Literature DB >> 2719894

Cardiovascular (ECG and systolic time intervals) and anticholinergic effects of repeated doses of femoxetine--a comparison with amitriptyline and placebo in healthy men.

S J Warrington1, P Turner, B K Skrumsager.   

Abstract

1. The cardiovascular and anticholinergic effects of femoxetine and amitriptyline were compared with those of placebo in a double-blind cross-over trial in 12 healthy men. The daily doses administered were therapeutic: 600 mg femoxetine and 150 mg amitriptyline. Duration of treatment with each drug was 13 days. 2. The statistically significant effects on systolic time intervals and ECG comprised a larger decrease of QS2 index during femoxetine than during amitriptyline, and an increase of PEP/LVET ratio and QRS duration by amitriptyline. These results suggest that femoxetine and, to a lesser extent, amitriptyline increase contractility compared with placebo, and amitriptyline, but not femoxetine, causes delay in intracardiac conduction. 3. The effects of amitriptyline on the systolic time intervals are difficult to interpret because of the changes in heart rate and intracardiac electrical conduction caused by the drug. These problems of interpretation are discussed. 4. No significant changes in blood pressure were observed. The heart rate during both femoxetine and amitriptyline periods was significantly faster than during the placebo period, amitriptyline causing a significantly greater increase. 5. Salivary secretion was decreased more by amitriptyline (26%) than by femoxetine (8%), the latter being not significantly different from placebo. Femoxetine tended to increase pupil diameter and amitriptyline to increase accommodation near point, but no visual disturbances were reported on any treatment. Symptoms such as dry mouth, constipation and sedation were significantly less frequently reported during femoxetine than during amitriptyline treatment.

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Year:  1989        PMID: 2719894      PMCID: PMC1379833          DOI: 10.1111/j.1365-2125.1989.tb05375.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  30 in total

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Journal:  J Chromatogr       Date:  1977-03-11

5.  Systolic time interval v heart rate regression equations using atropine: reproducibility studies.

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Journal:  Br J Clin Pharmacol       Date:  1981-07       Impact factor: 4.335

6.  Antidepressant evaluation and the pharmacological actions of FG4963 in depressive patients.

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Journal:  Eur J Pharmacol       Date:  1977-03-07       Impact factor: 4.432

7.  The cardiac effects of therapeutic plasma concentrations of imipramine.

Authors:  S J Kantor; A H Glassman; J T Bigger; J M Perel; E V Giardina
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8.  Electrocardiogram changes and plasma desipramine levels during treatment of depression.

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9.  Cardiovascular effect of imipramine and nortriptyline in elderly patients.

Authors:  P Thayssen; M Bjerre; P Kragh-Sørensen; M Møller; O L Petersen; C B Kristensen; L F Gram
Journal:  Psychopharmacology (Berl)       Date:  1981       Impact factor: 4.530

10.  Paroxetine: pharmacokinetics, tolerance and depletion of blood 5-HT in man.

Authors:  J Lund; B Lomholt; J Fabricius; J A Christensen; E Bechgaard
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1979-04
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  3 in total

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2.  The bioavailability of digoxin from three oral formulations measured by a specific h.p.l.c. assay.

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3.  Physiologically based pharmacokinetic-quantitative systems toxicology and safety (PBPK-QSTS) modeling approach applied to predict the variability of amitriptyline pharmacokinetics and cardiac safety in populations and in individuals.

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  3 in total

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