-
2
-
-
0029860967
-
Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity
-
Carrillo JA, Dahl ML, Svensson JO, Alm C, Rodriguez I, Bertilsson L. Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity. Clin Pharmacol Ther 1996;60:183-90.
-
(1996)
Clin Pharmacol Ther
, vol.60
, pp. 183-190
-
-
Carrillo, J.A.1
Dahl, M.L.2
Svensson, J.O.3
Alm, C.4
Rodriguez, I.5
Bertilsson, L.6
-
3
-
-
0027406654
-
Fluvoxamine is a potent inhibitor of cytochrome P4501A2
-
Brøsen K, Skjelbo E, Rasmussen BB, Poulsen HE, Loft S. Fluvoxamine is a potent inhibitor of cytochrome P4501A2. Biochem Pharmacol 1993;45:1211-4.
-
(1993)
Biochem Pharmacol
, vol.45
, pp. 1211-1214
-
-
Brøsen, K.1
Skjelbo, E.2
Rasmussen, B.B.3
Poulsen, H.E.4
Loft, S.5
-
4
-
-
0026725007
-
Interaction between fluvoxamine and imipramine/desipramine in four patients
-
Spina E, Campo GM, Avenoso A, Pollicino MA, Caputi AP. Interaction between fluvoxamine and imipramine/desipramine in four patients. Ther Drug Monit 1992;14:194-6.
-
(1992)
Ther Drug Monit
, vol.14
, pp. 194-196
-
-
Spina, E.1
Campo, G.M.2
Avenoso, A.3
Pollicino, M.A.4
Caputi, A.P.5
-
5
-
-
0025921081
-
Possible interaction between theophylline and fluvoxamine
-
Diot P, Jonville AP, Gerard F, Bonnelle M, Autret E, Breteau M, et al. Possible interaction between theophylline and fluvoxamine [letter]. Therapie 1991;46: 170-1.
-
(1991)
Therapie
, vol.46
, pp. 170-171
-
-
Diot, P.1
Jonville, A.P.2
Gerard, F.3
Bonnelle, M.4
Autret, E.5
Breteau, M.6
-
6
-
-
0026041851
-
Toxic interaction between fluvoxamine and sustained release theophylline in an 11-year-old boy
-
Sperber AD. Toxic interaction between fluvoxamine and sustained release theophylline in an 11-year-old boy. Drug Saf 1991;6:460-2.
-
(1991)
Drug Saf
, vol.6
, pp. 460-462
-
-
Sperber, A.D.1
-
7
-
-
0026019728
-
Fluvoxamine-tricyclic antidepressant interaction: An accidental finding
-
Bertschy G, Vandel S, Vandel B, Allers G, Volmat R. Fluvoxamine-tricyclic antidepressant interaction: an accidental finding [letter]. Eur J Clin Pharmacol 1991; 40:119-20.
-
(1991)
Eur J Clin Pharmacol
, vol.40
, pp. 119-120
-
-
Bertschy, G.1
Vandel, S.2
Vandel, B.3
Allers, G.4
Volmat, R.5
-
8
-
-
0028016505
-
Elevated levels of clozapine in serum after addition of fluvoxamine
-
Hiemke C, Weigmann H, Härtter S, Dahmen N, Wetzel H, Müller H. Elevated levels of clozapine in serum after addition of fluvoxamine. J Clin Psychopharmacol 1994;14:279-81.
-
(1994)
J Clin Psychopharmacol
, vol.14
, pp. 279-281
-
-
Hiemke, C.1
Weigmann, H.2
Härtter, S.3
Dahmen, N.4
Wetzel, H.5
Müller, H.6
-
9
-
-
0028318482
-
Fluvoxamine inhibition and carbamazepine induction of the metabolism of clozapine: Evidence from a therapeutic drug monitoring service
-
Jerling M, Lindstrom L, Bondesson U, Bertilsson L. Fluvoxamine inhibition and carbamazepine induction of the metabolism of clozapine: evidence from a therapeutic drug monitoring service. Ther Drug Monit 1994;16:368-74.
-
(1994)
Ther Drug Monit
, vol.16
, pp. 368-374
-
-
Jerling, M.1
Lindstrom, L.2
Bondesson, U.3
Bertilsson, L.4
-
10
-
-
0029974521
-
A fluvoxamine-caffeine interaction study
-
Jeppesen U, Loft S, Poulsen HE, Brøsen K. A fluvoxamine-caffeine interaction study, Pharmacogenetics 1996;6:213-22.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 213-222
-
-
Jeppesen, U.1
Loft, S.2
Poulsen, H.E.3
Brøsen, K.4
-
11
-
-
0026787192
-
The effect of selective serotonin reuptake inhibitors on cytochrome P4502D6 (CYP2D6) activity in human liver microsomes
-
Crewe HK, Lennard MS, Tucker GT, Woods FR, Haddock RE. The effect of selective serotonin reuptake inhibitors on cytochrome P4502D6 (CYP2D6) activity in human liver microsomes. Br J Clin Pharmacol 1992;34:262-5.
-
(1992)
Br J Clin Pharmacol
, vol.34
, pp. 262-265
-
-
Crewe, H.K.1
Lennard, M.S.2
Tucker, G.T.3
Woods, F.R.4
Haddock, R.E.5
-
12
-
-
0026795695
-
Inhibitors of imipramine metabolism by human liver microsomes
-
Skjelbo E, Brøsen K. Inhibitors of imipramine metabolism by human liver microsomes. Br J Clin Pharmacol 1992;34:256-61.
-
(1992)
Br J Clin Pharmacol
, vol.34
, pp. 256-261
-
-
Skjelbo, E.1
Brøsen, K.2
-
13
-
-
0027254118
-
Effect of fluvoxamine on the pharmacokinetics of imipramine and desipramine in healthy subjects
-
Spina E, Pollicino AM, Avenoso A, Campo GM, Perucca E, Caputi AP. Effect of fluvoxamine on the pharmacokinetics of imipramine and desipramine in healthy subjects. Ther Drug Monit 1993;15:243-6.
-
(1993)
Ther Drug Monit
, vol.15
, pp. 243-246
-
-
Spina, E.1
Pollicino, A.M.2
Avenoso, A.3
Campo, G.M.4
Perucca, E.5
Caputi, A.P.6
-
14
-
-
0029738965
-
Dose dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine
-
Jeppesen U, Gram LF, Vistisen K, Loft S, Poulsen HE, Brøsen K. Dose dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine. Eur J Clin Pharmacol 1996;51:73-8.
-
(1996)
Eur J Clin Pharmacol
, vol.51
, pp. 73-78
-
-
Jeppesen, U.1
Gram, L.F.2
Vistisen, K.3
Loft, S.4
Poulsen, H.E.5
Brøsen, K.6
-
15
-
-
0029068546
-
Fluvoxamine and fluoxetine: Interaction studies with amitriptyline, clomipramine and neuroleptics in phenotyped patients
-
Vandel S, Bertschy G, Baumann P, Bouquet S, Bonin B, Francois T, et al. Fluvoxamine and fluoxetine: interaction studies with amitriptyline, clomipramine and neuroleptics in phenotyped patients. Pharmacol Res 1995;31:347-53.
-
(1995)
Pharmacol Res
, vol.31
, pp. 347-353
-
-
Vandel, S.1
Bertschy, G.2
Baumann, P.3
Bouquet, S.4
Bonin, B.5
Francois, T.6
-
16
-
-
0028898044
-
Selective serotonin reuptake inhibitors and theophylline metabolism in human liver microsomes: Potent inhibition by fluvoxamine
-
Rasmussen BB, Maenpaa J, Pelkonen O, Loft S, Poulsen HE, Lykkesfeldt J, et al. Selective serotonin reuptake inhibitors and theophylline metabolism in human liver microsomes: potent inhibition by fluvoxamine. Br J Clin Pharmacol 1995;39:151-9.
-
(1995)
Br J Clin Pharmacol
, vol.39
, pp. 151-159
-
-
Rasmussen, B.B.1
Maenpaa, J.2
Pelkonen, O.3
Loft, S.4
Poulsen, H.E.5
Lykkesfeldt, J.6
-
17
-
-
0000924175
-
A metabolite of "Paludrine" with high antimalarial activity
-
Carrington HC, Crowther AF, Davey DG, Levi AA, Rose FL. A metabolite of "Paludrine" with high antimalarial activity. Nature 1951;168:1080.
-
(1951)
Nature
, vol.168
, pp. 1080
-
-
Carrington, H.C.1
Crowther, A.F.2
Davey, D.G.3
Levi, A.A.4
Rose, F.L.5
-
18
-
-
0024371975
-
Inter-subject variability in the metabolism of proguanil to the active metabolite cycloguanil in man
-
Ward SA, Watkins WM, Mberu E, Saunders JE, Koech DK, Gilles HM, et al. Inter-subject variability in the metabolism of proguanil to the active metabolite cycloguanil in man. Br J Clin Pharmacol 1989;27: 781-7.
-
(1989)
Br J Clin Pharmacol
, vol.27
, pp. 781-787
-
-
Ward, S.A.1
Watkins, W.M.2
Mberu, E.3
Saunders, J.E.4
Koech, D.K.5
Gilles, H.M.6
-
19
-
-
0025307263
-
In vitro metabolism of the biguanide antimalarials in human liver microsomes: Evidence for a role of the mephenytoin hydroxylase (P450 MP) enzyme
-
Helsby NA, Ward SA, Howells RE, Breckenridge AM. In vitro metabolism of the biguanide antimalarials in human liver microsomes: evidence for a role of the mephenytoin hydroxylase (P450 MP) enzyme. Br J Clin Pharmacol 1990;30:287-91.
-
(1990)
Br J Clin Pharmacol
, vol.30
, pp. 287-291
-
-
Helsby, N.A.1
Ward, S.A.2
Howells, R.E.3
Breckenridge, A.M.4
-
20
-
-
0025735576
-
The activation of the biguanide antimalarial proguanil co-segregates with the mephenytoin oxidation polymorphism: A panel study
-
Ward SA, Helsby NA, Skjelbo E, Brøsen K, Gram LF, Breckenridge AM. The activation of the biguanide antimalarial proguanil co-segregates with the mephenytoin oxidation polymorphism: a panel study. Br J Clin Pharmacol 1991;31:689-92.
-
(1991)
Br J Clin Pharmacol
, vol.31
, pp. 689-692
-
-
Ward, S.A.1
Helsby, N.A.2
Skjelbo, E.3
Brøsen, K.4
Gram, L.F.5
Breckenridge, A.M.6
-
21
-
-
0026582038
-
Relation between chloroguanide bioactivation to cycloguanil and the genetically determined metabolism of mephenytoin in humans
-
Funck-Brentano C, Bosco O, Jacqz Aigrain E, Keundjian A, Jaillon P. Relation between chloroguanide bioactivation to cycloguanil and the genetically determined metabolism of mephenytoin in humans. Clin Pharmacol Ther 1992;51:507-12.
-
(1992)
Clin Pharmacol Ther
, vol.51
, pp. 507-512
-
-
Funck-Brentano, C.1
Bosco, O.2
Jacqz Aigrain, E.3
Keundjian, A.4
Jaillon, P.5
-
22
-
-
0027272518
-
Proguanil metabolism is determined by the mephenytoin oxidation polymorphism in Vietnamese living in Denmark
-
Brøsen K, Skjelbo E, Flachs H. Proguanil metabolism is determined by the mephenytoin oxidation polymorphism in Vietnamese living in Denmark. Br J Clin Pharmacol 1993;36:105-8.
-
(1993)
Br J Clin Pharmacol
, vol.36
, pp. 105-108
-
-
Brøsen, K.1
Skjelbo, E.2
Flachs, H.3
-
23
-
-
0028919941
-
Metabolic disposition of proguanil in extensive and poor metabolisers of 5-mephenytoin 4′-hydroxylation recruited from an Indonesian population
-
Setiabudy R, Kusaka M, Chiba K, Darmansjah I, Ishizaki T. Metabolic disposition of proguanil in extensive and poor metabolisers of 5-mephenytoin 4′-hydroxylation recruited from an Indonesian population. Br J Clin Pharmacol 1995;39:297-303.
-
(1995)
Br J Clin Pharmacol
, vol.39
, pp. 297-303
-
-
Setiabudy, R.1
Kusaka, M.2
Chiba, K.3
Darmansjah, I.4
Ishizaki, T.5
-
24
-
-
0029960882
-
Chloroguanide metabolism in relation to the efficacy in malaria prophylaxis and the S-mephenytoin oxidation in Tanzanians
-
Skjelbo E, Mutabingwa TK, Bygbjerg Ib, Nielsen KK, Gram LF, Brøsen K. Chloroguanide metabolism in relation to the efficacy in malaria prophylaxis and the S-mephenytoin oxidation in Tanzanians. Clin Pharmacol Ther 1996;59:304-11.
-
(1996)
Clin Pharmacol Ther
, vol.59
, pp. 304-311
-
-
Skjelbo, E.1
Mutabingwa, T.K.2
Bygbjerg, Ib.3
Nielsen, K.K.4
Gram, L.F.5
Brøsen, K.6
-
25
-
-
0028228630
-
In vitro proguanil activation to cycloguanil by human liver microsomes is mediated by CYP3A isoforms as well as by S-mephenytoin hydroxylase
-
Birkett DJ, Rees D, Andersson T, Gonzalez FJ, Miners JO, Veronese ME. In vitro proguanil activation to cycloguanil by human liver microsomes is mediated by CYP3A isoforms as well as by S-mephenytoin hydroxylase. Br J Clin Pharmacol 1994;37:413-20.
-
(1994)
Br J Clin Pharmacol
, vol.37
, pp. 413-420
-
-
Birkett, D.J.1
Rees, D.2
Andersson, T.3
Gonzalez, F.J.4
Miners, J.O.5
Veronese, M.E.6
-
26
-
-
0028279041
-
Evidence that CYP2C19 is the major (S)-mephenytoin 4′-hydroxylase in humans
-
Goldstein JA, Faletto MB, Romkes Sparks M, Sullivan T, Kitareewan S, Raucy JL, et al. Evidence that CYP2C19 is the major (S)-mephenytoin 4′-hydroxylase in humans. Biochemistry 1994;33:1743-52.
-
(1994)
Biochemistry
, vol.33
, pp. 1743-1752
-
-
Goldstein, J.A.1
Faletto, M.B.2
Romkes Sparks, M.3
Sullivan, T.4
Kitareewan, S.5
Raucy, J.L.6
-
27
-
-
0028260641
-
The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans
-
de Morais SM, Wilkinson GR, Blaisdell J, Nakamura K, Meyer UA, Goldstein JA. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. J Biol Chem 1994;269:15419-22.
-
(1994)
J Biol Chem
, vol.269
, pp. 15419-15422
-
-
De Morais, S.M.1
Wilkinson, G.R.2
Blaisdell, J.3
Nakamura, K.4
Meyer, U.A.5
Goldstein, J.A.6
-
28
-
-
0028131815
-
Simultaneous determination of urinary free cortisol and 6 beta-hydroxycortisol by high-performance liquid chromatography to measure human CYP3A activity
-
Lykkesfeldt J, Loft S, Poulsen HE. Simultaneous determination of urinary free cortisol and 6 beta-hydroxycortisol by high-performance liquid chromatography to measure human CYP3A activity. J Chromatogr B Biomed Appl 1994;660:23-9.
-
(1994)
J Chromatogr B Biomed Appl
, vol.660
, pp. 23-29
-
-
Lykkesfeldt, J.1
Loft, S.2
Poulsen, H.E.3
-
29
-
-
0000257683
-
The absorption and excretion of Paludrine in the human subject
-
Maegraith BG, Tottey HH, Adams ARD, Horner Andrews WH, Sing JD. The absorption and excretion of Paludrine in the human subject. Ann Trop Med Parasitol 1946;40:493-506.
-
(1946)
Ann Trop Med Parasitol
, vol.40
, pp. 493-506
-
-
Maegraith, B.G.1
Tottey, H.H.2
Adams, A.R.D.3
Horner Andrews, W.H.4
Sing, J.D.5
-
30
-
-
0029807319
-
Population pharmacokinetics of proguanil in patients with acute P. falciparum malaria after combined therapy with atovaquone
-
Hussein Z, Eaves C, Hutchinson D, Canfield C. Population pharmacokinetics of proguanil in patients with acute P. falciparum malaria after combined therapy with atovaquone. Br J Clin Pharmacol 1996;42:589-97.
-
(1996)
Br J Clin Pharmacol
, vol.42
, pp. 589-597
-
-
Hussein, Z.1
Eaves, C.2
Hutchinson, D.3
Canfield, C.4
-
31
-
-
0028864296
-
Comparison of chloroguanide and mephenytoin for the in vivo assessment of genetically determined CYP2C19 activity in humans
-
Partovian C, Jacqz Aigrain E, Keundjian A, Jaillon P, Funck-Brentano C. Comparison of chloroguanide and mephenytoin for the in vivo assessment of genetically determined CYP2C19 activity in humans. Clin Pharmacol Ther 1995;58:257-63.
-
(1995)
Clin Pharmacol Ther
, vol.58
, pp. 257-263
-
-
Partovian, C.1
Jacqz Aigrain, E.2
Keundjian, A.3
Jaillon, P.4
Funck-Brentano, C.5
-
32
-
-
0029824249
-
In vivo inhibition of CYP2C19 but not CYP2D6 by fluvoxamine
-
Xu ZH, Xie HG, Zhou HH. In vivo inhibition of CYP2C19 but not CYP2D6 by fluvoxamine. Br J Clin Pharmacol 1996;42:518-21.
-
(1996)
Br J Clin Pharmacol
, vol.42
, pp. 518-521
-
-
Xu, Z.H.1
Xie, H.G.2
Zhou, H.H.3
-
33
-
-
0029558898
-
N-Demethylation of amitriptyline in vitro: Role of cytochrome P-450 3A (CYP3A) isoforms and effect of metabolic inhibitors
-
Schmider J, Greenblatt DJ, von Moltke LL, Harmatz JS, Shader RI. N-Demethylation of amitriptyline in vitro: role of cytochrome P-450 3A (CYP3A) isoforms and effect of metabolic inhibitors. J Pharmacol Exp Ther 1995;275:592-7.
-
(1995)
J Pharmacol Exp Ther
, vol.275
, pp. 592-597
-
-
Schmider, J.1
Greenblatt, D.J.2
Von Moltke, L.L.3
Harmatz, J.S.4
Shader, R.I.5
-
34
-
-
0027230584
-
Major pathway of imipramine metabolism is catalyzed by cytochromes P-450 1A2 and P-450 3A4 in human liver
-
Lemoine A, Gautier JC, Azoulay D, Kiffel L, Belloc C, Guengerich FP, et al. Major pathway of imipramine metabolism is catalyzed by cytochromes P-450 1A2 and P-450 3A4 in human liver. Mol Pharmacol 1993;43:827-32.
-
(1993)
Mol Pharmacol
, vol.43
, pp. 827-832
-
-
Lemoine, A.1
Gautier, J.C.2
Azoulay, D.3
Kiffel, L.4
Belloc, C.5
Guengerich, F.P.6
-
35
-
-
0024427759
-
The increase in urinary excretion of 6 beta-hydroxycortisol as a marker of human hepatic cytochrome P450IIIA induction
-
Ged C, Rouillon JM, Pichard L, Combalbert J, Buessot N, Bories P, et al. The increase in urinary excretion of 6 beta-hydroxycortisol as a marker of human hepatic cytochrome P450IIIA induction. Br J Clin Pharmacol 1989;28:373-87.
-
(1989)
Br J Clin Pharmacol
, vol.28
, pp. 373-387
-
-
Ged, C.1
Rouillon, J.M.2
Pichard, L.3
Combalbert, J.4
Buessot, N.5
Bories, P.6
-
36
-
-
0026601064
-
Heterogeneity of CYP3A isoforms metabolizing erythromycin and cortisol
-
Hunt CM, Watkins PB, Saenger P, Stave GM, Barlascini N, Watlington CO, et al. Heterogeneity of CYP3A isoforms metabolizing erythromycin and cortisol. Clin Pharmacol Ther 1992;51:18-23.
-
(1992)
Clin Pharmacol Ther
, vol.51
, pp. 18-23
-
-
Hunt, C.M.1
Watkins, P.B.2
Saenger, P.3
Stave, G.M.4
Barlascini, N.5
Watlington, C.O.6
|