Raloxifene Hydrochloride
Categoria
Raloxifene Hydrochloride Nombres de marca, Raloxifene Hydrochloride Analogos
Raloxifene Hydrochloride Marca los nombres de mezcla
Raloxifene Hydrochloride Formula quimica
C28H27NO4S
Raloxifene Hydrochloride RX enlace
http://www.rxlist.com/cgi/generic/raloxif.htm
Raloxifene Hydrochloride FDA hoja
Raloxifene Hydrochloride MSDS (hoja de seguridad de materiales)
Raloxifene Hydrochloride Sintesis de referencia
CD Jones et al., J. Med. Cem. 27, 1057 (1984)
Raloxifene Hydrochloride Peso molecular
473.584 g/mol
Raloxifene Hydrochloride Punto de fusion
143-147oC
Raloxifene Hydrochloride H2O Solubilidad
0.25 mg / L
Raloxifene Hydrochloride Estado
Solid
Raloxifene Hydrochloride LogP
5.749
Raloxifene Hydrochloride Formas de dosificacion
Tableta
Raloxifene Hydrochloride Indicacion
Para la prevención de la osteoporosis en mujeres post-menopáusicas
Raloxifene Hydrochloride Farmacologia
El raloxifeno, un modulador selectivo del receptor de estrógeno (SERM) de la clase benzotiofeno, es similar al tamoxifeno, ya que produce efectos similares al estrógeno en el hueso y el metabolismo lipídico, mientras que antagonizar los efectos del estrógeno sobre el tejido mamario. El raloxifeno disminuye la resorción ósea, aumenta la densidad mineral ósea (DMO) y disminuye la incidencia de fracturas. El raloxifeno se utiliza en la prevención de la menopausia la osteoporosis y el cáncer de mama.
Raloxifene Hydrochloride Absorcion
Aproximadamente el 60% de una dosis oral se absorbe, pero glucuronoconjugación presistémico es muy amplia. La biodisponibilidad absoluta de raloxifeno es del 2,0%
Raloxifene Hydrochloride Toxicidad
No hay información disponible
Raloxifene Hydrochloride Informacion de Pacientes
PATIENT INFORMATION
For safe and effective use of EVISTA, the physician should inform patients about the following:
Patient Immobilization: EVISTA should be discontinued at least 72 hours prior to and during prolonged immobilization
(e.g., post-surgical recovery, prolonged bed rest), and patients should be advised to avoid prolonged restrictions of
movement during travel because of the increased risk of venous thromboembolic events.
Hot flashes or flushes: EVISTA is not effective in reducing hot flashes or flushes associated with estrogen deficiency.
In some asymptomatic patients, hot flashes may occur upon beginning EVISTA therapy.
Other Preventive Measures: Patients should be instructed to take supplemental calcium and vitamin D, if daily dietary
intake is inadequate. Weight-bearing exercise should be considered along with the modification of certain behavioral
factors, such as cigarette smoking, and/or alcohol consumption, if these factors exist.
Physicians should instruct their patients to read the patient package insert before starting therapy with EVISTA and to
re-read it each time the prescription is renewed.
For safe and effective use of EVISTA, the physician should inform patients about the following:
Patient Immobilization: EVISTA should be discontinued at least 72 hours prior to and during prolonged immobilization
(e.g., post-surgical recovery, prolonged bed rest), and patients should be advised to avoid prolonged restrictions of
movement during travel because of the increased risk of venous thromboembolic events.
Hot flashes or flushes: EVISTA is not effective in reducing hot flashes or flushes associated with estrogen deficiency.
In some asymptomatic patients, hot flashes may occur upon beginning EVISTA therapy.
Other Preventive Measures: Patients should be instructed to take supplemental calcium and vitamin D, if daily dietary
intake is inadequate. Weight-bearing exercise should be considered along with the modification of certain behavioral
factors, such as cigarette smoking, and/or alcohol consumption, if these factors exist.
Physicians should instruct their patients to read the patient package insert before starting therapy with EVISTA and to
re-read it each time the prescription is renewed.
Raloxifene Hydrochloride Organismos afectados
Humanos y otros mamíferos
