World Health Organization Ensures More Children Die from Vaccines by Revising Vaccine Adverse Reaction Reporting

In April 2017, the World Health Organization (WHO) coordinated a joint project between teams of experts from the National AEFI (adverse events following immunization) committees of India and Zimbabwe with each country’s Ministry of Health. However, doctors in private practice did not necessarily agree that the new guidelines helped protect the children of the world. In fact, they suspected just the opposite. Instead of accurately assessing potential vaccine-reactions, the new guidelines seemed to further hinder the discovery of real vaccine-reactions, particularly when a death occurred after vaccine administration. In a letter published in the prestigious Indian Journal of Medical Ethics, two prestigious doctors from India, Dr. Jacob Puliyel and Dr. Anant Phadke, expressed their concerns over this new classification system. “By simply denying deaths, the new AEFI classification is liable to miss the safety signals and therefore potential dangers with new vaccines.” They note that Sri Lanka suspended the use of a pentavalent vaccine after five deaths within four months after its introduction in January 2008 and, in 2013 Viet Nam shelved the pentavalent vaccine because it had been associated with 12 deaths. However, in both cases, the WHO teams which investigated the deaths declared they were ‘unlikely’ to be related to the vaccines used. The authors point out that the consequences of using the new classification are illustrated starkly in the causality assessment of 134 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare in India. 78 of these babies survived and 58 died. Who is WHO protecting – children or vaccine manufacturers?

World Health Organization’s New Lax Vaccine Safety Policy Leads to More Child Deaths by Vaccines

Two leading pediatricians in India have published a critique of the World Health Organization's (WHO) newly revised manual on the classification of Adverse Events Following Immunization (AEFI). The doctors claim that the new guidelines are too lax, resulting in more children dying from adverse reactions to vaccines, with no accountability for the vaccine manufacturers to produce safer vaccines. In the U.S., pharmaceutical companies manufacturing vaccines cannot be sued due to faulty vaccines, which allows them to put as many vaccines into the market as they want, with no repercussions if the vaccine proves to be faulty or have a high injury and death rate. Victims must sue the U.S. government and top DOJ attorneys who protect the drug companies. This move by the WHO may very well be an attempt to protect drug companies manufacturing vaccines by preventing lawsuits in the rest of the world for faulty vaccines. According to the report of these two doctors, the consequence of India adopting WHO's new classification can be seen from the causality assessment of 132 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare. Of the total AEFI cases, 54 babies died and 78 survived, "but not even one death was classified as vaccine-related. Nearly all the deaths were simply classified as unclassifiable or coincidental."