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2001, Número 5

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Rev Fac Med UNAM 2001; 44 (5)


El resurgimiento de la talidomida

Sigala C, Nelle H, Halabe J
Texto completo Cómo citar este artículo

Idioma: Español
Referencias bibliográficas: 33
Paginas: 212-215
Archivo PDF: 35.53 Kb.


PALABRAS CLAVE

Sin palabras Clave

FRAGMENTO

La talidomida se sintetizó por primera vez en el ańo de 1954 por los laboratorios Chemie Grünenthal, en Alemania, con el nombre molecular de alfa-phtalyglutamic-acid-imida. Conocida por sus efectos sedantes e hipnóticos, y utilizada en el tratamiento del vómito asociado al primer trimestre del embarazo, a mediados de los 50 era la tercera droga más vendida, sin toxicidad entonces reconocida, ya que fue probada en ratones a dosis 10,000 mg/kg sin observar efectos colaterales fatales.1,2


REFERENCIAS (EN ESTE ARTÍCULO)

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  32. Vogelsang G, Farmer E, Hess A, Altamonte V et al. Thalidomide for the treatment of chronic graft-versus-host disease. NEJM 1992; 326(16): 1055-1058.

  33. Norfolk H, Bailey W et al. Thalidomide treatment for chronic graft-versus. Host disease. British Journal of Haematology 1991; 78: 23-227.




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