Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Anita C. Rudy"'
Publikováno v:
The Journal of Pain. 11:24-31
We conducted a prospective multicenter, open-label, escalating dose-range trial to compare, across patients, single intranasal doses (2, 4, 6, 8, and 10 mg) of hydromorphone HCl in the treatment of acute trauma pain The main outcome measure of pain-i
Publikováno v:
Epilepsy Research. 83:124-132
Summary Purpose To compare 2.5mg and 5.0mg single-dose pharmacokinetics (PK), pharmacodynamics (PD) and tolerability of an intranasal (IN) midazolam formulation, to a 2.5-mg intravenous (IV) dose. Methods Design was an open-label, three-way crossover
Publikováno v:
Clinical Therapeutics. 27:430-440
Butorphanol tartrate (BT) nasal spray is currently marketed as a multidose spray pump product. However, access to excessive amounts of drug in a single bottle (up to 15 doses) creates the potential for misuse, diversion, and abuse.This study evaluate
Publikováno v:
Clinical Drug Investigation. 24:633-639
Narcotic analgesics such as hydromorphone undergo an extensive first-pass effect resulting in a low systemic bioavailability following oral administration. Alternative dosing routes, such as rectal and intranasal (IN) routes, have been suggested as o
Publikováno v:
Pharmacotherapy. 24:26-32
Study Objective. To investigate the effect of the nasal corticosteroid fluticasone propionate on the bioavailability and pharmacokinetics of single-dose intranasal hydromorphone hydrochloride in patients with allergic rhinitis. Design. Randomized, th
Publikováno v:
Pharmacotherapy. 23:153-158
Study Objectives. To determine the distribution of hydromorphone into breast milk and the potential exposure of the suckling infant, and whether the distribution of hydromorphone into milk can be predicted accurately by a passive diffusion model. Des
Publikováno v:
The Journal of Clinical Pharmacology. 41:1225-1231
The purpose of this study was to evaluate the pharmacokinetic profile of intranasal lorazepam in comparison to currently established administration routes. Eleven healthy volunteers completed this randomized crossover study. On three occasions, each
Publikováno v:
British Journal of Clinical Pharmacology. 37:1-5
1. Piroxicam pharmacokinetics were assessed in three groups of subjects: (1) young healthy volunteers, (2) healthy elderly subjects (mean +/- s.d. creatinine clearance 88 +/- 13 ml min-1), and (3) elderly patients with renal insufficiency (creatinine
Autor:
Qian Xiaotao, Anita C. Rudy, Stephen D. Hall, Sarah I. Ryan, Lorrie A. Kalasinski, John D. Bradley
Publikováno v:
Therapeutic Drug Monitoring. 14:464-470
The pharmacokinetics of the enantiomers of ibuprofen have been investigated following oral administration of 300 or 600 mg of racemic ibuprofen four times daily to 45 patients with osteoarthritis. Fifteen of these patients also received single doses
Publikováno v:
Pharmacotherapy. 28(7)
Study Objective. To evaluate the pharmacokinetics of haloperidol after intranasal administration compared with intravenous and intramuscular administration, and to evaluate systemic and local tolerance of intranasal administration. Design. Randomized