Base de dados : HANSEN
Pesquisa : HANSENOSTATICOS/TOX [Descritor de assunto]
Referências encontradas : 5 [refinar]
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Id:22351
Autor:S, B. B. M. Dharmendra; Chatterjee, K. R.
Título:Thiosemicarbazone in the treatment of leprosy.
Fonte:Lepr Ind;24(3):93-, july, 1952. tab.
Resumo:(I) The previous work with thiosemicarbazone in the treatment of leprosy is summarised. (2) Siocarbazone brand of thiosemicarbazone has been used in 52 cases of leprosy, 9 untraeded neural cases, 27 untreated lepromatous cases and 16 previously treated lepromatous cases, 15 with sulphones, and I with hydnocarpus oil. The duration of treatment has from 2 months to 16 months with an average of I0 months. (3) The patients have stood the drug well and there has been satisfactory clinical and bacteriological response. In addition to usual therapeutic affects, special features with thiosemicarbazone treatment have been the complete or partial restoration of sensation in the anaesthetic patches and in the limbs with polyneuritic type of anaesthesia, replacement of deseased nails by new ones, and growth of new hair in depilated areas. Considering the short period of treatment those features are rather remarkable. (4) In the toxicity of thiosemicarbazone seems to be less than that of the sulphones specially in relation to its effect on the haemopoietic system. However, the thiosemicarbazone is not as free from toxicity as described by some workers eho have used it in leprosy. A special kind of toxicity which indicates specific intolerance has been noticed and this has been manifested by sudden rise of temperature even after small doses of the drug (AU).
Descritores:HANSENIASE/quimioter
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/farmacol
HANSENOSTATICOS/tox
HANSENOSTATICOS/uso terap
Localização:BR191.1


  2 / 5 HANSEN  
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Id:20441
Autor:Emmerson, George A; Anderson, Hamiilton H.
Título:Toxicity of certain proposed antileprosy dyes: fluorescein, eosin, erythrosin, and others.
Fonte:Int. J. Lepr;2(3):257-263, Aug.-Oct. 1934. tab.
Resumo:Fluorescein, eosin, erythrosin and methylene green were found to be lethal at 300, 350, 200 and 150 mgm. per kilogram, respectively when administered intravenously to rabbits, and at 600, 500, 300 and 125 mgm. per kilogram intraperitoneally in rats. Methylene green is lethal for anesthetized cats in doses of 50 to 75 mgm. per kilogram. Orally in rats these dyes are tolerated in doses of 1.0 gm. per kilogram with the exception of methylene green, which killed 2 of 5 rats at 500 mgm. per kilogram. Data are presented on the chronic toxicity of trypan blue, gentian violet, brillant green and mercurochrome. Three of 6 rabbits dying under repeated intravenous administrations of trypan blue had received a total cumulative dose, approximately equivalent to but one acute lethal dose, i.e., 120 to 150 mgm. per kilogram. The dangers of repeatedly using high doses in human lepers, the superiority of oral administration over intravenous, and the danger of certain synergizing agents, including photodynamic effects, are discussed. (AU).
Descritores:HANSENIASE/quimioter
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/tox
Limites:ANIMAL
Localização:BR191.1


  3 / 5 HANSEN  
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Id:20358
Autor:Ryrie, Gordon A.
Título:A preliminary report on the action of certain dyes in leprosy.
Fonte:Int. J. Lepr;1(4):469-475, Oct. 1933. .
Resumo:1- A number of indications and analogies suggest the trial of coal-tar dyes and their derivatives in leprosy. 2- Intravenous injections of a large number of dyes have been given to 85 patients. 3- A number of these dyes show marked selective concentration in the leprotic lesions, a phenomenon not seen in certain non-leprotic lesions. 4- With trypan blue, brilliant green, fluorescein and perhaps eosin a definite diminution of the external manifestations of leprosy has been observed, accompanied by other signs of clinical improvement. 5- With the other dyes administered no signs of clinical improvement were observed. 6- This report is a study of the immediate reaction of the lesions; we have as yet no knowledge of the later effects of the injection of these dyes. We consider from this preliminary report that further trial and study of these dyes is definitely indicated in the hope that it may lead to further possibilities in the chemotherapy of this disease. (AU).
Descritores:HANSENIASE/quimioter
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/tox
HANSENOSTATICOS/uso terap
HANSENIASE/diag
Limites:HUMANO
Localização:BR191.1


  4 / 5 HANSEN  
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Id:20355
Autor:Muir, Ernest.
Título:Treatment of leprosy: a review.
Fonte:Int. J. Lepr;1(4):407-458, Oct. 1933. ilus.
Descritores:HANSENOSTATICOS/hist
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/isol
HANSENOSTATICOS/farmacol
HANSENOSTATICOS/farmacocin
HANSENOSTATICOS/tox
HANSENOSTATICOS/uso terap
HANSENIASE/quimioter
 HANSENIASE/terap
Limites:HUMANO
Localização:BR191.1


  5 / 5 HANSEN  
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Id:20328
Autor:Read, Bernard E.
Título:The toxicity of sodium hydnocarpate.
Fonte:Int. J. Lepr;1(3):293-307, July 1933. tab.
Resumo:1-High concentrations and large doses of commercial preparations of sodium hydnocarpate administered to rabbits and dogs intravenously and subcutaneouly produce albuminuria, hematuria, and emaciation. 2- There is loss os weight when either the sodium salts or the ethyl esters are given subcutaneously in amounts more than 50 milligrams per kilogram of body weight. A certain degree of tolerance can be developed with suitable dosage. 3-Pronounced albuminuria is observed in rabbits after subcutaneous injection of 12.5 milligrams of the salts. With larger or smaller doses it is not so pronunced. In dogs, a 4 per cent solution of esters in olive oil is apparently most rapidly absorbed and gives the earliest traces of albumen. $- The less readily absorbed and less reactive concentrations also produce albuminuria, but only after an interval of several days...(AU).
Descritores:CHAULMOOGRA/admin
CHAULMOOGRA/tox
CHAULMOOGRA/farmacocin
HANSENOSTATICOS/admin
HANSENOSTATICOS/ef adv
HANSENOSTATICOS/farmacocin
HANSENOSTATICOS/tox
Limites:ANIMAL
Localização:BR191.1



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