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NEPHARM: A pharmacokinetic database for adjusting drug dosage to impaired renal function

  • Keller F. 
  • Arnold R. 
  • Frankewitsch T. 
  • Zellner D. 
  • Giehl M. 
Posters
Part of the Lecture Notes in Computer Science book series (LNCS, volume 934)

References

  1. Benet LZ, Williams RL. Design and optimization of dosage regimens: pharmacokinetic data. In (Ed) Gilman AG, Rall RW, Nies AS, Taylor P. Goodman and Gilman's: The Pharmacological Basis of Therapeutics. Pergamon, New York 1990: 1650–1735Google Scholar
  2. Proost JH, Meijer DKF. MW/Pharm, an integrated software package for drug dosage regimen calculation and therapeutic drug monitoring. Comp Biol Med 1992, 22: 155–63CrossRefGoogle Scholar
  3. Sheiner LB, Rubin DB. Intention-to-treat analysis and the goals of clinical trials. Clin Pharmacol Therap 1995, 57: 6–15CrossRefGoogle Scholar
  4. Swanson DJ, Reitberg DP, Smith IL, Wels PB, Schentag JP. Steady-state moxalactam pharmacokinetics in patients: noncompartmental versus two-compartmental analysis. J Pharmacokinet Biopharm 1983, 11:337–353PubMedGoogle Scholar
  5. Wolter K, Claus M, Wagner K, Fritschka E. Teicoplanin pharmacokinetics and dosage recommendations in chronic hemodialysis patients and in patients undergoing continuous veno-venous hemodialysis. Clin Nephrol 1994, 42: 389–397PubMedGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1995

Authors and Affiliations

  • Keller F. 
    • 1
  • Arnold R. 
    • 1
  • Frankewitsch T. 
    • 1
  • Zellner D. 
    • 1
  • Giehl M. 
    • 1
    • 2
  1. 1.Medical Department, Division of NephrologyUniversity HospitalUlm
  2. 2.Body CounterUniversity Hospital Banjamin FranklinBerlin

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