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The Pediatric Perils of PEG: From MiraLAX to COVID Shots, FDA and CDC Ignore Safety Signals

By Children’s Health Defense Team

 

Last year, the U.S. Food and Drug Administration warned that some ultrasound contrast agents contain polyethylene glycol (PEG) and therefore shouldn’t be administered to patients with known or suspected allergies to PEG — but there are no similar warnings for adults or children who get PEG-containing COVID-19 shots or MiraLAX, an over-the-counter laxative.

On Oct. 20 — the very same day the Centers for Disease Control and Prevention’s (CDC) crooked vaccine advisory committee members voted to add COVID-19 shots to the Child and Adolescent Immunization Schedule — Indonesia’s Ministry of Health took a bold step in a different direction: It banned the sale and prescription of pediatric cough syrups and other liquid medications, at least temporarily.

The ministry linked the cough syrups to kidney injuries that recently killed almost 100 Indonesian children and nearly 70 children in The Gambia in West Africa, and it voiced the suspicion that those numbers could be the tip of a much larger iceberg.

After the rash of West African deaths, the World Health Organization issued a medical product alert for four brands of cough syrup manufactured in India and imported into The Gambia through a U.S. company — warning of the products’ possibly global distribution and calling for the substandard products’ removal from circulation.

 

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