FDA Approved H1N1 Vaccines Contain Ingredients Known to Cause Cancer and Death

Most health experts will agree that vaccine reactions can occur. It is estimated that roughly 1 in every million people will react to their vaccine. Even then, health officials maintain that it is usually a simple case of inflammation at the injection site and/or a slight fever. On a rare occasion, anaphylactic shock may occur due to the patient reacting to a substance that they are allergic to. However, the FDA recently approved four H1N1 vaccines that not only contain very questionable ingredients, but some of those ingredients have even been proven to cause cancer and death.

The FDA has awarded H1N1 contracts to the following companies: MedImmune, LLC (1), CSL Limited (2), Novartis Vaccines and Diagnostics Limited (3), and Sanofi Pasteur (4). Their package inserts became public knowledge in recent weeks.

All four vaccines list hypersensitivity to eggs as a contraindication (1) (2) (3) (4). This means that it is not advisable to administer any one of these products to a person suffering from a severe egg allergy or egg protein allergy. This contraindication may affect as many as 15 million people (based on a population of 300 million). (5). While parents are instructed not to feed their infant eggs until 1 year of age, these same infants will be exposed to eggs by way of their H1N1 vaccine and/or seasonal flu vaccine beginning at 6 months of age.

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