FUNDAMENTAL AND CLINICAL STUDIES ON LATAMOXEF IN THE PERINATAL PERIOD

Fundamental and clinical studies on latamoxef (LMOX) in the perinatal period were carried out, and following results were obtained. 1. Concentration of LMOX was showed high peak levels in maternal serum, umbilical serum and amniotic fluid. LMOX seemed to be a very transferable compound to human tiss...

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Published inJapanese journal of antibiotics Vol. 37; no. 6; pp. 991 - 1005
Main Authors TAKASE, ZENJIRO, KOHMOTO, YOSHIYUKI, SHIRAFUJI, HIROKO, SHIMIZU, TETSUYA, ISHIKAWA, MUTSUO, SAKURABA, MAMORU, ICHINOHE, KIHYOE, SUGAHARA, SUGURU, HAYASHI, HIROSHI, CHO, NANKUN, SUZUKI, HIDENOBU, AKIYAMA, TOSHIO, KAWAMURA, EIICHI, TOGO, MITSUMASA, NISHIMOTO, SEKIO, HIDAKA, TERUO, FUKUNAGA, KANGO, KUNII, KATSUAKI, MATSUDA, SEIJI, KASHIWAKURA, TAKASHI, NOJIMA, MICHIO, TAKASE, SACHIKO, NINOMIYA, KEIU, HASEGAWA, YUKIO, NODA, KATSUMI, HAYASAKI, MOTOKI, TAKADA, YASUHIRO, KONDOH, HIDEAKI, ITOH, KUNIHIKO, IIDA, MITSUO, CHIN, CHOKEN, YAMADA, YOSHITAKA, OHSUGI, SATORU, KATOH, RYUHJI, LIN, YIHUNG, BABA, YOSHITAKA, WAKITA, KATSUJI, OKADA, HIROJI, YAMAMOTO, TAKAO, YASUDA, JINSUKE, KANAO, MASAAKI, MOTOMURA, RYUTARO
Format Journal Article
LanguageJapanese
Published Japan Japan Antibiotics Research Association 01.06.1984
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Summary:Fundamental and clinical studies on latamoxef (LMOX) in the perinatal period were carried out, and following results were obtained. 1. Concentration of LMOX was showed high peak levels in maternal serum, umbilical serum and amniotic fluid. LMOX seemed to be a very transferable compound to human tissues. 2. LMOX was administered to 28 cases of various perinatal infections. Clinical responses were excellent in 13 cases, good in 15 cases and poor in none. And 140 cases of prophylactic use in the field of perinatal period were evaluated in good. 3. No side effect was seen and an abnormal laboratory finding, the increase of GPT, was observed in only 1 case. 4. LMOX was a highly useful antibiotic in perinatal infections, the safe dose range of LMOX into the perinatal mothers was estimated to be 2g/day, with the maximum safe dose being 4g/day.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0368-2781
2186-5477
DOI:10.11553/antibiotics1968b.37.991