-
1
-
-
0030899302
-
Rupatadine, a new potent, orally active dual antagonist of histamine and platelet-activating factor (PAF)
-
Merlos M., Giral M., Balsa D., et al. Rupatadine, a new potent, orally active dual antagonist of histamine and platelet-activating factor (PAF). J Pharmacol Exp Ther 280 (1997) 114-121
-
(1997)
J Pharmacol Exp Ther
, vol.280
, pp. 114-121
-
-
Merlos, M.1
Giral, M.2
Balsa, D.3
-
2
-
-
33947310075
-
Rupatadine: A review of its use in the management of allergic disorders
-
Keam S.J., and Plosker G.L. Rupatadine: A review of its use in the management of allergic disorders. Drugs 67 (2007) 457-474
-
(2007)
Drugs
, vol.67
, pp. 457-474
-
-
Keam, S.J.1
Plosker, G.L.2
-
3
-
-
0043256677
-
Rupatadine in allergic rhinitis: Pooled analysis of efficacy data
-
Pérez I., de la Cruz G., Villa M., and Izquierdo I. Rupatadine in allergic rhinitis: Pooled analysis of efficacy data. Allergy 57 Suppl 73 (2002) 245
-
(2002)
Allergy
, vol.57
, Issue.SUPPL. 73
, pp. 245
-
-
Pérez, I.1
de la Cruz, G.2
Villa, M.3
Izquierdo, I.4
-
4
-
-
17444422490
-
Rupatadine 10 mg and cetirizine 10 mg in seasonal allergic rhinitis: A randomised, double-blind parallel study
-
Spanish Rupatadine Rhinitis Study Group
-
Martínez-Cócera C., De Molina M., Martí-Guadaño E., et al., Spanish Rupatadine Rhinitis Study Group. Rupatadine 10 mg and cetirizine 10 mg in seasonal allergic rhinitis: A randomised, double-blind parallel study. J Investig Allergol Clin Immunol 15 (2005) 22-29
-
(2005)
J Investig Allergol Clin Immunol
, vol.15
, pp. 22-29
-
-
Martínez-Cócera, C.1
De Molina, M.2
Martí-Guadaño, E.3
-
5
-
-
1942505919
-
A randomized, double-blind, parallel-group study, comparing the efficacy and safety of rupatadine (20 and 10 mg), a new PAF and H1 receptor-specific histamine antagonist, to loratadine 10 mg in the treatment of seasonal allergic rhinitis
-
French Rupatadine-Rhinitis Study Group
-
Saint-Martin F., Dumur J.P., Pérez I., Izquierdo I., and French Rupatadine-Rhinitis Study Group. A randomized, double-blind, parallel-group study, comparing the efficacy and safety of rupatadine (20 and 10 mg), a new PAF and H1 receptor-specific histamine antagonist, to loratadine 10 mg in the treatment of seasonal allergic rhinitis. J Investig Allergol Clin Immunol 14 (2004) 34-40
-
(2004)
J Investig Allergol Clin Immunol
, vol.14
, pp. 34-40
-
-
Saint-Martin, F.1
Dumur, J.P.2
Pérez, I.3
Izquierdo, I.4
-
6
-
-
3042702887
-
Rupatadine 10 mg and ebastine 10 mg in seasonal allergic rhinitis: A comparison study
-
Rupatadine Study Group
-
Guadańo E.M., Serra-Batlles J., Meseguer J., et al., Rupatadine Study Group. Rupatadine 10 mg and ebastine 10 mg in seasonal allergic rhinitis: A comparison study. Allergy 59 (2004) 766-771
-
(2004)
Allergy
, vol.59
, pp. 766-771
-
-
Guadańo, E.M.1
Serra-Batlles, J.2
Meseguer, J.3
-
7
-
-
8344261734
-
Central and peripheral evaluation of rupatadine, a new antihistamine/platelet-activating factor antagonist, at different doses in healthy volunteers
-
Barbanoj M.J., García-Gea C., Morte A., et al. Central and peripheral evaluation of rupatadine, a new antihistamine/platelet-activating factor antagonist, at different doses in healthy volunteers. Neuropsychobiology 50 (2004) 311-321
-
(2004)
Neuropsychobiology
, vol.50
, pp. 311-321
-
-
Barbanoj, M.J.1
García-Gea, C.2
Morte, A.3
-
8
-
-
33645833853
-
Drug interactions during therapy with three major groups of antimicrobial agents
-
Shakeri-Nejad K., and Stahlmann R. Drug interactions during therapy with three major groups of antimicrobial agents. Expert Opin Pharmacother 7 (2006) 639-651
-
(2006)
Expert Opin Pharmacother
, vol.7
, pp. 639-651
-
-
Shakeri-Nejad, K.1
Stahlmann, R.2
-
9
-
-
10744232330
-
The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
-
Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism/Clinical Pharmacology Technical Working Group and FDA Center for Drug Evaluation and Research (CDER)
-
Bjornsson T.D., Callaghan J.T., Einolf H.J., et al., Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism/Clinical Pharmacology Technical Working Group and FDA Center for Drug Evaluation and Research (CDER). The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab Dispos 31 (2003) 815-832
-
(2003)
Drug Metab Dispos
, vol.31
, pp. 815-832
-
-
Bjornsson, T.D.1
Callaghan, J.T.2
Einolf, H.J.3
-
10
-
-
0033770638
-
Macrolide-induced clinically relevant drug interactions with cytochrome P-450A (CYP) 3A4: An update focused on clarithromycin, azithromycin and dirithromycin
-
Westphal J.F. Macrolide-induced clinically relevant drug interactions with cytochrome P-450A (CYP) 3A4: An update focused on clarithromycin, azithromycin and dirithromycin. Br J Clin Pharmacol 50 (2000) 285-295
-
(2000)
Br J Clin Pharmacol
, vol.50
, pp. 285-295
-
-
Westphal, J.F.1
-
11
-
-
16444377083
-
Mechanism-based inhibition of cytochrome P450 3A4 by therapeutic drugs
-
Zhou S., Yung Chan S., Cher Goh B., et al. Mechanism-based inhibition of cytochrome P450 3A4 by therapeutic drugs. Clin Pharmacokinet 44 (2005) 279-304
-
(2005)
Clin Pharmacokinet
, vol.44
, pp. 279-304
-
-
Zhou, S.1
Yung Chan, S.2
Cher Goh, B.3
-
12
-
-
0035049380
-
Pharmacokinetic and safety profile of desloratadine and fexofenadine when coadministered with azithromycin: A randomized, placebocontrolled, parallel-group study
-
Gupta S., Banfield C., Kantesaria B., et al. Pharmacokinetic and safety profile of desloratadine and fexofenadine when coadministered with azithromycin: A randomized, placebocontrolled, parallel-group study. Clin Ther 23 (2001) 451-466
-
(2001)
Clin Ther
, vol.23
, pp. 451-466
-
-
Gupta, S.1
Banfield, C.2
Kantesaria, B.3
-
13
-
-
0034111043
-
P-glycoprotein inhibitor erythromycin increases oral bioavailability of talinolol in humans
-
Schwarz U.I., Gramatté T., Krappweis J., et al. P-glycoprotein inhibitor erythromycin increases oral bioavailability of talinolol in humans. Int J Clin Pharmacol Ther. 38 (2000) 161-167
-
(2000)
Int J Clin Pharmacol Ther.
, vol.38
, pp. 161-167
-
-
Schwarz, U.I.1
Gramatté, T.2
Krappweis, J.3
-
14
-
-
0034649020
-
Doctors revise declaration of Helsinki
-
Christie B. Doctors revise declaration of Helsinki. BMJ 321 (2000) 913
-
(2000)
BMJ
, vol.321
, pp. 913
-
-
Christie, B.1
-
15
-
-
53049089188
-
-
European Agency for the Evaluation of Medicinal Products, International Conference on Harmonisation-World Health Organization. Guideline for Good Clinical Practice [EMEA Web site]. ICH Topic E6. Step 5. Note for guidance on Good Clinical Practice (CPMP/ICH/135/95). Geneva, Switzerland: WHO; 2002. http://www.emea.eu.int. Accessed April 11, 2007.
-
European Agency for the Evaluation of Medicinal Products, International Conference on Harmonisation-World Health Organization. Guideline for Good Clinical Practice [EMEA Web site]. ICH Topic E6. Step 5. Note for guidance on Good Clinical Practice (CPMP/ICH/135/95). Geneva, Switzerland: WHO; 2002. http://www.emea.eu.int. Accessed April 11, 2007.
-
-
-
-
16
-
-
53049085092
-
-
Guidance for Industry. Bioanalytical Method Validation US Dept of Health and Human Services. Food and Drug Administration, Center for Drug Evaluation and Research (CDER) Center for Veterinary Medicine (CVM), May 2001.
-
Guidance for Industry. Bioanalytical Method Validation US Dept of Health and Human Services. Food and Drug Administration, Center for Drug Evaluation and Research (CDER) Center for Veterinary Medicine (CVM), May 2001.
-
-
-
-
17
-
-
0034469255
-
Bioanalytical method validation-A revisit with a decade of progress
-
Shah V.P., Midha K.K., Findlay J.W., et al. Bioanalytical method validation-A revisit with a decade of progress. Pharm Res 17 (2000) 1551-1557
-
(2000)
Pharm Res
, vol.17
, pp. 1551-1557
-
-
Shah, V.P.1
Midha, K.K.2
Findlay, J.W.3
-
18
-
-
53049102646
-
-
Guidance for Industry. Statistical approaches to establishing bioequivalence. US Dept of Health and Human Services. Food and Drug Administration, Center for Drug Evaluation and Research (CDER), January 2001.
-
Guidance for Industry. Statistical approaches to establishing bioequivalence. US Dept of Health and Human Services. Food and Drug Administration, Center for Drug Evaluation and Research (CDER), January 2001.
-
-
-
-
19
-
-
53049109869
-
-
Zithromax (azithromycin) clinical pharmacology. Pharmacokinetics [Rxlist Web site]. http://www.rxlist.com/cgi/generic/azith_cp.htm. Accessed May 11, 2005.
-
Zithromax (azithromycin) clinical pharmacology. Pharmacokinetics [Rxlist Web site]. http://www.rxlist.com/cgi/generic/azith_cp.htm. Accessed May 11, 2005.
-
-
-
-
20
-
-
0029130840
-
Macrolide antibacterials. Drug interactions of clinical significance
-
von Rosensteil N.A., and Adam D. Macrolide antibacterials. Drug interactions of clinical significance. Drug Saf 13 (1995) 105-122
-
(1995)
Drug Saf
, vol.13
, pp. 105-122
-
-
von Rosensteil, N.A.1
Adam, D.2
-
21
-
-
10744233896
-
Possible involvement of the drug transporters P glycoprotein and multidrug resistance-associated protein Mrp2 in disposition of azithromycin
-
Sugie M., Asakura E., Zhao Y.L., et al. Possible involvement of the drug transporters P glycoprotein and multidrug resistance-associated protein Mrp2 in disposition of azithromycin. Antimicrob Agents Chemother 48 (2004) 809-814
-
(2004)
Antimicrob Agents Chemother
, vol.48
, pp. 809-814
-
-
Sugie, M.1
Asakura, E.2
Zhao, Y.L.3
-
22
-
-
0036122644
-
The effects of steady-state erythromycin and azithromycin on the pharmacokinetics of sildenafil in healthy volunteers
-
Muirhead G.J., Faulkner S., Harness J.A., and Taubel J. The effects of steady-state erythromycin and azithromycin on the pharmacokinetics of sildenafil in healthy volunteers. Br J Clin Pharmacol. 53 Suppl 1 (2002) 37S-43S
-
(2002)
Br J Clin Pharmacol.
, vol.53
, Issue.SUPPL. 1
-
-
Muirhead, G.J.1
Faulkner, S.2
Harness, J.A.3
Taubel, J.4
-
23
-
-
0344081226
-
No clinically significant effect of erythromycin or azithromycin on the pharmacokinetics of voriconazole in healthy male volunteers
-
Purkins L., Wood N., Ghahramani P., et al. No clinically significant effect of erythromycin or azithromycin on the pharmacokinetics of voriconazole in healthy male volunteers. Br J Clin Pharmacol. 56 Suppl 1 (2003) 30-36
-
(2003)
Br J Clin Pharmacol.
, vol.56
, Issue.SUPPL. 1
, pp. 30-36
-
-
Purkins, L.1
Wood, N.2
Ghahramani, P.3
-
24
-
-
53049101202
-
-
Clarinex (desloratadine). Summary product characteristics [Web site]. http://www.spfiles.com/piclarinex.pdf. Accessed April 7, 2008.
-
Clarinex (desloratadine). Summary product characteristics [Web site]. http://www.spfiles.com/piclarinex.pdf. Accessed April 7, 2008.
-
-
-
-
25
-
-
53049098031
-
Prevalence of the slow metabolizer (SM) phenotype and single dose pharmacokinetics (PK) of desloratadine (DCL) in a population of healthy adults
-
Frick G.S., Blum R.A., Kovacs S.J., et al. Prevalence of the slow metabolizer (SM) phenotype and single dose pharmacokinetics (PK) of desloratadine (DCL) in a population of healthy adults. Clin Pharmacol Ther 75 (2004) 9
-
(2004)
Clin Pharmacol Ther
, vol.75
, pp. 9
-
-
Frick, G.S.1
Blum, R.A.2
Kovacs, S.J.3
-
26
-
-
33644906907
-
Adult and paediatric poor metabolisers of desloratadine: An assessment of pharmacokinetics and safety
-
Prenner B., Kim K., Gupta S., et al. Adult and paediatric poor metabolisers of desloratadine: An assessment of pharmacokinetics and safety. Expert Opin Drug Saf 5 (2006) 211-223
-
(2006)
Expert Opin Drug Saf
, vol.5
, pp. 211-223
-
-
Prenner, B.1
Kim, K.2
Gupta, S.3
|