A systematic comparison of the properties of clinically used angiotensin II type 1 receptor antagonists
MC Michel, C Foster, HR Brunner, L Liu - Pharmacological reviews, 2013 - ASPET
Angiotensin II type 1 receptor antagonists (ARBs) have become an important drug class in
the treatment of hypertension and heart failure and the protection from diabetic nephropathy …
the treatment of hypertension and heart failure and the protection from diabetic nephropathy …
Clinical pharmacokinetics of angiotensin II (AT1) receptor blockers in hypertension
ZH Israili - Journal of human hypertension, 2000 - nature.com
Angiotensin II receptor blockers (ARBs) represent a new class of effective and well tolerated
orally active antihypertensive agents. Recent clinical trials have shown the added benefits of …
orally active antihypertensive agents. Recent clinical trials have shown the added benefits of …
Effects of renal failure on drug transport and metabolism
H Sun, L Frassetto, LZ Benet - Pharmacology & therapeutics, 2006 - Elsevier
Renal failure not only alters the renal elimination, but also the non-renal disposition of drugs
that are extensively metabolized by the liver. Although reduced metabolic enzyme activity in …
that are extensively metabolized by the liver. Although reduced metabolic enzyme activity in …
Angiotensin II AT1 receptor antagonists. Clinical implications of active metabolites
B Schmidt, B Schieffer - Journal of medicinal chemistry, 2003 - ACS Publications
The renin angiotensin system (RAS) is one of the most powerful regulators of blood pressure
and volume homeostasis in mammals. Its effector peptide angiotensin II (ANG II) is cleaved …
and volume homeostasis in mammals. Its effector peptide angiotensin II (ANG II) is cleaved …
Hepatic clearance, but not gut availability, of erythromycin is altered in patients with end‐stage renal disease
H Sun, LA Frassetto, Y Huang… - Clinical Pharmacology & …, 2010 - Wiley Online Library
Nonrenal clearance of drugs can be significantly lower in patients with end‐stage renal
disease (ESRD) than in those with normal renal function. Using erythromycin (ER) as a …
disease (ESRD) than in those with normal renal function. Using erythromycin (ER) as a …
Pharmacokinetics of the oral direct renin inhibitor aliskiren alone and in combination with irbesartan in renal impairment
S Vaidyanathan, H Bigler, CM Yeh, MN Bizot… - Clinical …, 2007 - Springer
Background Aliskiren is an orally active direct renin inhibitor approved for the treatment of
hypertension. This study assessed the effects of renal impairment on the pharmacokinetics …
hypertension. This study assessed the effects of renal impairment on the pharmacokinetics …
Effect of severe renal failure and haemodialysis on the pharmacokinetics of levosimendan and its metabolites
J Puttonen, S Kantete, M Kivikko, S Häkkinen… - Clinical …, 2007 - Springer
Background and objectives Levosimendan is a calcium sensitiser developed for the
treatment of congestive heart failure. It increases myocardial contractility, reduces the filling …
treatment of congestive heart failure. It increases myocardial contractility, reduces the filling …
Effects of uremic toxins on transport and metabolism of different biopharmaceutics drug disposition classification system xenobiotics
M Reyes, LZ Benet - Journal of pharmaceutical sciences, 2011 - Elsevier
Chronic kidney disease (CKD) is recognized to cause pharmacokinetic changes in renally
excreted drugs; however, pharmacokinetic changes are also reported for drugs that are …
excreted drugs; however, pharmacokinetic changes are also reported for drugs that are …
A physiologically based pharmacokinetic model of ertapenem in pediatric patients with renal impairment
L Ye, M Ke, X You, P Huang, C Lin - Journal of pharmaceutical sciences, 2020 - Elsevier
Ertapenem is a widely used antibiotic; however, its pharmacokinetics has not been fully
evaluated in children with renal impairment. A physiologically based pharmacokinetic …
evaluated in children with renal impairment. A physiologically based pharmacokinetic …
Pharmacokinetics of eprosartan in healthy subjects, patients with hypertension, and special populations
MB Bottorff, DM Tenero - Pharmacotherapy: The Journal of …, 1999 - Wiley Online Library
After oral administration of eprosartan to healthy volunteers, bioavailability is approximately
13%, with peak plasma concentrations occurring 1–2 hours after an oral dose in the fasted …
13%, with peak plasma concentrations occurring 1–2 hours after an oral dose in the fasted …