Australia’s FDA (the Therapeutic Goods Administration or TGA) hides from questions about sudden infant deaths after vaccination

A string of sudden unexpected deaths in infants following the Infanrix Hexa® vaccine has forced the drug regulator to go to ground. India also warned about deaths following this vaccine.

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. [All in one syringe each time—Nass]

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. 

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

For the rest go here:

Maryanne Demasi, reports
TGA hides from questions about sudden infant deaths after vaccination
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…
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Australia only has 8% of the US population (27 million people). 287,000 babies were born in Australia last year.

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