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Journal Abstract Search


635 related items for PubMed ID: 18343242

  • 1. Comparison of two marketed nifedipine modified-release formulations: an exploratory clinical food interaction study.
    Wonnemann M, Schug B, Anschütz M, Brendel E, De Nucci G, Blume H.
    Clin Ther; 2008 Jan; 30(1):48-58. PubMed ID: 18343242
    [Abstract] [Full Text] [Related]

  • 2. Dosage form-related food interaction observed in a marketed once-daily nifedipine formulation after a high-fat American breakfast.
    Schug BS, Brendel E, Wonnemann M, Wolf D, Wargenau M, Dingler A, Blume HH.
    Eur J Clin Pharmacol; 2002 May; 58(2):119-25. PubMed ID: 12012144
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Bioavailability of two oral suspension and two oral tablet formulations of acyclovir 400 mg: two single-dose, open-label, randomized, two-period crossover comparisons in healthy Mexican adult subjects.
    Palma-Aguirre JA, Absalón-Reyes JA, Novoa-Heckel G, de Lago A, Oliva I, Rodríguez Z, González-de la Parra M, Burke-Fraga V, Namur S.
    Clin Ther; 2007 Jun; 29(6):1146-52. PubMed ID: 17692728
    [Abstract] [Full Text] [Related]

  • 5. Bioavailability of two oral-tablet and two oral-suspension formulations of naproxen sodium/paracetamol (acetaminophen): single-dose, randomized, open-label, two-period crossover comparisons in healthy Mexican adult subjects.
    Palma-Aguirre JA, Villalpando-Hernández J, Novoa-Heckel G, Oliva I, Cariño L, López-Bojórquez E, Burke-Fraga V, Namur S, González-de la Parra M.
    Clin Ther; 2009 Feb; 31(2):399-410. PubMed ID: 19302912
    [Abstract] [Full Text] [Related]

  • 6. Single-dose relative bioavailability of a new quetiapine fumarate extended-release formulation: a postprandial, randomized, open-label, two-period crossover study in healthy Uruguayan volunteers.
    Estevez-Carrizo FE, Parrillo S, Ercoli MC, Estevez-Parrillo FT.
    Clin Ther; 2011 Jun; 33(6):738-45. PubMed ID: 21704238
    [Abstract] [Full Text] [Related]

  • 7. Bioequivalence of a single 10-mg dose of finasteride 5-mg oral disintegrating tablets and standard tablets in healthy adult male Han Chinese volunteers: a randomized sequence, open-label, two-way crossover study.
    Chen L, Jiang X, Huang L, Lan K, Wang H, Hu L, Ren J, Li X, Zou Q.
    Clin Ther; 2009 Oct; 31(10):2242-8. PubMed ID: 19922895
    [Abstract] [Full Text] [Related]

  • 8. Differences in bioavailability between 60 mg of nifedipine osmotic push-pull systems after fasted and fed administration.
    Anschütz M, Wonnemann M, Schug B, Toal C, Donath F, Pontius A, Pauli K, Brendel E, Blume H.
    Int J Clin Pharmacol Ther; 2010 Feb; 48(2):158-70. PubMed ID: 20137768
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Bioavailability of two oral formulations of a single dose of levofloxacin 500 mg: an open-label, randomized, two-period crossover comparison in healthy Mexican volunteers.
    Galan-Herrera JF, Poo JL, Rosales-Sanchez O, Fuentes-Fuentes E, Cariño L, Burke-Fraga V, Namur S, Parra MG.
    Clin Ther; 2009 Aug; 31(8):1796-803. PubMed ID: 19808138
    [Abstract] [Full Text] [Related]

  • 11. A phase I, randomized, open-label, crossover study of the single-dose pharmacokinetic properties of guanfacine extended-release 1-, 2-, and 4-mg tablets in healthy adults.
    Swearingen D, Pennick M, Shojaei A, Lyne A, Fiske K.
    Clin Ther; 2007 Apr; 29(4):617-25. PubMed ID: 17617285
    [Abstract] [Full Text] [Related]

  • 12. Significant food interactions observed with a nifedipine modified-release formulation marketed in the European Union.
    Wonnemann M, Schug B, Schmücker K, Brendel E, van Zwieten PA, Blume H.
    Int J Clin Pharmacol Ther; 2006 Jan; 44(1):38-48. PubMed ID: 16425970
    [Abstract] [Full Text] [Related]

  • 13. Bioequivalence of two levothyroxine tablet formulations without and with mathematical adjustment for basal thyroxine levels in healthy Argentinian volunteers: a single-dose, randomized, open-label, crossover study.
    Di Girolamo G, Keller GA, de Los Santos AR, Schere D, Gonzalez CD.
    Clin Ther; 2008 Nov; 30(11):2015-23. PubMed ID: 19108789
    [Abstract] [Full Text] [Related]

  • 14. Bioavailability of two oral formulations of loratadine 20 mg with concomitant ketoconazole: an open-label, randomized, two-period crossover comparison in healthy Mexican adult volunteers.
    Piñeyro-López A, Pineyro-Garza E, Torres-Alanís O, Reyes-Araiza R, Gómez Silva M, Wacksman N, Lujàn Rangel R, de Lago A, Trejo D, Gonzàlez-de la Parra M, Namur S.
    Clin Ther; 2006 Jan; 28(1):110-5. PubMed ID: 16490584
    [Abstract] [Full Text] [Related]

  • 15. [Role of food interaction pharmacokinetic studies in drug development. Food interaction studies of theophylline and nifedipine retard and buspirone tablets].
    Drabant S, Klebovich I, Gachályi B, Renczes G, Farsang C.
    Acta Pharm Hung; 1998 Sep; 68(5):294-306. PubMed ID: 9805816
    [Abstract] [Full Text] [Related]

  • 16. Relative bioavailability of sapropterin from intact and dissolved sapropterin dihydrochloride tablets and the effects of food: a randomized, open-label, crossover study in healthy adults.
    Musson DG, Kramer WG, Foehr ED, Bieberdorf FA, Hornfeldt CS, Kim SS, Dorenbaum A.
    Clin Ther; 2010 Feb; 32(2):338-46. PubMed ID: 20206791
    [Abstract] [Full Text] [Related]

  • 17. Pharmacokinetics of a once-daily extended-release formulation of pramipexole in healthy male volunteers: three studies.
    Jenner P, Könen-Bergmann M, Schepers C, Haertter S.
    Clin Ther; 2009 Nov; 31(11):2698-711. PubMed ID: 20110012
    [Abstract] [Full Text] [Related]

  • 18. Bioavailability and bioequivalence of two oral formulations of alendronate sodium 70 mg: an open-label, randomized, two-period crossover comparison in healthy Korean adult male volunteers.
    Rhim SY, Park JH, Park YS, Lee MH, Kim DS, Shaw LM, Yang SC, Kang JS.
    Clin Ther; 2009 May; 31(5):1037-45. PubMed ID: 19539104
    [Abstract] [Full Text] [Related]

  • 19. In vitro dissolution and in vivo oral absorption of methylphenidate from a bimodal release formulation in healthy volunteers.
    Wang Y, Lee L, Somma R, Thompson G, Bakhtiar R, Lee J, Rekhi GS, Lau H, Sedek G, Hossain M.
    Biopharm Drug Dispos; 2004 Mar; 25(2):91-8. PubMed ID: 14872557
    [Abstract] [Full Text] [Related]

  • 20. Determination of nifedipine in human plasma and its use in bioequivalence study.
    Guo Y, Dai J, Qian G, Guo N, Ma Z, Guo X.
    Int J Pharm; 2007 Aug 16; 341(1-2):91-6. PubMed ID: 17507190
    [Abstract] [Full Text] [Related]


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