Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters











Database
Language
Publication year range
2.
Am J Cardiol ; 67(1): 59-62, 1991 Jan 01.
Article in English | MEDLINE | ID: mdl-1846057

ABSTRACT

The antihypertensive effects and safety profiles of lisinopril (10 to 40 mg) and atenolol (50 to 100 mg) were compared in a randomized, double-blind, parallel group trial in 144 patients with essential hypertension. After 8 weeks of therapy, seated blood pressure (BP) decreased by 26/15 mm Hg with lisinopril and by 19/14 mm Hg with atenolol. Lisinopril produced a greater reduction (p less than 0.05) in sitting systolic BP than did atenolol. Standing BP decreased by 25/15 mm Hg with lisinopril and by 19/14 mm Hg with atenolol. No important changes in hematologic and biochemical profiles were seen with either drug. Eleven patients, 7 receiving lisinopril and 4 receiving atenolol, were withdrawn because of adverse experiences; another 3 patients defaulted during treatment, 1 in the lisinopril group and 2 in the atenolol group. Both drugs were well-tolerated and are therefore suitable for first-line therapy in essential hypertension.


Subject(s)
Antihypertensive Agents/therapeutic use , Atenolol/therapeutic use , Enalapril/analogs & derivatives , Hypertension/drug therapy , Antihypertensive Agents/adverse effects , Atenolol/adverse effects , Double-Blind Method , Enalapril/adverse effects , Enalapril/therapeutic use , Female , Humans , Lisinopril , Male , Middle Aged
3.
Br J Clin Pharmacol ; 9(3): 233-7, 1980 Mar.
Article in English | MEDLINE | ID: mdl-6988003

ABSTRACT

1 Labetalol has been compared with propranolol in a double-blind, double-dummy study of 24 patients with mild or moderate essential hypertension. 2 Two patients were unable to tolerate propranolol and five labetalol, because of symptom side effects; this difference was not significant (P greater than 0.1). 3 On a self-administered questionnaire, labetalol was associated with a greater number of side effects per patient than propranolol, but no individual side effect was significantly more common with either drug. 4 There was no difference in the number of spontaneously reported side effects between the two drugs. 5 Both drugs impaired pulmonary function, but propranolol caused a greater reduction than labetalol after 8 weeks of treatment. 6 We conclude that labetalol and propranolol are similarly effective and acceptable to the patient.


Subject(s)
Ethanolamines/therapeutic use , Hypertension/drug therapy , Labetalol/therapeutic use , Propranolol/therapeutic use , Adult , Aged , Blood Pressure , Clinical Trials as Topic , Double-Blind Method , Female , Humans , Hypertension/physiopathology , Labetalol/adverse effects , Male , Middle Aged , Propranolol/adverse effects , Time Factors
SELECTION OF CITATIONS
SEARCH DETAIL