Experience with ceftazidime in obstetrics and gynaecology in Japan

The effects of ceftazidime weTe evaluated in 238 patients. Among these patients 221 (93%) were assessed as having either 'excellent ' or 'good ' clinical responses. Bacteriologically, in 102 (87%) out of 117 cases, the causative organisms were either eliminated or replaced. Adverse events noted were limited to mild rashes in 2 patients and gastric discomfort in another. Penetration of ceftazidime into uterine tissues was studied and, following an intravenous bolus dose of 1 g, concentrations in various parts of the uterus averaged 36 to 57 mg/kg at 11 to 26 min. Concentrations in intrapelvic fluid in patients undergoing radical hysterectomy averaged 37 mg/1 at 30 min after an intravenous bolus injection of 1 g, and 23 mg/1 at 30 min after completion of a 60-min infusion