On February 11, NBC News reported that Pfizer-BioNTech is postponing its applicated to the Food and Drug Administration for the expansion of COVID-19 “vaccines” for children ages six months to 4 years.

Pfizer said they expect “more data” from testing in April on its three-dose series for young children. The drug company said two doses “didn’t generate a strong enough immune response” in a trial of children ages 2 to 4.

The company in February asked the FDA to approve the first two doses.

But experts outside the FDA have told the agency that Pfizer’s data wasn’t sufficient to approve the drug. Those same experts said their warnings “were falling on deaf ears” in the FDA.

Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, said regulators chose to not approve the two-dose treatment until they studied the three-dose proposal.

Marks said parents should be “reassured” because the FDA takes these tests “seriously.”

John Moore, a professor of microbiology and immunology at Weill Cornell Medical College, said Pfizer took a guess at the best dosage for young and “they got it wrong, they underdosed.”

How can you trust these people with the health of your youngest children? The government has been wrong so many times with the Chinese coronarvirus and now they could approve more drugs from Pfizer?

This is madness.

The coronavirus is least deadly to young children. Why submit a child to an experimental “vaccine?”

Many parents will have their babies vaccinated but they need to be completely appraised of the risk they are taking with their child’s health.