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Pfizer Covid-19 Vaccine : European & United States Reporting Systems Flag SEVERE Safety Issues

Updated: Apr 28, 2021

(Part 1 of a series documenting safety issues with the three US Emergency Use Covid-19 vaccinations - part two MODERNA here and part 3 Johnson & Johnson HERE

For full review of Vaccine Safety Concerns: Please See Part Six of Health Professionals for Covid-19 Policy Correction HERE

Pfizer Covid-19 vaccinations were approved in the United States, on December 11, 2020 for Emergency Investigational Use only, with many other countries quickly following suit.

Read the FDA Emergency Use Investigational permissions letter HERE:

"Pfizer-BioNTech COVID‑19 Vaccine is for use for active immunization to prevent COVID-19 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 16 years of age and older. The vaccine contains a nucleoside-modified messenger RNA (modRNA) encoding the viral spike (S) glycoprotein of SARS-CoV-2 formulated in lipid particles. It is an investigational vaccine not licensed for any indication"

Media claims around Covid-19 safety are contradicted by pharmaceutical trial data, and vaccine adverse event monitoring reports , in the US & abroad, Media has disingenuously cited lack of evidence as THE evidence the vaccines are safe. This holds no merit when pharmaceutical companies bypassed the normal safety trial period of five to twelve years, and there is no standard method by the CDC for Covid-19 postmortem assessment.

United States Covid-19 mass vaccination program launched without appropriate monitoring system in place, with VAERS CDC system estimated to capture only 1% of vaccine injuries/deaths. according to Harvard Study. (Data is credible as far as it goes, with 83% generated from medical providers, state reporting agencies, and pharmaceutical agencies).

Additionally, CDC appears to have adopted a 'plausible deniability' standard for attributing post vaccination deaths to Covid-19 vaccinations. The agency dismisses deaths occurring within minutes of vaccine administration with symptoms matching listed FDA side effects for Covid-19 vaccines, as unrelated to vaccines. Often, no autopsies are performed and there is no set standard for post Covid-19 vaccination portmortem review.

European & Japanese Post Vaccine Injury monitoring systems capturing exponentially higher rates of injury post Pfizer Covid-19 vaccination than inadequate US systems.

Contrary to US reporting that no correlation has been made between Pfizer Covid-19 vaccinations and post vaccination deaths, Norway changed its recommendations for administration of the vaccine after autopsy investigation correlated vaccine side effects to elderly deaths in care homes

By the Numbers: United States Data

Pfizer Comiraty Covid-19 Vaccination Injury Statistics:

VAERS CDC Reports :

Total adverse reports: 31,549

Notes: CDC reports total 3,456 deaths following ALL Covid-19 vaccinations, VAERS search only reflects 2,470 of these reports, unknown which Covid-19 vaccines compose the other 1,000 death reports, Outreach to CDC has generated no reply with inquiry seeking information on the discrepancy in reporting numbers, and why 1,000 cases are not accessible through VAERS data search:

Deaths, Time Period Death Occurred Post Vaccination

Total: 1,174

0 Days: 174 (minutes to hours post Pfizer Covid-19 Vaccination)

1 Days: 180

2: Days: 83

37.7% of Post Pfizer Covid-19 deaths reported occurred within 48 hours of vaccine

31% within minutes to one day post vaccination

Half of all deaths occurred within a 7 day time period (as of /2021)

Go to Vaers Data CDC search for more information

Additional Severe Reactions Reported to VAERS CDC for Pfizer Covid-19 Vaccinations Include:

750 life threatening events reports

487 permanent disability reports

2,443 hospitalization reports

5,399 Emergency Room Visits

UK Data: Pfizer Covid-19 Vaccinations:

UK Assets Monitoring System:

  • 4210 Blood disorders including 1 death

  • 1675 Cardiac disorders including 46 deaths

  • 12 Congenital disorders

  • 1374 Ear disorders

  • 28 Endocrine disorders

  • 2034 Eye disorders

  • 14,140 Gastrointestinal disorders including 15 deaths

  • 38,968 General disorders including 130 deaths

  • 35 Hepatic disorders

  • 723 Immune system disorders including 1 death

  • 3070 Infections including 57 deaths

  • 847 Injuries including 2 deaths

  • 1525 Investigations including 1 death

  • 821 Metabolic disorders including 1 death

  • 17,756 Muscle & tissue disorders including

  • 60 Neoplasms including 1 death

  • 24,917 Nervous system disorders including 23 deaths

  • 63 Pregnancy conditions including 3 deaths

  • 2115 Psychiatric disorders

  • 340 Renal & urinary disorders including 2 deaths

  • 768 Reproductive & breast disorders

  • 5537 Respiratory disorders including 26 deaths

  • 9622 Skin disorders including 1 death

  • 35 Social circumstances

  • 100 Surgical & medical procedures

  • 1724 Vascular disorders including 4 deaths

Here is the summary data through April 10, 2021.

Total reactions for the experimental mRNA vaccine Tozinameran (code BNT162b2, Comirnaty) from BioNTech/ Pfizer: 3,760 deaths and 134,606 injuries to 10/04/2021

  • 10,021 Blood and lymphatic system disorders incl. 31 deaths

  • 6,413 Cardiac disorders incl. 442 deaths

  • 44 Congenital, familial and genetic disorders incl. 2 deaths

  • 3,620 Ear and labyrinth disorders incl. 2 deaths

  • 93 Endocrine disorders

  • 3,997 Eye disorders incl. 5 deaths

  • 30,091 Gastrointestinal disorders incl. 196 deaths

  • 93,635 General disorders and administration site conditions incl. 1,279 deaths

  • 171 Hepatobiliary disorders incl. 14 deaths

  • 2,808 Immune system disorders incl. 15 deaths

  • 8,451 Infections and infestations incl. 380 deaths

  • 3,210 Injury, poisoning and procedural complications incl. 66 deaths

  • 6,560 Investigations incl. 147 deaths

  • 2,207 Metabolism and nutrition disorders incl. 79 deaths

  • 48,571 Musculoskeletal and connective tissue disorders incl. 40 deaths

  • 109 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 7 deaths

  • 59,021 Nervous system disorders incl. 335 deaths

  • 152 Pregnancy, puerperium and perinatal conditions incl. 6 deaths

  • 70 Product issues

  • 5,208 Psychiatric disorders incl. 52 deaths

  • 807 Renal and urinary disorders incl. 57 deaths

  • 806 Reproductive system and breast disorders incl. 1 death

  • 12,075 Respiratory, thoracic and mediastinal disorders incl. 432 deaths

  • 14,257 Skin and subcutaneous tissue disorders incl. 31 deaths

  • 352 Social circumstances incl. 5 deaths

  • 101 Surgical and medical procedures incl 5 deaths

  • 6,996 Vascular disorders incl. 131 de

Pfizer Covid-19 injury reports in the news: (Click on Headline to Read Story):

Anaphylactic reactions are occurring up to 120x rate reported by CDC according to independent hospital studies, no adequate screening protocol for Polyethylene Glycol contraindication, see below articles:

Japan Sees High Rates of Anaphylaxis with Pfizer Vaccine ( more evidence US monitoring not capturing events, same vaccine)

Fertility concerns have been flagged with Pfizer & Moderna mRNA vaccination. News media has dismissed concern due to lack of evidence, however, the experts flagging the concerns state studies have not been done to study for the issue and there is potential for a antibody reaction to occur which could interfere with placenta formation. Here is the specific concern, with link to Emergency Stay source directly below excerpt:

"Severalv vaccine candidate sare expected to induce the formation of humoral antibodies against spike proteins of SARS-CoV-2.Syncytin-1 (see Gallaher, B., “Response to nCoV2019 Against Backdrop of Endogenous Retroviruses” -,which is derived from human endogenous retroviruses (HERV) and is responsible for the development of a placenta in mammals and humans and is therefore an essential prerequisite for a successful pregnancy, is also found in homologous form in the spike proteins of SARS viruses.There is no indication whether antibodies against spike proteins of SARSviruses would also act like anti-Syncytin-1 antibodies. However, if this were to be the case this would then also prevent the formation of a placentawhich would result in vaccinated womenessentially becominginfertile.To my knowledge, Pfizer/BioNTech has yet to release any samples of written materials provided to patients, so it is unclear what, if any,informationregarding (potential) fertility-specific risks caused by antibodiesis included.According to section 10.4.2 of the Pfizer/BioNTech trial protocol, a woman of childbearing potential (WOCBP) is eligible to participate if she is not pregnant or breastfeeding, and is using an acceptable contraceptive method as described in the trial protocol during the intervention period (for a minimum of 28 days after the last dose of study intervention). This means that it could take a relatively longtime before a noticeable number of cases of post-vaccination infertility could be observed'.

Health Care professionals have serious concerns over Covid 19 vaccination safety Please refer to Section 6 of the petition for full documentation and evidence regarding this issue:

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Notices of Liability for COVID-19 Vaccine Harms and Deaths Served on All Members of the European Parliament

On April 20, 2021, ahead of the April 28 vote on EU vaccine passports (the ‘Digital Green Certificate’), notices of liability for vacccine harms and deaths were served on all Members of the European Parliament. The full list of recipients can be viewed here.

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