[Pharmacokinetics and clinical efficacy of flomoxef in neonates]. 1991

S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
Department of Pediatrics, School of Medicine, Keio University.

Clinical pharmacology and efficacy of flomoxef (FMOX) in neonates were investigated. And the following results were obtained. 1. Mean serum concentrations of FMOX at 30 minutes after administration were 24.3 micrograms/ml, 47.6 micrograms/ml, and 85.8 micrograms/ml at doses of 10 mg/kg, 20 mg/kg, and 40 mg/kg administered, respectively. 2. Mean serum half-lives of FMOX were 3.4 hours in 0-3 day-old neonates, and 2.6 hours in 4 day-old or older subjects. 3. A dose response was evident among different dose groups given 10 mg/kg, 20 mg/kg, and 40 mg/kg. 4. Urinary recovery rates of FMOX in the first 6 hours after administration ranged between 12.8 and 51.1%. 5. FMOX was effective in 7 out of 8 cases in which causative pathogens were identified. 6. Diarrhea was observed in 1 case as a side effect of the drug, but the symptom was relieved soon after the completion of the treatment. There was no case in which any abnormal laboratory results were observed. 7. FMOX has a broad spectrum of activities against Gram-positive and Gram-negative aerobes and anaerobes. It is stable against most of beta-lactamases. It was demonstrated to be highly effective in our study, and yet without any serious side effects. FMOX is therefore considered to be one of the useful agents of the first choice for the treatment of bacterial infections such as sepsis and urinary tract infections in neonates and infants.

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007275 Injections, Intravenous Injections made into a vein for therapeutic or experimental purposes. Intravenous Injections,Injection, Intravenous,Intravenous Injection
D008297 Male Males
D002511 Cephalosporins A group of broad-spectrum antibiotics first isolated from the Mediterranean fungus ACREMONIUM. They contain the beta-lactam moiety thia-azabicyclo-octenecarboxylic acid also called 7-aminocephalosporanic acid. Antibiotics, Cephalosporin,Cephalosporanic Acid,Cephalosporin,Cephalosporin Antibiotic,Cephalosporanic Acids,Acid, Cephalosporanic,Acids, Cephalosporanic,Antibiotic, Cephalosporin,Cephalosporin Antibiotics
D004341 Drug Evaluation Any process by which toxicity, metabolism, absorption, elimination, preferred route of administration, safe dosage range, etc., for a drug or group of drugs is determined through clinical assessment in humans or veterinary animals. Evaluation Studies, Drug,Drug Evaluation Studies,Drug Evaluation Study,Drug Evaluations,Evaluation Study, Drug,Evaluation, Drug,Evaluations, Drug,Studies, Drug Evaluation,Study, Drug Evaluation
D005260 Female Females
D006207 Half-Life The time it takes for a substance (drug, radioactive nuclide, or other) to lose half of its pharmacologic, physiologic, or radiologic activity. Halflife,Half Life,Half-Lifes,Halflifes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000367 Age Factors Age as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or the effect of a circumstance. It is used with human or animal concepts but should be differentiated from AGING, a physiological process, and TIME FACTORS which refers only to the passage of time. Age Reporting,Age Factor,Factor, Age,Factors, Age
D001424 Bacterial Infections Infections by bacteria, general or unspecified. Bacterial Disease,Bacterial Infection,Infection, Bacterial,Infections, Bacterial,Bacterial Diseases

Related Publications

S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
July 1993, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
July 1993, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
November 1991, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
August 1987, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
November 1991, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
November 1991, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
August 1987, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
November 1988, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
November 1991, The Japanese journal of antibiotics,
S Azagami, and E Isohata, and S Takeda, and Y Kin, and T Oikawa, and M Osano, and H Shiro
July 1993, The Japanese journal of antibiotics,
Copied contents to your clipboard!