States that the Food and Drug Administration has approved a surgical procedure which is designed to combat snoring. Details on the estimated number of Americas that suffer from habitual snoring; Name of the procedure; Infor...
A week after Apple heldan event revealing its new iPhone, Apple Watch and AirPod models, the U.S. Food and Drug Administration has approved an Apple Watch function that can detect sleep apnea in device-wearers. The sleep apnea detection tool comes four days before the launch date of Apple...
Inspire has been approved for individuals with moderate or severe obstructive sleep apnea who are not able to use a Continuous Positive Airway Pressure (CPAP) device, the external mask that's often recommended for patients with the disorder. Many patients find the CPAP uncomfortable and don't use...
Galaxy Watch users in the United States can now access another health feature approved by the FDA. Reportedly, the sleep apnea detection feature was recently approved by the FDA for the Samsung Galaxy Watch. Samsung is the first company to receive approval for this feature in the US. In ...
Idorsia Ltd today announced that the FDA has approved Quviviq (daridorexant) 25 mg and 50 mg for the treatment of adult patients with insomnia, characterized by difficulties with sleep onset and/or sleep maintenance1.
OnabotulinumtoxinA Approved for Pediatric Neurogenic Detrusor Overactivity The treatment can be used in children aged 5 years or older that are intolerant of or do not respond well to anticholinergic medication. FDA Approves MRI Labeling for Genio Obstructive Sleep Apnea Therapy The Genio system offer...
“We are seeking additional companion diagnostic claims for FoundationOne Liquid CDx, which, if approved, would further enhance utility of the test in clinical practice,” Brian Alexander, MD, MPH, chief medical officer at Foundation Medicine. “Additionally, this test is an important tool for ...
have untreated, severe breathing problems during your sleep (sleep apnea) take certain medicines called monoamine oxidase (MAO) inhibitors (such as selegiline, phenelzine, linezolid) Talk to your healthcare provider before taking ZEPOSIA if you have any of these conditions or do not know if you ...
17 PATIENT COUNSELING INFORMATION Advise the patient to read the FDA-approved patient labeling (Medication Guide). Tell patients not to discontinue GILENYA without first discussing this with the prescribing physician. Advise patients to contact their physician if they accidently take more GILENYA than ...
The US Food and Drug Administration (FDA)today announcedit has approved label changes specifying new dosing for products containing zolpidem (Ambien,Ambien CR,andEdluar), all widely prescribed sleep medications, because of the known risk for next-morning impairment with these drugs. ...