FDA authorizes first commercial monkeypox test, pertussis vaccine for young infants
The Food and Drug Administration Friday authorized for the first commercial test kit to detect monkeypox in lesion swab specimens. Only laboratories certified under the Clinical Laboratory Improvement Amendments to perform moderate or high complexity tests are authorized to perform the Abbott Molecular test.
In other news, the FDA the first vaccine to administer to mothers during pregnancy to prevent whooping cough (pertussis) in infants under two months old. The Boostrix vaccine previously was approved to protect pregnant women, adults and children age 10 and older.
Related News Articles
Headline
The American College of Obstetricians and Gynecologists April 17 released guidance recommending a new approach to prenatal care delivery. The guidance calls…
Headline
The National Institutes of Health April 7 released a study that found twins — smaller at birth on average than singletons — develop slower in early pregnancy…
Headline
A National Institutes of Health study published April 2 found that blood pressure patterns observed during the first half of pregnancy can determine a woman's…
Headline
The U.S. birth rate fell 2% in 2023 to about 3.6 million, according to final data released March 18 by the Centers for Disease Control and Prevention. The…
Headline
A study by the Penn State Department of Nutritional Sciences found that low vitamin D levels in the first trimester of pregnancy are associated with higher…
Headline
The U.S. maternal mortality rate decreased to 18.6 deaths per 100,000 live births in 2023, down from 22.3 in 2022, according to new data from the Centers for…