Absolute bioavailability and metabolic disposition of valaciclovir, the L-valyl ester of acyclovir, following oral administration to humans.

Ítems similars

• Lack of interaction between valaciclovir, the L-valyl ester of aciclovir, and digoxin
  per: Soul-Lawton, J H, et al.
  Publicat: (1998)
• Phase I trial of valaciclovir, the L-valyl ester of acyclovir, in patients with advanced human immunodeficiency virus disease.
  per: Jacobson, M A, et al.
  Publicat: (1994)
• The absolute bioavailability and metabolic disposition of the novel antimigraine compound zolmitriptan (311C90)
  per: Seaber, E., et al.
  Publicat: (1997)
• Multiple Interactions of Cimetidine and Probenecid with Valaciclovir and Its Metabolite Acyclovir
  per: De Bony, F., et al.
  Publicat: (2002)
• Absolute oral bioavailability and disposition kinetics of puerarin in female rats
  per: Anukunwithaya, Tosapol, et al.
  Publicat: (2018)