This Perspective discusses new FDA guidance for pulse oximeters that aims to reduce disparities in device performance related to skin pigment.
Risultati per: La FDA approva il sistema di riabilitazione dell’ictus
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Aritmie, ad Ancona il sistema innovativo di ablazione con Affera
Rapidità, sicurezza, efficacia. Primo ospedale pubblico a usarla
Aritmie, ad Ancona il sistema innovativo di ablazione con Affera
Rapidità, sicurezza, efficacia. Primo ospedale pubblico a usarla
FDA Approval of Obecabtagene Autoleucel for B-Cell Acute Lymphoblastic Leukemia
This JAMA Insights discusses the recent FDA approval of obecabtagene autoleucel for adults with relapsed or refractory B-cell acute lymphoblastic leukemia and provides regulatory considerations.
FDA Approves First Fast-Acting Insulin Biosimilar for Diabetes
The US Food and Drug Administration (FDA) recently approved the rapid-acting human insulin analog insulin-aspart-szjj, marketed as Merilog, as a biosimilar to insulin aspart (Novolog).
Suzetrigine, a New Nonopioid Pain Medication, Gains U.S. FDA Approval
So far, studies suggest modest benefits for acute postoperative pain, but many questions remain.
FDA Approves Semaglutide to Reduce Risk of Kidney Disease Progression
Semaglutide, marketed as Ozempic, recently became the first glucagon-like peptide 1 (GLP-1) receptor agonist approved by the US Food and Drug Administration (FDA) to reduce the risk of worsening kidney disease, kidney failure, and death due to cardiovascular disease in adults with type 2 diabetes (T2D) and chronic kidney disease (CKD), a common complication of T2D.
Antidiabete che fa anche dimagrire riduce infarti e ictus
Ampio studio sul New England, protegge il cuore anche in pillola
Melanoma e tumore del polmone, Aifa approva l'immunoterapia in fase precoce
Ok alla rimborsabilità negli stadi iniziali della malattia, può aumentare le guarigioni
Per riabilitazione bambini giochi high-tech e realtà virtuale
Al Don Gnocchi Firenze il Computer assisted rehabilitation lab
FDA Authorizes Marketing of ZYN Nicotine Pouch Products
The US Food and Drug Administration (FDA) recently authorized the marketing of 20 ZYN nicotine pouch products, the first of their kind to receive such approval. The decision followed an extensive scientific review that concluded that the benefits of these cigarette alternatives outweighed the risks, in line with the public health standards set by the 2009 Family Smoking Prevention and Tobacco Control Act.
FDA Issues Warning of Guillain-Barré Syndrome Risk for 2 RSV Vaccines
The respiratory syncytial virus (RSV) vaccines marketed as Abrysvo by Pfizer and Arexvy by GSK will now require a warning about the risk of Guillain-Barré syndrome (GBS), the US Food and Drug Administration (FDA) announced recently.
Diagnosi precoce dell'ictus, a Chieti c'è la Risonanza portatile
Prima in Italia, finanziata dal ministero della Salute
“Prevenzione Insieme!”, progetto in Valle d'Aosta sull'ictus
Sono previste sei giornate di screening gratuiti
Donare spesso il sangue migliora forma fisica sistema sanguigno
Aumenta le cellule ematiche vantaggiose,migliora i globuli rossi
Diabete, un sistema 'Smart' permetterà dosaggio preciso insulina
Invia notifiche tramite app in caso di dosi dimenticate