-
1
-
-
24744457296
-
Assessment of CYP1A2 activity in clinical practice: Why, how, and when?
-
Faber MS, Jetter A, Fuhr U. Assessment of CYP1A2 activity in clinical practice: why, how, and when? Basic Clin Pharmacol Toxicol 2005 97 : 125 34.
-
(2005)
Basic Clin Pharmacol Toxicol
, vol.97
, pp. 125-34
-
-
Faber, M.S.1
Jetter, A.2
Fuhr, U.3
-
2
-
-
0036667961
-
The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors
-
Rasmussen BB, Brix TH, Kyvik KO, Brøsen K. The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors. Pharmacogenetics 2002 12 : 473 8.
-
(2002)
Pharmacogenetics
, vol.12
, pp. 473-8
-
-
Rasmussen, B.B.1
Brix, T.H.2
Kyvik, K.O.3
Brøsen, K.4
-
3
-
-
20144370197
-
Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors
-
Korhonen LE, Rahnasto M, Mahonen NJ, Wittekindt C, Poso A, Juvonen RO et al. Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors. J Med Chem 2005 48 : 3808 15.
-
(2005)
J Med Chem
, vol.48
, pp. 3808-15
-
-
Korhonen, L.E.1
Rahnasto, M.2
Mahonen, N.J.3
Wittekindt, C.4
Poso, A.5
Juvonen, R.O.6
-
4
-
-
0025848751
-
Evidence for the involvement of several cytochromes P-450 in the first steps of caffeine metabolism by human liver microsomes
-
Berthou F, Flinois JP, Ratanasavanh D, Beaune P, Riche C, Guillouzo A. Evidence for the involvement of several cytochromes P-450 in the first steps of caffeine metabolism by human liver microsomes. Drug Metab Dispos 1991 19 : 561 7.
-
(1991)
Drug Metab Dispos
, vol.19
, pp. 561-7
-
-
Berthou, F.1
Flinois, J.P.2
Ratanasavanh, D.3
Beaune, P.4
Riche, C.5
Guillouzo, A.6
-
5
-
-
0029018483
-
Characterization of human cytochromes P450 involved in theophylline 8-hydroxylation
-
Zhang ZY, Kaminsky LS. Characterization of human cytochromes P450 involved in theophylline 8-hydroxylation. Biochem Pharmacol 1995 50 : 205 11.
-
(1995)
Biochem Pharmacol
, vol.50
, pp. 205-11
-
-
Zhang, Z.Y.1
Kaminsky, L.S.2
-
7
-
-
0032878034
-
Determination of the human cytochrome P450 isoforms involved in the metabolism of zolmitriptan
-
Wild MJ, McKillop D, Butters CJ. Determination of the human cytochrome P450 isoforms involved in the metabolism of zolmitriptan. Xenobiotica 1999 29 : 847 57.
-
(1999)
Xenobiotica
, vol.29
, pp. 847-57
-
-
Wild, M.J.1
McKillop, D.2
Butters, C.J.3
-
8
-
-
0022263133
-
Purification and characterization of the human liver cytochromes P-450 involved in debrisoquine 4-hydroxylation and phenacetin O-deethylation, two prototypes for genetic polymorphism in oxidative drug metabolism
-
Distlerath LM, Reilly PE, Martin MV, Davis GG, Wilkinson GR, Guengerich FP. Purification and characterization of the human liver cytochromes P-450 involved in debrisoquine 4-hydroxylation and phenacetin O-deethylation, two prototypes for genetic polymorphism in oxidative drug metabolism. J Biol Chem 1985 260 : 9057 67.
-
(1985)
J Biol Chem
, vol.260
, pp. 9057-67
-
-
Distlerath, L.M.1
Reilly, P.E.2
Martin, M.V.3
Davis, G.G.4
Wilkinson, G.R.5
Guengerich, F.P.6
-
9
-
-
0027985726
-
Clozapine disposition covaries with CYP1A2 activity determined by a caffeine test
-
Bertilsson L, Carrillo JA, Dahl ML, Llerena A, Alm C, Bondesson U et al. Clozapine disposition covaries with CYP1A2 activity determined by a caffeine test. Br J Clin Pharmacol 1994 38 : 471 3.
-
(1994)
Br J Clin Pharmacol
, vol.38
, pp. 471-3
-
-
Bertilsson, L.1
Carrillo, J.A.2
Dahl, M.L.3
Llerena, A.4
Alm, C.5
Bondesson, U.6
-
10
-
-
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. 1211-4
-
-
Brøsen, K.1
Skjelbo, E.2
Rasmussen, B.B.3
Poulsen, H.E.4
Loft, S.5
-
11
-
-
0026718146
-
Inhibitory potency of quinolone antibacterial agents against cytochrome P450IA2 activity in vivo and in vitro
-
Fuhr U, Anders EM, Mahr G, Sorgel F, Staib AH. Inhibitory potency of quinolone antibacterial agents against cytochrome P450IA2 activity in vivo and in vitro. Antimicrob Agents Chemother 1992 36 : 942 8.
-
(1992)
Antimicrob Agents Chemother
, vol.36
, pp. 942-8
-
-
Fuhr, U.1
Anders, E.M.2
Mahr, G.3
Sorgel, F.4
Staib, A.H.5
-
12
-
-
0027380074
-
Isoform-selective mechanism-based inhibition of human cytochrome P450 1A2 by furafylline
-
Kunze KL, Trager WF. Isoform-selective mechanism-based inhibition of human cytochrome P450 1A2 by furafylline. Chem Res Toxicol 1993 6 : 649 56.
-
(1993)
Chem Res Toxicol
, vol.6
, pp. 649-56
-
-
Kunze, K.L.1
Trager, W.F.2
-
13
-
-
1842636952
-
Fluvoxamine drastically increases concentrations and effects of tizanidine: A potentially hazardous interaction
-
Granfors MT, Backman JT, Neuvonen M, Ahonen J, Neuvonen PJ. Fluvoxamine drastically increases concentrations and effects of tizanidine: a potentially hazardous interaction. Clin Pharmacol Ther 2004 75 : 331 41.
-
(2004)
Clin Pharmacol Ther
, vol.75
, pp. 331-41
-
-
Granfors, M.T.1
Backman, J.T.2
Neuvonen, M.3
Ahonen, J.4
Neuvonen, P.J.5
-
14
-
-
33747072651
-
Rofecoxib is a potent inhibitor of cytochrome P450 1A2: Studies with tizanidine and caffeine in healthy subjects
-
Backman JT, Karjalainen MJ, Neuvonen M, Laitila J, Neuvonen PJ. Rofecoxib is a potent inhibitor of cytochrome P450 1A2: studies with tizanidine and caffeine in healthy subjects. Br J Clin Pharmacol 2006 62 : 345 57.
-
(2006)
Br J Clin Pharmacol
, vol.62
, pp. 345-57
-
-
Backman, J.T.1
Karjalainen, M.J.2
Neuvonen, M.3
Laitila, J.4
Neuvonen, P.J.5
-
15
-
-
10044260714
-
Ciprofloxacin greatly increases concentrations and hypotensive effect of tizanidine by inhibiting its cytochrome P450 1A2-mediated presystemic metabolism
-
Granfors MT, Backman JT, Neuvonen M, Neuvonen PJ. Ciprofloxacin greatly increases concentrations and hypotensive effect of tizanidine by inhibiting its cytochrome P450 1A2-mediated presystemic metabolism. Clin Pharmacol Ther 2004 76 : 598 606.
-
(2004)
Clin Pharmacol Ther
, vol.76
, pp. 598-606
-
-
Granfors, M.T.1
Backman, J.T.2
Neuvonen, M.3
Neuvonen, P.J.4
-
16
-
-
25844501496
-
Oral contraceptives containing ethinyl estradiol and gestodene markedly increase plasma concentrations and effects of tizanidine by inhibiting cytochrome P450 1A2
-
Granfors MT, Backman JT, Laitila J, Neuvonen PJ. Oral contraceptives containing ethinyl estradiol and gestodene markedly increase plasma concentrations and effects of tizanidine by inhibiting cytochrome P450 1A2. Clin Pharmacol Ther 2005 78 : 400 11.
-
(2005)
Clin Pharmacol Ther
, vol.78
, pp. 400-11
-
-
Granfors, M.T.1
Backman, J.T.2
Laitila, J.3
Neuvonen, P.J.4
-
17
-
-
33751558274
-
Rofecoxib is a potent, metabolism-dependent inhibitor of CYP1A2: Implications for in vitro prediction of drug interactions
-
Karjalainen MJ, Neuvonen PJ, Backman JT. Rofecoxib is a potent, metabolism-dependent inhibitor of CYP1A2: implications for in vitro prediction of drug interactions. Drug Metab Dispos 2006 34 : 2091 6.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 2091-6
-
-
Karjalainen, M.J.1
Neuvonen, P.J.2
Backman, J.T.3
-
18
-
-
34547781271
-
Tolfenamic acid is a potent CYP1A2 inhibitor in vitro but does not interact in vivo: Correction for protein binding is needed for data interpretation
-
Karjalainen MJ, Neuvonen PJ, Backman JT. Tolfenamic acid is a potent CYP1A2 inhibitor in vitro but does not interact in vivo: correction for protein binding is needed for data interpretation. Eur J Clin Pharmacol 2007 63 : 829 36.
-
(2007)
Eur J Clin Pharmacol
, vol.63
, pp. 829-36
-
-
Karjalainen, M.J.1
Neuvonen, P.J.2
Backman, J.T.3
-
19
-
-
33644861762
-
Inhibition constants, inhibitor concentrations and the prediction of inhibitory drug drug interactions: Pitfalls, progress and promise
-
Bachmann KA. Inhibition constants, inhibitor concentrations and the prediction of inhibitory drug drug interactions: pitfalls, progress and promise. Curr Drug Metab 2006 7 : 1 14.
-
(2006)
Curr Drug Metab
, vol.7
, pp. 1-14
-
-
Bachmann, K.A.1
-
20
-
-
0036771085
-
Inhibition-based metabolic drug-drug interactions: Predictions from in vitro data
-
Yao C, Levy RH. Inhibition-based metabolic drug-drug interactions: predictions from in vitro data. J Pharm Sci 2002 91 : 1923 35.
-
(2002)
J Pharm Sci
, vol.91
, pp. 1923-35
-
-
Yao, C.1
Levy, R.H.2
-
21
-
-
84971395861
-
Which concentration of the inhibitor should be used to predict in vivo drug interactions from in vitro data?
-
25.
-
Ito K, Chiba K, Horikawa M, Ishigami M, Mizuno N, Aoki J et al. Which concentration of the inhibitor should be used to predict in vivo drug interactions from in vitro data? AAPS Pharm Sci 2002 4 : article 25.
-
(2002)
AAPS Pharm Sci
, vol.4
-
-
Ito, K.1
Chiba, K.2
Horikawa, M.3
Ishigami, M.4
Mizuno, N.5
Aoki, J.6
-
22
-
-
1942455361
-
Database analyses for the prediction of in vivo drug-drug interactions from in vitro data
-
Ito K, Brown HS, Houston JB. Database analyses for the prediction of in vivo drug-drug interactions from in vitro data. Br J Clin Pharmacol 2004 57 : 473 86.
-
(2004)
Br J Clin Pharmacol
, vol.57
, pp. 473-86
-
-
Ito, K.1
Brown, H.S.2
Houston, J.B.3
-
23
-
-
29244447987
-
The utility of in vitro cytochrome P450 inhibition data in the prediction of drug-drug interactions
-
Obach RS, Walsky RL, Venkatakrishnan K, Gaman EA, Houston JB, Tremaine LM. The utility of in vitro cytochrome P450 inhibition data in the prediction of drug-drug interactions. J Pharmacol Exp Ther 2006 316 : 336 48.
-
(2006)
J Pharmacol Exp Ther
, vol.316
, pp. 336-48
-
-
Obach, R.S.1
Walsky, R.L.2
Venkatakrishnan, K.3
Gaman, E.A.4
Houston, J.B.5
Tremaine, L.M.6
-
24
-
-
33748946044
-
Prediction of in vivo drug-drug interactions from in vitro data: Factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4
-
Brown HS, Galetin A, Hallifax D, Houston JB. Prediction of in vivo drug-drug interactions from in vitro data: factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4. Clin Pharmacokinet 2006 45 : 1035 50.
-
(2006)
Clin Pharmacokinet
, vol.45
, pp. 1035-50
-
-
Brown, H.S.1
Galetin, A.2
Hallifax, D.3
Houston, J.B.4
-
25
-
-
15244345304
-
Prediction of drug metabolism and interactions on the basis of in vitro investigations
-
Pelkonen O, Turpeinen M, Uusitalo J, Rautio A, Raunio H. Prediction of drug metabolism and interactions on the basis of in vitro investigations. Basic Clin Pharmacol Toxicol 2005 96 : 167 75.
-
(2005)
Basic Clin Pharmacol Toxicol
, vol.96
, pp. 167-75
-
-
Pelkonen, O.1
Turpeinen, M.2
Uusitalo, J.3
Rautio, A.4
Raunio, H.5
-
26
-
-
27444445468
-
Prediction of in vivo drug-drug interactions from in vitro data: Impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant
-
Brown HS, Ito K, Galetin A, Houston JB. Prediction of in vivo drug-drug interactions from in vitro data: impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant. Br J Clin Pharmacol 2005 60 : 508 18.
-
(2005)
Br J Clin Pharmacol
, vol.60
, pp. 508-18
-
-
Brown, H.S.1
Ito, K.2
Galetin, A.3
Houston, J.B.4
-
27
-
-
0028093134
-
Kinetic applications using high substrate and competitive inhibitor concentrations to determine Ki or Km
-
Tornheim K. Kinetic applications using high substrate and competitive inhibitor concentrations to determine Ki or Km. Anal Biochem 1994 221 : 53 6.
-
(1994)
Anal Biochem
, vol.221
, pp. 53-6
-
-
Tornheim, K.1
-
28
-
-
0013212389
-
In vitro approaches for studying the inhibition of drug-metabolizing enzymes and identifying the drug-metabolizing enzymes responsible for the metabolism of drugs
-
In: Rodrigues, A.D. (ed.). Merkel Dekker Inc., West Point, NY
-
Madan A, Usuki E, Burton L, Ogilvie B, Parkinson A. In vitro approaches for studying the inhibition of drug-metabolizing enzymes and identifying the drug-metabolizing enzymes responsible for the metabolism of drugs. In : Rodrigues AD (ed.). Drug-Drug Interactions. Merkel Dekker Inc., West Point, NY, 2002 217 94.
-
(2002)
Drug-Drug Interactions.
, pp. 217-94
-
-
Madan, A.1
Usuki, E.2
Burton, L.3
Ogilvie, B.4
Parkinson, A.5
-
30
-
-
10744232330
-
The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
-
Bjornsson TD, Callaghan JT, Einolf HJ, Fischer V, Gan L, Grimm S et al. The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab Dispos 2003 31 : 815 32.
-
(2003)
Drug Metab Dispos
, vol.31
, pp. 815-32
-
-
Bjornsson, T.D.1
Callaghan, J.T.2
Einolf, H.J.3
Fischer, V.4
Gan, L.5
Grimm, S.6
-
31
-
-
0027364928
-
Specificity of substrate and inhibitor probes for human cytochromes P450 1A1 and 1A2
-
Tassaneeyakul W, Birkett DJ, Veronese ME, McManus ME, Tukey RH, Quattrochi LC et al. Specificity of substrate and inhibitor probes for human cytochromes P450 1A1 and 1A2. J Pharmacol Exp Ther 1993 265 : 401 7.
-
(1993)
J Pharmacol Exp Ther
, vol.265
, pp. 401-7
-
-
Tassaneeyakul, W.1
Birkett, D.J.2
Veronese, M.E.3
McManus, M.E.4
Tukey, R.H.5
Quattrochi, L.C.6
-
32
-
-
0025601732
-
Quinolone inhibition of cytochrome P-450-dependent caffeine metabolism in human liver microsomes
-
Fuhr U, Wolff T, Harder S, Schymanski P, Staib AH. Quinolone inhibition of cytochrome P-450-dependent caffeine metabolism in human liver microsomes. Drug Metab Dispos 1990 18 : 1005 10.
-
(1990)
Drug Metab Dispos
, vol.18
, pp. 1005-10
-
-
Fuhr, U.1
Wolff, T.2
Harder, S.3
Schymanski, P.4
Staib, A.H.5
-
33
-
-
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. 73-8
-
-
Jeppesen, U.1
Gram, L.F.2
Vistisen, K.3
Loft, S.4
Poulsen, H.E.5
Brøsen, K.6
-
34
-
-
0035215519
-
Fluvoxamine-theophylline interaction: Gap between in vitro and in vivo inhibition constants toward cytochrome P4501A2
-
Yao C, Kunze KL, Kharasch ED, Wang Y, Trager WF, Ragueneau I et al. Fluvoxamine-theophylline interaction: gap between in vitro and in vivo inhibition constants toward cytochrome P4501A2. Clin Pharmacol Ther 2001 70 : 415 24.
-
(2001)
Clin Pharmacol Ther
, vol.70
, pp. 415-24
-
-
Yao, C.1
Kunze, K.L.2
Kharasch, E.D.3
Wang, Y.4
Trager, W.F.5
Ragueneau, I.6
-
35
-
-
0024330642
-
Ciprofloxacin-caffeine: A drug interaction established using in vivo and in vitro investigations
-
Harder S, Fuhr U, Staib AH, Wolff T. Ciprofloxacin-caffeine: a drug interaction established using in vivo and in vitro investigations. Am J Med 1989 87 : 89S 91S.
-
(1989)
Am J Med
, vol.87
-
-
Harder, S.1
Fuhr, U.2
Staib, A.H.3
Wolff, T.4
-
36
-
-
33645961595
-
The impact of in vitro binding on in vitro-in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions
-
Grime K, Riley RJ. The impact of in vitro binding on in vitro-in vivo extrapolations, projections of metabolic clearance and clinical drug-drug interactions. Curr Drug Metab 2006 7 : 251 64.
-
(2006)
Curr Drug Metab
, vol.7
, pp. 251-64
-
-
Grime, K.1
Riley, R.J.2
-
37
-
-
28444449875
-
Inhibitory effect of several fluoroquinolones on hepatic microsomal cytochrome P-450 1A activities in dogs
-
Regmi NL, Abd El-Aty AM, Kuroha M, Nakamura M, Shimoda M. Inhibitory effect of several fluoroquinolones on hepatic microsomal cytochrome P-450 1A activities in dogs. J Vet Pharmacol Ther 2005 28 : 553 7.
-
(2005)
J Vet Pharmacol Ther
, vol.28
, pp. 553-7
-
-
Regmi, N.L.1
Abd El-Aty, A.M.2
Kuroha, M.3
Nakamura, M.4
Shimoda, M.5
-
38
-
-
0027452618
-
Quinolone antibacterial agents: Relationship between structure and in vitro inhibition of the human cytochrome P450 isoform CYP1A2
-
Fuhr U, Strobl G, Manaut F, Anders EM, Sorgel F, Lopez-de-Brinas E et al. Quinolone antibacterial agents: relationship between structure and in vitro inhibition of the human cytochrome P450 isoform CYP1A2. Mol Pharmacol 1993 43 : 191 9.
-
(1993)
Mol Pharmacol
, vol.43
, pp. 191-9
-
-
Fuhr, U.1
Strobl, G.2
Manaut, F.3
Anders, E.M.4
Sorgel, F.5
Lopez-De-Brinas, E.6
-
40
-
-
0021824615
-
Impairment of caffeine clearance by chronic use of low-dose oestrogen-containing oral contraceptives
-
Abernethy DR, Todd EL. Impairment of caffeine clearance by chronic use of low-dose oestrogen-containing oral contraceptives. Eur J Clin Pharmacol 1985 28 : 425 8.
-
(1985)
Eur J Clin Pharmacol
, vol.28
, pp. 425-8
-
-
Abernethy, D.R.1
Todd, E.L.2
-
42
-
-
33846674113
-
Pharmacokinetic drug interactions involving 17alpha- ethinylestradiol: A new look at an old drug
-
Zhang H, Cui D, Wang B, Han YH, Balimane P, Yang Z et al. Pharmacokinetic drug interactions involving 17alpha- ethinylestradiol: a new look at an old drug. Clin Pharmacokinet 2007 46 : 133 57.
-
(2007)
Clin Pharmacokinet
, vol.46
, pp. 133-57
-
-
Zhang, H.1
Cui, D.2
Wang, B.3
Han, Y.H.4
Balimane, P.5
Yang, Z.6
-
43
-
-
29944446317
-
Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: Implications for drug-drug interactions
-
Ogilvie BW, Zhang D, Li W, Rodrigues AD, Gipson AE, Holsapple J et al. Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions. Drug Metab Dispos 2006 34 : 191 7.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 191-7
-
-
Ogilvie, B.W.1
Zhang, D.2
Li, W.3
Rodrigues, A.D.4
Gipson, A.E.5
Holsapple, J.6
-
44
-
-
0032239288
-
The role of CYP2C in the in vitro bioactivation of the contraceptive steroid desogestrel
-
Gentile DM, Verhoeven CH, Shimada T, Back DJ. The role of CYP2C in the in vitro bioactivation of the contraceptive steroid desogestrel. J Pharmacol Exp Ther 1998 287 : 975 82.
-
(1998)
J Pharmacol Exp Ther
, vol.287
, pp. 975-82
-
-
Gentile, D.M.1
Verhoeven, C.H.2
Shimada, T.3
Back, D.J.4
-
45
-
-
0019523789
-
Human pharmacokinetics of tolfenamic acid, a new anti-inflammatory agent
-
Pentikäinen PJ, Neuvonen PJ, Backman C. Human pharmacokinetics of tolfenamic acid, a new anti-inflammatory agent. Eur J Clin Pharmacol 1981 19 : 359 65.
-
(1981)
Eur J Clin Pharmacol
, vol.19
, pp. 359-65
-
-
Pentikäinen, P.J.1
Neuvonen, P.J.2
Backman, C.3
-
46
-
-
0004047129
-
-
2nd edn. Churchill Livingstone, Edinburgh, UK
-
Dollery C. Therapeutic Drugs, 2nd edn. Churchill Livingstone, Edinburgh, UK, 1999.
-
(1999)
Therapeutic Drugs
-
-
Dollery, C.1
-
47
-
-
47649094023
-
-
FDA Celebrex (Celecoxib) Capsules Application No.: 21-156 & 20998/S007 Clinical Pharmacology. Biopharmaceutics reviews section. URL
-
FDA Celebrex (Celecoxib) Capsules Application No.: 21-156 & 20998/S007 Clinical Pharmacology Biopharmaceutics reviews section. 1999. URL: http://www.fda.gov/CDER/foi/nda/99/21156-S007_Celebrex.htm
-
(1999)
-
-
-
48
-
-
0042126736
-
Celecoxib inhibits metabolism of cytochrome P450 2D6 substrate metoprolol in humans
-
Werner U, Werner D, Rau T, Fromm MF, Hinz B, Brune K. Celecoxib inhibits metabolism of cytochrome P450 2D6 substrate metoprolol in humans. Clin Pharmacol Ther 2003 74 : 130 7.
-
(2003)
Clin Pharmacol Ther
, vol.74
, pp. 130-7
-
-
Werner, U.1
Werner, D.2
Rau, T.3
Fromm, M.F.4
Hinz, B.5
Brune, K.6
-
49
-
-
47649105473
-
-
EMEA Celecoxib BILAG I PRODUKTRESUME. URL
-
EMEA Celecoxib BILAG I PRODUKTRESUME. 2006. URL: http://www.emea.europa. eu/humandocs/PDFs/EPAR/onsenal/H-466-PI-da.pdf
-
(2006)
-
-
-
50
-
-
0035000968
-
Role of human liver cytochrome P4503A in the metabolism of etoricoxib, a novel cyclooxygenase-2 selective inhibitor
-
Kassahun K, McIntosh IS, Shou M, Walsh DJ, Rodeheffer C, Slaughter DE et al. Role of human liver cytochrome P4503A in the metabolism of etoricoxib, a novel cyclooxygenase-2 selective inhibitor. Drug Metab Dispos 2001 29 : 813 20.
-
(2001)
Drug Metab Dispos
, vol.29
, pp. 813-20
-
-
Kassahun, K.1
McIntosh, I.S.2
Shou, M.3
Walsh, D.J.4
Rodeheffer, C.5
Slaughter, D.E.6
-
51
-
-
34247381685
-
The effect of etoricoxib on the pharmacodynamics and pharmacokinetics of warfarin
-
Schwartz JI, Agrawal NG, Hartford AH, Cote J, Hunt TL, Verbesselt R et al. The effect of etoricoxib on the pharmacodynamics and pharmacokinetics of warfarin. J Clin Pharmacol 2007 47 : 620 7.
-
(2007)
J Clin Pharmacol
, vol.47
, pp. 620-7
-
-
Schwartz, J.I.1
Agrawal, N.G.2
Hartford, A.H.3
Cote, J.4
Hunt, T.L.5
Verbesselt, R.6
-
52
-
-
0020679387
-
In vitro activity of Bay
-
09867, a new quinoline derivative, compared with those of other antimicrobial agents.
-
Wise R, Andrews JM, Edwards LJ. In vitro activity of Bay 09867, a new quinoline derivative, compared with those of other antimicrobial agents. Antimicrob Agents Chemother 1983 23 : 559 64.
-
(1983)
Antimicrob Agents Chemother
, vol.23
, pp. 559-64
-
-
Wise, R.1
Andrews, J.M.2
Edwards, L.J.3
-
53
-
-
0023737762
-
Effect of magnesium hydroxide on the absorption of tolfenamic and mefenamic acids
-
Neuvonen PJ, Kivistö KT. Effect of magnesium hydroxide on the absorption of tolfenamic and mefenamic acids. Eur J Clin Pharmacol 1988 35 : 495 501.
-
(1988)
Eur J Clin Pharmacol
, vol.35
, pp. 495-501
-
-
Neuvonen, P.J.1
Kivistö, K.T.2
-
54
-
-
47649092919
-
-
Merck & Co. Inc. VIOXX (rofecoxib tablets and oral suspension). URL
-
Merck & Co. Inc. VIOXX (rofecoxib tablets and oral suspension). 2002. URL: http://www.merck.com/product/usa/pi_circulars/v/vioxx/vioxx_pi.pdf
-
(2002)
-
-
-
55
-
-
0037372154
-
Single- and multiple-dose pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase-2, in man
-
Agrawal NG, Porras AG, Matthews CZ, Rose MJ, Woolf EJ, Musser BJ et al. Single- and multiple-dose pharmacokinetics of etoricoxib, a selective inhibitor of cyclooxygenase-2, in man. J Clin Pharmacol 2003 43 : 268 76.
-
(2003)
J Clin Pharmacol
, vol.43
, pp. 268-76
-
-
Agrawal, N.G.1
Porras, A.G.2
Matthews, C.Z.3
Rose, M.J.4
Woolf, E.J.5
Musser, B.J.6
-
56
-
-
10744219874
-
Pharmacokinetics of etoricoxib in patients with renal impairment
-
Agrawal NG, Matthews CZ, Mazenko RS, Kline WF, Woolf EJ, Porras AG et al. Pharmacokinetics of etoricoxib in patients with renal impairment. J Clin Pharmacol 2004 44 : 48 58.
-
(2004)
J Clin Pharmacol
, vol.44
, pp. 48-58
-
-
Agrawal, N.G.1
Matthews, C.Z.2
Mazenko, R.S.3
Kline, W.F.4
Woolf, E.J.5
Porras, A.G.6
-
57
-
-
0030859745
-
The clinical pharmacokinetics of zolmitriptan
-
Dixon R, Warrander A. The clinical pharmacokinetics of zolmitriptan. Cephalalgia 1997 18 : 15 20.
-
(1997)
Cephalalgia
, vol.18
, pp. 15-20
-
-
Dixon, R.1
Warrander, A.2
-
58
-
-
23644446491
-
Comparison of ethinylestradiol pharmacokinetics in three hormonal contraceptive formulations: The vaginal ring, the transdermal patch and an oral contraceptive
-
van den Heuvel MW, van Bragt AJ, Alnabawy AK, Kaptein MC. Comparison of ethinylestradiol pharmacokinetics in three hormonal contraceptive formulations: the vaginal ring, the transdermal patch and an oral contraceptive. Contraception 2005 72 : 168 74.
-
(2005)
Contraception
, vol.72
, pp. 168-74
-
-
Van Den Heuvel, M.W.1
Van Bragt, A.J.2
Alnabawy, A.K.3
Kaptein, M.C.4
-
59
-
-
0025062383
-
Protein binding of the contraceptive steroids gestodene, 3-keto-desogestrel and ethinylestradiol in human serum
-
Kuhnz W, Pfeffer M, al-Yacoub G. Protein binding of the contraceptive steroids gestodene, 3-keto-desogestrel and ethinylestradiol in human serum. J Steroid Biochem 1990 35 : 313 8.
-
(1990)
J Steroid Biochem
, vol.35
, pp. 313-8
-
-
Kuhnz, W.1
Pfeffer, M.2
Al-Yacoub, G.3
-
60
-
-
0030791647
-
Pharmacokinetics of the new progestogens and influence of gestodene and desogestrel on ethinylestradiol metabolism
-
Stanczyk FZ. Pharmacokinetics of the new progestogens and influence of gestodene and desogestrel on ethinylestradiol metabolism. Contraception 1997 55 : 273 82.
-
(1997)
Contraception
, vol.55
, pp. 273-82
-
-
Stanczyk, F.Z.1
-
61
-
-
0023757438
-
Alterations in the serum levels of gestodene and SHBG during 12 cycles of treatment with 30 micrograms ethinylestradiol and 75 micrograms gestodene
-
Kuhl H, Jung-Hoffmann C, Heidt F. Alterations in the serum levels of gestodene and SHBG during 12 cycles of treatment with 30 micrograms ethinylestradiol and 75 micrograms gestodene. Contraception 1988 38 : 477 86.
-
(1988)
Contraception
, vol.38
, pp. 477-86
-
-
Kuhl, H.1
Jung-Hoffmann, C.2
Heidt, F.3
|