Portolés A - Search Results

1

Bioequivalence study of two formulations of enalapril, at a single oral dose of 20 mg (tablets): A randomized, two-way, open-label, crossover study in healthy volunteers.

Portolés A, Terleira A, Almeida S, García-Arenillas M, Caturla MC, Filipe A, Vargas E. Portolés A, et al. Curr Ther Res Clin Exp. 2004 Jan;65(1):34-46. doi: 10.1016/S0011-393X(04)90003-3. Curr Ther Res Clin Exp. 2004. PMID: 24936102 Free PMC article.

2

Bioequivalence study of two different tablet formulations of carvedilol in healthy volunteers.

Portolés A, Filipe A, Almeida S, Terleira A, Vallée F, Vargas E. Portolés A, et al. Arzneimittelforschung. 2005;55(4):212-7. doi: 10.1055/s-0031-1296847. Arzneimittelforschung. 2005. PMID: 15901044 Clinical Trial.

3

A new high-absorption-rate Paracetamol 500-mg formulation: a comparative bioavailability study in healthy volunteers.

Portolés A, Puerro M, Terleira A, Rodríguez A, Caturla MC, Fernández N, Vargas E. Portolés A, et al. Curr Ther Res Clin Exp. 2003 Jul;64(7):401-11. doi: 10.1016/S0011-393X(03)00110-3. Curr Ther Res Clin Exp. 2003. PMID: 24944391 Free PMC article.

4

Truncated AUC in the evaluation of fluconazole bioequivalence. A cross-over, randomised, open-label study in healthy volunteers.

Portolés A, Almeida S, Terleira A, de Pablo I, Filipe A, Cruz Caturla M, Moreno A. Portolés A, et al. Arzneimittelforschung. 2004;54(11):752-6. doi: 10.1055/s-0031-1297032. Arzneimittelforschung. 2004. PMID: 15612616 Clinical Trial.

5

Comparative bioavailability/ bioequivalence of two different sertraline formulations: a randomised, 2-period x 2-sequence, crossover clinical trial in healthy volunteers.

Almeida S, Portolés A, Terleira A, Filipe A, Cea E, Caturla MC. Almeida S, et al. Among authors: portoles a. Arzneimittelforschung. 2005;55(4):191-7. doi: 10.1055/s-0031-1296844. Arzneimittelforschung. 2005. PMID: 15901041 Clinical Trial.

6

Lack of pharmacokinetic interaction between omeprazole or lansoprazole and ivabradine in healthy volunteers: an open-label, randomized, crossover, pharmacokinetic interaction clinical trial.

Portolés A, Calvo A, Terleira A, Laredo L, Resplandy G, Gorostiaga C, Moreno A. Portolés A, et al. J Clin Pharmacol. 2006 Oct;46(10):1195-203. doi: 10.1177/0091270006291624. J Clin Pharmacol. 2006. PMID: 16988209 Clinical Trial.

7

Effects of Hypericum perforatum on ivabradine pharmacokinetics in healthy volunteers: an open-label, pharmacokinetic interaction clinical trial.

Portolés A, Terleira A, Calvo A, Martínez I, Resplandy G. Portolés A, et al. J Clin Pharmacol. 2006 Oct;46(10):1188-94. doi: 10.1177/0091270006291623. J Clin Pharmacol. 2006. PMID: 16988208 Clinical Trial.

8

Effect of adverse drug reactions on length of stay in surgical intensive care units.

Vargas E, Terleira A, Hernando F, Perez E, Cordón C, Moreno A, Portolés A. Vargas E, et al. Among authors: portoles a. Crit Care Med. 2003 Mar;31(3):694-8. doi: 10.1097/01.CCM.0000049947.80131.ED. Crit Care Med. 2003. PMID: 12626971

9

Effect of drug-test interactions on length of hospital stay.

Terleira A, Portolés A, Rojas A, Vargas E. Terleira A, et al. Among authors: portoles a. Pharmacoepidemiol Drug Saf. 2007 Jan;16(1):39-45. doi: 10.1002/pds.1330. Pharmacoepidemiol Drug Saf. 2007. PMID: 17013947

10

Truncated area under the urinary excretion rate curve in the evaluation of alendronate bioequivalence after a single dose in healthy volunteers.

Portolés A, Prieto E, Calvo A, Laredo L, Fernández N, Vargas E. Portolés A, et al. Arzneimittelforschung. 2009;59(8):397-402. doi: 10.1055/s-0031-1296414. Arzneimittelforschung. 2009. PMID: 19813462 Clinical Trial.

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