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Fitbit's health care business is showing considerable gains in a rapidly growing market with competitors like Apple and Garmin.
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The FDA has denied Sarepta Therapeutics’ application for its second Duchenne muscular dystrophy treatment, despite the company producing twice the amount of data behind its controversial first product approval in 2016.
Sarepta (Nasdaq: SR read more »
Sarepta (Nasdaq: SR read more »
Wine and money flowed and glasses clinked at the 32nd annual Auction of Washington Wines on Saturday, when the dinner/auction at Chateau Ste. Michelle raised $4.5 million to benefit Seattle Children’s Hospital’s uncompensated care fund, and wine edu
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The Food and Drug Administration approved Nabriva Therapeutics' drug application for its antibiotic Xenleta.
Xenleta treats community-acquired bacterial pneumonia (CABP), a leading cause of infection-related deaths in the United States. read more »
Xenleta treats community-acquired bacterial pneumonia (CABP), a leading cause of infection-related deaths in the United States. read more »
Legislators, nonprofit groups and business leaders attended a blessing ceremony for the the new Joint Outreach Center medical clinic in Kaneohe on Friday. The following day, the center held an open house that allowed members of the community to lear
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(Reuters Health) - Seniors may be more likely than younger adults to choke on vitamins and dietary supplements, or to have other problems swallowing them, especially when the pills are on the larger side, a new study suggests.
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NEW YORK (Reuters Health) - Measuring blood pressure outside the clinic using 24-hour monitoring equipment is important for identifying and managing hypertension in African-Americans, a new study shows.
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Sarepta Therapeutics Inc said on Monday the U.S. Food and Drug Administration declined to approve its newest treatment for Duchenne muscular dystrophy (DMD), citing safety concerns including the risk of infection and kidney toxicity.
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