Abstract | AIMS: METHODOLOGY: After an informed consent, 16 patients with essential hypertension were recruited. After a wash out period, the patients received increasing doses of Moxonidine (maximum dose 0.6 mg) for four weeks to control the blood pressure. RESULTS: The mean reduction in blood pressure (systolic/diastolic) was 17.6/14.5 mm Hg in supine position and 18.2/12.6 mm Hg in standing position. The significant side effect was observed only in one patient. CONCLUSIONS:
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Authors | S Jain, P Malhotra, S Kumari, S Varma |
Journal | The Journal of the Association of Physicians of India
(J Assoc Physicians India)
Vol. 49
Pg. 829-30
(Aug 2001)
ISSN: 0004-5772 [Print] India |
PMID | 11837474
(Publication Type: Clinical Trial, Journal Article)
|
Chemical References |
- Antihypertensive Agents
- Imidazoles
- moxonidine
|
Topics |
- Adult
- Aged
- Antihypertensive Agents
(adverse effects, therapeutic use)
- Blood Pressure
(drug effects, physiology)
- Epistaxis
(chemically induced)
- Female
- Humans
- Hypertension
(drug therapy, physiopathology)
- Imidazoles
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Severity of Illness Index
|