Anaphylactic Reaction   21.0
Suicide 18.3
Convulsion   16.3
Thrombotic thrombocytopenic purpura (TTP)   16.3
Paralysis 16.0
Neuropathy 11.2
Multiple organ dysfunction syndromes   11.1

Table 3 clearly shows that Pfizer’s nothing-to-worry-about smug attitude is not only misplaced. It is deeply arrogant, insulting, and deadly.

Let us take myocarditis, for example. Pfizer’s secret document above claims that all is well with their vaccine. Yet independent and creative researchers like Kirsch clearly show that these safety claims are not only bogus. They are outright fraudulent and dangerous.

Table 3 shows that the Covid vaccines are producing myocarditis at a 4,320 % rate more than ALL vaccines in the last 5 years. And Pfizer is telling the FDA not to worry?

Note that, in Table 3 above, the Factor X for death is 58.1 or 5,810% higher than all vaccines in the last five years. This “vaccine” is definitely not safe and effective!

The same is true with ALL the serious negative side effects listed in Table 3. Pulmonary embolism has a Multiplication Factor X of 473 or 47,300%. Contrary to Pfizer’s smooth assurances, this is surely something to do intense investigation on.

But no, FDA continues to give authorizations after authorizations for the dangerous and destructive Pfizer “vaccines” which can become death shots for some people. Pfizer and FDA have a cozy and mutually beneficial relationship. This is why Pfizer can get away with murder as far as FDA is concerned. This is why FDA has no problem asking the Court to allow it 55 years to release all the data connected with Pfizer’s EUA with FDA. Obviously, such a request is not only preposterous but also fraudulent. FDA is a captured regulatory agency. It has been captured by Pfizer, which provides monetary rewards and lucrative post-FDA positions to its compliant regulators[19] For the details on the 55 years release time, see Reference # 5 … Continue reading.

Kirsch also reports on the work of vaccine safety expert, Albert Benavides.  Here are the overview comments of Kirsch on this new research work that confirms his earlier research[20]

“In a brand new VAERS data analysis performed by our friend Albert Benavides (aka WelcomeTheEagle88), we found hundreds of serious adverse events that were completely missed by the CDC that should have been mentioned in the informed consent document that is given to patients. And we found over 200 symptoms that occur at a higher relative rate than myocarditis (relative to all previous vaccines over the last 5 years). [See Table 3 above.] Altogether, there were over 4,000 VAERS adverse event codes that were elevated by these vaccines by a factor of 10 or more over baseline that the CDC should have warned people about. [Multiplier Factor X]

“As of November 1, 2021, there have been more adverse events reported for the COVID vaccines than for all 70+ vaccines combined since they started tracking adverse events 30 years ago. That’s a stunning statistic, nobody can deny it, but nobody in the mainstream medical community (or mainstream media) seems to care much. It’s not even worth noting in passing. Wow.” [Emphasis added] [Note on Table 3 added.]

Finally, there is another analysis, which totally destroys that FDA, CDC, and DOH narrative that the vaccines are safe and effective as well as confirming CCH’s analysis of the secret Pfizer document for FDA.

The Bradford-Hill criteria are an accepted method for determining whether causality exists between a vaccine injection and the resulting adverse impacts that follow vaccination. It lays out the following criteria in determining whether a vaccine injection caused an adverse reaction or not.

These are the criteria:  consistency, the strength of association, specificity, temporal relation, and biological plausibility[21]

Consistency: Adverse events following Covid vaccination follow are consistent the world over.  The WHO’s global VigiFlow database reports over 2 million adverse events following vaccination[22]

Strength of Association:  The association is definitely strong as can be clearly seen in the thousands of stories of death and harm following vaccination, including experiences with the second dose of the vaccine[23]

Specificity:  The adverse events are indeed reported commonly as specific to Covid vaccinations and not other causes. However, CDC, FDA, and DOH try to muddle the issue and say that co-morbidities are the source of death. We have already rebutted this point in our comments above.

Temporal Relation: More than fifty percent of those who had a fatal reaction to the vaccines, died with three days[24] In addition, the global data is showing that the most deaths occur in the most vaccinated nations of the world[25]

Biological Plausibility. All the vaccines use the spike proteins as the antigen. Tragically, the spike proteins in and by themselves are toxic as cited above.  Scientists have measured micro-clotting due to the spike proteins in vaccinated people[26] Antibody-dependent enhancement (ADE) is a known side-effect of all Covid vaccines for almost two decades[27]; … Continue reading. Now, science is also discovering that vaccines are destroying the effectiveness of the immune system[28] as well as disrupting the DNA repair mechanism of our body[29]


It is clear that Pfizer’s vaccines can cause harm and death. The science is clear. Pfizer’s “vaccine” is a deadly product that can harm or kill you. Avoid it like you would avoid a plague. Your life depends on it.

Stand up against mandatory vaccination. For your friends still making the choice, inform them of the Pfizer assassination project. Ignorance can kill. Lies can enslave you. To be forewarned is to be forearmed! Step forward to the Truth! Defend your true humanity, freedom, and health.


1 To get the Multiplier Factor X, divide the number of AEs from the Covid vaccines by the number of AEs from ALL vaccines from 2015-2019.
9 and
12 Caldwell Esselstyn, M.D., Prevent and Reverse Heart Disease by  New York: Avery (Penguin Books).
13 Conversation with Governor Gwen Garcia of Cebu Province, around 22 February 2021.
15 See references #8 and 1 above.
18 To get the Multiplier Factor X, divide the number of AEs from the Covid vaccines by the number of AEs from ALL vaccines from 2015-2019.
19 For the details on the 55 years release time, see Reference # 5 above..
27;;  20 Mechanisms of Injuries (MOI) How COVID-19 Injections Can Make You Sick; Even Kill You, Dr. Sherri Tenpenny Cleveland, Ohio;  20 MORE MECHANISMS OF INJURY (MOI) Compiled by Dr. Sherri Tenpenny.

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