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Confidence interval criteria for assessment of dose proportionality

Pharmaceutical research, 2000-10, Vol.17 (10), p.1278-1283

2000

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Pharmacokinetics, Safety, and Tolerability of Atomoxetine and Effect of CYP2D610/10 Genotype in Healthy Japanese Men

Journal of clinical pharmacology, 2012-03, Vol.52 (3), p.388-403

2012

Volltextzugriff (PDF)

Sensitive and specific radioimmunoassay for fialuridine: initial assessment of pharmacokinetics after single oral doses to healthy volunteers

Antimicrobial Agents and Chemotherapy, 1994-09, Vol.38 (9), p.2134-2142

1994

Volltextzugriff (PDF)

Why rate of absorption inferences in single dose bioequivalence studies are often inappropriate

Pharmaceutical research, 1998-02, Vol.15 (2), p.276-279

1998

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Pharmacokinetics of dirithromycin

Journal of antimicrobial chemotherapy, 1993-03, Vol.31 (suppl-C), p.65-75

1993

Volltextzugriff (PDF)

Tmax : an unconfounded metric for rate of absorption in single dose bioequivalence studies

Pharmaceutical research, 1996-02, Vol.13 (2), p.324-328

1996

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Effects of renal dysfunction on the pharmacokinetics of loracarbef

Clinical pharmacology and therapeutics, 1993-09, Vol.54 (3), p.311-316

1993

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Disposition of zatosetron, a serotonin (5-HT3) receptor antagonist, in humans

Drug metabolism and disposition, 1993-03, Vol.21 (2), p.249

1993

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The penetration of dirithromycin into bronchoalveolar lavage fluid and alveolar macrophages

Journal of antimicrobial chemotherapy, 1994-05, Vol.33 (5), p.1045-1050

Baughman, Robert P.

1994

Volltextzugriff (PDF)

Clinical Pharmacokinetics of Pinacidil, A Potassium Channel Opener, in Hypertension

Journal of clinical pharmacology, 1989-01, Vol.29 (1), p.33-40

1989

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Disposition of [14c]Pinacidil in Humans

Journal of pharmaceutical sciences, 1988-02, Vol.77 (2), p.153-156

1988

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Sensitive, specific radioimmunoassay for quantifying pergolide in plasma

Clinical chemistry (Baltimore, Md.), 1992-10, Vol.38 (10), p.1975

1992

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Disposition in humans of racemic picenadol, an opioid analgesic

Drug metabolism and disposition, 1990-11, Vol.18 (6), p.968

1990

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Pharmacokinetics of cefaclor AF: effects of age, antacids and H2-receptor antagonists

Postgraduate medical journal, 1992, Vol.68 Suppl 3, p.S3-S9

1992

Volltextzugriff (PDF)

A comprehensive review of the clinical pharmacology and pharmacokinetics of cefaclor

Clinical therapeutics, 1988, Vol.11 Suppl A, p.5-19

1988

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Effect of probenecid on the pharmacokinetics of moxalactam

Antimicrobial Agents and Chemotherapy, 1982-01, Vol.21 (1), p.58-61

1982

Volltextzugriff (PDF)

Disposition and metabolic fate of atomoxetine hydrochloride: the role of CYP2D6 in human disposition and metabolism

Drug metabolism and disposition, 2003-01, Vol.31 (1), p.98

2003

Volltextzugriff (PDF)

Pharmacokinetic profile of loracarbef

The American journal of medicine, 1992-06, Vol.92 (6), p.S16-S19

1992

Volltextzugriff (PDF)

Bioavailability and pharmacokinetics of prednisone in humans

Journal of pharmaceutical sciences, 1975-01, Vol.64 (1), p.109-112

1975

Volltextzugriff (PDF)

Single- and multiple-dose pharmacokinetics of moxalactam in normal subjects

Antimicrobial Agents and Chemotherapy, 1982-07, Vol.22 (1), p.94-102

1982

Volltextzugriff (PDF)

Atomoxetine hydrochloride: clinical drug-drug interaction prediction and outcome

The Journal of pharmacology and experimental therapeutics, 2004-02, Vol.308 (2), p.410

2004

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Effect of hepatic impairment on the pharmacokinetics of atomoxetine and its metabolites

Clinical pharmacology and therapeutics, 2003-03, Vol.73 (3), p.178-191

2003

Volltextzugriff (PDF)

Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability

Journal of pharmaceutical sciences, 1978-11, Vol.67 (11), p.1582-1586

1978

Volltextzugriff (PDF)

Pharmacokinetic Evaluation of a Drug Interaction between Kaolin-Pectin and Clindamycin

Journal of pharmaceutical sciences, 1978-11, Vol.67 (11), p.1579-1582

1978

Volltextzugriff (PDF)

Double Latin Square Study to Determine Variability and Relative Bioavailability of Methylprednisolone

Journal of pharmaceutical sciences, 1979-10, Vol.68 (10), p.1312-1316

1979

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Confidence interval criteria for assessment of dose proportionality

Pharmacokinetics, Safety, and Tolerability of Atomoxetine and Effect of CYP2D610/10 Genotype in Healthy Japanese Men

Sensitive and specific radioimmunoassay for fialuridine: initial assessment of pharmacokinetics after single oral doses to healthy volunteers

Why rate of absorption inferences in single dose bioequivalence studies are often inappropriate

Pharmacokinetics of dirithromycin

Tmax : an unconfounded metric for rate of absorption in single dose bioequivalence studies

Effects of renal dysfunction on the pharmacokinetics of loracarbef

Disposition of zatosetron, a serotonin (5-HT3) receptor antagonist, in humans

The penetration of dirithromycin into bronchoalveolar lavage fluid and alveolar macrophages

Clinical Pharmacokinetics of Pinacidil, A Potassium Channel Opener, in Hypertension

Disposition of [14c]Pinacidil in Humans

Sensitive, specific radioimmunoassay for quantifying pergolide in plasma

Disposition in humans of racemic picenadol, an opioid analgesic

Pharmacokinetics of cefaclor AF: effects of age, antacids and H2-receptor antagonists

A comprehensive review of the clinical pharmacology and pharmacokinetics of cefaclor

Effect of probenecid on the pharmacokinetics of moxalactam

Disposition and metabolic fate of atomoxetine hydrochloride: the role of CYP2D6 in human disposition and metabolism

Pharmacokinetic profile of loracarbef

Bioavailability and pharmacokinetics of prednisone in humans

Single- and multiple-dose pharmacokinetics of moxalactam in normal subjects

Atomoxetine hydrochloride: clinical drug-drug interaction prediction and outcome

Effect of hepatic impairment on the pharmacokinetics of atomoxetine and its metabolites

Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability

Pharmacokinetic Evaluation of a Drug Interaction between Kaolin-Pectin and Clindamycin

Double Latin Square Study to Determine Variability and Relative Bioavailability of Methylprednisolone

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