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Results of consecutive trials in 255 patients mark kris, md 1 * , richard gralla, md 1 , leslie tyson, rn 1 , rebecca clark, rn 1 , david kelsen, md 2 , laura reilly, rn 1 , susan groshen, phd 3 , george bosl, md 2 , leonard kalman, md 1 developmental chemotherapy, memorial sloan-kettering cancer center, cornell university medical college, new york, new york 2 solid tumor services, department of medicine, memorial sloan-kettering cancer center, cornell university medical college, new york, new york 3 biostatistics laboratory, memorial sloan-kettering cancer center, cornell university medical college, new york, new york * correspondence to mark kris, developmental chemotherapy service, memorial sloan-kettering cancer center, 1275 york avenue, new york, ny 10021 this journal is listed in the national library of medicine's pubmed index.
What drugs are covered? a. All generic drugs are covered without prior authorization, except: i. benzoyl peroxide erythromycin gel, ticlopidine, nizatidine, cimetidine, omeprazole 20 mg & 40 mg, nefazodone, topical tretinoin, fluoxetine 40 mg capsule. b. All of the brand drugs listed in the table below are covered: Accucheck Advantage monitors Accucheck Advantage test strips and supplies Activella Actonel Actonel with Calcium Advair Advicor Aggrenox Alphagan Altace Amaryl Ambien Amerge Anusol-HC cream and suppositories Aricept Asmanex Astelin Atrovent Avodart Axert Azopt Betoptic-S Caduet Cefzil Cenestin Cerumenex Claritin OTC Claritin-D OTC Climara Pro Clozaril Combipatch Combivent Coreg Cosopt Coumadin Covera HS Cozaar Detrol Detrol LA Diflucxn Dilantin Diovan Diovan HCT Duragesic Duricef oral suspension Emtriva Epzicom Evista Exelon Famvir Fem HRT Flomax Florinef Flovent Foradil Fosamax Frova Gengraf Geodon Glucophage XR Glucovance Humalog Humulin Hyzaar Imitrex Lanoxin Lantus Lexapro Levaquin Lipitor Loprressor HCT Lotrel Maxalt Metaglip Migranal Monopril HCT Nasalcrom Neoral Niacin Nicotrol inhaler Norvasc Novolin Novolog Omnicef Ortho-Prefest OTC nicotine gum, lozenges, patches Plavix Plendil Pravachol Premarin Premphase Prempro Prevpac Prilosec OTC ProAir HFA Proctocort ProctoKit Proscar QVAR Reminyl Risperdal Sandimmune Serevent Sonata Spiriva Sular Synthroid Tarka Tegretol Tigan suppositories Toprol XL Tricor Trusopt Truvada Valtrex Verelan Vytorin Welchol Xalatan Zaditor OTC Zarontin Zetia Zithromax Zomig Zyprexa and effexor.
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36. Oral H, Knight BP, Tada H, et al. Pulmonary vein isolation for paroxysmal and persistent atrial fibrillation. Circulation. 2002; 105: 1077-1081. Oral H, Scharf C, Chugh A, et al. Catheter ablation for paroxysmal atrial fibrillation: segmental pulmonary vein ostial ablation versus left atrial ablation. Circulation. 2003; 108: 2355-2360. Haissaguerre M, Jais P, Shah DC, et al. Electrophysiological end point for catheter ablation of atrial fibrillation initiated from multiple pulmonary venous foci. Circulation 2000; 101: 1409-1417 Pappone C, Oreto G, Rosanio S, et al. Atrial electroanatomic remodeling after circumferential radiofrequency pulmonary vein ablation: efficacy of an anatomic approach in a large cohort of patients with atrial fibrillation. Circulation 2001; 104: 2539-2544. Marrouche NF, Dresing T, Cole C, et al. Circular mapping and ablation of the pulmonary vein for treatment of atrial fibrillation: impact of different catheter technologies. J Coll Cardiol. 2002; 40: 464-474. Pappone C, Rosanio S, Augello G, et al. Mortality, morbidity, and quality of life after circumferential pulmonary vein ablation for atrial fibrillation: outcomes from a controlled nonrandomized long-term study. J Coll Cardiol. 2003; 42: 185-197. Wazni OM, Marrouche NF, Martin DO, et al. Radiofrequency ablation vs antiarrhythmic drugs as first-line treatment of symptomatic atrial fibrillation: a randomized trial. JAMA. 2005; 293: 2634-2640. Oral H, Pappone C, Chugh A, et al. Circumferential pulmonary-vein ablation for chronic atrial fibrillation. N Engl J Med. 2006; 354: 934-941. Sanchez-Quintana D, Cabrera JA, Climent V, Farre J, Mendonca MC, Ho SY. Anatomic relations between the esophagus and left atrium and relevance for ablation of atrial fibrillation. Circulation. 2005; 112: 1400-1405. Cox JL, Schuessler RB, Lappas DG, Boineau JP. An 8 1 2year clinical experience with surgery for atrial fibrillation. Ann Surg. 1996; 224: 267-273. Cox JL, Ad N, Palazzo T, Fitzpatrick S, et al. Current status of the Maze procedure for the treatment of atrial fibrillation. Semin Thorac Cardiovasc Surg. 2000; 12: 15-19. Prasad SM, Maniar HS, Camillo CJ, et al. The Cox maze III procedure for atrial fibrillation: long-term efficacy in patients and evista.
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Age structures of hospitalised are very different from one State to the other, reflecting the differences in the recruitment of data collection sites and in the age structure of the populations ; - For a given injury, a fracture for example, the percentage of hospitalised varies considerably between States. These results confirm that the inter-State macro-accidentologic analysis is a very delicate job due to the strong variability of the indicators. This variability can originate from factors that are difficult to isolate: difference in the data collection methodology, non stable hospital samples, evolution of data collection quality, difference in the structure health care systems or evolutions in practices. Nevertheless, for States with long and relatively homogeneous time series two trends can be observed: - A slow but relatively continuous decrease of the average RH can be seen for BE, DK, FR, IE, NL, PT between 1991 8, 62% ; and 1997 7, 42% ; . - The average ALS is relatively stable for BE, DK, FR, IE, NL between 1991 7, 91 days ; and 1997 7, 13 days ; , with the beginning of a slow decrease from 1995 on 7, 84 days ; . - Finally, over time we notice a convergence of the RH of all the States over time AT excepted ; towards the European average deviations between States decrease for those having more than two years of observations and flonase.
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Through a local formulary or insurance company. In acute arthritis, such as gout, full-dose NSAIDs should be started. For chronic musculoskeletal pain, the starting daily dose should be half the maximum, and the maintenance dose should be determined by assessing the benefits and side effects. When an NSAID has been tried at full dose for 2 weeks without satisfactory results, another NSAID from a different chemical class should be tried. Different forms of the same drug are often available. For example, sustained-release, controlled-release, entericcoated and suppository formulations may be available for many NSAIDs. Sustained-release and controlled-release formulations and NSAIDs with a long half-life may be more convenient because these are taken only once a day. Sustained-release, controlled-release and suppository formulations may be more effective in reducing morning stiffness in patients with inflammatory joint disease. Suppository and enteric-coated formulations may reduce upper GI symptoms of dyspepsia, but there is no evidence that they reduce serious upper GI complications.6, 7 In many instances the choice of formulation becomes one of personal preference and the preference of local third-party payers.
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Fourth, all information gathered on the implementation of the Decision shall be brought to the attention of the TRIPS Council in its annual review as set out in paragraph 8 of the Decision. In addition, as stated in footnote 3 to paragraph 1 b ; of the Decision, the following Members have agreed to opt out of using the system as importers: Australia, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Japan, Luxembourg, Netherlands, New Zealand, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom and United States of America. Until their accession to the European Union, Czech Republic, Cyprus, Estonia, Hungary, Latvia, Lithuania, Malta, Poland, Slovak Republic and Slovenia agree that they would only use the system as importers in situations of national emergency or other circumstances of extreme urgency. These countries further agree that upon their accession to the European Union, they will opt out of using the system as importers. As we have heard today, and as the Secretariat has been informed in certain communications, some other Members have agreed that they would only use the system as importers in situations of national emergency or other circumstances of extreme urgency: Hong Kong China, Israel, Korea, Kuwait, Macao China, Mexico, Qatar, Singapore, Chinese Taipei, Turkey, United Arab Emirates. Companies have often used special labelling, colouring, shaping, sizing, etc. to differentiate products supplied through donor or discounted pricing programmes from products supplied to other markets. Examples of such measures include the following: Bristol Myers Squibb used different markings imprints on capsules supplied to sub Saharan Africa. Novartis has used different trademark names, one Riamet ; for an anti-malarial drug provided to developed countries, the other Coartem ; for the same products supplied to developing countries. Novartis further differentiated the products through distinctive packaging. GlaxoSmithKline GSK ; used different outer packaging for its HIV AIDS medications Combivir, Epivir and Trizivir supplied to developing countries. GSK further differentiated the products by embossing the tablets with a different number than tablets supplied to developed countries, and plans to further differentiate the products by using different colours. Merck differentiated its HIV AIDS antiretroviral medicine CRIXIVAN through special packaging and labelling, i.e., gold-ink printing on the capsule, dark green bottle cap and a bottle label with a light-green background. Pfizer used different colouring and shaping for Difljcan pills supplied to South Africa.
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