Componente que se encarga de estabilizar el fármaco para evitar su alteración
Eje que compone la curva farmacocinética que permite hablar de la cantidad de fármaco en sangre
Forma farmacéutica que tiene un vehículo lipídico en mayor proporción que el vehículo acuoso
Nombre del proceso o fase donde se logra aumento de la hidrosoloubilidad de un fármaco para aumentar su metabolización
Nombre del fármaco que, a pesar de saturar todos sus receptores diana, no logra provocar un efecto máximo
Factor que condiciona la biodisponibilidad del fármaco al tener igual estructura química que él, pero que presenta diferente ubicación espacial
Cantidad del fármaco que llega a la circulación sistèmica después de que se realice el proceso de absorción
Molécula inactiva que necesita un proceso de metabolización y/o activación para poder cumplir una función terapéutica
Fármaco de vía oral que presenta gran contenido de alcohol
Factor que modifica el metabolismo de un fármaco debido al déficit de ingesta de proteínas que impide la formación de enzimas que lleven a cabo dicho proceso.
La rifampicina es un fármaco altamente liposoluble, para su excreción el cuerpo necesita disminuir el ph del túbulo contorneado distal, esto con el objetivo de disminuir su reabsorción, ¿Cómo se denomina este proceso?
Verticales
Factor que condiciona la absorción del medicamento mediante una posible ionización del fármaco
Nombre de la vía donde solo se usan fármacos liposolubles y no hay absorción del medicamento ya que se pretende que este quede sobre la piel
Valor de concentración en la que puede variar un fármaco, siempre y cuando este tenga efecto biológico positivo sin causar daño en el paciente
Zona del cuerpo donde se dificulta la distribución del fármaco debido a la ausencia de perfusión sanguínea
Factor que condiciona la absorción del fármaco debido a la capacidad de que este se disuelva en determinada sustancia.
Después de la unión del fármaco a las proteínas tisulares hay un secuestro en vasos sanguíneos, ¿Cómo se le denomina a la inversión del gradiente del fármaco que causa que este se acumule en mayor cantidad en el tejido que en sangre?
Vía de administración que permite usar fármacos en vehículos acuosos y lipídicos pero solo en pequeñas cantidades
Cantidad de medicamento que es necesario especificar en la prescripción médica
Magnitud del efecto del fármaco que depende de la velocidad de asociación y disociación de este sus receptores diana
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