author_facet Kramer, M
Kramer, M
author Kramer, M
spellingShingle Kramer, M
British Journal of Clinical Pharmacology
Chronic toxicity of pyrazolones: the problem of nitrosation.
Pharmacology (medical)
Pharmacology
author_sort kramer, m
spelling Kramer, M 0306-5251 1365-2125 Wiley Pharmacology (medical) Pharmacology http://dx.doi.org/10.1111/j.1365-2125.1980.tb01815.x <jats:p>1 During 6‐month oral toxicity studies of dipyrone in rats and dogs, there was an increase in the number of reticulocytes and Heinz bodies at the highest dose, and a slight haemosiderosis was induced. 2 Similar results were obtained after parenteral administration (intravenously and subcutaneously). 3 These studies fail to contribute to the knowledge of the mechanism of allergic reactions in man. 4 In vitro studies in conditions imitating the physiological environment, show to what extent nitrosation of dipyrone takes place. 5 Subsequent toxicological investigations with the two reaction compounds, or the nitrosation product itself, are powerful instruments to show whether the nitrosamine or nitrosamide formed is dangerous. 6 In the case of pyrazolones, only aminopyrine forms a carcinogenic nitrosamine.</jats:p> Chronic toxicity of pyrazolones: the problem of nitrosation. British Journal of Clinical Pharmacology
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title Chronic toxicity of pyrazolones: the problem of nitrosation.
title_unstemmed Chronic toxicity of pyrazolones: the problem of nitrosation.
title_full Chronic toxicity of pyrazolones: the problem of nitrosation.
title_fullStr Chronic toxicity of pyrazolones: the problem of nitrosation.
title_full_unstemmed Chronic toxicity of pyrazolones: the problem of nitrosation.
title_short Chronic toxicity of pyrazolones: the problem of nitrosation.
title_sort chronic toxicity of pyrazolones: the problem of nitrosation.
topic Pharmacology (medical)
Pharmacology
url http://dx.doi.org/10.1111/j.1365-2125.1980.tb01815.x
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description <jats:p>1 During 6‐month oral toxicity studies of dipyrone in rats and dogs, there was an increase in the number of reticulocytes and Heinz bodies at the highest dose, and a slight haemosiderosis was induced. 2 Similar results were obtained after parenteral administration (intravenously and subcutaneously). 3 These studies fail to contribute to the knowledge of the mechanism of allergic reactions in man. 4 In vitro studies in conditions imitating the physiological environment, show to what extent nitrosation of dipyrone takes place. 5 Subsequent toxicological investigations with the two reaction compounds, or the nitrosation product itself, are powerful instruments to show whether the nitrosamine or nitrosamide formed is dangerous. 6 In the case of pyrazolones, only aminopyrine forms a carcinogenic nitrosamine.</jats:p>
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description <jats:p>1 During 6‐month oral toxicity studies of dipyrone in rats and dogs, there was an increase in the number of reticulocytes and Heinz bodies at the highest dose, and a slight haemosiderosis was induced. 2 Similar results were obtained after parenteral administration (intravenously and subcutaneously). 3 These studies fail to contribute to the knowledge of the mechanism of allergic reactions in man. 4 In vitro studies in conditions imitating the physiological environment, show to what extent nitrosation of dipyrone takes place. 5 Subsequent toxicological investigations with the two reaction compounds, or the nitrosation product itself, are powerful instruments to show whether the nitrosamine or nitrosamide formed is dangerous. 6 In the case of pyrazolones, only aminopyrine forms a carcinogenic nitrosamine.</jats:p>
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spelling Kramer, M 0306-5251 1365-2125 Wiley Pharmacology (medical) Pharmacology http://dx.doi.org/10.1111/j.1365-2125.1980.tb01815.x <jats:p>1 During 6‐month oral toxicity studies of dipyrone in rats and dogs, there was an increase in the number of reticulocytes and Heinz bodies at the highest dose, and a slight haemosiderosis was induced. 2 Similar results were obtained after parenteral administration (intravenously and subcutaneously). 3 These studies fail to contribute to the knowledge of the mechanism of allergic reactions in man. 4 In vitro studies in conditions imitating the physiological environment, show to what extent nitrosation of dipyrone takes place. 5 Subsequent toxicological investigations with the two reaction compounds, or the nitrosation product itself, are powerful instruments to show whether the nitrosamine or nitrosamide formed is dangerous. 6 In the case of pyrazolones, only aminopyrine forms a carcinogenic nitrosamine.</jats:p> Chronic toxicity of pyrazolones: the problem of nitrosation. British Journal of Clinical Pharmacology
spellingShingle Kramer, M, British Journal of Clinical Pharmacology, Chronic toxicity of pyrazolones: the problem of nitrosation., Pharmacology (medical), Pharmacology
title Chronic toxicity of pyrazolones: the problem of nitrosation.
title_full Chronic toxicity of pyrazolones: the problem of nitrosation.
title_fullStr Chronic toxicity of pyrazolones: the problem of nitrosation.
title_full_unstemmed Chronic toxicity of pyrazolones: the problem of nitrosation.
title_short Chronic toxicity of pyrazolones: the problem of nitrosation.
title_sort chronic toxicity of pyrazolones: the problem of nitrosation.
title_unstemmed Chronic toxicity of pyrazolones: the problem of nitrosation.
topic Pharmacology (medical), Pharmacology
url http://dx.doi.org/10.1111/j.1365-2125.1980.tb01815.x