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- NAKAZAWA SUSUMU
- Department of Pediatrics, Tokyo Ebara Municipal Hospital Department of Pediatrics, School of Medicine, Showa University
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- SATO HAJIME
- Department of Pediatrics, Tokyo Ebara Municipal Hospital Department of Pediatrics, School of Medicine, Showa University
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- NIINO KENJI
- Department of Pediatrics, Tokyo Ebara Municipal Hospital Department of Pediatrics, School of Medicine, Showa University
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- HIRAMA YUICHI
- Department of Pediatrics, Tokyo Ebara Municipal Hospital Department of Pediatrics, School of Medicine, Showa University
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- NARITA AKIRA
- Department of Pediatrics, Tokyo Ebara Municipal Hospital Department of Pediatrics, School of Medicine, Showa University
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- NAKAZAWA SHIN-ICHI
- Department of Pediatrics, Tokyo Ebara Municipal Hospital Department of Pediatrics, School of Medicine, Showa University
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- CHIKAOKA HIDEJIRO
- Department of Pediatrics, Takatsu Central Hospital
Bibliographic Information
- Other Title
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- 新生児並びに幼若乳児におけるLatamoxefの基礎的, 臨床的検討
- シンセイジ ナラビニ ヨウジャク ニュウジ ニ オケル Latamoxef ノ
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Description
1. Fundamental and clinical studies in infants including neonates on latamoxef (LMOX) were carried out, and following results were obtained.<BR>2. In fundamental studies, half-lives of LMOX were 5.79, 4.38 hours, at dose 10 mg/kg by intravenous injection and intravenous drip infusion in neonates, respectively.And urinary excretions were 6.8, 15.6% for 6 hours, respectively.In 28-50 day-old neonates, half-lives were 2.26-4.3 hours at dose 20mg/kg, and urinary excretions were renged from 14.3 to 37.0%.<BR>3. Clinical results were following.In 8 cases of bronchopneumonia and 2 cases of pertussis, the clinical efficacy rate was 100% at daily dose 38-100 mg/kg twice or third a day by intravenous injection or intravenous drip infusion for 6-9 days duration.<BR>4. All causative organisms (K. pneumoniae 1, S.aureus 1) were eliminated after LMOX 43 or 38 mg/kg/day dose administration.<BR>5. Side effect and laboratory abnormal value were not noticed in all cases. We finally have a conclusion that LMOX should be administered 40-70 mg/kg/day, and given twice or third a day by intravenous injection or intravenous drip infusion.
Journal
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- The Japanese Journal of Antibiotics
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The Japanese Journal of Antibiotics 36 (9), 2302-2311, 1983
Japan Antibiotics Research Association
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Details 詳細情報について
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- CRID
- 1390282680466464128
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- NII Article ID
- 130004393966
- 40000017574
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- NII Book ID
- AN00002626
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- COI
- 1:STN:280:DyaL2c%2FptVOnsw%3D%3D
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- ISSN
- 21865477
- 03682781
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- NDL BIB ID
- 2639588
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- PubMed
- 6655849
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed