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PUBMED FOR HANDHELDS

Journal Abstract Search


634 related items for PubMed ID: 7859239

  • 1. Effect of meals and dosage-form modification on theophylline bioavailability from a 24-hour sustained-release delivery system.
    González MA, Straughan AB.
    Clin Ther; 1994; 16(5):804-14. PubMed ID: 7859239
    [Abstract] [Full Text] [Related]

  • 2. Pharmacokinetic comparison of a once-daily and twice-daily theophylline delivery system.
    González MA, Kisicki J, Straughn AB.
    Clin Ther; 1994; 16(4):686-92. PubMed ID: 7982257
    [Abstract] [Full Text] [Related]

  • 3. Biopharmaceutic characteristics of a new extended-release theophylline formulation (Uni-Dur).
    Oosterhuis B, Brannan MD, Groen H, Peeters PA, Hempenius J, Radwanski E, Nomeir AA, Affrime MB, Jonkman JH.
    Ann Allergy Asthma Immunol; 1995 Aug; 75(2):157-61. PubMed ID: 7648380
    [Abstract] [Full Text] [Related]

  • 4. Evaluation of the effect of 3 different diets on the bioavailability of 2 sustained release theophylline matrix tablets.
    Gai MN, Isla A, Andonaegui MT, Thielemann AM, Seitz C.
    Int J Clin Pharmacol Ther; 1997 Dec; 35(12):565-71. PubMed ID: 9455715
    [Abstract] [Full Text] [Related]

  • 5. Effect of food on bioavailability and pharmacokinetics of theophylline following administration of two sustained release dosage forms: Part I.
    Ohmori N, Inotsume N, Matsukura M, Higashi A, Iwaoku R, Tobino Y, Nakano M, Matsuda I.
    Int J Clin Pharmacol Ther Toxicol; 1986 Mar; 24(3):148-52. PubMed ID: 3699941
    [Abstract] [Full Text] [Related]

  • 6. Assessment of the bioequivalence of two formulations of clarithromycin extended-release 500-mg tablets under fasting and fed conditions: a single-dose, randomized, open-label, two-period, two-way crossover study in healthy Jordanian male volunteers.
    Alkhalidi BA, Tamimi JJ, Salem II, Ibrahim H, Sallam AA.
    Clin Ther; 2008 Oct; 30(10):1831-43. PubMed ID: 19014838
    [Abstract] [Full Text] [Related]

  • 7. Relative bioavailability of tizanidine 4-mg capsule and tablet formulations after a standardized high-fat meal: a single-dose, randomized, open-label, crossover study in healthy subjects.
    Henney HR, Shah J.
    Clin Ther; 2007 Apr; 29(4):661-9. PubMed ID: 17617289
    [Abstract] [Full Text] [Related]

  • 8. Comparative steady-state bioavailability of sustained-release theophylline preparations: Theo-Dur, Uni-Dur and Xanthium.
    Rojanasthien N, Kovjiriyapan K, Manorot M, Pothirat C.
    Asian Pac J Allergy Immunol; 2001 Jun; 19(2):69-78. PubMed ID: 11699723
    [Abstract] [Full Text] [Related]

  • 9. Influence of food on the rate and extent of absorption of theophylline after single dose oral administration of a controlled release tablet.
    Lagas M, Jonkman JH.
    Int J Clin Pharmacol Ther Toxicol; 1985 Aug; 23(8):424-6. PubMed ID: 4044074
    [Abstract] [Full Text] [Related]

  • 10. Steady-state pharmacokinetic properties of a 24-hour prolonged-release formulation of ropinirole: results of two randomized studies in patients with Parkinson's disease.
    Tompson DJ, Vearer D.
    Clin Ther; 2007 Dec; 29(12):2654-66. PubMed ID: 18201581
    [Abstract] [Full Text] [Related]

  • 11. Therapeutic equivalence of a generic slow-release theophylline tablet.
    Hendeles L, Breton AL, Beaty R, Harman E.
    Pharmacotherapy; 1995 Dec; 15(1):26-35. PubMed ID: 7739942
    [Abstract] [Full Text] [Related]

  • 12. Comparative steady-state bioavailability of Theo-24 and Theo-Dur in healthy men.
    Dockhorn RJ, Cefali EA, Straughn AB.
    Ann Allergy; 1994 Mar; 72(3):218-22. PubMed ID: 8129214
    [Abstract] [Full Text] [Related]

  • 13. Study of bioavailability and pharmacokinetics of theophylline following administration of two sustained release dosage forms as assessed by salivary data: Part II.
    Ohmori N, Inotsume N, Matsukura M, Higashi A, Iwaoku R, Tobino Y, Nakano M, Matsuda I.
    Int J Clin Pharmacol Ther Toxicol; 1986 Apr; 24(4):196-201. PubMed ID: 3710632
    [Abstract] [Full Text] [Related]

  • 14. Pharmacokinetic profile of a new sustained-release theophylline pellet formulation for once-daily evening administration.
    Steinijans VW, Sauter R, Böhm A, Staudinger H.
    Arzneimittelforschung; 1988 Aug; 38(8A):1241-50. PubMed ID: 3190813
    [Abstract] [Full Text] [Related]

  • 15. A single-dose, two-way crossover, bioequivalence study of dexmethylphenidate HCl with and without food in healthy subjects.
    Teo SK, Scheffler MR, Wu A, Stirling DI, Thomas SD, Stypinski D, Khetani VD.
    J Clin Pharmacol; 2004 Feb; 44(2):173-8. PubMed ID: 14747426
    [Abstract] [Full Text] [Related]

  • 16. NTP Toxicology and Carcinogenesis Studies of Theophylline (CAS No. 58-55-9) in F344/N Rats and B6C3F1 Mice (Feed and Gavage Studies).
    National Toxicology Program .
    Natl Toxicol Program Tech Rep Ser; 1998 Aug; 473():1-326. PubMed ID: 12571677
    [Abstract] [Full Text] [Related]

  • 17. Bioequivalence of a new sustained-release formulation of sodium valproate, valproate modified-release granules, compared with existing sustained-release formulations after once- or twice-daily administration.
    Dulac O, Alvarez JC.
    Pharmacotherapy; 2005 Jan; 25(1):35-41. PubMed ID: 15767218
    [Abstract] [Full Text] [Related]

  • 18. Absorption of theophylline from conventional and sustained-release tablets.
    Mellstrand T, Svedmyr N, Fagerström PO.
    Eur J Respir Dis Suppl; 1980 Jan; 109():54-60. PubMed ID: 6934088
    [Abstract] [Full Text] [Related]

  • 19. [The effect of food on theophylline absorption].
    Pabst G, Weber W, Müller M, Barkworth MF.
    Arzneimittelforschung; 1998 May; 48(5A):569-73. PubMed ID: 9676346
    [Abstract] [Full Text] [Related]

  • 20. Pharmacokinetic properties of combination oxycodone plus racemic ibuprofen: two randomized, open-label, crossover studies in healthy adult volunteers.
    Kapil R, Nolting A, Roy P, Fiske W, Benedek I, Abramowitz W.
    Clin Ther; 2004 Dec; 26(12):2015-25. PubMed ID: 15823765
    [Abstract] [Full Text] [Related]


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