Abstract
This was a 2-period randomized, crossover study in 8 healthy males to determine the effects of cimetidine (400 mg q.i.d. for 6 days) on the pharmacokinetics and pharmacodynamic effects of the angiotensin II receptor antagonist, losartan (100 mg). Cimetidine increased the AUC for losartan 18% without affecting the AUC for E-3174, the active metabolite of losartan. The increase in plasma renin activity following losartan was not affected by cimetidine (maximum mean increases 12.6 and 12.1 ng Ang I.ml-1.h-1 without and with cimetidine, respectively). These results indicate that cimetidine does not appear to alter the pharmacokinetics or pharmacodynamics of losartan to a clinically significant extent.
Publication types
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Clinical Trial
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Randomized Controlled Trial
MeSH terms
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Adult
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Angiotensin Receptor Antagonists*
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Antihypertensive Agents / therapeutic use
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Biphenyl Compounds / antagonists & inhibitors
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Biphenyl Compounds / pharmacokinetics*
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Cimetidine / pharmacology*
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Cross-Over Studies
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Histamine H2 Antagonists / pharmacology*
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Humans
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Hypertension / drug therapy
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Imidazoles / antagonists & inhibitors
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Imidazoles / pharmacokinetics*
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Imidazoles / therapeutic use
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Losartan
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Male
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Tetrazoles / antagonists & inhibitors
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Tetrazoles / pharmacokinetics*
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Tetrazoles / therapeutic use
Substances
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Angiotensin Receptor Antagonists
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Antihypertensive Agents
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Biphenyl Compounds
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Histamine H2 Antagonists
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Imidazoles
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Tetrazoles
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Cimetidine
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losartan carboxylic acid
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Losartan