Contents Pages by Subject

Food And Drug Administration / F.D.A

Article Image News Link • Global, CNBC and Fox News

The Food and Drug Administration on Monday approved Pfizer and BioNTech's request to allow their Covid-19 vaccine to be given to kids ages 12 to 15 on an emergency use basis, allowing states to get middle school students vaccinated before the fall.

Article Image News Link • Global BY JACK PHILLIPS

Former Food and Drug Administration Commissioner Scott Gottlieb said that the six-foot social distancing mandate that was employed across much of the United States and the world to deal with the CCP virus pandemic "wasn't based on clear science.

Article Image News Link • Global By Alliance for

In the U.S., vaccines granted Emergency Use Authorization by the FDA, as is the case with the Pfizer and Moderna COVID vaccines, are considered experimental. Administrators of emergency use vaccines are required by law to inform vaccine recipients of

Article Image News Link • Global

By Environmental Health News

Investigation reveals FDA's failure to account for the cumulative effect of chemicals on public health, particularly for communities already facing significant health and socio-economic disparities and for children who are uniquely susceptible to d

Article Image News Link • Global, Spiro Skouras

The US has already begun to roll out 2.9-million doses of the Pfizer vaccine, and on Friday, the FDA authorized a second COVID-19 vaccine from Moderna for emergency use and plans to ship 7.9-million doses to 3,700 locations this week. Neither the Pfi

Article Image News Link • Global

U.S. Food and Drug Administration staff recommends monitoring people who get Pfizer or Moderna's Covid-19 vaccine shots for possible cases of Bell's Palsy, saying it's not necessarily a side effect but worth watching out for, reports CNBC.

Article Image News Link • Global

Natural News - Ethan Huff

After declaring its own experimental Wuhan coronavirus (Covid-19) vaccine to be "safe," "effective," and ready to go, drug giant Pfizer is now planning to file for emergency use authorization from the U.S. Food and Drug Administration (FDA).