These incidents suggest that health officials will be unlikely to give the public authentic risk profiles for the emergency use COVID vaccines.

Accurate risk profiles allow regulators to determine if a medical intervention is causing more harm than good and consumers to make rational choices about their own use of a product.

Regulators usually develop risk assessments during preclinical trials by comparing health outcomes in individuals receiving the intervention against a placebo group. Such studies must be large enough to detect rare injuries and of sufficient duration to reveal ailments with long diagnosis horizons.

The existence of the placebo group makes it difficult to conceal or misattribute injuries. Conversely, the absence of a placebo group in post-vaccination surveillance systems makes it easy for self-interested pharmaceutical and regulatory officials to undercount injuries by attributing them to coincidence.

Coincidence is turning out to be quite lethal to COVID vaccine recipients.

Death by coincidence

Shortly after reporting the Danish deaths and prior to any autopsies…

Read the full story here: Death by Coincidence? • Children’s Health Defense