PARENTS OF NEWBORN BABIES

 

Newborn babies are MANDATED to be injected w/SYNTHETIC K1 (refer to "BOXED WARNING") w/benzyl alcohol (from petroleum; a toxic chemical), aluminum, and dextrose (cornstarch sugar/D-glucose), 21CFR184.1857, a glucose (blood sugar)-elevating agent -- MANDATORY OR PARENTAL RIGHTS THREATENED.
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c204c720-88d3-a6d6-e053-2a95a90a3de5

 

Mandatory neonatal SYNTHETIC K1 (Phytonadione) injectable emulsions administered within hours of birth routinely utilize hydrous dextrose (cornstarch sugar/D-glucose) as a formulation vehicle. Due to the FDA's blank classification in 21CFR184.1857, molecular formula C6H12O6, this sugar carries trace, biologically active corn polypeptides from the biological source: CORNSTARCH.

BREACH OF STANDARD MEDICAL PROTCOL

Hospital protocols mandate the injection of this dextrose-containing vehicle without requiring clinicians to verify the newborn baby’s blood glucose levels prior to or after administration. Dextrose is an active glucose (blood sugar)-elevating agent; injecting it into a neonate blindly without pre- and post-labs bypasses foundational clinical monitoring guidelines. This unmonitored practice forces direct intravenous/intramuscular exposure to a highly processed corn carbohydrate matrix before the infant's immune profiles can be evaluated, masking potential excipient hypersensitivity beneath Phytonadione's existing FDA Boxed Warning for fatal anaphylaxis.

Corn Allergy Advocacy/Resources, Email: cornallergyinitiative@gmail.com
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