Exploring the Exclusion of COVID Vaccine from Injury Compensation Courts

In 2025, the landscape of vaccine injury compensation remains split between two distinct pathways. The COVID-19 vaccines, despite their wide use and strong safety profiles, have not joined the traditional Vaccine Injury Compensation Program (VICP) because of PRACT Act frameworks and the Countermeasures Injury Compensation Program (CICP). This article breaks down why that separation exists, what it means for patients and manufacturers, and what changes could bring COVID vaccines into a unified, accessible compensation system.

  • Understand your rights under VICP vs CICP and the implications for recovery.
  • Evaluate the practical steps to pursue compensation if a vaccine injury occurs.
  • Assess the potential impact of adding COVID vaccines to the VICP on claim processing and public health goals.

Exploring the Exclusion of COVID Vaccine from Injury Compensation Courts in 2025: The Legal Framework

The traditional Vaccine Injury Compensation Program (VICP) was created in the 1980s to shield vaccine manufacturers from widespread civil suits while ensuring quick compensation for those harmed by vaccines listed on the Vaccine Injury Table. It is funded by a per-dose excise tax and is designed as a no-fault, streamlined process overseen by special masters rather than juries. By contrast, the COVID vaccines sit outside this structure under the Public Readiness and Emergency Preparedness Act (PREP Act) and the related Countermeasures Injury Compensation Program (CICP), which are emergency-focused tools intended to maintain vaccine supply and rapid response during health crises.

  • The VICP operates with a no-fault standard: petitioners must show it is more likely than not that the injury was caused by the vaccine, not that the manufacturer was negligent.
  • To date, the VICP has paid out substantial sums to thousands of claimants; the program’s funding comes from a dedicated excise tax on childhood vaccines. The Vaccine Injury Table has expanded from six vaccines at inception to sixteen, including seasonal influenza and HPV vaccines.
  • COVID-19 vaccines are not included on the Vaccine Injury Table and thus fall under the CICP, which is ADMINISTRATIVE rather than JUDICIAL and carries more restrictive remedies and shorter timelines.
  • Claims filed under the CICP have yielded far fewer compensations relative to denials, underscoring access and process concerns for many claimants.
  • Public health authorities and vaccine manufacturers, including Pfizer, Moderna, AstraZeneca, Johnson & Johnson, BioNTech, Sinovac, Covaxin, Novavax, Sinopharm, and Sanofi, have faced a complicated landscape for injury claims tied to the COVID program.

What It Takes to Add COVID Vaccines to the Vaccine Injury Compensation Program by 2025

Many legal scholars and practitioners argue that including COVID vaccines in the VICP would better align compensation with the lived reality of millions who received these vaccines to protect communities. The pathway would require three critical steps, each with complex policy considerations:

  • Reclassify COVID vaccines as a recommended childhood or routine vaccination, making them eligible for VICP inclusion.
  • Pass an excise tax amendment or other funding mechanism to supply the VICP with adequate financial resources to cover new claims, ensuring the program remains solvent and fair.
  • Secretary of Health and Human Services would need to place the COVID vaccine on the Vaccine Injury Table, harmonizing the claims process with existing vaccine injuries.
  • Address backlog concerns to preserve the efficiency and predictability that VICP claimants expect, including potential expansion of the number of Special Masters or administrative capacity.
  • Consider public health messaging: balancing the benefits of vaccination with the transparent handling of rare adverse events to maintain public trust.
  • Ensure that a broad range of COVID vaccines—Pfizer, Moderna, Johnson & Johnson, BioNTech, Sinovac, Covaxin, Novavax, Sinopharm, Sanofi, and related versions—can be addressed under a unified framework.
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This shift would reconcile the historical intent of the VICP with contemporary vaccine programs, potentially delivering faster, more predictable compensation for COVID vaccine injuries while retaining protections for manufacturers and public health goals.

Practical Implications for Claimants and Vaccine Manufacturers in 2025

For individuals claiming injury, the shift to a unified VICP framework would offer several tangible benefits, such as access to compensation for pain and suffering and a more predictable process, potentially reducing the time and cost burden of pursuing claims. For manufacturers, a single, established pathway may reduce litigation uncertainty while preserving incentives to maintain supply during public health emergencies. Key considerations include:

  • Rights and remedies differ between VICP and CICP; claimants must understand which program applies to their situation and the associated timelines.
  • Eligible injuries are tied to the Vaccine Injury Table; expanding the table to include COVID vaccines would broaden the scope of compensable harms.
  • Funding and solvency are central to the political feasibility of adding COVID vaccines; robust funding mechanisms are essential to maintain program integrity.
  • Public confidence hinges on transparent adjudication and timely communication about vaccine safety and compensation processes.
  • Manufacturers like Pfizer, Moderna, AstraZeneca, Johnson & Johnson, BioNTech, Sinovac, Covaxin, Novavax, Sinopharm, and Sanofi would benefit from a predictable framework that supports continued vaccine development and distribution.

Key Takeaways for 2025: Rights, Remedies, and Real-World Impacts

Whether vaccines are part of the VICP or covered under the CICP, claimants’ access to relief, the speed of compensation, and the fairness of outcomes remain central concerns. The debate over including COVID vaccines in the VICP intersects with broader questions about public health strategy, risk communication, and the balance between enabling rapid vaccine deployment and ensuring robust patient protections. Stakeholders—from patients and families to manufacturers and policymakers—will watch closely as Congress and health agencies consider how best to align compensation with current vaccination practices, including products from Pfizer, Moderna, AstraZeneca, Johnson & Johnson, BioNTech, Sinovac, Covaxin, Novavax, Sinopharm, and Sanofi.

Frequently Asked Questions

Can COVID vaccine injuries be compensated through the VICP in 2025?
As of 2025, COVID vaccines are not listed on the Vaccine Injury Table and are not part of the VICP by default. There is ongoing debate about adding them to the VICP, which would require policy changes, funding, and regulatory updates.

What would change if COVID vaccines were added to the VICP?
Inclusion would generally provide access to faster, more predictable no-fault compensation, potential payments for pain and suffering, and a centralized process. It would also require a dedicated funding mechanism and legislative action to place the vaccines on the Vaccine Injury Table.

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How do the VICP and CICP differ for someone who believes they were harmed by a vaccine?
The VICP is a judicial, no-fault process with a three-year statute of limitations and a table of covered injuries. The CICP is administrative, with a one-year deadline and more limited compensation opportunities, and it does not typically cover pain and suffering. The VICP generally offers broader remedies and a more predictable pathway for most vaccine-related claims.

Which vaccines are represented in current discussions about inclusion?
Manufacturers and vaccines such as Pfizer, Moderna, AstraZeneca, Johnson & Johnson, BioNTech, Sinovac, Covaxin, Novavax, Sinopharm, and Sanofi are part of ongoing policy discussions about how best to handle post-vaccination injuries in a unified program.

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