Inicialmente, la FDA autorizó en septiembre de 1998 los comprimidos de 200 mg del fármaco (en tres tomas diarias) para ser utilizado en combinación con otros antirretrovirales.
Se espera que la nueva formulación de este inhibidor de la proteasa constituya un régimen terapéutico más sencillo para los pacientes al suponer menor cantidad de comprimidos que debe tomar cada día, lo cual puede traducirse en un mejor cumplimiento del tratamiento.
Webs Relacionadas
Información sobre Sustiva (efavirenz)
http://www.sustiva.com/
FDA
http://www.fda.gov/
Bristol-Myers Squibb
http://www.bms.com/
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