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Efficacy and safety of formoterol in Japanese patients with COPD.

Efficacy and safety of formoterol in Japanese patients with COPD. Research Abstract Details 

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  • Efficacy and safety of formoterol in Japanese patients with COPD. Abstract Text:

    yoshiaki minakataYoshiaki Minakata,hideya iijimaHideya Iijima,tsuneyuki takahashiTsuneyuki Takahashi,motohiko miuraMotohiko Miura,hiromasa ogawaHiromasa Ogawa,keiji kimuraKeiji Kimura,takeharu kogaTakeharu Koga,masaharu kinoshitaMasaharu Kinoshita,tohru tsudaTohru Tsuda,hisamichi aizawaHisamichi Aizawa,masakazu ichinoseMasakazu Ichinose,yoshiaki minakataYoshiaki Minakata,hideya iijimaHideya Iijima,tsuneyuki takahashiTsuneyuki Takahashi,motohiko miuraMotohiko Miura,hiromasa ogawaHiromasa Ogawa,keiji kimuraKeiji Kimura,takeharu kogaTakeharu Koga,masaharu kinoshitaMasaharu Kinoshita,tohru tsudaTohru Tsuda,hisamichi aizawaHisamichi Aizawa,masakazu ichinoseMasakazu Ichinose,

    OBJECTIVE: This study evaluated the efficacy and safety of the formoterol Turbuhaler at dosages of 4.5, 9 and 18 microg bid compared with placebo in Japanese patients with COPD. METHODS: In this randomized, double-blind, placebo-controlled, multicenter study, 36 patients with a pre-bronchodilator FEV(1) value within 40 to 70% of the predicted value were randomized to receive formoterol at doses of 4.5, 9, and 18 microg bid, and placebo, for 1 week in a crossover fashion. RESULTS: The primary outcome variable, one hour post-dose FEV(1) on the last day of the one week treatment period, was significantly higher for all formoterol dosages compared with placebo (p<0.001 for all doses); adjusted g-means for formoterol 4.5, 9 and 18 microg bid, and placebo, were 1.510 L, 1.491 L, 1.520 L and 1.342 L, respectively. All three dosages of formoterol also provided significantly better improvements than placebo in the secondary variables FVC, inspiratory capacity (IC) and morning and evening PEF. Results for IC and PEF indicated a trend towards a larger improvement at higher dosages. CONCLUSION: Treatment with formoterol at dosages of 4.5, 9 and 18 microg bid showed significantly superior effects to placebo on FEV(1) in Japanese patients with COPD. The results for some of the secondary variables (IC and PEF) indicated a trend towards larger improvements at higher dosages. All dosages of formoterol were well tolerated in Japanese patients.

    Efficacy and safety of formoterol in Japanese patients with COPD. Publishing Authors By Initials

    y minakataY Minakata,h iijimaH Iijima,t takahashiT Takahashi,m miuraM Miura,h ogawaH Ogawa,k kimuraK Kimura,t kogaT Koga,m kinoshitaM Kinoshita,t tsudaT Tsuda,h aizawaH Aizawa,m ichinoseM Ichinose,y minakataY Minakata,h iijimaH Iijima,t takahashiT Takahashi,m miuraM Miura,h ogawaH Ogawa,k kimuraK Kimura,t kogaT Koga,m kinoshitaM Kinoshita,t tsudaT Tsuda,h aizawaH Aizawa,m ichinoseM Ichinose,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Efficacy and safety of formoterol in Japanese patients with COPD. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Internal medicine (Tokyo, Japan)

    VOLUME: 47

    Page Numbers: 217-23

    Journal Abbreviation: Intern. Med.

    ISSN: 1349-7235

    DAY: 15

    MONTH: 02

    YEAR: 2008

    Efficacy and safety of formoterol in Japanese patients with COPD. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9204241

    Efficacy and safety of formoterol in Japanese patients with COPD. Keywords Mesh Terms:

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    Grant and Affiliation Information for Efficacy and safety of formoterol in Japanese patients with COPD.

    AFFILIATION: The Third Department of Internal Medicine, Wakayama Medical University, Wakayama, Japan. masakazu@wakayama-med.ac.jp

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: Intern Med

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