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
X (nee Twitter): Corn Allergy
Mgmt. @AllergyMgmt911