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Olmesartan
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| Systematic (IUPAC) name | |
| (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 5-(2-hydroxypropan-2-yl)-2-propyl-3-[ [4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]imidazole-4-carboxylate | |
| Identifiers | |
| CAS number | |
| ATC code | C09 |
| PubChem | |
| DrugBank | |
| Chemical data | |
| Formula | C29H30N6O6 |
| Mol. mass | 558.585 g/mol |
| SMILES | & |
| Pharmacokinetic data | |
| Bioavailability | 26% (olmesartan medoxomil) |
| Metabolism | Hepatic (cannot be removed by hemodialysis) |
| Half life | 13 hours |
| Excretion | Renal 40%, biliary 60% |
| Therapeutic considerations | |
| Pregnancy cat. |
C (D if used in second or third trimester) |
| Legal status |
℞ Prescription only |
| Routes | Oral |
Olmesartan (Benicar,Olmetec) belongs to the class of medicines called angiotensin II receptor antagonists to treat high blood pressure. It is marketed worldwide by Daiichi Sankyo, Ltd. and in the United States by Daiichi Sankyo, Inc. and Forest Laboratories. Olmesartan works by blocking the binding of angiotensin II to the AT1 receptors in vascular muscle; it is therefore independent of angiotensin II synthesis pathways, unlike ACE inhibitors. By blocking binding rather than synthesis of angiotensin II, olmesartan inhibits the negative regulatory feedback on renin secretion. As a result of this blockage, olmesartan restricts vasoconstriction and the secretion of aldosterone. This lowers blood pressure by producing vasodilation, and decreasing peripheral resistance.Olmesartan also has high affinity for the Vitamin D Receptor[1] and because of the role of the Vitamin D receptor in innate immunity[2], olmesartan has immune modulatory properties.
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Administration
Olmesartan is available in 5, 20, and 40 mg tablets. A normal dose for an adult (including the elderly and mild renal or hepatic impairment) is 20 mg/day in one dosage. This may be increased after two weeks to 40 mg/day if further blood pressure reduction is needed.
Myocardial infarction
A recent meta-analysis published in the peer-reviewed journal Circulation demonstrated that angiotensin II receptor antagonist induce myocardial infarction compared to placebo.[3]
Side effects
Side effects include:
- Dizziness
- Headache
- Diarrhea
- Upper respiratory tract infection
- Fast or slow heart rate [1]
- Cough, dry and unproductive, moderate to severe [2]
Notes
^1. Website of National Institute of Heath, US Government. http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a603006.html#side-effects
^2. Website of Daiichi Sankyo, Inc. Goto: http://www.benicar.com/prod_info/index.asp?ref=1001011101 and open .pdf files containing product information Benicar and Benicar HCT
References
- ^ http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=16403216
- ^ http://www.ncbi.nlm.nih.gov/pubmed/16497887?ordinalpos=17&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum - [PubMed]
- ^ Strauss MH, Hall AS. (2006). "Angiotensin receptor blockers may increase risk of myocardial infarction: unraveling the ARB-MI paradox.". Circulation 8 (114): 838–54. doi:. PMID 16923768.
Hodgson, Barbara B., and Kizior, Robert J. Saunders Nursing Drug Handbook 2006. St. Louis, MO: Elsevier, Saunders, 2006.
External links
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Wikipedia content modification information:
- This page was last modified on 1 July 2008, at 20:22.
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