Monarch eTNS, a Bioelectronic Medical Device for Pediatric ADHD, Now Available
The device gained FDA approval in 2019 based on data from a placebo-controlled clinical trial that included 62 children with moderate to severe ADHD.
The device gained FDA approval in 2019 based on data from a placebo-controlled clinical trial that included 62 children with moderate to severe ADHD.
Pedmark is the first FDA-approved therapy indicated to reduce the risk of cisplatin-induced hearing loss in children.
Girls experienced more significant BMI increases than boys
Authors say tool can be incorporated for routine screening in primary care settings
Bivalent COVID-19 booster vaccines for children; wearable device to help treat fluid overload in adults with chronic heart failure; real-world data insights into molnupiravir efficacy; vaccine for the third trimester of pregnancy to prevent pertussis; and an FDA update on apomorphine infusion in Parkinson disease.
The bivalent Moderna and Pfizer-BioNTech COVID-19 Vaccines are authorized as a single booster dose at least 2 months after the primary or booster vaccination.
The sBLA is supported by data from the phase 3 FIREFLEYE and BUTTERFLEYE trials that evaluated the efficacy and safety aflibercept in infants with ROP.
Early use of steroids in children hospitalized for COVID-19 without MIS-C not associated with shorter length of stay
Effectiveness in preventing pertussis among infants younger than 2 months of age when administered during the third trimester of pregnancy was based on a reanalysis of data from an observational case-control study.