MOZOM-analyse
First ask for trust, then seal the files: why vaccine injury needs transparency

- Source
- Western Standard, Health Canada, FDA, EMA, BMJ, Yale, CDC, MHRA, TGA, Medsafe, GVDN en wetenschappelijke publicaties
- MOZOM headline
- First ask for trust, then seal the files: why vaccine injury needs transparency
- Original headline
- Canada, the US and Europe show the same tension: recognized rare side effects, but slow access to underlying files
- Author
- Paul Giezen
- Date
- 26 juli 2026 om 12:10
- Subject
- MOZOM investigates why vaccine damage files, rough reports and assessment documents are often delayed, limited or redacted worldwide, while citizens had to quickly give confidence during the corona period.
Summary of the original report
The immediate cause is a report from the Canadian Western Standard that Health Canada has allegedly shielded vaccine damage data for up to 15 years. Legally, this is more precise: according to reports, this concerns an exceptionally long extension for an extensive information request about vaccine and drug side effects, not a general law that automatically seals all vaccine damage files for 15 years. Yet the issue fits into a broader pattern. Canada publishes global figures on recognized vaccine damage claims, the US had to release Pfizer documents more quickly after a lawsuit, EMA publishes clinical data but edits personal data and commercially sensitive documents, and countries such as the UK, Australia and New Zealand mainly publish summaries. The tension is the same everywhere: governments recognize rare side effects, but full underlying insight remains limited.
Own source research: acknowledge damage, limit files
MOZOM has raised the issue with several countries. Canada has a Vaccine Impact Assistance Program and publishes totals: thousands of claims, hundreds of approvals and millions of Canadian dollars in benefits. This confirms that recognized vaccine damage exists. At the same time, individual files and the underlying assessment remain largely shielded. In the US, the FDA initially wanted to release vaccine documents very slowly; a federal judge forced acceleration. In the EU, EMA publishes clinical data, but with redactions and limitations. In the UK, Australia and New Zealand, regulations, reporting systems and summaries are visible, but the public debate is usually not given direct access to all raw files. In addition, there are critical flows of experts: BMJ authors who demand raw data, Yale researchers who seriously investigate post-vaccination complaints, and non-mainstream doctors/pathologists who point out signals that they believe are not sufficiently investigated. The strong point is not that all these claims have been proven, but that transparency is not sufficiently fast and open to dampen mistrust.
From safety promise to file delay
The frame during the pandemic was often certainty: safe, effective, necessary, solidarity. The post-pandemic frame is more bureaucratic: privacy, editorial, corporate confidentiality, capacity issues, procedure. It is precisely that transition that is grating. When the citizen had to act quickly, but the government needs years to provide verifiable substantiation, an asymmetry arises: trust in advance, accountability afterwards. This asymmetry fuels the suspicion that unwelcome data is being pushed away, even when this has not been proven.
What has been proven, what has not?
Evidence shows that serious vaccine-related side effects are rare but real. Major studies and regulators cite myocarditis/pericarditis, TTS/VITT, Guillain-Barré and CVST, among others, as signals or recognized risks with certain vaccines and age groups. It has not been proven that all long-term complaints after vaccination are caused by vaccination. It has also not been proven that white clots, excess mortality or broad chronic complaints are consciously hidden worldwide. It has been proven that access to raw files and assessment documents is often slow or limited. That is exactly the journalistically relevant core: transparency is not a luxury when the subject concerns social trust, medical coercive pressure and possible damage.
Possible message behind the news
The visible message from governments is: we monitor safety and protect privacy. The critical counter-message is: trust without rapid file inspection is not verifiable trust. The MOZOM reading is that delayed transparency undermines trust, even when some reasons for restriction are legally defensible.
Neutral conclusion
A global cover-up has not been proven based on public sources. But the pattern of delayed, limited and often only opened vaccine files after a lot of pressure is certainly newsworthy. Governments recognize rare damage and publish summaries, but the verifiable underlying documents often become available slowly or in a filtered manner. The sharp, legally safe conclusion: anyone who asks for trust during a crisis should not organize years of file fog after the crisis. Transparency about vaccine damage is not an anti-vaccine position, but a necessary condition for regaining credibility.
Source:
- Western Standard: Health Canada seals vaccine injury records for 15 years
- Canada: Vaccine Impact Assistance Program statistics
- Health Canada: Vaccine Impact Assistance Program
- Health Canada: 2024-2025 annual report access to information
- Health Canada: clinical trial record retention reduced to 15 years
- FDA: biologics electronic reading room
- US federal court: FDA must release Pfizer vaccine documents faster
- EMA: clinical data publication
- BMJ: Covid-19 vaccines and treatments: we must have raw data, now
- GVDN / PubMed: adverse events of special interest in 99 million vaccinated people
- Yale: immune markers in post-vaccination syndrome indicate future research directions
- CDC: VAERS limitations and vaccine safety monitoring
- UK: Vaccine Damage Payment Scheme
- Australia: COVID-19 Vaccine Claims Scheme
- New Zealand: COVID-19 vaccine data and monitoring