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Plasma pharmacokinetics of sulfadiazine administered twice daily versus four times daily are similar in human immunodeficiency virus-infected patients.

AbstractThe pharmacokinetics of 2,000 mg of sulfadiazine administered twice daily (BID) versus those of 1,000 mg administered four times a day were compared in eight human immunodeficiency virus-infected patients. No differences in pharmacokinetic parameters were detected between the regimens. These data provide a pharmacokinetic rationale for BID dosing of sulfadiazine for the treatment and suppression of toxoplasmosis.
AuthorsM Kelli Jordan, Aaron H Burstein, Diane Rock-Kress, Raul M Alfaro, Alice K Pau, Joseph A Kovacs, Stephen C Piscitelli (Affiliation: Pharmacy Department, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.)
JournalAntimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 48 Issue 2 Pg. 635-7 (Feb 2004) ISSN: 0066-4804 United States
PMID14742225 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Anti-Infective Agents
  • Sulfadiazine
Topics
  • Anti-Infective Agents (administration & dosage, blood, pharmacokinetics)
  • Area Under Curve
  • Cross-Over Studies
  • HIV Infections (complications, metabolism)
  • Half-Life
  • Humans
  • Models, Biological
  • Sulfadiazine (administration & dosage, blood, pharmacokinetics)
  • Toxoplasmosis (drug therapy, etiology)