Publicaciones en las que colabora con ANA ISABEL TERLEIRA FERNÁNDEZ (18)

2022

  1. Against All Odds? Addiction History Associated with Better Viral Hepatitis Care: A Dutch Nationwide Claims Data Study

    Journal of Clinical Medicine, Vol. 11, Núm. 4

  2. Carisoprodol Single and Multiple Dose PK-PD. Part II: Pharmacodynamics Evaluation Method for Central Muscle Relaxants. Double-Blind Placebo-Controlled Clinical Trial in Healthy Volunteers

    Journal of Clinical Medicine, Vol. 11, Núm. 4

2020

  1. Effect of enantiomerism on the bioequivalence of a new ibuprofen 600-mg tablet formulation obtained by roller compaction

    Chirality, Vol. 32, Núm. 2, pp. 185-190

2019

  1. Effect of Roux-en-Y gastric surgery on ciprofloxacin pharmacokinetics: an obvious effect?

    European Journal of Clinical Pharmacology, Vol. 75, Núm. 5, pp. 647-654

2010

  1. Better sexual acceptability of agomelatine (25 and 50 mg) compared with paroxetine (20 mg) in healthy male volunteers. An 8-week, placebo-controlled study using the PRSEXDQ-SALSEX scale

    Journal of Psychopharmacology, Vol. 24, Núm. 1, pp. 111-120

2009

  1. Estudio piloto de utilizaeión de antifúngieos sistémieos en el Hospital Clínieo San Carlos. Propuesta de un método de estudio

    Revista Espanola de Quimioterapia, Vol. 22, Núm. 3, pp. 127-134

2007

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

    Pharmacoepidemiology and Drug Safety, Vol. 16, Núm. 1, pp. 39-45

2006

  1. Effects of Hypericum perforation on ivabradine pharmacokinetics in healthy volunteers: An open-label, pharmacokinetic interaction clinical trial

    Journal of Clinical Pharmacology, Vol. 46, Núm. 10, pp. 1188-1194

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

    Journal of Clinical Pharmacology, Vol. 46, Núm. 10, pp. 1195-1203

2005

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

    Arzneimittel-Forschung/Drug Research, Vol. 55, Núm. 4, pp. 212-217

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

    Arzneimittel-Forschung/Drug Research, Vol. 55, Núm. 4, pp. 191-197

  3. Erratum: Bioequivalence study of two different tablet formulations of carvedilol in healthy volunteers (Arzneimittel-Forschung/Drug Research (2005) 55, 4 (212-217))

    Arzneimittel-Forschung/Drug Research

2004

  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

    Current Therapeutic Research - Clinical and Experimental, Vol. 65, Núm. 1, pp. 34-46

2003

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

    Current Therapeutic Research - Clinical and Experimental, Vol. 64, Núm. 7, pp. 401-411

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

    Critical Care Medicine, Vol. 31, Núm. 3, pp. 694-698

2002

  1. Pharmacokinetic study of a new ibuprofen 600mg plus codeine 30mg combination versus ibuprofen or codeine alone in single oral doses in healthy volunteers

    Clinical Drug Investigation, Vol. 22, Núm. 1, pp. 41-49

2001

  1. Comparative single-dose bioavailability study of two oral formulations of ibuprofen in healthy volunteers

    Clinical Drug Investigation, Vol. 21, Núm. 5, pp. 383-389

2000

  1. Modification of albumin use pattern after an educational intervention

    Disease Management and Health Outcomes, Vol. 8, Núm. 1, pp. 43-50