1.Comparison of the Effect of Cefadroxil and Kanamycin Sulfate in the Treatment of Male Gonorrhoea.
Chang Hoon KWAK ; Young Suck RO ; Young Tae KIM ; Jae Hong KIM ; Joong Hwan KIM
Korean Journal of Dermatology 1984;22(6):599-603
No abstract available.
Cefadroxil*
;
Humans
;
Kanamycin*
;
Male*
2.Hypersensitivity myocarditi caused by ceused by cafadroxil.
Tae Rim SHIN ; Hae Young CHOI ; Yoon Hye CHANG ; Young Joo CHO
Korean Journal of Allergy 1997;17(2):186-191
Hypersensitivity myocarditis is an inflammatory disease of the myocardium usually related to drug allergy. The clinical manifestation may be nonspecific, and the diagnosis is seldom suspected or established during the life. So in most of the reported patients, the diagnosis was made at autopsy. Although, retrospectively, more than 90% of the patients described have had clinically recognizable cardiac involvement before death, tole clinical suspicion of hypersensitivity myocarditis is rare. The presence of nonspecific cardiac finding in a patient receiving any drug associated with hypersensitivity should alert the clinician to the possibility of drug related myocarditis. We experienced a case of hypersensitivity myocarditis accompanying allergic skin lesion in a 58 years old man with a history of taking cefadroxil. Fortunately, the outcome was favorable, therefore we do not have histologic confirmation of the diagnosis.
Autopsy
;
Cefadroxil
;
Diagnosis
;
Drug Hypersensitivity
;
Humans
;
Hypersensitivity*
;
Middle Aged
;
Myocarditis
;
Myocardium
;
Retrospective Studies
;
Skin
3.A Simple and Sensitive Assay for Cefepime in Human Plasma Using High Performance Liquid Chromatography.
Young Sun KIM ; Dong Seok YIM ; Dong Gun LEE ; Sang Bok LEE
The Korean Journal of Physiology and Pharmacology 2003;7(4):247-250
A simple and sensitive assay method was developed for cefepime in human plasma using high performance liquid chromatography (HPLC). Cefepime and cefadroxil (the internal standard) were extracted from heparinized human plasma by simple deproteination with perchloric acid. The extract was injected into an Atlantis dC18 column (250 X 4.6 mm; particle size 5micrometer, Waters) and the column was eluted with methanol and 0.01 M dihydrogen phosphate at pH 3.0 (15 : 85 v : v) as a mobile phase at a flow rate of 0.7 mL/min. Linearity was confirmed for the range 0.25 to 200 micro L/mL and the limit of quantitation was 0.25 micro L/mL. The retention times were 10.2 min and 13.4 min for cefepime and cefadroxil, respectively. This method was successfully applied to a pharmacokinetic study of cefepime in plasma from bone marrow transplant patients.
Bone Marrow
;
Cefadroxil
;
Chromatography, High Pressure Liquid
;
Chromatography, Liquid*
;
Heparin
;
Humans*
;
Hydrogen-Ion Concentration
;
Methanol
;
Particle Size
;
Plasma*
4.Efficacy of Cefadroxil Monohydrate (Duricef.
Korean Journal of Urology 1982;23(8):1165-1169
Effect of Cefadroxil monohydrate was evaluated on 37 patients with urinary tract infection in our department during past 6 months periods. Cefadroxil was given Orally at a dose of 1.0 gm - 3.0 gm bid per day for 3 - 15 days and following results were obtained. 1. Excellent or good results was observed in 31 out of 34 patients in whom complete follow up study were done, giving success rate of 91.2%. 2. Therapeutic effects were obtained in 10 out of 11 patients with urethritis and all patients with cystitis and pyelonephritis, but not in 1 with urethritis, 1 with prostatitis and 1 out of 9 urinary tract infections with predisposing factors. 3. In this clinical settings, Cefadroxil was effective against E. coli infection in 10 patients, mixed infection in 2 and Staphylococcus aureus infection in 5. However it was ineffective against Serratia infection in 1 patient and Staphylococcus infection in 1. 4. As to the side effects, only mild dizziness was observed in 2 patient.
Causality
;
Cefadroxil*
;
Coinfection
;
Cystitis
;
Dizziness
;
Follow-Up Studies
;
Humans
;
Prostatitis
;
Pyelonephritis
;
Serratia Infections
;
Staphylococcus
;
Staphylococcus aureus
;
Urethritis
;
Urinary Tract Infections*
;
Urinary Tract*
5.A case of bronchial asthma due to cefadroxil in a housewife.
Jeong Hee CHOI ; Yu Jin SUH ; Jae Wook JUNG ; Hyun Joo SONG ; Chang Hee SUH ; Dong Ho NAHM ; Hae Sim PARK
Journal of Asthma, Allergy and Clinical Immunology 2002;22(4):736-741
Cephalosporins are the most important -lactams that induce IgE-mediated reactions. Also, cephalosporins have been known as a causative agent for occupational asthma in pharmaceutical workers. To our knowledge, this is the first report of cephalosporin-induced bronchial asthma in a housewife with no history of occupational exposure. We experienced a 30-year old female who had developed shortness of breath, coughing and itching sensation of the skin since 3 years ago whenever she handled drug powder for upper respiratory infections (URI) prescribed for her two sons with bronchial asthma. She had handled drug powder for 7 years because her sons had experienced frequent URI. Skin prick test with cefadroxil (10mg/ml) and cefaclor (10mg/ml) showed positive reactions. Bronchial challenge test with cefadroxil showed immediate asthmatic reaction, and bronchial challenge with cefaclor showed immediate urticaria and angioedema without significant fall in FEV1. We confirmed cefadroxil-induced bronchial asthma sensitized by intermittent inhalation in a non-occupational setting.
Adult
;
Angioedema
;
Asthma*
;
Asthma, Occupational
;
Bronchial Provocation Tests
;
Cefaclor
;
Cefadroxil*
;
Cephalosporins
;
Cough
;
Dyspnea
;
Female
;
Humans
;
Inhalation
;
Occupational Exposure
;
Pruritus
;
Respiratory Tract Infections
;
Sensation
;
Skin
;
Urticaria
6.Antibacterial Activity of Ceftizoxime Against Gram Negative Enteric Bacteria in vitro and in vivo.
Woo Mok BYUN ; Jae Chun CHANG ; Bok Hwan PARK ; Hee Sun KIM ; Sung Kwang KIM
Yeungnam University Journal of Medicine 1989;6(1):59-68
Ceftizoxime sodium is a new synthetic β-lactam antibiotic combining potent antibacterial activity with high stability to a wide range of bacterial β-lactamase. This experiment was achieved to evaluate the antibacterial activities of ceftizoxime sodium against. Gram negative enteric bacteria isolated from in outpatient visiting Yeungnam university hospital and to study the emergence of drug induced bacterial variants which resist to ceftizoxime in vitro. The antibacterial activity of the ceftizoxime was compared with that of antibiotics and its effect on population of normal intestinal flora in mice was observed. The results are summarized as follows: 1. Highly effective antibacterial activity of ceftizoxime against Gram negative enteric bacilli was demonstrated and this antibacterial activity was superior to that of ampicillin. 2. Several test strains shows multiple antibiotic resistance. Among 15 strains of Escherichia coli, 1 strain was resistant to ampicillin, cefadroxil, gentamicin, tetracycline, and 2 strains were resistant to ampicillin, cefadroxil, tetracycline, five strains of Escherichia coli and Enterobacter cloacae was resistant to ampicillin, tetracycline and Shigella dysenteriae was resistant to ampicillin, gentamicin, tetracycline. 3. The frequency of in vitro emergence of resistant variants among ceftizoxime sensitive bacteria in the presence of increasing concentrations of the compound was found to be low. 4. Plasmid was isolated in 6 of 9 strains (6 strains of Escherichia coli, Shigella dysenteriae, Enterobacter cloacae and Salmonella typhi). That showed different antibiotic resistance. They were 5 strains of Escherichia coli and 1 strain of Shigella dysenteriae. However, plasmid could not be considered as a hallmark for antibiotic resistance by this Further studies with curing experiment are to be accomplished for this purpose. 5. Changes in the bacterial count of normal intestinal flora following 25 mg/kg/day administration of ceftizoxime over 5 consecutive days were not significant. In conclusion, ceftizoxime appeared to be a drug of choice in the treatment of Gram negative enteric bacilli infection.
Ampicillin
;
Animals
;
Anti-Bacterial Agents
;
Bacteria
;
Bacterial Load
;
Cefadroxil
;
Ceftizoxime*
;
Drug Resistance, Microbial
;
Enterobacter cloacae
;
Enterobacteriaceae*
;
Escherichia coli
;
Gastrointestinal Microbiome
;
Gentamicins
;
Humans
;
In Vitro Techniques*
;
Mice
;
Outpatients
;
Plasmids
;
Salmonella
;
Shigella dysenteriae
;
Tetracycline