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Sudden Deaths among Babies after GSK Hexavalent. Australian TGA is Investigating. “UE EMA to Ignore…”

by Gospa News

by Marianne Demasi, phd – originally published on her Substack

All links to previous Gospa News investigation have been added in the aftermath

A more in-depth investigation will be published soon, subscribe Gospa News Newesletter

VERSIONE IN ITALIANO

The Therapeutic Goods Administration (TGA) (regulatory agency of the Australian Government – Gospa News ed) has gone to ground after being confronted with questions about a series of sudden deaths in infants who received the Infanrix-Hexa® vaccine.

Sudden unexpected death in infancy (SUDI) and sudden infant death syndrome (SIDS) are names for the sudden and unexpected death of a baby when there is no apparent cause of death.

The “hexavalent” vaccine protects against six diseases (diphtheria, tetanus, whooping cough, polio, hepatitis B and Hib) and is administered to infants at 2, 4 and 6 months of age.

Approved by the TGA in 2006, the vaccine lies at the heart of the National Immunisation Program, and has been administered to millions of babies across the country.

FOI request

A freedom of information (FOI) request for the number of deaths reported after use of the Infanrix-Hexa® vaccine has revealed some worrying data.The Database of Adverse Event Notifications (DAEN) shows 17 reported deaths in infants.

Screenshot

A further 26 reported deaths exist in the TGA’s ‘internal’ database, the Adverse Event Management System (AEMS), according to a recent FOI report.

Overall, 43 sudden unexpected deaths have been reported in babies mostly under 12 months of age, which have occurred within a day or two of vaccination…

READ FULL ARTICLE HERE… (gospanews.net)Live Stream + Chat (zutalk.com)

 


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