Articles related to FDA

GE HealthCare’s Portrait Mobile, recently cleared by the FDA, offers a novel approach to patient monitoring, allowing continuous oversight without confining patients to their beds. Explore how this innovative technology could redefine hospital care practices.

The recent FDA approval of brexpiprazole for Alzheimer’s dementia patients has ignited concerns among healthcare professionals. Physicians are urged to carefully consider the drug’s minimal efficacy and increased mortality risk in their treatment decisions.

The FDA’s approval of Daxxify offers a promising new treatment for cervical dystonia. Explore the comprehensive clinical data that supports this peptide-formulated neuromodulator’s efficacy and safety profile.

The FDA’s recent approval of Akeega, a combination therapy for BRCA-mutated mCRPC, marks a significant advancement in targeted treatment. This approval, based on the MAGNITUDE study, offers a new therapeutic option for patients, supported by robust clinical data.

The FDA’s accelerated approval of elranatamab offers a new therapeutic pathway for adults with relapsed or refractory multiple myeloma. With promising response rates and an established safety profile, this treatment may provide a much-needed option for those struggling with relapsed myeloma.

The updated prescribing guidelines for Wegovy (semaglutide) offer new maintenance dosing options for adults, reflecting recent research findings.