Pfizer COVID Vaccine Authorization for Children Under 5 Delayed as FDA Seeks More Data; CDC Says Booster Shots' Efficacy Wanes

Pfizer COVID Vaccine Authorization for Children Under 5 Delayed as FDA Seeks More Data; CDC Says Booster Shots' Efficacy Wanes

The approval of Pfizer COVID-19 vaccines for children under five years old hits another delay as the Food and Drug Administration (FDA) needed more data.
Vaccination in California

U.S. FDA to Allow Americans With Different Brand of Booster Vaccine Shot

U.S. FDA will allow Americans to use the "mix and match" approach on booster vaccine shots.
Former FDA Chief Says COVID Vaccines for Children Age 5-11 Could Be Approved by Late October

Former FDA Chief Says COVID Vaccines for Children Age 5-11 Could Be Approved by Late October

Former FDA chief Scott Gottlieb said that children aged five to 11 years old could be eligible for the Pfizer vaccine by the end of October.
Convalescent plasma from a recovered coronavirus disease (COVID-19) patient at Bloodworks Northwest

FDA Puts Emergency Approval for Blood Plasma as COVID-19 Treatment on Hold

The U.S. Food and Drug Administration (FDA) put the emergency use authorization for blood plasma as a COVID-19 Treatment on hold, reported The New York Times.
Miners Tested For Coronavirus As Infections Persist In Polish Coal Country

COVID-19 Saliva Test Partly Funded by NBA Gets FDA Emergency Use Approval

A saliva-based COVID-19 Test received emergency-use approval from the U.S. Food and Drug Administration (FDA) on Saturday.
Mexico hand sanitizer FDA

FDA Warns Public of Several Toxic Mexican-Made Hand Sanitizers

The U.S. Food and Drug Administration (FDA) has reminded the public to avoid using hand sanitizer products containing toxic substance methanol.
Intravenous Test

100 Million COVID-19 Test a Month: FDA Approves Intravenous Antibody Test

U.S. Food and Drug Administration has approved Roche, the Swiss drugmaker, for antibody tests that will determine whether people have ever been infected by COVID-19.
U.S. FDA

FDA Approves First Rapid COVID-19 Test Gives Results in 45 Minutes

The United States Food and Drug Administration has announced its approval to use the COVID-19 testing kit that will give results or detections within 45 minutes.
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