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Clinical pharmacology of ramipril.
- Source :
-
The American journal of cardiology [Am J Cardiol] 1987 Apr 24; Vol. 59 (10), pp. 23D-27D. - Publication Year :
- 1987
-
Abstract
- Ramipril is a long-acting non-sulphydryl converting enzyme inhibitor that requires cleavage of its ester group to form the active diacid metabolite, ramiprilat. Renal excretion largely determines the drug's duration of action and the dosage should be reduced in patients with renal impairment. Oral ramipril given daily at dosages of 5 mg or more can control blood pressure over a 24-hour period; lower doses may be effective in patients with heart failure inadequately controlled by diuretics alone. No serious idiosyncratic adverse reactions have been reported. Ramipril is one of the most potent long-acting converting enzyme inhibitors developed; it is effective given once daily in the treatment of all grades of hypertension and of heart failure.
- Subjects :
- Antihypertensive Agents metabolism
Blood Pressure drug effects
Bridged Bicyclo Compounds metabolism
Half-Life
Humans
Ramipril
Renin-Angiotensin System drug effects
Angiotensin-Converting Enzyme Inhibitors
Antihypertensive Agents therapeutic use
Bridged Bicyclo Compounds therapeutic use
Bridged-Ring Compounds therapeutic use
Heart Failure drug therapy
Hypertension drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 0002-9149
- Volume :
- 59
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- The American journal of cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 3034028
- Full Text :
- https://doi.org/10.1016/0002-9149(87)90048-8