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If there is a new pandemic before 2032, how long (in days) will it be from the first US laboratory-confirmed case until the first FDA-approved vaccine?

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"This decision protects children, respects families, and rebuilds trust in public health."

"This [2026] decision recommits HHS to all three [transparency, rigorous science, and respect for families]."

"This decision commits NIH, CDC, and FDA to gold standard science, greater transparency, and ongoing reassessment as new data emerge."

"No family will lose access.This [2026] framework empowers parents and physicians to make individualized decisions based on risk, while maintaining strong protection against serious disease."

"The data support a more focused schedule that protects children from the most serious infectious diseases while improving clarity, adherence, and public confidence."

“I think that a reduced schedule is going to endanger children and lay the groundwork for a resurgence in preventable disease.”

"This wildly irresponsible decision will put lives at risk."

“Changing the pediatric vaccine schedule based on no scientific input on safety risks and little transparency will cause unnecessary fear for patients and doctors, and will make America sicker.”

“There will be more diseases, more infection, more hospitalizations.”

Will Secretary Kennedy's U.S. Childhood Vaccine Schedule Overhaul Risk Public Health?

Dr. Helmut Sterz, a former chief toxicologist for Pfizer's European operations, testified before the German Bundestag's Corona Enquete Commission on March 19, 2026, arguing that key preclinical safety studies were skipped before the Comirnaty mRNA vaccine received approval.

Dr. Helmut Sterz, a former chief toxicologist for Pfizer's European operations, testified before the German Bundestag's Corona Enquete Commission on March 19, 2026, arguing that key preclinical safety studies were skipped before the Comirnaty mRNA vaccine received approval.

Sterz told the commission that no carcinogenicity study was conducted before the vaccine's approval, citing time constraints, and that a reproductive toxicity study in rats was carried out inadequately, making reliable estimates of the vaccine's effect on pregnancy impossible.

The Epoch Times

Sterz told the commission that no carcinogenicity study was conducted before the vaccine's approval, citing time constraints, and that a reproductive toxicity study in rats was carried out inadequately, making reliable estimates of the vaccine's effect on pregnancy impossible.

Germany's Paul-Ehrlich-Institut recorded approximately 2,133 deaths reported after Comirnaty vaccination. Sterz applied a 30-times multiplier — drawn from a U.S.-based underreporting estimate — to arrive at a figure of up to 60,000 possible vaccine-related deaths in Germany.

Germany's Paul-Ehrlich-Institut recorded approximately 2,133 deaths reported after Comirnaty vaccination. Sterz applied a 30-times multiplier — drawn from a U.S.-based underreporting estimate — to arrive at a figure of up to 60,000 possible vaccine-related deaths in Germany.

German Health Minister Karl Lauterbach, who was present at the hearing, rejected Sterz's claims, stating that toxicity and carcinogenicity had been studied and that steps normally conducted sequentially were run in parallel to accelerate the process without compromising safety.

German Health Minister Karl Lauterbach, who was present at the hearing, rejected Sterz's claims, stating that toxicity and carcinogenicity had been studied and that steps normally conducted sequentially were run in parallel to accelerate the process without compromising safety.

Sterz also alleged that the vaccine distributed to the public differed from the substance used in clinical trials, stating that mass production relied on the bacterium Escherichia coli, which he said resulted in bacterial DNA contamination and a theoretical increased cancer risk.

Sterz also alleged that the vaccine distributed to the public differed from the substance used in clinical trials, stating that mass production relied on the bacterium Escherichia coli, which he said resulted in bacterial DNA contamination and a theoretical increased cancer risk.

The U.S. Food and Drug Administration updated warning labels for Comirnaty and Spikevax in June 2025 to include new safety information on myocarditis and pericarditis, noting the estimated incidence was approximately 27 cases per million doses in males aged 12 through 24.

The U.S. Food and Drug Administration updated warning labels for Comirnaty and Spikevax in June 2025 to include new safety information on myocarditis and pericarditis, noting the estimated incidence was approximately 27 cases per million doses in males aged 12 through 24.

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