Causality assessment of adverse drug reactions: comparison of the results obtained from published decisional algorithms and from the evaluations of an expert panel.
Causality assessment of adverse drug reactions: comparison of the results obtained from published decisional algorithms and from the evaluations of an expert panel.
AF Macedo, FB Marques, CA Fontes Ribeiro, F Teixeira
Pharmacoepidemiol. Drug Saf. 14(12): 885 890, 2005
2005
Single or Multiple Injections of Metamphetamine Increased Dopamine Turnover but Did Not Decrease Tyrosine Hydroxylase Levels or Cleave Caspase-3 in Caudate-Putamen
Single or Multiple Injections of Metamphetamine Increased Dopamine Turnover but Did Not Decrease Tyrosine Hydroxylase Levels or Cleave Caspase-3 in Caudate-Putamen
F. C. Pereira, E. S. Lourenço, F. Borges, T. Morgadinho, C. A. Fontes Ribeiro, T. R. Macedo, S. F. Ali.
Synapse, 60: 185 193, 2006
2006
Can Decisional Algorithms Replace Global Introspection in the Individual Causality Assessment of Spontaneously Reported ADRs?
Can Decisional Algorithms Replace Global Introspection in the Individual Causality Assessment of Spontaneously Reported ADRs?
AF Macedo, FB Marques, CA Fontes Ribeiro
Drug Safety. 29(8):697-702, 2006
2006
Brain Blood Flow SPET Imaging in Heroin Abusers
Brain Blood Flow SPET Imaging in Heroin Abusers
M. F. Botelho, J. S. Relvas, M. Abrantes, M. J. Cunha, T. R. Marques, E. Rovira, C. A. Fontes Ribeiro and Tice Macedo.
Ann NY Acad Sci 1074: 466477, 2006
2006
Methamphetamine, Morphine, and Their Combination: Acute Changes in Striatal Dopaminergic Transmission Evaluated by Microdialysis in Awake Rats
Methamphetamine, Morphine, and Their Combination: Acute Changes in Striatal Dopaminergic Transmission Evaluated by Microdialysis in Awake Rats
FC Pereira, E Lourenço, N Milhazes, T Morgadinho, C A Fontes Ribeiro, Syed F Ali, T R Macedo
Ann NY Acad Sci 1074: 160173, 2006
2006
Mecanismos neurobiológicos da toxicodependência
Mecanismos neurobiológicos da toxicodependência
TRA Macedo e CA Fontes Ribeiro
Coimbra Médica, 2 (1): 3 19, 2006.
2006
Electromyographyc analysis of an abdominal exercise performed in trained and untrained subjects
Electromyographyc analysis of an abdominal exercise performed in trained and untrained subjects
P Tavares , E Ribeiro, M Marcelino, G Fontes Ribeiro, F Rosado and C. A. Fontes Ribeiro
Journal of the Coimbra Network of Exercise Sciences, 3(1): 55 59, 2006. (Ediction online of: Journal of the Coimbra Network of Exercise Sciences, 2006).
2006
Characterization of the human basilar artery contractile response to 5-HT and triptans
Characterization of the human basilar artery contractile response to 5-HT and triptans
SA Silva, FB Marques, CA Fontes Ribeiro
Fundamental and Clinical Pharmacology, 21(3): 265 72, 2007
2007
Pre- and postjunctional effects of ATP and NPY on sympathetic control of human uterine artery
Pre- and postjunctional effects of ATP and NPY on sympathetic control of human uterine artery
C. Cavadas, C.A. Fontes Ribeiro, C. Neta, J. Silva, S. Gulbenkian, M.T. Morgadinho, S.A.R. Silva, T.R.A Macedo
Poster with oral discussion in 3th Meeting of the Portuguese Society for Neuroscience (Espinho, December de 1996)
1996
Effect of nebicapone on the pharmacokinetics and pharmacodynamics of warfarin in healthy subjects
Effect of nebicapone on the pharmacokinetics and pharmacodynamics of warfarin in healthy subjects
Luis Almeida, Amílcar Falcão, Manuel Vaz-da-Silva, Teresa Nunes, Ana-Teresa Santos, José-Francisco Rocha, Carla Neta, Tice Macedo, C. Fontes-Ribeiro and P. Soares-da-Silva
Abstract
Objective Nebicapone is a new catechol-O-methyltransferase inhibitor. In vitro, nebicapone has showed an inhibitory effect upon CYP2C9, which is responsible for the metabolism of S-warfarin. The objective of this study was to investigate the effect of nebicapone on warfarin pharmacokinetics and pharmacodynamics in healthy subjects.
Methods Single-centre, open-label, randomised, two-period crossover study in 16 healthy volunteers. In one period, subjects received nebicapone 200 mg thrice daily for 9 days and a racemic warfarin 25-mg single dose concomitantly with the nebicapone morning dose on day 4 (test). In the other period, subjects received a racemic warfarin 25-mg single dose alone (reference). The treatment periods were separated by a washout of 14 days.
Results For R-warfarin, mean ± SD C
max was 1,619 ± 284 ng/mL for test and 1,649 ± 357 ng/mL for reference, while AUC
0-t was 92,796 ± 18,976 ng·h/mL (test) and 73,597 ± 11,363 ng·h/mL (reference). The R-warfarin test-to-reference geometric mean ratio (GMR) and 90% confidence interval (90%CI) were 0.973 (0.878–1.077) for C
max and 1.247 (1.170–1.327) for AUC
0-t . For S-warfarin, mean ± SD C
max was 1,644 ± 331 ng/mL for test and 1,739 ± 392 ng/mL for reference, while AUC
0-t was 66,627 ± 41,199 ng·h/mL (test) and 70,178 ± 42,560 ng·h/mL (reference). The S-warfarin test-to-reference GMR and 90%CI were 0.932 (0.845–1.028) for C
max and 0.914 (0.875–0.954) for AUC
0-t . No differences were found for the pharmacodynamic parameter (INR).
Conclusion Nebicapone showed no significant effect on S-warfarin pharmacokinetics or on the coagulation endpoint (INR). A mild inhibition of the R-warfarin metabolism was found but is unlikely to be of clinical relevance
Eur J Clin Pharmacol(October, 2008-Volume 64, Number 10 )
2008
http://www.springerlink.com/content/m3617087h1347604/