rifampin and Glucosephosphate-Dehydrogenase-Deficiency

rifampin has been researched along with Glucosephosphate-Dehydrogenase-Deficiency* in 5 studies

Trials

1 trial(s) available for rifampin and Glucosephosphate-Dehydrogenase-Deficiency

ArticleYear
Efficacy of WHO regimens in the management of leprosy patients with G6PD deficiency.
    International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association, 1999, Volume: 67, Issue:2

    Topics: Adolescent; Adult; Clofazimine; Dapsone; Drug Therapy, Combination; Female; Glucosephosphate Dehydrogenase Deficiency; Humans; Leprostatic Agents; Leprosy; Male; Middle Aged; Oman; Practice Guidelines as Topic; Rifampin; World Health Organization

1999

Other Studies

4 other study(ies) available for rifampin and Glucosephosphate-Dehydrogenase-Deficiency

ArticleYear
Successful rifampin desensitization in a pediatric patient with latent tuberculosis.
    Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2014, Volume: 25, Issue:4

    Topics: Child; Clinical Protocols; Contraindications; Desensitization, Immunologic; Diphenhydramine; Drug Dosage Calculations; Drug Hypersensitivity; Exanthema; Glucosephosphate Dehydrogenase Deficiency; Humans; Immune Tolerance; Isoniazid; Latent Tuberculosis; Male; Rifabutin; Rifampin

2014
Brucellosis triggering hemolytic anemia in glucose-6-phosphate dehydrogenase deficiency.
    Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2009, Volume: 18, Issue:4

    To present a case of acute brucellosis triggering acute hemolytic anemia in a subject with glucose-6-phosphate dehydrogenase (G6PD) deficiency.. A 17-year-old male patient presented with fever, malaise and jaundice. His blood and bone marrow cultures yielded Brucella species. In addition, he was found to have acute hemolytic anemia due to previously undiagnosed G6PD deficiency. He was started on folic acid supplementation and given a combination of doxycycline and rifampicin for 6 weeks. His response to antibiotic therapy was optimal; the hemolytic anemia resolved. There were no further episodes of hemolysis.. This case showed that the differential diagnosis of acute hemolytic anemia in subjects with G6PD deficiency should include brucellosis, especially in regions where the infection is endemic.

    Topics: Adolescent; Anemia, Hemolytic; Anti-Bacterial Agents; Brucellosis; Doxycycline; Folic Acid; Glucosephosphate Dehydrogenase Deficiency; Hematinics; Humans; Male; Rifampin

2009
Pathology of bactericidal power of neutrophils.
    Seminars in hematology, 1975, Volume: 12, Issue:2

    Topics: Agranulocytosis; Blood Bactericidal Activity; Candida; Chediak-Higashi Syndrome; Chromosome Aberrations; Chromosome Disorders; Female; Glucosephosphate Dehydrogenase Deficiency; Glutathione Peroxidase; Granulomatous Disease, Chronic; Heterozygote; Humans; Infant, Newborn; Leukocytes; Lupus Erythematosus, Discoid; Male; Neoplasms; Neutropenia; Neutrophils; Peroxidases; Phagocytosis; Pregnancy; Rifampin; Sulfonamides; Vitamin B 6 Deficiency

1975
Electrophoretic heterogeneity of erythrocyte and leucocyte glucose-6-phosphate dehydrogenase in Italians from various ethnic groups.
    Nature, 1966, Aug-20, Volume: 211, Issue:5051

    Topics: Aminopyrine; Anemia, Hemolytic; Electrophoresis; Erythrocytes; Ethnology; Favism; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Italy; Leukocytes; Molecular Biology; Mutation; Rifampin

1966