primaquine phosphate

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• primaquine phosphate — An antimalarial agent especially effective against Plasmodium vivax, terminating relapsing vivax malaria; usually administered with chloroquine. p. sensitivity a sensitivity to p. observed in individuals with glucose 6 phosphate dehydrogenase… …   Medical dictionary

• Primaquine — Systematic (IUPAC) name (RS) N (6 methoxyquinolin 8 yl)pentane 1,4 diamine Clinical data AHFS/Drugs.com …   Wikipedia

• primaquine — /pruy meuh kween /, n. Pharm. a viscous liquid, C15H21N3O, used in the treatment of malaria. [1945 50; < NL prima PRIME + QUIN(OLIN)E] * * * ▪ drug       synthetic drug used in the treatment of malaria, an infection caused by the protozoan… …   Universalium

• Deficit en glucose-6-phosphate deshydrogenase — Déficit en glucose 6 phosphate déshydrogénase Déficit en glucose 6 phosphate déshydrogénase Autre nom Favisme Référence MIM …   Wikipédia en Français

• Déficit En Glucose-6-Phosphate Déshydrogénase — Autre nom Favisme Référence MIM …   Wikipédia en Français

• Déficit en glucose 6 phosphate déshydrogénase — Autre nom Favisme Référence MIM …   Wikipédia en Français

• Déficit en glucose-6-phosphate déshydrogénase — Référence MIM 305900 Transmission Récessive liée à l X Chromosome Xq28 Mutation Ponctuelle Diagnostic prénatal …   Wikipédia en Français

• Glucose-6-phosphate dehydrogenase deficiency — ] The discovery of G6PD deficiency relieved heavily upon the testing of prisoner volunteers at Illinois State Penitentiary, although today such studies cannot be performed. When some prisoners were given the drug primaquine, some developed… …   Wikipedia

• glucose-6-phosphate dehydrogenase deficiency — n a hereditary metabolic disorder affecting red blood cells that is controlled by a variable gene on the X chromosome, that is characterized by a deficiency of glucose 6 phosphate dehydrogenase conferring marked susceptibility to hemolytic anemia …   Medical dictionary

• Deficiency, glucose-6-phosphate dehydrogenase (G6PD) — Deficiency of G6PD is the commonest disease causing enzyme defect in humans affecting an estimated 400 million people. The G6PD gene is on the X chromosome. Males with the enzyme deficiency develop anemia due to breakup of their red blood cells… …   Medical dictionary

• Glucose-6-phosphate dehydrogenase (G6PD) — Deficiency of G6PD is the commonest disease causing enzyme defect in humans affecting an estimated 400 million people. The G6PD gene is on the X chromosome. Males with the enzyme deficiency develop anemia due to breakup of their red blood cells… …   Medical dictionary