Government Negligence in Pandemic Response
Legal Accountability for Officials Who Continued Harmful Treatments Despite Early Warnings
Introduction
In this ‘hypothetical scenario,’ government officers responsible for the health and well-being of the State's population faces a pandemic. Various scientifically unproven responses and a medical treatment, which later proved more deadly than the pandemic itself, were implemented. Despite early discoveries that the unproven responses and treatment did not protect the population, authorities continued its rollout, resulting in thousands of deaths. This report examines the potential defenses the officers and the government might employ if sued for negligence and considers the similarities to defenses used during the Nazi Nuremberg Trials.
Legal Framework for Negligence
Duty of Care: Government officials have a legal obligation to protect public health and ensure the safety of the population.
Breach of Duty: Plaintiffs must prove that the officials breached this duty by failing to act as reasonably prudent officials under similar circumstances.
Causation: There must be a direct link between the breach of duty and the harm suffered by the plaintiffs.
Damages: Plaintiffs must show that they suffered actual harm or loss as a result of the breach.
Potential Defenses and Challenges
Good Faith Actions
Challenge: Good faith actions imply that the officials believed they were acting in the best interest of the public based on the information available to them at the time. However, if it was discovered early on that the treatment was ineffective and potentially harmful, continuing the rollout undermines the claim of good faith.
Analysis: Officials are expected to act upon new and critical information promptly. Ignoring or disregarding evidence that the treatment was not protective and potentially deadly would indicate a lack of good faith. This could be seen as reckless disregard for public safety rather than a reasonable mistake.
Qualified Immunity
Challenge: Qualified immunity protects government officials from liability unless they violated clearly established statutory or constitutional rights that a reasonable person would have known. Continuing the rollout of a harmful treatment could be argued as a violation of individuals' rights to life and safety.
Analysis: Once it became clear that the treatment was harmful, continuing its administration would likely be seen as a violation of established rights. Qualified immunity would not protect officials who knowingly caused harm after receiving clear evidence of the treatment's dangers.
Reliance on Expert Advice
Challenge: Reliance on expert advice is a valid defense if the advice is followed reasonably. However, if new evidence emerges that contradicts the initial expert recommendations, continuing to follow outdated advice becomes indefensible.
Analysis: If experts initially recommended the treatment but later findings indicated it was ineffective and harmful, continuing its use despite new evidence would not be considered reasonable reliance on expert advice. Officials are expected to adjust their actions based on the most current and accurate information.
Emergency Powers and Discretionary Acts
Challenge: Emergency powers and discretionary acts allow officials to make rapid decisions in a crisis. However, these powers are not a carte blanche to ignore emerging evidence that indicates harm.
Analysis: The discretionary nature of emergency powers does not absolve officials from the responsibility of acting on new information. Continuing a harmful treatment after recognizing its dangers would likely be seen as an abuse of discretionary power rather than a legitimate emergency measure.
Comparative Risk Assessment
Challenge: Comparative risk assessment involves weighing the benefits and risks of different actions. If early evidence showed that the treatment was more harmful than the disease, continuing its rollout would not be a rational risk assessment.
Analysis: Effective comparative risk assessment requires officials to act on up-to-date information. Ignoring evidence of harm from the treatment indicates a failure to properly assess and mitigate risks, undermining this defense.
Comparisons to the Nuremberg Trials
Following Orders (Superior Orders)
Nazi Defense: Many defendants argued that they were simply following orders from higher authorities (the "Nuremberg Defense" or "Superior Orders").
Modern Perspective: The Nuremberg Principles established that following orders is not a sufficient defense for committing war crimes or crimes against humanity. Individuals are responsible for their actions, especially if they violate fundamental human rights.
State Authority and Sovereignty
Nazi Defense: Defendants claimed their actions were legal under the laws of Nazi Germany, and thus they were acting within the scope of their authority.
Modern Perspective: The Nuremberg Trials rejected the notion that state laws could legitimize actions that are fundamentally inhumane. International law holds individuals accountable for actions that violate human rights, regardless of domestic laws.
Public Health and Safety (Eugenics and Medical Experiments)
Nazi Defense: Some defendants justified their actions, including forced sterilizations and medical experiments, as being in the interest of public health and scientific advancement.
Modern Perspective: The Nuremberg Code, developed in response to these defenses, emphasizes the ethical principles of medical research, including informed consent and the prohibition of inhumane treatment. The intentional harm caused by these actions was deemed unjustifiable.
Conclusion
Given the specific hypothetical details that the treatment was known to be ineffective and harmful early in its rollout, the following points are critical:
Negligence and Recklessness: Continuing a harmful treatment despite clear evidence of its dangers would likely be considered negligence or even recklessness. Officials have a duty to protect public health, and knowingly causing harm breaches this duty.
Breach of Duty: There is a clear breach of duty when officials fail to act on critical information that impacts public safety.
Causation and Damages: The direct link between the continued rollout of the harmful treatment and the resulting deaths establishes causation and damages, strengthening the case against the officials.
In this context, the defenses of good faith actions, qualified immunity, reliance on expert advice, emergency powers, and discretionary acts would likely fail because they do not account for the deliberate continuation of a known harmful practice. The accountability and liability of the officials would be difficult to defend under these circumstances. The comparisons to the Nuremberg Trials highlight that justifications based on following orders, state authority, and supposed public health benefits do not absolve individuals from responsibility for actions that cause significant harm.
The FDA issued an EUA for the pfizer mRNA jabs in Dec 2020 and reported that there was "no evidence" that the vaccine prevents transmission of covid from person to person. They deliberately prevented known "safe and effective" (and early) treatments like ivermectin and hydroxychloroquine, presumably to force us to take their supposedly experimental toxic mRNA soup. The Commonwealth Immunisation Handbook and the Nuremburg Code both have strong similarities that require valid informed consent for vaccines and "experimental" treatments to be given. The evidence of harm and coverup is strong, and yet they still promote this poison as "safe and effective". Covid was never a pandemic, and positive readings from a super sensitive PCR test elevated the numbers. It is also likely that the PCR tests were positive to other viruses. Surely, what is already known should be sufficient evidence to prosecute these tyrants?
WA is still full of tyrants like that Deputy Commissioner who just fired 11 officers and some staff members for not getting the genetic therapy shots. The man needs to go to Rottenest Island and go swimming with the great white sharks.