[Clinical study of a macrolide antibiotic, azithromycin, in pediatric patients]. 1996

Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
Department of Pediatrics, Kansai Medical University.

Azithromycin (AZM), 10% fine granules or 100 mg capsules, were given orally to 27 children with various pediatric infections. The results of the study are shown below. 1. Pharmacokinetic investigation. We studied plasma and urinary concentrations after 100 mg AZM capsules were given. One patient received 8.3 mg/kg of AZM once a day for 3 days, and AZM concentration in plasma was 0.033 microgram/ml 48 hours after the final dosing. Doses of 8.3 and 12.5 mg/kg body weight of AZM were respectively given to two patients once daily for 3 days. As a result, AZM concentrations in urine during a period between 96 and 120 hours post-dosing were 1.67 and 4.53 micrograms/ml, respectively, and urinary excretion rate in 120 hours after the first dosing was 10.54% in the patient that was given 12.5 mg/kg. 2. Clinical investigation. Clinical efficacies were examined in 24 patients. Excellent results were obtained in 7 patients, good results in 14 patients, hence the clinical efficacy rate was 87.5%. Bacteriologically, Haemophilus influenzae strains isolates from 2 patients were eradicated in 1 and decreased in the other. Safety was evaluated in 26 patients. An adverse reaction was observed in 1 patient (urticaria). Abnormal laboratory test results were observed in 2 patients, decreased WBC in 1 and elevation of eosinophils in the other. The above results suggest that AZM is a useful oral antibiotic for pediatric patients with infection with susceptible organisms.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D008297 Male Males
D010612 Pharyngitis Inflammation of the throat (PHARYNX). Sore Throat,Pharyngitides,Sore Throats,Throat, Sore
D011019 Pneumonia, Mycoplasma Interstitial pneumonia caused by extensive infection of the lungs (LUNG) and BRONCHI, particularly the lower lobes of the lungs, by MYCOPLASMA PNEUMONIAE in humans. In SHEEP, it is caused by MYCOPLASMA OVIPNEUMONIAE. In CATTLE, it may be caused by MYCOPLASMA DISPAR. Mycoplasma Pneumonia,Pneumonia, Primary Atypical,Mycoplasma dispar Infection,Mycoplasma ovipneumoniae Infection,Mycoplasma pneumoniae Infection,Atypical Pneumonia, Primary,Atypical Pneumonias, Primary,Mycoplasma Pneumonias,Mycoplasma dispar Infections,Mycoplasma ovipneumoniae Infections,Mycoplasma pneumoniae Infections,Pneumonias, Mycoplasma,Pneumonias, Primary Atypical,Primary Atypical Pneumonia,Primary Atypical Pneumonias
D012141 Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. Respiratory System Infections,Upper Respiratory Tract Infection,Upper Respiratory Tract Infections,Infections, Respiratory,Infections, Respiratory Tract,Infections, Upper Respiratory,Infections, Upper Respiratory Tract,Respiratory Infections,Upper Respiratory Infections,Infection, Respiratory System,Infection, Respiratory Tract,Respiratory Infection, Upper,Respiratory System Infection,Respiratory Tract Infection
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths

Related Publications

Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
March 1997, The Japanese journal of antibiotics,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
June 2000, The Japanese journal of antibiotics,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
January 1988, Plucne bolesti : casopis Udruzenja pneumoftiziologa Jugoslavije = the journal of Yugoslav Association of Phthisiology and Pneumology,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
May 1988, Antimicrobial agents and chemotherapy,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
December 2009, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
October 1994, Immunitat und Infektion,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
February 1989, The Japanese journal of antibiotics,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
July 2007, Biochimica et biophysica acta,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
January 2017, PloS one,
Y Kobayashi, and M Kino, and H Higashino, and J Takaya, and Y Harada, and Y Kawamura, and H Kawasaki, and Y Nagao
September 1995, The Japanese journal of antibiotics,
Copied contents to your clipboard!