The Medical Letter n. 7 / 2021
Nr. 07 del 01/04/2021TML n.7 / 2021 BAMLANIVIMAB ED ETESEVIMAB PER LA COVID-19
La Food and Drug Administration (FDA) ha rilasciato l’autorizzazione all’uso d’emergenza (EUA) per gli anticorpi monoclonali sperimentali di Lilly bamlanivimab (LY-CoV555) ed etesevimab...
TML n.7 / 2021 ORIAHNN PER IL SANGUINAMENTO MESTRUALE ANOMALO ASSOCIATO A FIBROMA
La FDA ha approvato Oriahnn (Abbvie; non disponibile in commercio in Italia), una combinazione a dose fissa dell’antagonista del recettore dell’ormone di rilascio delle gonadotropine (GnRH)...
TML n.7 / 2021 SEMAGLUTIDE PER LA PERDITA DI PESO
In alcuni studi clinici di recente pubblicazione, l’iniezione sottocutanea una volta alla settimana dell’agonista del recettore del peptide 1 glucagone-simile (GLP-1) semaglutide (Ozempic-Novo...
TML n.7 / 2021 COLCHICINA A BASSO DOSAGGIO PER LA MALATTIA CORONARICA
La FDA ha approvato la colchicina, farmaco antinfiammatorio vecchio di secoli (Colchicina Lirca-Acarpia Farmaceutici), per la profilassi e il trattamento delle crisi di gotta e per il trattamento...
TML n.7 / 2021 IPERTENSIONE CON ERENUMAB
Nel 2018 la Food and Drug Administration (FDA) ha approvato l’antagonista del recettore del gene della calcitonina (CGRP), somministato per via sottocutanea una volta al mese, erenumab-aooe...
TML n.7 / 2021 ERRATA CORRIGE: VACCINO JOHNSON & JOHNSON PER LA COVID-19
Nel numero 6 del 15 marzo 2021, pag. 72, il testo del paragrafo “Effetti avversi” è il seguente con conseguente integrazione delle note EFFETTI AVVERSI – Nello studio ENSAMBLE sono stati...
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