Base de dados : HANSEN
Pesquisa : RIFAMPINA/EF ADV [Descritor de assunto]
Referências encontradas : 24 [refinar]
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Id:27305
Autor:Mane, Ibrahima; Cartel, Jean-Louis; Grosset, Jacques-Henri.
Título:Field trial on efficacy of supervised monthly dose of 600mg rifampin, 400mg ofloxacin and 100mg minocycline for the treatment of leprosy; first results.
Fonte:Int. J. Lepr;65(2):224-229, Jun. 1997. tab.
Resumo:In 1995, a field trial was implemented in Senegal in order to evaluate the efficacy of a regimen based on the monthly supervised intake of rifampin 600 mg, ofloxacin 400 mg and minocycline 100 mg to treat leprosy. During the first year of the trial, 220 patients with active leprosy (newly detected or relapsing after dapsone monotherapy) were recruited: 102 paucibacillary (PB) (60 males and 42 females) and 118 multibacillary (MB) (71 males and 47 females). All of them accepted the new treatment (none requested to be preferably put under standard WHO/MDT), no clinical sign which could be considered as a toxic effect of the drug was noted, and none of the patients refused to continue treatment because of any clinical trouble. The compliance was excellent: the 113 patients (PB and MB) detected during the first 6 months of the trial have taken six monthly doses in 6 months, as planned. The rate of clearance and the progressive decrease of cutaneous lesions was satisfactory. Although it is too soon to give comprehensive results, it should be noted that no treatment failure was observed in the 56 PB patients who have completed treatment and have been followed up for 6 months. The long-term efficacy of the new regimen is to be evaluated on the rate of relapse during the years following the cessation of treatment. If that relapse rate is acceptable (similar to that observed in patients after treatment with current standard WHO/ MDT), the new regimen could be a solution to treat, for instance, patients very irregular and/or living in remote or inaccessible areas since no selection of rifampin-resistant Mycobacterium leprae should be possible (a monthly dose of ofloxacin and minocycline being as effective as a dose of dapsone and clofazimine taken daily for 1 month). Nevertheless, until longer term results of this and other trials become available, there is no justification for any change in the treatment strategy, and all leprosy patients should be put under standard WHO/MDT. (AU)^ien.
Descritores:Hanseníase/quimioter
Rifampina/admin
Rifampina/ef adv
Rifampina/uso terap
Ofloxacino/admin
Ofloxacino/ef adv
Ofloxacino/uso terap
Minociclina/admin
Minociclina/ef adv
Minociclina/uso terap
Limites:Humanos
Masculino
Feminino
Localização:BR191.1


  2 / 24 HANSEN  
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Texto Completo-en
Id:26834
Autor:Namisato, Masako; Ogawa, Hideoki.
Título:Serious side effects of rifampin on the course of WHO/MDT: a case report.
Fonte:Int. J. Lepr;68(3):277-282, Sept., 2000. tab.
Resumo:A male born in 1935 was diagnosed as having lepromatous leprosy when he was 17 years old. In addition to dapsone (DDS) monotherapy, he had been treated with rifampin (RMP) for 2 terms: first with 450 mg a day for 2 years when he was 39 years old; second with 150 mg a day for 2 months after a 1-year interval from the first regimen. During these entire courses with RMP, no complication was noted. When he was 64 years old in 1999, a diagnosis of relapsed borderline tuberculoid (BT) leprosy was made, and he was started on the multibacillary (MB) regimen of the World Health Organization multidrug therapy (WHO/MDT). After the third dose of monthly RMP, he developed a flu-like syndrome and went into shock. A few hours later, intravascular hemolysis occurred followed by acute renal failure. He was placed on hemodialysis for 7 series and recovered almost completely about 2 months later. The immune complexes with anti-RMP antibody followed by complement binding may have accounted for these symptoms. Twenty-four reported cases of leprosy who had developed side effects of RMP under an intermittent regimen were analyzed; 9 of the cases had had prior treatment with RMP but 15 had not. Adverse effects were more likely to occur in MB cases and were more frequent during the first 6 doses of intermittent regimens. The cases with prior treatment with RMP had had a higher incidence of serious complications such as marked hypotension, hemolysis and acute renal failure. However, many exceptions were also found, and we could not verify any fully dependable factor(s) to predict the side effects of RMP. More field investigation is desirable, and monthly administration of RMP must be conducted under direct observation through the course of WHO/MDT. (AU)^ien.
Descritores:Hanseníase/quimioter
Hanseníase/imunol
Rifampina/ef adv
Rifampina/uso terap
Limites:Humanos
Meio Eletrônico:http://hansen.bvs.ilsl.br/textoc/revistas/intjlepr/2000/pdf/v68n3/v68n3a05.pdf - en.
Localização:BR191.1


  3 / 24 HANSEN  
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Id:25582
Autor:GIRLING, D . J
Título:Reaçoes adversas a rifampicina em esquemas contra a tuberculose
Adverse reactions to rifampicin in schemes against tuberculosis-
Fonte:s.l; s.n; 1977. 35 p. ilus, tab.
Descritores:RIFAMPINA/ef adv
RIFAMPINA/sint quim
RIFAMPINA/imunol
RIFAMPINA/farmacol
RIFAMPINA/uso terap
HANSENIASE/quimioter
Limites:ESTUDO COMPARATIVO
Localização:Br191.1; 01217/d.a


  4 / 24 HANSEN  
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Id:20765
Autor:Kaluarachchi, S. I; Fernandopulle, B. M. R; Gunawardane, B. P
Título:Hepatic and haematological adverse reactions associated with the use of multidrug therapy in leprosy - a five year retrospective study
..-
Fonte:s.l; s.n; 2001. 9 p. tab.
Resumo:This study analyses retrospectively some of the risks associated with the use of WHO-multidrug therapy (MDT) in Sri Lanka. Case records of 3,333 new cases of leprosy attending the Central Leprosy Clinic in Colombo during 1991-1995, were analysed for adverse drug reactions involving the liver and blood. There were 81 reports of suspected hepatic or haematological adverse reactions associated with the use of MDT, of which 39 were classified as haemolytic anaemia, 25 as toxic hepatitis, 2 as methaemoglobinaemia and 15 as anaemia. Dapsone, was incriminated in the majority of adverse reactions (72 per cent). Adverse drug reactions were more common in female than male subjects (55 per cent vs 45 per cent; P < 0.5), but there was no significant differences between the age groups. Majority of adverse reactions was seen within the first three months of initiation of MDT. This study in no way undermines the benefits of MDT but highlights the risks and suggests measures to minimize these risks. (AU).
Descritores:ANEMIA/ind quim
ANEMIA/epidemiol
CLOFAZIMINA/ef adv
DAPSONA/ef adv
QUIMIOTERAPIA COMBINADA
HEPATITE TOXICA/epidemiol
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/uso terap
HANSENIASE/quimioter
ESTUDOS RETROSPECTIVOS
RIFAMPINA/ef adv
RIFAMPINA/uso terap
METEMOGLOBINEMIA/ind quim
METEMOGLOBINEMIA/epidemiol
Limites:HUMANO
MASCULINO
FEMININO
CRIANÇA
ADULTO
MEIA-IDADE
ADOLESCENTE
Meio Eletrônico: - .
Localização:BR191.1; 09163/s


  5 / 24 HANSEN  
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Id:19791
Autor:Salafia, A; Ignatia.
Título:Tratamiento intermitente con rifampicina contra tratamiento intensivo en lepra.
Fonte:Fontilles - Revista de Leprología;16(5):585-590, May.-Ago. 1988. tab.
Resumo:Los autores informan y comparan los resultados obtenidos con tratamiento intensivo e intermitente con rifampicina en 244 pacientes. (AU).
Descritores:HANSENIASE/quimioter
HANSENIASE/prev
RIFAMPINA/admin
RIFAMPINA/ef adv
Meio Eletrônico: - .
Localização:BR191.1


  6 / 24 HANSEN  
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Id:19007
Autor:Terencio de las Aguas, José; Gómez Achevarría, José Ramón; López Pla, Jorge.
Título:Efectos secundarios y toxicidad de la rifampicina en el tratamiento de la lepra.
Fonte:Fontilles - Revista de Leprología;19(3):259-267, Sep.-Dic. 1993. ilus.
Resumo:Se analisa la toxicidad y los efectos de la rifampicina en el tratamiento de la lepra. En una experiencia terapéutica sobre 131 enfermos se ha observado una buena tolerancia general citándose algunas alteraciones gastro-intestinales y únicamente cuando se empleó como monoterapia la aparición de reacción lepromatosa en un 60%. Cuando se utilizó asociada a la clofazimina fueron escasos los episódios reaccionales. La tolerancia fue buena incluso asociada al isoprodian. En administración intermitente, mensual o semanal, hubo aparición del "Flu síndrome" en un 25% y 2 casos graves de insuficiencias renales agudas y una hepatitis tóxica. (AU).
Descritores:RIFAMPINA/admin
RIFAMPINA/ef adv
RIFAMPINA/tox
HANSENIASE/compl
HANSENIASE/quimioter
HANSENIASE/prev
Meio Eletrônico: - .
Localização:BR191.1


  7 / 24 HANSEN  
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Id:18503
Autor:Kaluarachchi, S. I; Fernandopulle, B. M. R; Gunawardane, B. P
Título:Hepatic and haematological adverse reactions associated with the use of multidrug therapy in leprosy - a five year retrospective study
..-
Fonte:s.l; s.n; 2001. 9 p. tab.
Resumo:This study analyses retrospectively some of the risks associated with the use of WHO-multidrug therapy (MDT) in Sri Lanka. Case records of 3,333 new cases of leprosy attending the Central Leprosy Clinic in Colombo during 1991-1995, were analysed for adverse drug reactions involving the liver and blood. There were 81 reports of suspected hepatic or haematological adverse reactions associated with the use of MDT, of which 39 were classified as haemolytic anaemia, 25 as toxic hepatitis, 2 as methaemoglobinaemia and 15 as anaemia. Dapsone, was incriminated in the majority of adverse reactions (72 per cent). Adverse drug reactions were more common in female than male subjects (55 per cent vs 45 per cent; P < 0.5), but there was no significant differences between the age groups. Majority of adverse reactions was seen within the first three months of initiation of MDT. This study in no way undermines the benefits of MDT but highlights the risks and suggests measures to minimize these risks. (AU).
Descritores:ANEMIA/ind quim
ANEMIA/epidemiol
CLOFAZIMINA/ef adv
DAPSONA/ef adv
QUIMIOTERAPIA COMBINADA
HEPATITE TOXICA/epidemiol
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/uso terap
HANSENIASE/quimioter
METEMOGLOBINEMIA/ind quim
METEMOGLOBINEMIA/epidemiol
ESTUDOS RETROSPECTIVOS
RIFAMPINA/ef adv
RIFAMPINA/uso terap
Limites:HUMANO
MASCULINO
FEMININO
CRIANÇA
ADULTO
ADOLESCENTE
Meio Eletrônico: - .
Localização:BR191.1; 09123/s


  8 / 24 HANSEN  
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Id:18489
Autor:Goulart, Isabela Maria Bernades; Arbex, Guilherme Leonel; Carneiro, Marcus Hubaide; Rodrigues, Mariana Scalia; Gadia, Rafael
Título:Efeitos adversos da poliquimioterapia em pacientes com hanseníase: um levantamento de cinco anos em um Centro de Saúde da Universidade Federal de Uberlândia
Adverse effects of multidrug therapy in leprosy patients: a five-year survey at a Health Center of the Federal University of Uberlandia-
Fonte:s.l; s.n; set.-out. 2002. 8 p. tab.
Resumo:The introduction of multidrug therapy (WHO/MDT)-composed by the drugs dapsone, clofazimine and rifampicin has enabled the cure of Hansen's disease, however, the adverse effects of these drugs were not given priority by the health team. Aiming to determine MDT's adverse effects' magnitude and relate them to the non-adhesion of patients to the treatment, a study of 187 charts of patients treated with MDT from January of 1995 to May 2000, was carried out at a Health Center of the Federal University of Uberlandia. Side effects were recorded in 71 patients' charts. Among the 113 side effects found, 80 (70.7 per cent) were related to dapsone, 7 (6.2 per cent) were caused by rifampicin and 26 (20.5 per cent) were attributed to clofazimine. These effects induced 28 (14.9 per cent), patients to change the therapeutic scheme, representing 39.4 per cent from the 71 patients with adverse effects. Throughout this study, the importance is discussed of considering MDT's adverse effects when training the health team to heighten the patient's adhesion to the treatment and thereby collaborating to eliminate Hansen's disease as a public health problem. (AU).
Descritores:CLOFAZIMINA/admin
CLOFAZIMINA/ef adv
DAPSONA/admin
DAPSONA/ef adv
QUIMIOTERAPIA COMBINADA
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENIASE/quimioter
COOPERACAO DO PACIENTE/estatíst
DESISTÊNCIA DO PACIENTE/estatíst
ESTUDOS RETROSPECTIVOS
RIFAMPINA/admin
RIFAMPINA/ef adv
Limites:PRÉ-ESCOLAR
CRIANÇA
ADOLESCENCIA
ADULTO
RESUMO EM INGLES
FEMININO
HUMANO
LACTENTE
RECEM-NASCIDO
MASCULINO
MEIA-IDADE
Localização:BR191.1; 09017/s


  9 / 24 HANSEN  
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Id:18476
Autor:Queiroz, Regina Helena Costa; Souza, Ana Maria de; Sampaio, Suely Vilela; Melchior Junior, Enzo
Título:Biochemical and hematological side effects of clofazimine in leprosy patients
..-
Fonte:s.l; s.n; 2002. 4 p. tab.
Resumo:Gastrointestinal toxicity and red skin discoloration were the major side effects observed in leprosy patients undergoing long-term treatment with clofazimine (CFZ). Hematological and biochemical alterations have been cited among other side effects; however, their real magnitude and clinical significance at the doses currently employed in therapy have not been sufficiently documented. We therefore investigated the correlation between CFZ plasma concentration and biochemical (transaminases, bilirubins, alkaline phosphatase, gamma-glutamyltransferase, amylase, urea, creatinine, and potassium plasma levels) as well as hematological changes blood and reticulocyte counts, osmotic fragility, detection of Heinz bodies and methemoglobinemia (MHM), following in two regimes of treatment: CFZ as a single drug and CFZ as part of multidrug (MDT) therapy, in combination with dapsone and rifampicin. MHM and hemolytic anemia were detected in the MDT group only. Eosinophilia was found in patients of either group. Determination of hepatic, pancreatic and renal biochemical parameters showed rare, occasional changes of apparently no clinical significance. We conclude that CFZ is a generally well tolerated and safe drug when given as a daily dose of 50mg, which is currently used in leprosy patients. (AU).
Descritores:CONTAGEM DE CELULAS SANGUINEAS
CLOFAZIMINA/admin
CLOFAZIMINA/ef adv
CLOFAZIMINA/uso terap
DAPSONA/admin
DAPSONA/ef adv
DAPSONA/uso terap
QUIMIOTERAPIA COMBINADA
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/uso terap
HANSENIASE/sangue
HANSENIASE/quimioter
RIFAMPINA/admin
RIFAMPINA/ef adv
RIFAMPINA/uso terap
Limites:SUPPORT, NON-U.S. GOV'T
FEMININO
HUMANO
MASCULINO
Meio Eletrônico: - .
Localização:BR191.1; 08998/s


  10 / 24 HANSEN  
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Id:18442
Autor:Winter, R. J; Banks, R. A; Collins, C. M; Hoffbrand, B. I
Título:Rifampicin induced light chain proteinuria and renal failure
..-
Fonte:s.l; s.n; dec. 1984. 2 p. .
Resumo:Light chain proteinuria is a recognised cause of renal disease and renal failure. In 1973 Graber et al described light chain proteinuria occuring in patients given rifampicin and there have since been two case reports of renal failure due to rifampicin induced light chain proteinuria.(AU).
Descritores:DESIDRATACAO/compl
IMUNOGLOBULINAS CADEIA LEVE/urina
INSUFICIÊNCIA RENAL AGUDA/ind quim
PROTEINURIA/ind quim
RIFAMPINA/ef adv
Limites:RELATO DE CASO
HUMANO
MASCULINO
MEIA-IDADE
Meio Eletrônico: - .
Localização:BR191.1; 01799/s


  11 / 24 HANSEN  
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Id:18312
Autor:Qunibi, Wajeh Y; Godwin, John; Eknoyan, Garabed
Título:Toxic nephropathy during continuous rifampin therapy
..-
Fonte:s.l; s.n; jun. 1980. 2 p. tab.
Resumo:A relatively mild nonoliguric acute renal failure developed early in the course of daily rifampin treatment in a 54-year-old man who was receiving concomitant steroid therapy. The renal lesion was an acute interstitial nephritis characterized by tubular dysfunction:inability to concentrate urine, increase in fractional excretion of sodium and uric acid, and glycosuria with normal blood glucose values. All abnormalities resolved promptly upon withdrawal of rifampin while steroid therapy was gradually reduced. The documents the fact that rifampin-induced nephropathy can occur in the course of a continuous daily regimen and may be favorably influenced by steroid administration.(AU).
Descritores:QUIMIOTERAPIA COMBINADA
INSUFICIÊNCIA RENAL AGUDA/ind quim
PREDNISONA/admin
PREDNISONA/uso terap
RIFAMPINA/admin
RIFAMPINA/ef adv
FATORES DE TEMPO
TUBERCULOSE PULMONAR/quimioter
Limites:RELATO DE CASO
HUMANO
MASCULINO
MEIA-IDADE
Meio Eletrônico: - .
Localização:BR191.1; 00442/s


  12 / 24 HANSEN  
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Id:16329
Autor:Muthukumar, Thangamani; Jayakumar, Matcha; Fernando, Edwin M; Muthusethupathi, Muthayeepalayam A
Título:Acute renal failure due to rifampicin: astudy of 25 patients
..-
Fonte:s.l; s.n; Oct. 2002. 7 p. ilus, tab.
Descritores:ANTIBIOTICOS ANTITUBERCULOSE
ANTIBIOTICOS ANTITUBERCULOSE
ESQUEMA DE MEDICAÇAO
INSUFICIENCIA RENAL AGUDA
INSUFICIENCIA RENAL AGUDA
INSUFICIENCIA RENAL AGUDA
HANSENIASE
OLIGURIA
PROGNOSTICO
RIFAMPINA
RIFAMPINA
TUBERCULOSE DOS LINFONODOS/DT
Localização:BR191.1; 08638/s


  13 / 24 HANSEN  
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Id:15972
Autor:Flageul, B; Wagner, L; Cottenot, F
Título:Accidents immuno-allergiques à la rifampicine
..-
Fonte:s.l; s.n; 2002. 8 p. tab.
Descritores:HANSENIASE
HANSENIASE DIMORFA
HANSENIASE LEPROMATOSA
HANSENIASE TUBERCULOIDE
RIFAMPINA
RIFAMPINA
RIFAMPINA
RIFAMPINA
SULFONAMIDAS
SULFONAMIDAS
TROMBOCITOPENIA
TROMBOCITOPENIA
ANTIBIOTICOS COMBINADOS
CLOFAZIMINA
CLOFAZIMINA
DAPSONA
DAPSONA
HIPERSENSIBILIDADE A DROGAS
LEPROSTATICOS
LEPROSTATICOS
LEPROSTATICOS
Localização:BR191.1; 08568/s


  14 / 24 HANSEN  
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Id:14995
Autor:Ji, Baohong; Sow, Samba; Perani, Evelyne; Lienhardt, Christian; Diderot, Vimala; Grosset, Jacques
Título:Bactericidal activity of a single-dos combination of ofloxacin plus minocycline, with or without rifampin, against mycobacterium leprae in mice and in lepromatous patients
..-
Fonte:s.l; s.n; may, 1998. 6 p. tab.
Descritores:HANSENIASE
MYCOBACTERIUM LEPRAE
OFLOXACINA
OFLOXACINA
MINOCICLINA
MINOCICLINA
RIFAMPINA
RIFAMPINA
LEPROSTATICOS
LEPROSTATICOS
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS COMBINADOS
Localização:BR191.1; 07327/s


  15 / 24 HANSEN  
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Id:14989
Autor:Pandey, V. P; Taneja, S; Talati, R
Título:Acute renal failure and hepatitis induced by intermittent rifampicin therapy
..-
Fonte:s.l; s.n; 1999. 1 p. .
Descritores:HANSENIASE TUBERCULOIDE
LEPROSTATICOS
LEPROSTATICOS
HEPATITE TOXICA
HEPATITE TOXICA
INSUFICIENCIA RENAL AGUDA
INSUFICIENCIA RENAL AGUDA
RIFAMPINA
RIFAMPINA
Limites:RELATO DE CASO
HUMANO
MASCULINO
ADULTO
Localização:BR191.1; 07461/s


  16 / 24 HANSEN  
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Id:14984
Autor:Naafs, Ben
Título:Viewpoint: Leprosy after the year 2000
..-
Fonte:s.l; s.n; 2000. 4 p. .
Descritores:HANSENIASE
HANSENIASE
HANSENIASE
LEPROSTATICOS
PELE
CLOFAZIMINA
QUIMIOTERAPIA COMBINADA
HIPERSENSIBILIDADE TARDIA
PREVALENCIA
SAUDE PUBLICA
RIFAMPINA
Localização:BR191.1; 07425/s


  17 / 24 HANSEN  
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Id:14197
Autor:Queiroz, Regina Helena Costa; Melchior Junior, Enzo; Souza, Ana Maria de; Gouveia, Elias; Barbosa, Jose Carlos; Carvalho, Dermeval de
Título:Haematological and biochemical alterations in leprosy patients already treated with dapsone and MDT
..-
Fonte:s.l; s.n; 1997. 5 p. tab.
Descritores:HANSENIASE
HANSENIASE
CLOFAZIMINA
CLOFAZIMINA
DAPSONA
DAPSONA
QUIMIOTERAPIA COMBINADA
LEPROSTATICOS
METEMOGLOBINEMIA
RIFAMPINA
RIFAMPINA
Localização:BR191.1; 07131/s


  18 / 24 HANSEN  
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Id:14128
Autor:Baohong, J. I; Jamet, Pierre; Sow, Samba; Perani, Evelyne G; Traore, Issa; Grosset, Jacques H
Título:High relapse rate among lepromatous leprosy patients treated with rifampin plus ofloxacin daily for 4 weeks
..-
Fonte:s.l; s.n; 1997. 4 p. tab.
Descritores:AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
DAPSONA
ESQUEMA DE MEDICAÇAO
QUIMIOTERAPIA COMBINADA
SEGUIMENTOS
LEPROSTATICOS
LEPROSTATICOS
HANSENIASE LEPROMATOSA
HANSENIASE LEPROMATOSA
OFLOXACINA
OFLOXACINA
RECIDIVA
RIFAMPINA
RIFAMPINA
Localização:BR191.1; 07038


  19 / 24 HANSEN  
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Id:13785
Autor:Lau, Gilbert
Título:A fatal case of drug-induced multi-organ damage in a patient with Hansen's disease: dapsone syndrome or rifampicin toxicity?
..-
Fonte:s.l; s.n; 1995. 7 p. ilus.
Descritores:FIGADO
MIOCARDITE
MIOCARDIO
NEFRITE INTERSTICIAL
RIFAMPINA
Localização:BR191.1; 06761/s


  20 / 24 HANSEN  
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Id:13383
Autor:Cusumano, A; Caldentey, D; Marise, C; Raimondo, M; Ibarra, R
Título:Renal cortical necrosis as complication of leprosy treatment (Letter)
..-
Fonte:s.l; s.n; 1992. 2 p. ilus, graf.
Descritores:ESQUEMA DE MEDICAÇAO
NECROSE DO CORTEX RENAL
HANSENIASE LEPROMATOSA
RIFAMPINA
RIFAMPINA
Localização:BR191.1; 06410/s



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