WHO’s own world-wide ADR reporting system shows almost 3.6 million adverse events ranging from mild to very serious disease and even death!
What is VigiBase?
VigiBase is UMC’s starting-point for the journey from data to wisdom about safer use of medicines and wise therapeutic decisions in clinical practice. It is the driving-force at the heart of the work of UMC and the WHO Programme. The purpose is to ensure that early signs of previously unknown medicines-related safety problems are identified as rapidly as possible.
What is VigiAccess?
VigiAccess was launched by the World Health Organization (WHO) in 2015 to provide public access to information in VigiBase, the WHO global database of reported potential side effects of medicinal products. Side effects – known technically as adverse drug reactions (ADRs) and adverse events following immunization (AEFIs) – are reported by national pharmacovigilance centres or national drug regulatory authorities that are members of the WHO Programme for International Drug Monitoring (PIDM). WHO PIDM was created in 1968 to ensure the safer and more effective use of medicinal products.
Go ahead and pull your own reports of not only the COVID vaccine, but also compare it with other vaccines such as the “Influenza vaccine”, “Measles vaccine” or “Mumps vaccine”. For example Compare the COVID vaccine ADR’s in the last 2 years with the Flu vaccinne over decades.
CLICK THE REPORT IMAGES BELOW TO SEE THE INCREASE OF ADR’s OVER TIME

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