들이마신 경우,호흡이 어려운 경우 환자를 신선한 공기가 있는 곳으로 옮기고 호흡하기 편한 자세로 안정을 취하게 함
P321
(…) 처치를 하시오.
P333+P313
피부자극성 또는 홍반이 나타나면 의학적인 조치·조언를 구하시오.
P342+P311
호흡기 증상이 나타나면 의료기관(의사)의 진찰을 받으시오.
P363
다시 사용전 오염된 의류는 세척하시오.
P501
...에 내용물 / 용기를 폐기 하시오.
세포니이드나트륨 C화학적 특성, 용도, 생산
개요
Cefonicid sodium is the first of the second-generation cephalosporin antibiotics
with a long enough serum half-life b4.5 hr.) to allow once-daily i.v. administration.
Cefonicid is resistant to β-lactamases produced by S. aureus, H. influenzae,
-N. gonorrhea, and related organisms. As with other drugs of this class, it is useful in
the treatment of urinary tract and lower respiratory tract infections, skin and skin
structure infections, and bone and joint infections, as well as in surgical
prophylaxis.
화학적 성질
White Powder
Clinical Use
Cefonicid Sodium (Monocid) is a second-generationcephalosporin that is structurally similar to cefamandole,except that it contains a methane sulfonic acid groupattached to the N-1 position of the tetrazole ring. Theantimicrobial spectrum and limited β-lactamase stabilityof cefonicid are essentially identical with those ofcefamandole. Cefonicid is unique among the second-generationcephalosporins in that it has an unusually long serum halflifeof approximately 4.5 hours. High plasma protein bindingcoupled with slow renal tubular secretion are apparentlyresponsible for the long duration of action. Despite the high fraction of drug bound in plasma, cefonicid is distributedthroughout body fluids and tissues, with the exception of thecerebrospinal fluid. Cefonicid is supplied as a highly water-soluble disodiumsalt, in the form of a sterile powder to be reconstituted forinjection. Solutions are stable for 24 hours at 25°C and for72 hours when refrigerated.
