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Coronavirus Disease 2019 (COVID-19)

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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
 
Based on a review of safety and effectiveness data from clinical trials in the United States and the expanded emergency authorization by the U.S. Food and Drug Administration
Based on a review of safety and effectiveness data from clinical trials in the United States and the expanded emergency authorization by the U.S. Food and Drug Administration
 
The Food and Drug Administration (FDA) on Wednesday released its analysis of Johnson & Johnson’s one-shot dose COVID-19 vaccine, supporting its authorization for emergency use.
The Food and Drug Administration (FDA) on Wednesday released its analysis of Johnson & Johnson’s one-shot dose COVID-19 vaccine, supporting its authorization for emergency use.
 
The Food and Drug Administration announced late last week that it reversed its position and will not seek to charge distillers a $14,000 fine for operating as “drug facilities.”
The Food and Drug Administration announced late last week that it reversed its position and will not seek to charge distillers a $14,000 fine for operating as “drug facilities.”
 
Agency says vaccine about 94% effective for most people
 
On Tuesday, the Food and Drug Administration announced it had approved the first rapid coronavirus test capable of being taken at home.
On Tuesday, the Food and Drug Administration announced it had approved the first rapid coronavirus test capable of being taken at home.
 
COVID-19 treatment tested by ECU, Vidant receives FDA emergency use authorization
COVID-19 treatment tested by ECU, Vidant receives FDA emergency use authorization
 
President Donald Trump claimed on Monday that the U.S. Food and Drug Administration and Democrats delayed releasing news on a potential vaccine to hurt his reelection chances.
President Donald Trump claimed on Monday that the U.S. Food and Drug Administration and Democrats delayed releasing news on a potential vaccine to hurt his reelection chances.
 
John Cochran — “The Grumpy Economist” — has been arguing for a long time that “cheap, fast, tests can stop this pandemic quickly, even if they are not very accurate.”
John Cochran — “The Grumpy Economist” — has been arguing for a long time that “cheap, fast, tests can stop this pandemic quickly, even if they are not very accurate.”
 
Former Food and Drug Administration Commissioner Scott Gottlieb warned people about trusting Moscow’s claims that it had developed a successful coronavirus vaccine.
Former Food and Drug Administration Commissioner Scott Gottlieb warned people about trusting Moscow’s claims that it had developed a successful coronavirus vaccine.
 
ABR is a non-profit firm which has been the subject of criminal referrals from House and Senate committees investigating whether Planned Parenthood or any other entity was illegally profiting from the handling of fetal tissue from aborted babies.
ABR is a non-profit firm which has been the subject of criminal referrals from House and Senate committees investigating whether Planned Parenthood or any other entity was illegally profiting from the handling of fetal tissue from aborted babies.
 
FDA advises consumers not to use any hand sanitizer manufactured by Eskbiochem SA de CV in Mexico, due to the potential presence of methanol (wood alcohol), a substance that can be toxic when absorbed through the skin or ingested.
FDA advises consumers not to use any hand sanitizer manufactured by Eskbiochem SA de CV in Mexico, due to the potential presence of methanol (wood alcohol), a substance that can be toxic when absorbed through the skin or ingested.
 
A blood test to determine who has been infected by SARS-CoV-2 is one thing, but a test to find out who has already had it is a whole different kettle of fish.
A blood test to determine who has been infected by SARS-CoV-2 is one thing, but a test to find out who has already had it is a whole different kettle of fish.
 
The FDA is getting closer to a vaccine.
 
On Sunday night, the Food and Drug Administration (FDA) issued an emergency use authorization for hydroxychloroquine and chloroquine
On Sunday night, the Food and Drug Administration (FDA) issued an emergency use authorization for hydroxychloroquine and chloroquine
 
With the help of the Food and Drug Administration, which has fast-tracked the effort, the state of New York is trying out potential treatments for people who have contracted COVID-19.
With the help of the Food and Drug Administration, which has fast-tracked the effort, the state of New York is trying out potential treatments for people who have contracted COVID-19.
 
The FDA and the Federal Trade Commission have already issued warning letters to seven companies for selling fraudulent COVID-19 products.
The FDA and the Federal Trade Commission have already issued warning letters to seven companies for selling fraudulent COVID-19 products.
 
We've had no shortage of goofiness at the General Assembly in the past few weeks. And we're not just talking about the recently convened short session, which seems to have little purpose other than trying to fix embarrassing mistakes in the election process the same General Assembly
We've had no shortage of goofiness at the General Assembly in the past few weeks. And we're not just talking about the recently convened short session, which seems to have little purpose other than trying to fix embarrassing mistakes in the election process the same General Assembly
 
This month, Congressman Walter B. Jones (NC-3) secured language which encourages the Department of Veterans Affairs to study and use advancements in prostheses, most notably, hydraulic technology
This month, Congressman Walter B. Jones (NC-3) secured language which encourages the Department of Veterans Affairs to study and use advancements in prostheses, most notably, hydraulic technology
 
One of my greatest priorities is to reduce the price of prescription drugs.
 
Today, the Council of Economic Advisers (CEA) released a report on how the government can help to effectively reduce the prices of lifesaving drugs while stimulating innovation in the pharmaceutical industry
Today, the Council of Economic Advisers (CEA) released a report on how the government can help to effectively reduce the prices of lifesaving drugs while stimulating innovation in the pharmaceutical industry
 
Congressman Walter B. Jones (NC-3) is continuing his long-standing fight to level the playing field for shrimping families in Eastern North Carolina and across the country
Congressman Walter B. Jones (NC-3) is continuing his long-standing fight to level the playing field for shrimping families in Eastern North Carolina and across the country
 
Hundreds of thousands of Americans have lost their lives to drug abuse, and it will only get worse unless action is taken
Hundreds of thousands of Americans have lost their lives to drug abuse, and it will only get worse unless action is taken
 
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