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PUBMED FOR HANDHELDS

Journal Abstract Search


125 related items for PubMed ID: 7095920

  • 1. The bioavailability and kinetics of dihydroquinidine in patients with heart disease.
    Regazzi Bonora M, Salerno JA, Rondanelli R, Cristiani D, Chimienti M.
    Int J Clin Pharmacol Ther Toxicol; 1982 May; 20(5):212-8. PubMed ID: 7095920
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  • 2. Disposition kinetics of dihydroquinidine following quinidine administration.
    Ueda CT, Williamson BJ, Dzindzio BS.
    Res Commun Chem Pathol Pharmacol; 1976 Jun; 14(2):215-25. PubMed ID: 940955
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  • 6. Steady-state bioavailability of two sustained-release quinidine preparations: quinidine gluconate versus quinidine sulfate.
    Taggart WV, Holyoak W.
    Clin Ther; 1983 Jun; 5(4):357-64. PubMed ID: 6871920
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  • 7. Pharmacokinetics of dihydroquinidine in congestive heart failure patients after intravenous quinidine administration.
    Ueda CT, Dzindzio BS.
    Eur J Clin Pharmacol; 1979 Sep; 16(2):101-5. PubMed ID: 499305
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  • 8. Pharmacokinetics of hydroxy-3(S)-dihydroquinidine in healthy volunteers after intravenous and oral administration.
    Jaillon P, Poirier JM, Lecocq B, Jarreau C, Pays M, Richard MO, Cheymol G.
    Eur J Drug Metab Pharmacokinet; 1986 Sep; 11(3):233-8. PubMed ID: 3816879
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  • 11. Pharmacokinetics of tramadol and bioavailability of enteral tramadol formulations. 3rd Communication: suppositories.
    Lintz W, Barth H, Osterloh G, Schmidt-Böthelt E.
    Arzneimittelforschung; 1998 Sep; 48(9):889-99. PubMed ID: 9793614
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  • 12. Bioavailability of theophylline from a sustained-release aminophylline formulation (Euphyllin retard tablets)--plasma levels after single and multiple oral doses.
    Schuppan D, Molz KH, Staib AH, Rietbrock N.
    Int J Clin Pharmacol Ther Toxicol; 1981 May; 19(5):223-7. PubMed ID: 7251238
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  • 13. Pharmacokinetics of valproic acid obtained after administration of three oral formulations to humans.
    Bialer M, Hussein Z, Dubrovsky J, Raz I, Abramsky O.
    Isr J Med Sci; 1984 Jan; 20(1):46-9. PubMed ID: 6421770
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  • 15. Bioavailability of quinidine in slow-release form. A comparison between two preparations containing quinidine bisulphate as the active constituent.
    Regårdh CG, Johnsson G, Lundborg P, Perrson BA.
    Arzneimittelforschung; 1977 Jan; 27(9):1716-8. PubMed ID: 21671
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  • 16. Comparative bioavailability of a metoprolol controlled release formulation and a bisoprolol normal release tablet after single oral dose administration in healthy volunteers.
    Deroubaix X, Lins RL, Lens S, Demblon C, Jeanbaptiste B, Poelaert D, Stockis A.
    Int J Clin Pharmacol Ther; 1996 Feb; 34(2):61-70. PubMed ID: 8929748
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  • 18. Pharmacokinetics of etofylline after intravenous and oral administration to humans.
    Zuidema J, Verhoeven J, Merkus FW.
    Int J Clin Pharmacol Ther Toxicol; 1981 Jul; 19(7):310-3. PubMed ID: 7263108
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  • 20. [Pharmacokinetics and relative bioavailability of KC-404 sustained release tablets in healthy volunteers].
    Li T, Pang Y, Wang Z, Jia Y, Cheng Q, Sun J.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2003 Jul; 34(3):541-3. PubMed ID: 12910715
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