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Acella Pharmaceuticals is recalling two lots of its thyroid medication after testing found they may not be strong enough, the Food and Drug Administration announced last week.

The Food and Drug Administration announced Thursday that Acella Pharmaceuticals is voluntarily recalling one lot of 15-milligram and one lot of 120-milligram NP Thyroid®, Thyroid Tablets.

RECALL ALERT: Two types of thyroid medication have been recalled by their manufacturer after reports that they may not be strong enough, according to the Food and Drug Administration.

Two types of thyroid medications are being voluntarily recalled by the manufacturer, according to the Food and Drug Administration. The NP Thyroid tablets made by Acella Pharmaceuticals, LLC have possibly led to at least four reports of adverse effects.

Silicon Valley medical equipment startup Visby Medical has received Emergency Use Authorization by the U.S. Food and Drug Administration for a portable COVID-19 test kit, the first company to do so

In 'power grab', US Health Secretary asserts authority over Food and Drug Administration

In 'power grab', US Health Secretary asserts authority over Food and Drug Administration

The list of recalled hand sanitizer products that the U.S. Food and Drug Administration is warning consumers not to use due to potential methanol contamination has grown to nearly 150.

Silicon Valley startup Visby's portable COVID-19 test gets Emergency Use Authorization by the U.S. Food and Drug Administration

Roche announced the launch of its Elecsys® Anti-SARS-CoV-2 S antibody test for markets accepting the CE Mark. Roche has filed for Emergency Use Authorisation (EUA) from the U.S. Food and Drug Administration (FDA) #COVID19  #coronavirus  #SARSCoV2  #vaccine 

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The U.S. Food and Drug Administration is banning the use of electric shock devices to discipline school students. The ban is national, but it is targeted at a single Massachusetts school that has been using electric shocks for decades.

The first video game-based treatment for ADHD has been approved by the US Food and Drug Administration. The video game, called EndeavorRx, will be prescription only and aimed at children between the ages of eight and 12 with certain types of ADHD.

U.S. President Donald Trump says the drug Hydroxychloroquine has been approved by the Food and Drug administration and will be available for prescription immediately

The US Food and Drug Administration is requesting that manufacturers pull all prescription and over-the-counter ranitidine drugs, known by the brand name Zantac, from the market immediately, the agency announced on Wednesday.

It should not require the Governor of Ohio calling the President of the United States to get the Food and Drug Administration to allow a company to sterilize masks in large quantities. All these bureaucratic bottlenecks should be permanently fixed in the next phase.

Fact check: President Trump claimed the Food and Drug Administration had approved the "very powerful" drug chloroquine to treat coronavirus. But chloroquine has not been approved by the FDA to treat the coronavirus -- and nor has any other drug.

US Food and Drug Administration Commissioner Dr. Stephen Hahn: As of Friday at 6 p.m. ET, 5,861 tests for coronavirus have been completed by the US Centers for Disease Control and Prevention and public health labs.

The head of the U.S. Food and Drug Administration, Dr. Stephen Hahn, said each kit should allow a lab to run about 500 tests. That would work out to 1.25 million tests. Context: The U.S. has an estimated population of 331 million people.

The US Food and Drug Administration has warned leading e-cigarette maker Juul Labs about illegally marketing its product as a safer alternative to cigarettes.

Thanks to Trump's shutdown the Food and Drug Administration has suspended all routine inspections of domestic food-processing facilities. This tantrum is jeopardizing the health and safety of the American people.

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