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Coronavirus Disease 2019 (COVID-19)

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refuses FOI request - what are they hiding
 
The Food and Drug Administration (FDA) issued a safety alert after reviewing some reports of patients who had been diagnosed with cancer after receiving breast implants.
The Food and Drug Administration (FDA) issued a safety alert after reviewing some reports of patients who had been diagnosed with cancer after receiving breast implants.
 
This week, we begin a new phase in our COVID-19 response. We are launching a new vaccine – our first in almost two years – with a new approach.
This week, we begin a new phase in our COVID-19 response. We are launching a new vaccine – our first in almost two years – with a new approach.
 
The Food and Drug Administration (FDA) authorized updated COVID booster shots on Wednesday created to specifically target subvariants of Omicron.
The Food and Drug Administration (FDA) authorized updated COVID booster shots on Wednesday created to specifically target subvariants of Omicron.
 
The Food and Drug Administration (FDA) could rule this week that COVID booster shots may be distributed to Americans before the completion of testing in humans.
The Food and Drug Administration (FDA) could rule this week that COVID booster shots may be distributed to Americans before the completion of testing in humans.
 
Wednesday, the FDA authorized both the Moderna and Pfizer-BioNTech bivalent COVID-19 booster dose, which protects against the original as well as the Omicron strain.
Wednesday, the FDA authorized both the Moderna and Pfizer-BioNTech bivalent COVID-19 booster dose, which protects against the original as well as the Omicron strain.
 
Pfizer and BioNTech have requested that the Food and Drug Administration (FDA) grant an emergency use authorization for its COVID vaccine adapted to the BA.4/BA.5 versions of the Omicron variant.
Pfizer and BioNTech have requested that the Food and Drug Administration (FDA) grant an emergency use authorization for its COVID vaccine adapted to the BA.4/BA.5 versions of the Omicron variant.
 
President Joe Biden touted news Tuesday that the Food and Drug Administration is making hearing aids available over the counter — a move begun through a law signed under former President Donald Trump’s administration.
President Joe Biden touted news Tuesday that the Food and Drug Administration is making hearing aids available over the counter — a move begun through a law signed under former President Donald Trump’s administration.
 
Pharmaceutical companies have lost tens of billions in stock market value this week ahead of a trial regarding the heartburn drug Zantac.
Pharmaceutical companies have lost tens of billions in stock market value this week ahead of a trial regarding the heartburn drug Zantac.
 
FDA Emergency Use Authorization allows for alternative dosing regimen; increases JYNNEOS supply by up to five-fold
 
With the Food and Drug Administration (FDA) prepping yet another booster shot for this fall — this one to target the Omicron variant known as BA.5 — scientists and immunologists are working on a whole new approach that includes nasal spray vaccines and body patches.
With the Food and Drug Administration (FDA) prepping yet another booster shot for this fall — this one to target the Omicron variant known as BA.5 — scientists and immunologists are working on a whole new approach that includes nasal spray vaccines and body patches.
 
Puberty blockers, known as gonadotropin-releasing hormone (GnRH) substances, received a warning from U.S. Food and Drug Administration (FDA) officials earlier this month, saying the drug could cause brain swelling, loss of vision, and serious risks for children injecting the hormone.
Puberty blockers, known as gonadotropin-releasing hormone (GnRH) substances, received a warning from U.S. Food and Drug Administration (FDA) officials earlier this month, saying the drug could cause brain swelling, loss of vision, and serious risks for children injecting the hormone.
 
The Food and Drug Administration (FDA) authorized Novavax’s COVID vaccine for adults on Wednesday, offering a protein-based alternative to mRNA shots from other pharmaceutical companies.
The Food and Drug Administration (FDA) authorized Novavax’s COVID vaccine for adults on Wednesday, offering a protein-based alternative to mRNA shots from other pharmaceutical companies.
 
The Food and Drug Administration and the Centers for Disease Control and Prevention announced the Novavax COVID-19 vaccine can be used as an additional vaccine option for adults ages 18 years and older.
The Food and Drug Administration and the Centers for Disease Control and Prevention announced the Novavax COVID-19 vaccine can be used as an additional vaccine option for adults ages 18 years and older.
 
A panel of independent advisers that works with the Food and Drug Administration (FDA) has recommended producing new COVID-19 vaccines to target the Omicron variant.
A panel of independent advisers that works with the Food and Drug Administration (FDA) has recommended producing new COVID-19 vaccines to target the Omicron variant.
 
On Thursday, The Food and Drug Administration officially ordered all Juul electronic cigarettes to be removed from the United States market, the Associated Press reported.
On Thursday, The Food and Drug Administration officially ordered all Juul electronic cigarettes to be removed from the United States market, the Associated Press reported.
 
Reformulated Covid shots approved WITHOUT further clinical trials
Reformulated Covid shots approved WITHOUT further clinical trials
 
North Carolina Democratic Gov. Roy Cooper signed three bills into law yesterday, June 14, including one that legalizes FDA-approved THC medications.
North Carolina Democratic Gov. Roy Cooper signed three bills into law yesterday, June 14, including one that legalizes FDA-approved THC medications.
 
S.B. 448 Controlled Substances Act could fast track only FDA approved drugs containing marijuana in North Carolina.
S.B. 448 Controlled Substances Act could fast track only FDA approved drugs containing marijuana in North Carolina.
 
The Biden Administration and FDA are being scrutinized for their handling of the baby formula shortage across the U.S.
The Biden Administration and FDA are being scrutinized for their handling of the baby formula shortage across the U.S.
 
On May 20th, the Centers for Disease Control and Prevention (CDC), in addition to the FDA, recommended a booster dose of the Pfizer-BioNTech COVID-19 vaccine for children between the ages of 5 to 11.
On May 20th, the Centers for Disease Control and Prevention (CDC), in addition to the FDA, recommended a booster dose of the Pfizer-BioNTech COVID-19 vaccine for children between the ages of 5 to 11.
 
The U.S. Food and Drug Administration (FDA) announced late Thursday afternoon that it has limited the authorized use of the Johnson & Johnson vaccine to adults who cannot receive other coronavirus vaccines.
The U.S. Food and Drug Administration (FDA) announced late Thursday afternoon that it has limited the authorized use of the Johnson & Johnson vaccine to adults who cannot receive other coronavirus vaccines.
 
On March 30th, the FDA authorized and the CDC recommended certain immunocompromised individuals and people over the age of 50 receive an additional mRNA booster, at least 4 months after their initial booster.
On March 30th, the FDA authorized and the CDC recommended certain immunocompromised individuals and people over the age of 50 receive an additional mRNA booster, at least 4 months after their initial booster.
 
The North Carolina Department of Health and Human Services is cautioning families about certain infant formula that has been recalled by Abbott for potentially containing a bacteria that can lead to hospitalization in infants.
The North Carolina Department of Health and Human Services is cautioning families about certain infant formula that has been recalled by Abbott for potentially containing a bacteria that can lead to hospitalization in infants.
 
The Biden administration and the U.S. Food and Drug Administration (FDA) took heat online this week after the FDA announced the removal of emergency use authorization for two monoclonal antibodies, which effectively shut down treatment sites statewide in Florida.
The Biden administration and the U.S. Food and Drug Administration (FDA) took heat online this week after the FDA announced the removal of emergency use authorization for two monoclonal antibodies, which effectively shut down treatment sites statewide in Florida.
 
The Florida Department of Health announced Monday that the U.S. Food and Drug Administration (FDA) made an “abrupt decision to remove emergency use authorization for two monoclonal antibodies,” which effectively shut down treatment sites statewide.
The Florida Department of Health announced Monday that the U.S. Food and Drug Administration (FDA) made an “abrupt decision to remove emergency use authorization for two monoclonal antibodies,” which effectively shut down treatment sites statewide.
 
White House Press Secretary Jen Psaki defended the FDA during Tuesday’s press briefing for revoking its emergency use authorization for monoclonal antibody treatments for COVID-19.
White House Press Secretary Jen Psaki defended the FDA during Tuesday’s press briefing for revoking its emergency use authorization for monoclonal antibody treatments for COVID-19.
 
revoke emergency use of monoclonal antibodies with no basis for doing so but politics
revoke emergency use of monoclonal antibodies with no basis for doing so but politics
 
The FDA now authorizes and the Centers for Disease Control and Prevention recommends individuals who received the Moderna COVID-19 vaccine get a booster dose after five months.
The FDA now authorizes and the Centers for Disease Control and Prevention recommends individuals who received the Moderna COVID-19 vaccine get a booster dose after five months.
 
several states implement discrimination based on FDA standards
several states implement discrimination based on FDA standards
 
Info on Comirnaty and conflicts of interest at the FDA
Info on Comirnaty and conflicts of interest at the FDA
 
The Food and Drug Administration approved a new drug for Alzheimer’s disease Monday
The Food and Drug Administration approved a new drug for Alzheimer’s disease Monday
 
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