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schwit1 shared this article from the Washington Post: The House on Tuesday passed "right to try" legislation that would allow people with life-threatening illnesses to... [Read More]
The U.S. Food and Drug Administration issued a safety announcement May 23 warning consumers not to use teething products containing benzocaine in infants and children... [Read More]
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The ultimate goal is to gather data from 100 users and present it to the Food and Drug Administration to get clearance. [Read More]
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Federal health officials warned parents Wednesday about the dangers of teething remedies that contain a popular numbing ingredient and asked manufacturers to stop selling their... [Read More]
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(The Hill) President Trump will sign legislation next week allowing terminally ill patients to access experimental drugs not yet approved by the Food and Drug... [Read More]
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Palynziq (pegvaliase-pqpz) has been approved by the U.S. Food and Drug Administration to treat phenylketonuria, commonly called PKU. [Read More]
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In order to save their skin from the harmful effects of the scorching sun, many people are willing to try any product that boasts of... [Read More]
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Merrick Pet Care recalls Good Buddy and Backcountry Treats that likely have elevated levels of Thyroid Hormone. According to the U.S. Food and Drug Administration,... [Read More]
Photo Illustration by The Daily Beast In April, a committee at the Food and Drug Administration took the unprecedented step to recommend for approval Epidiolex,... [Read More]
SCI COMMUNIn science news around the world, the U.S. Food and Drug Administration approves the first drug to prevent migraine headaches. Swedish universities and research... [Read More]
A study of pollution in shellfishing areas in Plymouth Harbor, Kingston Bay and Duxbury Bay is scheduled to start in June.Scientists from the U.S. Food... [Read More]
The Food and Drug Administration is warning that Biotin, also known as vitamin B7, can cause misleading test results. This can lead to unnecessary procedures,... [Read More]
but it is not fun. You have apply it before you go outside, then reapply every two hours or after you swim or sweat,... [Read More]
President Trump will sign legislation next week allowing terminally ill patients to access experimental drugs not yet approved by the Food and Drug Administration (FDA).White House... [Read More]
The Food and Drug Administration issued parents some stern warnings about teething medicines for their babies, and simultaneously told manufacturers and retailers that if they... [Read More]
Twenty-seven years after the US Food and Drug Administration (FDA) approved a mild oral painkiller for over-the-counter use, the agency is reversing its stance. ... [Read More]
The Food and Drug Administration advises parents to stop using Orajel and other products marketed for teething babies containing benzocaine. [Read More]
The US Food and Drug Administration issued a warning to consumers Wednesday to stop using over-the-counter teething products that contain benzocaine. [Read More]
On March 6, 2018, the US Food and Drug Administration (FDA) authorised the DNA testing company 23andMe's Personal Genome Service that offers mail-order testing for... [Read More]
Kratom is an opioid derived from a plant native to Southeast Asia. It can be consumed in the form of pills, powder, or tea. The... [Read More]
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