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Tom Nijenhuis1 , Joost G.J. Hoenderop1 , Johannes Loffing2 , Annemiete W.C.M. van der Kemp1 , Carel H. van Os1 , Rene J.M. Bindels1 . 1 Department of Cell Physiology, University Medical Center Nijmegen, Netherlands; 2 Institute of Anatomy, University of Zurich, Switzerland Thiazide diuretics have the unique characteristic of increasing renal Na + excretion, while decreasing Ca2 + excretion. However, the molecular mechanism responsible for this thiazide-induced hypocalciuria remains unclear.
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1162. Angerman-Stewart, J. A., Eling, T. A. and Glasgow, W. C. 1995 ; . Prostaglandin H Synthase-2 Is Induced in Syrian Hamster Embryo Cells in Response to Basic Fibroblast Growth Factor. Arch. Biochem. Biophys. vol.318, No.2, April 20, pp. 378-386. 1163. Chandrasekaran, A., Osman, M., Scatina, J. A. and Sisenwine, S. F. 1995 ; . Metabolism of Equilin Sulfate in the Dog. J eroid Biochem.Molec.Biol. vol.55, No.2, pp. 271-278. 1164. Span, P. N., Smals, A. G. H., Sweep, C. G. J. and Benraad, ThJ. 1995 ; . Rat Steroid 5 alpha-Reductase Kinetic Characteristics: Extreme pH-dependency of the Type II Isozyme in Prostate and Epididymis Homogenates. J eroid Biochem.Molec.Biol. vol.54, No.3 4, pp. 185-192. 1165. Iehle, C., Delos, S., Guirou, O., Tate, R., Raynaud, J.-P. and Martin, P.-M. 1995 ; . Human Prostatic Steroid 5alpha-Reductase Isoforms-A Comparative Study of Selective Inhibitors. J eroid Biochem.Molec.Biol. vol.54, No.5 6, pp. 273-279. 1166. Castagnetta, L. A. M., Montesanti, A. M., Granata, O. M., Oliveri, G., Sorci, C. M. G., Amodio, R., Liquori, M. and Carruba, G. 1995 ; . 17 b-Hydroxysteroid Dehydrogenase Activity in Endometrial Cancer Cells: Different Metabolic Pathways of Estadiol in Hormone-responsive and Non-responsive Intact Cells. J eroid Biochem.Molec.Biol. vol.55, No.5 6, pp. 573-579. 1167. Spaldin, V., Madden, S., Adams, D. A., Edwards, R. J., Davies, D. S. and Park, B. K. 1995 ; . Determination of Human Hepatic Cytochrome P4501A2 Activity In Vitro Use of Tacrine As An Isoenzyme-Specific Probe. Drug Metab. Dispos. vol.23, No.9, pp. 929-934]. 1169. Sizemore, N., Mukhtar, H., Couch, L. H., Howard, P. C. and Rorke, E. A. 1995 ; . Differential response of normal and HPV immortalized ectocervical epithelial cells to B[a]P. Carcinogenesis vol.16, No.10, pp. 2413-2418. 1170. Dragsted, L. O., Frandsen, H., Reistad, R., Alexander, J. and Larsen, J. C. 1995 ; . DNA-binding and disposition of 5b]pyridine PhIP ; in the rat. Carcinogenesis vol.16, No.11, pp. 2785-2793. 1171. Dragsted, L. O., Grivas, S., Frandsen, H. and Larsen, J. C. 1995 ; . Antibodis to the food mutagens, 5-b]pyridine and 2-amino3, 4, 8-trimethylimidazo[4, useful for immunoassay and immunoaffinity chromatography of biological samples. Carcinogenesis vol.16, No.11, pp. 2795-2806. 1172. Ralston, S. L., Seidel, A., Luch, A., Platt, K. L. and Baird, W. M. 1995 ; . Stereoselective activation dibenzo[a, l]pyrene to - ; -anti 11R, 12S, 13S, ; - and and zyprexa.
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GENERAL INFORMATION Participating Pharmacy Network All participating pharmacies that provide pharmacy services for eligible members of PHC are contracted with PHC's Pharmacy Benefit Manager, MEDIMPACT. Pharmacy providers located in PHC's State contracted counties are referred to as "in-network" pharmacy providers and all other PHC pharmacy providers are referred to as "out-of-network" pharmacy providers. All PHC members are provided with an updated list of "in-network" pharmacy providers at the time of their enrollment. Pharmacy Reimbursement Participating pharmacies receive reimbursement from MedImpact for pharmacy services provided as specified for a covered medication and or reimbursable service as identified in the MedImpact Pharmacy Network Agreement Plan Sheet. MedImpact reimbursement is based on the lower of: Average Wholesale Price AWP ; less the contracted discount plus the contracted dispensing fee; Maximum Allowable Cost MAC ; plus the contracted dispensing fee; or Usual & Customary U&C whichever is lowest. Reimbursements are paid on a bimonthly reimbursement cycle in a 30-day average time frame from MedImpact receipt of a reimbursable claim. Pharmacy & Therapeutics P&T ; Committee The Pharmacy & Therapeutics Committee meets four times per year and is responsible for making recommendations to the Physician Advisory Committee regarding the content of the PHC Drug Formulary, including new drug evaluations, therapeutic class reviews, development of Prior Authorization Criteria, Code 1 Restrictions and other matters regarding the PHC drug benefit. The committee's membership is comprised of the PHC Medical Director, the PHC Director of Pharmacy, the PHC Clinical Pharmacist and practicing physicians and pharmacists from the community. Community practitioners interested in becoming a P&T member may contact the PHC Medical Director or Pharmacy Director. Scope of Drug Coverage With very few exceptions, the scope of drug coverage for PHC members potentially includes all Food and Drug Administration FDA ; approved drugs as part of the drug benefit. Those FDA approved drugs not on the PHC Drug Formulary are covered benefits with an approved Treatment Authorization Request TAR ; . It is misrepresentation of the PHC drug benefit by pharmacy providers to attempt to collect cash payment from a PHC member and inform them that their prescriptions are "not covered". PHC is concerned that such responses misrepresent the scope of PHC drug coverage and result in members not receiving needed medications. Those pharmacies identified as misrepresenting the PHC scope of coverage will be subject to corrective action by PHC.
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To allow for out-patient administration. This dosing can be reviewed in: Blood. 2004; 104: 1437. Title: Randomized, double-blind, activecontrolled trial of every-3-week darbepoetin alfa ARANESP ; for the treatment of chemotherapyinduced anemia Authors: Canon J-L, Vansteenkiste J, Bodoky G, et al. Reference: J Natl Cancer Inst. 2006; 98: 273-284. Purpose: Anemia is a frequent complication of cancer treatment and effects patient's quality of life. Darbepoetin is a long-acting erythropoiesis-stimulating protein that is administered by a variety of different schedules. This study compares the efficacy and safety of weekly versus an every-3-week regimen. Methods: Patients with a diagnosis of a nonmyeloid malignancy, undergoing at least 12 weeks of cytotoxic chemotherapy and were anemic hemoglobin [Hbg] 11 g dL ; within 24 hours of randomization, were eligible for the study. Patients were randomly assigned in a 1: ratio to receive darbepoetin alfa at a fixed dose of 500 mcg every 3 weeks or a weight-based dose of 2.25 mcg kg weekly for 15 weeks. All injections were administered subcutaneously. Doses of the drug were held if the Hbg 13 g dL the Hbg concentration increased by 1 g greater over a 14-day period. When the Hbg dropped to 12 g dL, the study drug was decreased to 60% of and accolate.
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