The Medical Letter TML n. 12 / 2025
Nr. 12 del 09/06/2025TML n. 12 / 2025 Uno IUD al rame a dosaggio ridotto
Miudella (Sebela in USA; non disponibile in commercio in Italia), un dispositivo intrauterino (Intrauterine Device, IUD) al rame, è stato approvato dalla US Food and Drug Administration (FDA) per la...
TML n. 12 / 2025 Un esame del sangue per lo screening del cancro colorettale
La US Food and Drug Administration (FDA) ha approvato Shield, un test del DNA per lo screening del cancro colorettale (CRC) negli adulti a rischio medio, di età ≥45 anni. Shield è il secondo test...
TML n. 12 / 2025 Guselkumab - Un antagonista dell'IL-23 per la malattia di Crohn
L'antagonista iniettabile dell'interleuchina (IL)-23 guselkumab (Tremfya - Janssen Cilag; farmaco ospedaliero esitabile) è stato ora approvato dalla US Food and Drug Administration (FDA) per il...
TML n. 12 / 2025 Prevenzione del morbillo
Secondo i Centers for Disease Control (CDC) americani, al 15 maggio 2025 sono stati confermati 1024 casi di morbillo negli Stati Uniti; l'11% dei casi ha comportato il ricovero in ospedale e tre...
TML n. 12 / 2025 Programma REMS e clozapina: un aggiornamento
La US Food and Drug Administration (FDA) ha annunciato che i prescrittori, le farmacie e i pazienti non sono più tenuti, negli Stati Uniti, a partecipare al programma REMS (Risk Evaluation and...
TML n. 12 / 2025 Un biosimilare dell'omalizumab intercambiabile con Xolair
Omlyclo (omalizumab), un prodotto biosimilare intercambiabile con l'anticorpo monoclonale ricombinante anti-IgE Xolair (Novartis Farma), è stato approvato dalla US Food and Drug Administration (FDA)...
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