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https://repository.unad.edu.co/handle/10596/44646Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.advisor | Castro Espinosa, Jobany | |
| dc.coverage.spatial | cead_-_medellín | |
| dc.creator | Vásquez, Dalila | |
| dc.creator | Álvarez, Fernanda | |
| dc.creator | Uribe, Juan Diego | |
| dc.creator | Asprilla, Jaida | |
| dc.creator | Castro, Yuliana | |
| dc.date.accessioned | 2022-01-18T14:04:16Z | |
| dc.date.available | 2022-01-18T14:04:16Z | |
| dc.date.created | 2021-12-29 | |
| dc.identifier.uri | https://repository.unad.edu.co/handle/10596/44646 | |
| dc.description.abstract | La farmacovigilancia es una disciplina que se encarga de evaluar, detectar, y prevenir los efectos adversos de los medicamentos o cualquier otro problema que se relacione con estos. (Calderón-Ospina, 2011) En Colombia el programa está al cuidado del INVIMA. La primordial finalidad de dicho plan es ejecutar la observación después del comercio del fármaco, con el fin de determinar la seguridad de estos; es importante mencionar que gracias a este programa se han retirado del mercado medicamentos que ponían en riesgo la salud de los colombianos. (Calderón-Ospina, 2011pg. 57) Los eventos adversos de los medicamentos son los efectos indeseables e inesperados de estos y que se asocian con su uso, por lo que se puede decir que la importancia de la farmacovigilancia radica, en prevenir e identificar los eventos adversos teniendo en cuenta la categorización de estas complicaciones las cuales pueden ser: posibles, probables y definitivas, las cuales pueden examinarse e interpretarse acorde al nivel de complejidad (leve, moderado, severo o letal). En farmacovigilancia, las RAM se basan en reportes para ser estudiados y estos se catalogan en graves o no graves, y se define si tienen o no las características establecidas para un evento adverso, si este se debe o no a una interacción medicamentosas; Las interacciones farmacológicas se dividen en farmacocinéticas y farmacodinamias, y es donde se procede a realizar una evaluación en lo que se refiere a la seguridad y efectividad de los tratamientos farmacológicos antes de su venta. | |
| dc.format | ||
| dc.title | Generalidades de la Farmacovigilancia | spa |
| dc.type | Diplomado de profundización para grado | |
| dc.subject.keywords | Farmacovigilancia | spa |
| dc.subject.keywords | Reacciones adversas | spa |
| dc.subject.keywords | Interacciones medicamentosas | spa |
| dc.subject.keywords | Seguridad | spa |
| dc.description.abstractenglish | Pharmacovigilance is a discipline that is responsible for evaluating, detecting, and preventing the adverse effects of medicines or any other problems that relate to them. (Calderón-Ospina, 2011) In Colombia, the programme is run by INVIMA. The primary purpose of this plan is to implement post-trade monitoring of the drug in order to determine the safety of the drug; it is important to mention that thanks to this program medicines that put the health of Colombians at risk have been withdrawn from the market. (Calderón-Ospina, 2011pg. 57) Adverse events of medicines are the undesirable and unexpected effects of these and are associated with their use, so it can be said that the importance of pharmacovigilance lies, to prevent and identify adverse events taking into account the categorization of these complications which may be: possible, probable and definitive, which may be examined and interpreted according to the level of complexity (mild, moderate, severe or lethal). In pharmacovigilance, AMR is based on reports to be studied and these are classified as serious or not serious, and it is defined whether or not they have the characteristics established for an adverse event, whether or not it is due to a drug interaction; Pharmacological interactions are divided into pharmacokinetics and pharmacodynamics, and it is where an evaluation is carried out with regard to the safety and effectiveness of pharmacological treatments before their sale. | |
| dc.subject.category | Cultura política | |
| Appears in Collections: | Diplomado de Farmacovigilancia | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| jduribemu.pdf | 239.12 kB | Adobe PDF | ![]() View/Open |
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