La FDA finaliza la transición para recomendar una evaluación de riesgos individual a fin de determinar la elegibilidad para donaciones de sangre

In English  SILVER SPRING, Md., 11 de mayo de 2023 /PRNewswire-HISPANIC PR WIRE/ — Hoy, la Administración de Alimentos y Medicamentos de Estados Unidos (FDA, por sus siglas en inglés) finalizó las recomendaciones para evaluar la elegibilidad de los donantes de sangre mediante un conjunto de preguntas individuales basadas en el riesgo para reducir el riesgo … Read more

FDA Approves First Drug to Treat Agitation Symptoms Associated with Dementia due to Alzheimer’s Disease

SILVER SPRING, Md., May 11, 2023 /PRNewswire/ — Today, the U.S. Food and Drug Administration is announcing the supplemental approval of Rexulti (brexpiprazole) oral tablets for the treatment of agitation associated with dementia due to Alzheimer’s disease. This is the first FDA-approved treatment option for this indication. “Agitation is one of the most common and challenging aspects … Read more

FDA Finalizes Move to Recommend Individual Risk Assessment to Determine Eligibility for Blood Donations

SILVER SPRING, Md., May 11, 2023 /PRNewswire/ — Today, the U.S. Food and Drug Administration finalized recommendations for assessing blood donor eligibility using a set of individual risk-based questions to reduce the risk of transfusion-transmitted HIV. These questions will be the same for every donor, regardless of sexual orientation, sex or gender. Blood establishments may … Read more