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1.
Arzneimittelforschung ; 42(12): 1473-7, 1992 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-1288512

RESUMO

The efficacy and tolerance of a garlic preparation (Sapec, Kwai) was investigated in a randomized double-blind study vs. bezafibrate. This multi-centre study was conducted in 5 general medical practices and involved 98 patients with primary hyperlipoproteinaemia. The daily doses of the active substances were 900 mg of garlic powder (standardized as to 1.3% alliin) and 600 mg of bezafibrate, respectively. The pre-phase with placebo lasted 6 weeks, the treatment period covered 12 weeks. All patients were advised to observe a low-fat "step-1 diet" for the duration of the study. The 98 case report forms allowed the statistical evaluation of total cholesterol, HDL cholesterol and triglyceride levels for 94 patients, and of LDL cholesterol values for 92 patients. In the course of the treatment both study medications caused a statistically highly significant reduction in total cholesterol, in LDL cholesterol and triglycerides, and an increase in HDL cholesterol. However, there was no significant difference in the efficacies of both medication groups. Side effects were mentioned by 5 patients each in both treatment groups, none of which led to the withdrawal of the patients. Concerning the garlic preparation, there was no correlation between the perception of garlic odour and the influence on the cholesterol level.


Assuntos
Bezafibrato/farmacologia , Alho , Hiperlipoproteinemias/tratamento farmacológico , Plantas Medicinais , Idoso , Bezafibrato/efeitos adversos , Pressão Sanguínea/efeitos dos fármacos , Colesterol/sangue , HDL-Colesterol/sangue , LDL-Colesterol/sangue , Método Duplo-Cego , Feminino , Frequência Cardíaca/efeitos dos fármacos , Humanos , Hiperlipoproteinemia Tipo II/sangue , Hiperlipoproteinemia Tipo II/tratamento farmacológico , Hiperlipoproteinemia Tipo III/sangue , Hiperlipoproteinemia Tipo III/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Odorantes , Triglicerídeos/sangue
2.
Fortschr Med ; 108(28): 539-42, 1990 Sep 30.
Artigo em Alemão | MEDLINE | ID: mdl-2242840

RESUMO

In the treatment of cardiac arrhythmias of varying genesis, an "observational study" in 1,160 patients showed that a high-dose oral magnesium preparation (Magnesium-Diasporal N 300 Granulat) was effective. In 82% of the patients observed, a dose of at least 300 mg magnesium/day produced good to very good results. Adverse effects of the drug were observed in only 1.6% of the patients. For all groups, the "success parameters" improved significantly. High-rate arrhythmias showed a better response to magnesium treatment than did low-rate arrhythmias, with a close correlation being found with the heart rate at the start of treatment. High-dose oral magnesium had a positive effect on concomitant hypertension. At a dosage of 300 mg treatment should be continued for at least 6 weeks.


Assuntos
Arritmias Cardíacas/tratamento farmacológico , Ácidos Levulínicos/uso terapêutico , Adulto , Idoso , Relação Dose-Resposta a Droga , Feminino , Frequência Cardíaca/efeitos dos fármacos , Humanos , Ácidos Levulínicos/administração & dosagem , Ácidos Levulínicos/efeitos adversos , Masculino , Pessoa de Meia-Idade
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