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Practice Management News
Number of opioids prescribed falls as long-term prescriptions rise
Over a period of 12 years, the number of opioids prescribed per person decreased, whereas the prescribing rate for long-term prescriptions increased, according to findings published in JAMA Network Open.
Physician burnout rate increases, broad-based approaches alleviate causes
The rate of physician burnout increased 5% during a 3-year period, according to findings recently published in JAMA Network Open.
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FDA grants fast track designation to Revex for opioid overdose
The FDA granted Revex fast track designation for the emergency treatment of known or suspected opioid overdose, according to a press release issued by the drug’s manufacturer.
National Cancer Institute director named acting FDA commissioner
Norman E. “Ned” Sharpless, MD, director of National Cancer Institute, will replace resigning FDA commissioner Scott Gottlieb, MD, according to a tweet from Gottlieb.
Health IT tool in waiting room improves clinician, patient communication
A simple waiting room-based tool on an iPad that researchers dubbed the Visit Planner significantly improved visit communication between primary care physicians and patients, according to findings recently published in Annals of Family Medicine.
Dual opioid prescriptions from VA, Medicare linked to higher risk for overdose death
Receiving opioid prescriptions from both the U.S. Department of Veterans Affairs and Medicare Part D was independently associated with two to three times the odds of unintentional death from an opioid overdose, according to findings published in Annals of Internal Medicine.
Gottlieb leaves mixed legacy on drug prices, opioids, tobacco use
As a former adviser to several federal entities, FDA Commissioner Scott Gottlieb, MD was familiar with public service before he assumed his current position in early 2017.
Gottlieb to step down as FDA commissioner
FDA Commissioner Scott Gottlieb, MD, announced his resignation effective 1 month from Tuesday, March 5, according to an HHS press release.
FDA warns CanaRx to stop distributing ‘unapproved, misbranded’ drugs
The FDA recently posted a warning letter to CanaRx requesting it immediately stop dispensing “unapproved new drugs” and “misbranded, potentially dangerous drugs” to U.S. consumers.
Drug companies grilled on pricing in Senate hearing
Representatives from AbbVie, AstraZeneca, Bristol-Myers Squibb, Janssen Pharmaceuticals, Merck, Pfizer and Sanofi voiced support for drug rebate reform, value-based program creation, and increasing transparency, biologics and generics awareness to lower U.S. drug prices at a recent Senate Finance Committee hearing.
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Headline News
Screen use in bed associated with delayed sleep, psychological distress in children, teens
September 25, 20243 min read -
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Q&A: Barriers to STI self-testing among teens, young adults
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Inadequate sleep during pregnancy tied to neurodevelopmental delays for boys
September 26, 20243 min read
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Headline News
Screen use in bed associated with delayed sleep, psychological distress in children, teens
September 25, 20243 min read -
Headline News
Q&A: Barriers to STI self-testing among teens, young adults
September 25, 20243 min read -
Headline News
Inadequate sleep during pregnancy tied to neurodevelopmental delays for boys
September 26, 20243 min read