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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    BJOG 75 (1968), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 167 (1969), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of cardiovascular electrophysiology 4 (1986), S. 0 
    ISSN: 1540-8167
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In an investigation designed to study the nature and prevalence of side effects during long-term therapy and the degree of correlation between side effects and the drug serum level, starting in 1975, mexiletine was given to 12 patients for 4 to 128 months with a mean of 56.2 months. The patients were followed according to a strict protocol for the first 18 months of treatment and then returned to routine care. In August 1983, 5 patients had been taking mexiletine for 74 and 96 months (mean 85 months). At the latest follow-up in April 1986, two patients were still on mexiletine therapy after 117 and 128 months of medication, respectively. A third patient died of probable digitalis intoxication just prior to follow-up, having then been on mexiletine for 118 months, Mexiletine was well tolerated and no serious side effects were seen. In particular, there was no rise in antinuclear factor titer. The serum level of mexiletine was easily maintained within the therapeutic range. The cerebral side effects correlated closely with the drug level; the gastrointestinal with the amount of mexiletine per dose. It is concluded that mexiletine can be administered for a long time as a safe alternative to other anti arrhythmic drugs.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cardiovascular drugs and therapy 6 (1992), S. 219-223 
    ISSN: 1573-7241
    Keywords: adrenaline ; hypertension ; metabolism ; amiloride ; hydrochlorothiazide ; lisinopril ; electrocardiogram
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Twelve healthy male volunteers were given adrenaline infusions, 0.05 μg/kg body weight/min over 120 minutes in order to achieve serum adrenaline concentrations comparable with those seen in acute myocardial infarction. The infusions were given on four occasions, at intervals of at least 4 weeks. Before the infusions the subjects were given, in random order, 14 days of pretreatment with placebo, hydrochlorothiazide 50 mg once daily, amiloride 10 mg once daily, or lisinorpil 20 mg once daily. The adrenaline infusion induced a drop in serum potassium of the same magnitude in all four groups, with the lowest absolute value after hydrochlorothiazide because of the lowest pre-adrenaline level. The infusion-induced decreases in serum calcium and magnesium were of the same magnitude in all groups, with the absolute calcium being least low in the hydrochlorothiazide group because of the highest preinfusion value. Preinfusion serum urate was highest after hydrochlorothiazide and fell during the adrenaline infusion in all groups, although not significantly. Blood glucose increased during the adrenaline infusion in all groups, but significantly more after hydrochlorothiazide and amiloride than after lisinopril. Heart rate increased during the adrenaline infusion in all groups but least after lisinopril. QTc preinfusion was longer after hydrochlorothiazide than after amiloride and placebo, but the infusion-induced prolongation of QTc was of the same magnitude in all pretreatment groups. Since our results were obtained in short-term experiments in normal subjects, their clinical relevance is question-able, but they support the view that ACE inhibitors may have certain metabolic advantages over diuretics.
    Type of Medium: Electronic Resource
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