Search Results - "Comstock, Thomas J."

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  1. 1

    Evaluation of an in vitro dialysis system to predict drug removal by Hudson, Joanna Q., Comstock, Thomas J., Feldman, George M.

    Published in Nephrology, dialysis, transplantation (01-02-2004)
    “…Background. Variation in the extent of drug removal under different dialysis conditions presents a challenge for prediction of drug elimination and dosage…”
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  2. 2
  3. 3

    The Pharmacokinetics of Subcutaneous Enoxaparin in End-Stage Renal Disease by Brophy, Donald F., Wazny, Lori D., Gehr, Todd W. B., Comstock, Thomas J., Venitz, Jürgen

    Published in Pharmacotherapy (01-02-2001)
    “…Study Objective. To evaluate the pharmacokinetics of enoxaparin in end‐stage renal disease (ESRD), and determine if dosage reduction is necessary to maintain…”
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  4. 4
  5. 5

    Considerations for optimal iron use for anemia due to chronic kidney disease by Hudson, Joanna Q., Comstock, Thomas J.

    Published in Clinical therapeutics (01-10-2001)
    “…Background: Availability of recombinant human erythropoietin (rHuEPO) has improved the treatment of anemia due to chronic kidney disease (CKD). Iron deficiency…”
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  6. 6

    Pharmacokinetics of gabapentin in subjects with various degrees of renal function by Blum, R A, Comstock, T J, Sica, D A, Schultz, R W, Keller, E, Reetze, P, Bockbrader, H, Tuerck, D, Busch, J A, Reece, P A

    Published in Clinical pharmacology and therapeutics (01-08-1994)
    “…The pharmacokinetics of oral gabapentin (400 mg) was studied in normal subjects and in subjects with various degrees of renal function. Sixty subjects…”
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  7. 7

    Nephrology Pharmaceutical Care Preceptorship: A Programmatic and Clinical Outcomes Assessment by Matzke, Gary R, Peter, Wendy L St, Comstock, Thomas J, Foote, Edward F

    Published in The Annals of pharmacotherapy (01-05-2000)
    “…OBJECTIVE: The University of Pittsburgh Nephrology Pharmaceutical Care Preceptorship (NPCP) program was conceived to acquaint health system pharmacists with…”
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  8. 8

    Effect of two administration schedules of an enteral nutrient formula on phenytoin bioavailability by Krueger, K A, Garnett, W R, Comstock, T J, Fitzsimmons, W E, Karnes, H T, Pellock, J M

    Published in Epilepsia (Copenhagen) (01-12-1987)
    “…Continuous nasogastric (NG) administration of enteral nutrient formulas (ENFs) reportedly lowers phenytoin (PHT) concentrations. We studied the effects of two…”
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  9. 9

    Nephrology: Nephrology Pharmaceutical Care Preceptorship: A Programmatic and Clinical Outcomes Assessment by Matzke, Gary R, Peter, Wendy L St, Comstock, Thomas J, Foote, Edward F

    Published in The Annals of pharmacotherapy (01-11-2007)
    “…Objective: The University of Pittsburgh Nephrology Pharmaceutical Care Preceptorship (NPCP) program was conceived to acquaint health system pharmacists with…”
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    Journal Article
  10. 10

    Lidocaine anesthesia: comparison of iontophoresis, injection, and swabbing by Russo, Jr, J, Lipman, A G, Comstock, T J, Page, B C, Stephen, R L

    Published in American journal of hospital pharmacy (01-06-1980)
    “…The duration and depth of anesthesia produced by lidocaine with three methods of administration were studied. To test duration of anesthesia, either lidocaine…”
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  11. 11

    A dose-response trial of once-daily diltiazem by Felicetta, J V, Serfer, H M, Cutler, N R, Comstock, T J, Huber, G L, Weir, M R, Hafner, K, Park, G D

    Published in The American heart journal (01-04-1992)
    “…This trial was performed to determine the safe and effective dosage range of once daily diltiazem (diltiazem CD) capsules for treatment of essential…”
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  12. 12

    Temperature dependence of phenytoin-protein binding in serum: effects of uremia and hypoalbuminemia by Allison, T B, Comstock, T J

    Published in Therapeutic drug monitoring (01-01-1988)
    “…Phenytoin-protein binding was determined as a function of temperature in uremic patients with normal albumin and in uremic patients with hypoalbuminemia. Free…”
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  13. 13

    A comparative bioavailability study of carbamazepine tablets and a chewable tablet formulation by Maas, B, Garnett, W R, Pellock, J M, Comstock, T J

    Published in Therapeutic drug monitoring (1987)
    “…Differences in product formulations have been shown to affect the therapeutic response by altering the relative bioavailability and pharmacokinetics of a drug…”
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  14. 14

    Ranitidine bioavailability and disposition kinetics in patients undergoing chronic hemodialysis by Comstock, T J, Sica, D A, Harford, A, Eshelman, F

    Published in Nephron (2015) (1989)
    “…The absorption and disposition of single-dose intravenous (i.v.) and oral ranitidine were evaluated in 6 patients undergoing chronic hemodialysis. Ranitidine…”
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  15. 15

    Ranitidine accumulation in patients undergoing chronic hemodialysis by Comstock, T J, Sica, D A, Stone, S, Davis, J, Garnett, W R, Karnes, H T, Warner, C W

    Published in Journal of clinical pharmacology (01-12-1988)
    “…Ranitidine accumulation was assessed in 20 patients undergoing chronic hemodialysis following oral daily doses of 150 mg ranitidine for 10 days. Serum…”
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  16. 16

    Single dose comparison of the relative bioavailability of phenytoin suspension and extended capsules by Fitzsimmons, W E, Garnett, W R, Comstock, T J, Pellock, J M

    Published in Epilepsia (Copenhagen) (01-07-1986)
    “…There is presently only one preparation of phenytoin approved for once-daily dosing--extended phenytoin sodium capsules. We have observed many hospitalized…”
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  17. 17

    Binding of quinidine to plasma proteins in normal subjects and in patients with hyperlipoproteinemias by Kates, R E, Sokoloski, T D, Comstock, T J

    Published in Clinical pharmacology and therapeutics (01-01-1978)
    “…Quinidine in the plasma binds to various lipoproteins as well as to albumin. With the use of computer simulations the effect of varying the serum level of each…”
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  18. 18

    Rapid high-pressure liquid chromatographic determination of quinidine and dihydroquinidine in plasma samples by Kates, R E, McKennon, D W, Comstock, T J

    Published in Journal of pharmaceutical sciences (01-02-1978)
    “…A high-pressure liquid chromatographic assay for quinidine and dihydroquinidine was developed. A cation-exchange column was utilized with an eluting solvent pH…”
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