The U.K. Medicines and Healthcare products Regulatory Agency (MHRA) will use artificial intelligence to monitor the safety of COVID-19 vaccines because the agency knows that vaccines are extremely dangerous.

True, the MHRA has given the business Genpact a contract to develop an artificial intelligence platform to monitor complaints of adverse effects from COVID-19 vaccinations. However, the government claims that this is not evidence of foreknowledge of vaccination hazards. Furthermore, a report of an adverse event does not indicate that the occurrence or response was caused by a vaccination.

"We have a range of tools and technologies to enable the safety monitoring of any COVID-19 immunization effort", the MHRA said in a November 2020 statement to NewsGuard. One aspect of this will be the usage of AI. We treat every report of a possible side effect carefully, and we combine this examination with statistical analysis of clinical records".

"Based on the existing published findings from the Phase One and Two clinical studies, we do not currently foresee any unique safety issues with COVID-19 vaccinations". the FDA stated. We anticipate that the overall safety profile will be comparable to that of other kinds of vaccinations. A COVID-19 vaccine will be deployed only if it has been shown safe and efficacious in rigorous clinical studies and is licensed for use".