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The Food and Drug Administration approved the prescription cannabidiol medicine Monday to treat rare and severe forms of epilepsy.

The new drug, Epidiolex, is a formulation of cannabidiol — CBD for short. It’s derived from cannabis but doesn’t contain the THC that recreational users value for providing “highs."

“This is an important medical advance,” said FDA Commissioner Dr. Scott Gottlieb. “But it’s also important to note that this is not an approval of marijuana or all of its components. This is the approval of one specific CBD medication for a specific use.”

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(Photo: 5-Hour Energy)

Federal officials are looking into reports of 13 deaths possibly connected to 5-Hour Energy, a liquid “shot” that contains caffeine and other compounds, the New York Times reported on Thursday. But the reports, which track cases since 2009, don’t show how the drinks could have caused the deaths and there’s no evidence the products are harmful.

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Federal health officials have approved the first at-home test to detect HIV antibodies, a move aimed at identifying and treating the estimated 20 percent of infected people in the U.S. who don’t know they have the virus that causes AIDS.

Food and Drug Administration officials on Tuesday approved the OraQuick In-Home HIV Test, the first over-the-counter, self-administered test that rapidly detects possible HIV infection. Despite concerns about learning of the serious diagnosis at home, an FDA panel unanimously agreed that the benefits of the home test outweigh the risks. 

Source: MSN
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If it comes in here and it’s bad,” said Denise Williams, a supervisor in the FDA’s Division of Import Operations in Southern California, “we’re gonna get ‘em.” 
Except when they don’t. Critics, including the U.S. Government Accountability Office, say the FDA is simply not up to the task of ensuring the safety of food imports, which are entering this country in ever-growing numbers.

Story continued here.

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