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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Neuroradiology 32 (1990), S. 70-73 
    ISSN: 1432-1920
    Keywords: Intrathecal diatrizoate meglumine ; Lethal dysregulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A case of inadvertent intrathecal injection of diatrizoate meglumine is presented. After myelography with 10 ml i.e. 6.5 g Angiografin, a 76-year-old man rapidly developed myoclonus, drowsiness and excessive metabolic acidosis. He died only a few hours later. Postmortem showed non-specific brain edema. RP-HPL-Chromatography confirmed high concentration of the contrast medium in CSF (6 mg/ml) which must have induced refractory central nervous dysregulation. The lethal effects of the misapplication of this agent on the nervous system are discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1912
    Keywords: Furosemide ; Hydrochlorothiazide ; Tizolemide ; Amiloride ; Triamterene ; Interactions ; Pharmacokinetics ; Micropuncture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The interaction between furosemide on the one hand and hydrochlorothiazide, tizolemide, amiloride and triamterene on the other was studied by clearance and micropuncture techniques in rats. Simultaneous administration of furosemide with hydrochlorothiazide and tizolemide distinctly increased the natriuresis compared to that induced by furosemide alone, whereas the potassium excretion diminished. In contrast, amiloride and triamterene primarily decreased furosemide-induced fractional potassium excretion by about 30%, whereas sodium excretion increased only slightly compared to that produced by furosemide alone. Hydrochlorothiazide and triamterene significantly decreased furosemide secretion and changed its pharmacokinetics. Furosemide plasma concentration increased, thus possibly prolonging the salidiuretic effect. Amiloride and tizolemide did not influence the secretion of furosemide at all.
    Type of Medium: Electronic Resource
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