Laboratory and clinical studies on S-1108
The efficacy and safety of the new ester-type oral cephem antibiotic S-1108 was studied in treating various infections. There were 20 subjects (13 males and 7 females) ranging in age from 29 to 77 years (mean age: 59.7 years). The target diseases included pneumonia in 5 cases, bronchitis in 2 cases,...
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Published in | CHEMOTHERAPY Vol. 41; no. Supplement1; pp. 321 - 325 |
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Main Authors | , , , |
Format | Journal Article |
Language | Japanese |
Published |
Japanese Society of Chemotherapy
30.06.1993
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Online Access | Get full text |
ISSN | 0009-3165 1884-5894 |
DOI | 10.11250/chemotherapy1953.41.Supplement1_321 |
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Abstract | The efficacy and safety of the new ester-type oral cephem antibiotic S-1108 was studied in treating various infections. There were 20 subjects (13 males and 7 females) ranging in age from 29 to 77 years (mean age: 59.7 years). The target diseases included pneumonia in 5 cases, bronchitis in 2 cases, acute exacerbation of chronic bronchitis in 4 cases, bronchial asthma+lower respiratory infection in 2 cases, bronchiectasis and acute exacerbation of chronic pulmonary emphysema in 2 cases, upper respiratory tract infection in 3 cases, and periproctitis and cystitis in 1 case each, for a total of 20 cases. S-1108 was administered 3 times daily in doses of 100 mg, and the treatment period ranged from 3 to 25 days (mean 10.5days). S-1108 was judged effective in 14 cases, fair in 3 cases, poor in 2 cases, and in 1 case was unevaluable, for an efficacy rate of 73.7%. In 7 of the 8 cases evaluated for bacteriological efficacy the bacteria were eliminated. Side effects consisted of dizziness in 1 patient. No abnormal changes in laboratory findings were observed. |
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AbstractList | The efficacy and safety of the new ester-type oral cephem antibiotic S-1108 was studied in treating various infections. There were 20 subjects (13 males and 7 females) ranging in age from 29 to 77 years (mean age: 59.7 years). The target diseases included pneumonia in 5 cases, bronchitis in 2 cases, acute exacerbation of chronic bronchitis in 4 cases, bronchial asthma+lower respiratory infection in 2 cases, bronchiectasis and acute exacerbation of chronic pulmonary emphysema in 2 cases, upper respiratory tract infection in 3 cases, and periproctitis and cystitis in 1 case each, for a total of 20 cases. S-1108 was administered 3 times daily in doses of 100 mg, and the treatment period ranged from 3 to 25 days (mean 10.5days). S-1108 was judged effective in 14 cases, fair in 3 cases, poor in 2 cases, and in 1 case was unevaluable, for an efficacy rate of 73.7%. In 7 of the 8 cases evaluated for bacteriological efficacy the bacteria were eliminated. Side effects consisted of dizziness in 1 patient. No abnormal changes in laboratory findings were observed. |
Author | Arita, Kenichi Daido, Kazuhiro Yamakido, Michio Hozawa, Soichiro |
Author_xml | – sequence: 1 fullname: Arita, Kenichi organization: Division of Respiratory Disease, Hiroshima Red Cross Hospital & Atomic Bomb Survivors Hospital – sequence: 1 fullname: Daido, Kazuhiro organization: Division of Respiratory Disease, Hiroshima Red Cross Hospital & Atomic Bomb Survivors Hospital – sequence: 1 fullname: Yamakido, Michio organization: Second Department of Internal Medicine, Hiroshima University School of Medicine – sequence: 1 fullname: Hozawa, Soichiro organization: Second Department of Internal Medicine, Hiroshima University School of Medicine |
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References | 2) 由良二郎, 齋藤篤: 第40回日本化学療法学会総会, 新薬シンポジウム. S-1108, 名古屋, 1992 1) 五島瑳智子, 島田馨: 第33回日本化学療法学会総会, 新薬シンポジウムT-2588. 東京, 1985 3) 日本化学療法学会: 抗菌薬による治験症例における副作用, 臨床検査値異常の判定基準案. Chemotherapy 39: 687-689, 1991 |
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