FDA - Page 5

The U.S. Food and Drug Administration (FDA), citing the latest science and data, rescinded its emergency use authorization (EUA) for chloroquine and hydroxychloroquine, the anti-malaria drugs touted by President Donald Trump and some doctors to combat the Chinese coronavirus.

Sen. Kelly Loeffler asked four health experts that took part in a Senate hearing on Tuesday about their relationship with President Trump.

(UPI) — The U.S. Food and Drug Administration Tuesday approved a new test for COVID-19 that allows users to collect their own samples for evaluation, from the comfort of own homes.

Republicans urged the White House to maintain regulations on use of aborted fetal tissue for vaccine research and on drug-induced abortions.

The economic impact of the country’s being shut down could leave us facing 20-30 million unemployed, a very dangerous consequence of the panicked reactions by governors across the country.

The U.S. Food and Drug Administration (FDA) issued an emergency use authorization on Friday for a blood purification treatment for coronavirus patients with confirmed or imminent respiratory failure. 

Food and Drug Administration (FDA) administrator Dr. Stephen Hahn told Breitbart News exclusively on Wednesday that his agency is working with private industry leaders to bring more antibody testing and promising potential plasma-based treatments for the coronavirus to the American public.

The Food And Drug Administration (FDA) issued an emergency authorization Sunday for hydroxychloroquine, a drug already used to treat malaria and other ailments, which has shown anecdotal efficacy against coronavirus.

Companies, hospitals, and doctors can now use a variety of unapproved and experimental machines and techniques to breathe air into asphyxiating coronavirus patients, according to a March 24 policy announcement by the federal agency responsible for licensing medical equipment. 

Health and Human Services (HHS) Secretary Alex Azar told Breitbart News exclusively that President Donald Trump in the coming days will work with his medical and scientific advisers to make a determination on how and when to reopen the country after wide-scale closure in the effort to stop the spread of the Chinese coronavirus.

Waltz will introduce a bill this week to lessen America’s dependence on Chinese pharmaceuticals and reduce the risk to its supply chains.

Teva Pharmaceutical Industries, Israel’s leading drug producer, announced Thursday that it is donating six million doses of its malaria tablet to the United States as testimonies continue to roll in claiming that it could potentially treat people with the Chinese coronavirus.

German pharmaceutical giant Bayer AG announced Thursday that it donated 3 million tablets of the malaria drug Resochin to the United States amid reports that it could potentially treat individuals with the deadly Chinese coronavirus. 

Studies are showing malaria drug chloroquine can both “prevent and treat coronavirus” in the cells of primates, but it is not FDA-approved for COVID-19.

United States Surgeon General Jerome Adams said Americans can help fight the coronavirus outbreak by donating blood.

The FDA has approved emergency authorization of a coronavirus test developed by the Swiss diagnostic developer Roche.

Former Vice President Joe Biden’s proposal for combatting the coronavirus cribs heavily from actions the Trump administration has already taken against the pandemic. 

The FDA is stressing the safety of donating blood in the wake of the coronavirus and calls on the public to step up to ensure stable supply.

Trump admitted at the White House that he was taking his own precautions to prevent the spread of coronavirus. “I haven’t touched my face in weeks,” he said. “In weeks. I miss it.”

Sen. Josh Hawley (R-MO) introduced the Medical Supply Chain Security Act on Thursday to combat potential American drug shortages created in the wake of the coronavirus outbreak in China and to reveal America’s reliance on Chinese manufacturing of pharmaceuticals and medical devices.

The Food and Drug Administration has granted expanded access for treatments employing the drug commonly known as “ecstasy,” or MDMA.

Activists with Ajinomoto’s “Redefine CRS” campaign claim fears related to monosodium glutamate (MSG) are rooted not in health, but racism.

WASHINGTON (AP) — U.S. health officials will ban most flavored e-cigarettes popular with underage teenagers, but with major exceptions that benefit vaping manufacturers, retailers and adults who use the nicotine-emitting devices.

No reliable scientific evidence exists to prove “transgender” children benefit from impersonating the opposite sex or puberty blockers.

The FDA has documented thousands of deaths linked to the puberty blockers now given to children who suffer from gender dysphoria.

A European doctor who supplies drugs for inducing abortion to American women online has filed a lawsuit against the Food and Drug Administration (FDA).

The Centers for Disease Control and Prevention (CDC) is reportedly investigation 153 possible cases of lung disease that may be associated with e-cigarettes and vaping. The sudden lung problems are primarily occuring amongst adolescents and young adults.

The Food and Drug Administration (FDA) published on Monday a voluntary multi-state recall of produce by Grower’s Express after potentially deadly bacteria was discovered.

The U.S. Food and Drug Administration released a list of dog food brands Thursday that could potentially lead to canine heart disease.

The FDA has announced that “Pillsbury Best 5-Pound Bread Flour” has been recalled for possible E.coli contamination.

The U.S. Food and Drug Administration has issued a mass recall of several tattoo inks containing dangerous bacteria.

According to a recent study, health apps aimed at helping users quit smoking and beat depression are selling user data to the Masters of the Universe at Facebook and Google.

The Centers for Disease Control and Prevention (CDC) reported on Monday that 626 cases of measles had been reported in 22 states.

A device created by an Israeli company to treat Alzheimer’s disease was considered for approval in the United States this week.

The National Institutes of Health (NIH) — part of the Department of Health and Human Services (HHS) — announced Monday it would be seeking to find and develop human tissue models that do not rely on the use of aborted fetal tissue.

The U.S. Food and Drug Administration (FDA) issued a recall Monday warning consumers that at least eight brands of dry dog food may contain toxic levels of vitamin D.