Public Health and Natural Rights: A Tale of Two Cities
5 min read Humans’ natural capacities for reasoning and speech mean that politics should be based on persuasion, not censorship, and that government should be based on consent, not coercion.
5 min read Humans’ natural capacities for reasoning and speech mean that politics should be based on persuasion, not censorship, and that government should be based on consent, not coercion.
10 min read A recent article about growing vaccine hesitancy in the US, and how to counter it, relies on certain assumptions about vaccines and their efficacy. This article looks at some of these claims.
2 min read Hedley Rees explains how the fragmented supply chain for new pharma products has disrupted the time-tested practices that were key to drug safety.
< 1 min read Liberal democracies were turned upside down to “protect health services”. Billions were forced to accept the Covid injections. How were mandates allowed? How could the medical profession forsake their legal and ethical obligations?
12 min read One goal of databases such as VAERS is to eliminate background ‘noise’ from random events. What percentage of the reports can be linked to the Covid injections? PANDA’s inquiry into excess deaths continues.
12 min read This continuation of our inquiry into the drivers of excess deaths digs a little deeper into the vaccination data to see how many lives the Covid vaccines saved.
6 min read Due to the importance of the issue of Covid-19 vaccinations to society at large, PANDA calls on Lancet to retract a seminal paper that is demonstrably incorrect in its assumptions.
5 min read Those who took the mRNA vaccines, especially pregnant women, did so based on trust in health authorities. However a recent report contains previously suppressed information that raises serious concerns.
7 min read An estimate in the Lancet that Covid-19 vaccinations prevented 14.4 million deaths is so impossibly high that the error should have been recognised. We demonstrate as part of our ongoing inquiry into the drivers of excess deaths.
17 min read In this work, we review the reports provided by Pfizer to the FDA for the trial’s first interim analysis. The reports demonstrate severe flaws in the procedure of approving Pfizer’s Covid-19 vaccine based on data from the vaccine’s phase III clinical trial.