La tercanidipine, un inhibiteur calcique de troisieme generation. Quels avantages? [Lercanidipine, a third generation calcium antagonist. Which advantages?]

Details

Serval ID
serval:BIB_FBB719F76B34
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
La tercanidipine, un inhibiteur calcique de troisieme generation. Quels avantages? [Lercanidipine, a third generation calcium antagonist. Which advantages?]
Journal
Revue Médicale Suisse
Author(s)
Meier  P., Burnier  M.
ISSN
1660-9379 (Print)
Publication state
Published
Issued date
09/2006
Volume
2
Number
78
Pages
2047-50, 2052-3
Notes
Comparative Study
English Abstract
Journal Article
Review --- Old month value: Sep 13
Abstract
Lercanidipine is a new highly lipophylic dihydropyrdine derivative of the third generation with equal efficacy but an improved tolerability profile. Comparative therapeutic trials have shown that it is as effective as other dihydropyridines, in particular amlodipine, beta-blockers, and angiotensin-converting enzyme inhibitors. Lercanidipine is well tolerated, with most treatment-emergent events related to vasodilation. Lercanidipine produces less reflex tachycardia and peripheral oedema. Common adverse events included headache and flushing. Because of its efficacy and favorable safety profile, lercanidipine has the potential to improve blood pressure control in a wide range of patients, including those who have not responded to, or who have been unable to tolerate other antihypertensive agents.
Keywords
Antihypertensive Agents/pharmacology/*therapeutic use Blood Pressure/drug effects Calcium Channel Blockers/pharmacology/*therapeutic use Controlled Clinical Trials Dihydropyridines/pharmacology/*therapeutic use Humans Hypertension/*drug therapy Severity of Illness Index Treatment Outcome
Pubmed
Create date
25/01/2008 13:56
Last modification date
20/08/2019 17:26
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