Zobrazeno 1 - 7
of 7
pro vyhledávání: '"W. L. Schary"'
Autor:
I.L. Honigberg, Francis R. Pelsor, G. E. Francisco, W. L. Schary, Jeffrey A. Kotzan, Vinod P. Shah, James T. Stewart, W. J. Brown
Publikováno v:
Biopharmaceutics & Drug Disposition. 5:335-344
The purpose of the study was to examine the bioequivalence of five commercially available oral prednisone products. The in vivo study utilized 18 healthy males, each of whom was administered 20 mg of prednisone as a reference solution or as a tablet
Autor:
R. N. Fogoros, Charles C. Whitney, Denise L. Howrie, W. L. Schary, H. J. Pieniaszek, Randy P. Juhl, Lewis W. Dittert
Publikováno v:
European Journal of Clinical Pharmacology. 32:607-610
Moracizine (ethmozine) is a phenothiazine derivative with demonstrated antiarrhythmic activity. To characterize the pharmacokinetics and material balance relationships in humans, we have given 14C-moracizine X HCl as a single oral dose of 500 mg (50
Publikováno v:
The Journal of pharmacy and pharmacology.
Publikováno v:
Clinical therapeutics. 7(2)
This study was designed to assess the bioequivalence of intramuscular molindone hydrochloride and marketed oral molindone. Ten schizophrenic patients (mean age, 30.2 years) received oral molindone in single daily doses of 100 or 150 mg for four to ei
Publikováno v:
The Journal of clinical psychiatry. 45(9 Pt 2)
Healthy male volunteers (N = 24) participated in a four-way crossover study to compare the rate and extent of absorption of naltrexone after administration of 50 mg tablets as 50, 100, and 200 mg doses and a 10 mg/ml reference syrup. A high-performan
Publikováno v:
Research communications in chemical pathology and pharmacology. 10(4)
The effect of phenylbutazone on the disposition of warfarin was studied in a subject given warfarin daily for one month. During concomitant phenylbutazone administration, the total plasma warfarin concentration declined from 4.2 to 2.0 mg/L. In contr
Publikováno v:
European journal of clinical pharmacology. 33(3)
The pharmacokinetics of intravenously, intramuscularly, and subcutaneously administered nalbuphine were studied in three parallel groups of 12 healthy volunteers each. The subjects received single doses of 10 mg and 20 mg of nalbuphine separated by a