FDA approves generic Abilify
On April 28, the U.S. Food and Drug Administration (FDA) approved the first generic versions of Abilify (aripiprazole). Read more.
Web Exclusives
Variation in mortality
Compared to Whites, Blacks had lower risk adjusted mortality rates for several medical conditions and for abdominal aortic aneurysm repair, according to a study…
Elevated upper body position after childbirth improve respiratory safety
An elevated upper body position might improve respiratory safety in women early after childbirth without impairing sleep quality, according to a study in CHEST.…
Twitter can help predict asthma-related ED visits
Researchers have created a model to predict approximately how many asthma sufferers would visit the ED at a large hospital in Dallas on a…
2015 top patient safety concerns
Alarm hazards top the “Top 10 Patient Safety Concerns for Healthcare Organizations,” released by ECRI Institute. Data integrity and managing patient violence are second…
FDA approves new test for diagnosing gastroparesis.
On April 6, the U.S. Food and Drug Administration (FDA) approved Gastric Emptying Breath Test (GEBT), a new noninvasive test to help diagnose gastroparesis…
Infections associated with reprocessed duodenoscopes
The U.S. Food and Drug Administration (FDA) has taken several steps in response to infections associated with reprocessed duodenoscopes, including issuing a safety communication…
FDA approves new treatment for rare bile acid synthesis disorders
On March 17, the U.S. Food and Drug Administration (FDA) approved Cholbam (cholic acid) capsules, the first FDA-approved treatment for pediatric and adult patients…
Radial approach safer than femoral for coronary angiogram
Patients undergoing coronary angiography have a significantly lower risk of major bleeding and mortality if the procedure is performed by using the radial, instead…
FDA releases guidance on reprocessing reusable medical devices
On March 12, the U.S. Food and Drug Administration (FDA) released guidance that includes recommendations medical device manufacturers should follow for the safe and…
RDA for vitamin D may be too low
According to researchers, the Recommended Dietary Allowance (RDA) for vitamin D, from the National Academy of Sciences Institute of Medicine, is underestimated by a…
FDA approves CPR devices
On March 9 the U.S. Food and Drug Administration (FDA) approved the ResQCPR System, a system of two devices for first responders to use…
FDA approves generic Abilify
On April 28, the U.S. Food and Drug Administration (FDA) approved the first generic versions of Abilify (aripiprazole). Read more.
Variation in mortality
Compared to Whites, Blacks had lower risk adjusted mortality rates for several medical conditions and for abdominal aortic aneurysm repair, according to…
Elevated upper body position after childbirth improve respiratory safety
An elevated upper body position might improve respiratory safety in women early after childbirth without impairing sleep quality, according to a study…
Twitter can help predict asthma-related ED visits
Researchers have created a model to predict approximately how many asthma sufferers would visit the ED at a large hospital in Dallas…
2015 top patient safety concerns
Alarm hazards top the “Top 10 Patient Safety Concerns for Healthcare Organizations,” released by ECRI Institute. Data integrity and managing patient violence…
FDA approves new test for diagnosing gastroparesis.
On April 6, the U.S. Food and Drug Administration (FDA) approved Gastric Emptying Breath Test (GEBT), a new noninvasive test to help…
Infections associated with reprocessed duodenoscopes
The U.S. Food and Drug Administration (FDA) has taken several steps in response to infections associated with reprocessed duodenoscopes, including issuing a…
FDA approves new treatment for rare bile acid synthesis disorders
On March 17, the U.S. Food and Drug Administration (FDA) approved Cholbam (cholic acid) capsules, the first FDA-approved treatment for pediatric and…
Radial approach safer than femoral for coronary angiogram
Patients undergoing coronary angiography have a significantly lower risk of major bleeding and mortality if the procedure is performed by using the…
FDA releases guidance on reprocessing reusable medical devices
On March 12, the U.S. Food and Drug Administration (FDA) released guidance that includes recommendations medical device manufacturers should follow for the…
RDA for vitamin D may be too low
According to researchers, the Recommended Dietary Allowance (RDA) for vitamin D, from the National Academy of Sciences Institute of Medicine, is underestimated…
FDA approves CPR devices
On March 9 the U.S. Food and Drug Administration (FDA) approved the ResQCPR System, a system of two devices for first responders…
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