Livia Benigni DVM, MRCVS Post-graduate Trainee in Radiology Livia graduated in 1998 from the University of Pisa, Italy. After graduation she completed a one year internship in Internal Medicine Cardiology ; at the Ecole Nationale Veterinaire d'Alfort, Paris, France. During the two years following the internship Livia was a part-time clinical assistant at the Cardiology Unit of the Ecole Veterinaire d'Alfort and she also worked as a veterinary surgeon in private practice. In 2001 she moved to London and started a self-funded part time training in veterinary diagnostic imaging aiming for the Diploma of the European College of Veterinary Diagnostic Imaging. For the past two years Livia has provided diagnostic imaging services in small animal private practices in London. In September 2003 she joined the Royal Veterinary College as a Senior Clinical Training Scholar in Diagnostic Imaging. Livia's interests include applications of ultrasonography in the evaluation of middle ear diseases and analysis of usefulness of FLAIR and other particular sequences in small animal MRI.
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At Blue Cross of California and BC Life & Health Insurance Company Blue Cross ; we keep our members' financial and health information private as required by law, accreditation standards and our own policies. This Notice explains your rights, our legal duties and our privacy practices. We are required by federal laws to provide you with this Notice. ask a hospital for details about your treatment so that we may review and pay the claim for your care. For Health Care Operations: We use and disclose information about you for our operations. For example, we may use information about you: n To review the quality of care and services you receive; n To provide you case management or care coordination services, such as for asthma, diabetes or traumatic injury; or n For quality or accreditation reviews. For Treatment Activities: We may use and disclose information about you for treatment activities those activities performed by a health care provider related to the provision, coordination or management of health care provided to you ; . We may disclose information about you to your health care provider in order for that provider to provide treatment to you. We may contact you with information about treatment options or other healthrelated benefits and services. For example, when you or your dependents reach a certain age, we may notify you about other products or programs for which you may become eligible, such as Medicare supplements or individual coverage. We may also send you reminders about routine medical check-ups and tests. If you are in a group health plan, we may share certain health information with your employer the plan sponsor ; or other organizations that help pay for your membership in the plan, to enroll you in the plan or so the plan sponsor can manage the health plan. Plan sponsors that receive this information are required by law to have controls in place to protect it from improper uses. To Your Family or Person Designated by You: We may disclose your medical information, with your verbal permission and in circumstances where it is impracticable to get your written permission, to a family member or other person designated by you to the extent necessary to help with your health care or with payment for your health care. We may use or disclose your name, location and general condition or death to notify, or assist in the notification of including identifying or locating ; , a person involved in your care. Before we disclose your medical information to a person involved in your health care or payment for your health care, we will provide you with an opportunity to object to such uses or disclosures. If you are not present, or in the event of your incapacity or an emergency, we will disclose your medical information based on our professional judgment of whether the disclosure would be in your best interest. As Allowed or Required by Law: Information about you may be used and shared as required by law; for health oversight activities required or allowed by law; for judicial or administrative proceedings; to public health authorities; for law enforcement purposes; to coroners, funeral directors or medical examiners about decedents ; and to organ procurement organizations for certain purposes; for research purposes; to avert a serious threat to health or safety; for specialized government functions; for workers' compensation purposes; to respond to requests from the Secretary, U.S. Department of Health and Human Services; and to alert appropriate authorities if we reasonably believe that you are a possible victim of abuse, neglect, domestic violence or other crimes. Authorization: We will get your written permission before we use or share your protected health information for any other purpose, unless otherwise stated in this Notice. You may withdraw this permission at any time, in writing. We will then stop.
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However, we have also recognized that the "absolute destruction of property is an extreme exercise of the police power and is justified only within the narrowest limits of actual necessity, unless the state chooses to pay compensation." Corneal, 95 So. 2d at 4 emphasis supplied ; . We have explained that "[w]here property is destroyed in order to save property of greater value, a provision for indemnity is a plain dictate of justice and of the principle of equality, " and . that statutory regulation of the power to destroy property in this situation "is always accompanied by statutory duty of compensation." Id. quoting Ernst Freund, The Police Power: Public Policy and Constitutional Rights, 534-35, at 564-65 1904 alteration in original ; . In Corneal, this Court specifically addressed the State's destruction of healthy citrus trees as a means of controlling the spread of a citrus disease known as "spreading decline." See id. at 2-3. The rule adopted by the State Plant Board to control the disease required the removal and burning of both infected and uninfected trees within a certain distance from infected trees. See id. at 3. The Court cited domestic animals infected with a contagious disease and a burning building as examples of circumstances that justify the destruction of property and alendronate.
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Global pharmaceutical turnover in the fourth quarter of 2004 increased three per cent, reflecting a US turnover increase of four per cent to 2, 114 million; whereas in Europe turnover grew two per cent to 1, 397 million, and in International turnover grew five per cent to 976 million. Turnover in the USA was impacted by generic competition for Wellbutrin and Paxil. Excluding sales of these products, turnover grew 10 per cent in the USA. Pharmaceutical turnover by therapeutic area GlaxoSmithKline's ability to continue to deliver pharmaceutical turnover growth, despite generic competition to several of its products, is primarily due to an exceptionally broad product portfolio of fast-growing, high-value products. These include the respiratory product Seretide Advair, up 19 per cent 2.5 billion ; , the diabetes treatment Avandia Avandamet, up 32 per cent 1.1 billion ; , Lamictal for epilepsy bipolar disorder, up 32 per cent 0.7 billion ; , Valtrex for herpes 0.6 billion ; , up 24 per cent, Coreg for heart disease, up 34 per cent 0.4 billion ; and vaccines, up 11 per cent 1.2 billion ; . In all, 12 GlaxoSmithKline products each had sales of over 500 million in 2004. Respiratory GlaxoSmithKline continues to be the global leader in respiratory pharmaceuticals with sales of its three key products, Seretide Advair, Flixotide Flovent and Serevent, amounting to 3.4 billion, up nine per cent. Sales of Seretide Advair, the Group's largest product grew 19 per cent to 2.5 billion although this contributed to declines in Serevent and Flixotide, its constituent products. In the USA, Advai sales grew 20 per cent to 1.3 billion. Growth of Seretide in Europe was also strong up 18 per cent to 902 million ; , although reported growth in the fourth quarter was adversely impacted by a one-off rebate adjustment in Germany and wholesaler de-stocking in Italy. International sales grew 15 per cent, reflecting good growth in all geographic areas. The older respiratory products Ventolin and Becotide continued to decline as patients converted to newer products. Central nervous system CNS ; CNS sales declined 16 per cent to 3.5 billion. Sales declined in all regions. Total sales of the Paxil franchise were down 39 per cent to 1.1 billion as a result of generic competition to Paxil IR, sales of which declined 53 per cent to 667 million. Mitigating this decline was the strong performance of the product in Japan, up 25 per cent to 171 million and the performance of Paxil CR which generated sales of 396 million, up 14 per cent. Total sales of Wellbutrin products fell 12 per cent to 751 million. Wellbutrin IR and SR sales fell 64 per cent to 284 million as a result of generic competition. This impact was partially offset, however, by the exceptionally strong performance of Wellbutrin XL, the new once-daily product, which achieved sales of 467 million in its first full year on the market.
Address for reprint requests and other correspondence: S. J. Moat, Wales Heart Research Institute, Univ. of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, UK E-mail: moatsj cardiff.ac ; . : ajpheart and amoxycillin.
Sign up sign in shortcuts end test topix nav menu - home page • forums • most popular • top stories • local • us • world • sports • entertainment • offbeat • all topix healthcare law blog forum newswire asthma inhalers in short supply posted in the healthcare law forum comments showing posts 161 - 180 of 229 « prev next » jump to page: 1 2 3 arthur abramson joined: mar 30, 2007 comments: 137 san francisco, ca reply » flag #162 jun 9, 2007 jack50 wrote: quoted text i have been on xopenex hfa for 2 months now and just had my dr change advair to flovent.
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M. Gregory Papa, D.O.; Abbott Spoke on Tricor. n. Richard J humann, Jr., M.D.; Wilmington Neurology Consultants.P.A Spoke on Relpax o. Anne Camasso, Arthritis Foundation Spoke on grandfathering VI. 1. PDL Selection Proton Pump Inhibitors ON PDL: Prevacid OFF PDL: Aciphex, Nexium, omeprazole, Prilosec OTC, Protonix, Zegerid Motion passed unanimously Antimigraine Agents, Triptans ON PDL: Amerge, Imitrex nasal and oral ; , Maxalt, Maxalt MLT OFF PDL: Axert, Frova, Imitrex subq ; , Relpax, Zomig nasal and oral ; , Zomig ZMT NOTE: Relpax will be grandfathered for the current patients Motion passed unanimously Leukotriene Modifiers ON PDL: Accolate, Singulair Motion passed unanimously Intranasal Rhinitis ON PDL: ipratropium, Astelin, Flonase, Nasarel, Nasonex OFF PDL: Beconase AQ, flunisolide, Nasacort AQ, Rhinocort Aqua Motion passed unanimously Glucocorticoids, Inhaled ON PDL: Advair, Aerobid, Aerobid M, Azmacort, Flovent, Pulmicort Respules, Qvar OFF PDL: Pulmicort Turbuhaler. Motion passed unanimously Lipotropics, Statins ON PDL: Advicor, Altoprev, Lescol, Lescol XL, Lipitor, Pravachol, Vytorin, Zocor OFF PDL: Crestor, lovastatin, Pravigard PAC NOTE: Vytorin was tentatively accepted on PDL pending confirmation that its cost would not be significantly higher than its components NOTE: Crestor will be grand fathered for the current patients; Caduet decision will be pended until the CCB class is reviewed. Motion passed unanimously VII. VIII. Adjournment-meeting adjourned at 9: 40. Next meeting is scheduled for March 17th at 7 p.m and ampicillin.
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The woman whose health is already at risk may not want to undergo the increased risk that carrying the fetus to term would impose on her and arava and advair, for example, advait side affect.
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From the Department of Psychiatry JBW, KMO ; , and the General Medicine Division JBW ; of Massachusetts General Hospital; Harvard Medical School, Boston, Mass JBW, JBM Stanford Center for Research in Disease Prevention, Stanford University, Palo Alto, Calif RSS and Sloan School of Management, Massachusetts Institute of Technology, Cambridge, Mass SNF ; . This study was supported in part by a grant from Wyeth Pharmaceuticals who played no role in the collection, analysis, interpretation of, or decision to publish the data ; and by the Massachusetts General Hospital's Primary Care Operations Improvement and Clinical Research Programs. Address correspondence to: Jeffrey B. Weilburg, MD, Department of Psychiatry, Massachusetts General Hospital, Wang Ambulatory Care Center, Room 815, 55 Fruit St, Boston MA 02114. E-mail: jweilburg partners.
21. MEDOFF-COOPER, B., T. Verklan et S. Carlson. The development of sucking patterns and physiologic correlates in very low birth weight infants, Nursing Research, 1993, 42 : 100-5. 22. MEIER, P.P. et M.M. Palmer. Transitional suck patterns in premature infants, Journal of Perinatal & Neonatal Nursing, septembre 1994, 8 2 ; : vii-viii. 23. MEIER, P.P., J.L. Engstrom, C.L. Crichton, D.R. Clark, M.M. Williams et H.H. Mangurten. A new scale for in-home test-weighing for mothers of preterm and high risk infants, Journal of Human Lactation, septembre 1994, 10 3 ; : 163-8. 24. MEIER, P.P., J.L. Engstrom, H.H. Mangurten, E. Estrada, B. Zimmerman et R. Kopparthi. Breastfeeding support services in the neonatal intensive-care unit, JOGN Nursing, juillet-aot 1993, 22 4 ; : 338-47. 25. NYQVIST, K.H. et P. Sjoden. Advice concerning breastfeeding from mothers of infants admitted to a neonatal intensive care unit: the Roy adaptation model as a conceptual structure, Journal of Advanced Nursing, janvier 1993, 18 1 ; : 54-63. 26. NYQVIST, K.H., P. Sjoden et U. Ewald. Mothers' advice about facilitating breastfeeding in a neonatal intensive care unit, Journal of Human Lactation, dcembre 1994, 10 4 ; : 237-44. 27. SALAMON, Y. Care study: breast-feeding in the SCBU. Special Care Baby Unit, Midwives Chronicle, mai 1993, 106 1264 ; : 178-9. 28. SOCIT CANADIENNE DE PDIATRIE, COMIT DE NUTRITION. Nutrient needs and feeding of premature infants, Canadian Medical Association Journal, 1995, 152 11 ; : 1765. 29. STORR, G. Breastfeeding premature triplets one woman's experience, Journal of Human Lactation, 1989, 5 2 ; : 74-7. 30. VALENTINE, H. Hindmilk improves weight gain in low birth weight infants fed human milk, Journal of Pediatric Gasteroenterology and Nutrition., 1994, 18 : 474-7, for example, advai warning.
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Theravance, Inc. LABA Update Conference Call January 11, 2006 TRANSCRIPT The Phase 2b studies will be designed to provide definitive safety and efficacy data. These results will enable us to make a go no decision on `797 based on a robust Phase 2b data set. We will not be going into the specific design criteria of the studies at this point, except to comment that the Phase 2b will entail larger numbers of patients dosed for longer periods of time than our Phase 2a work with doses that have the potential to be the commercial dose. Importantly, given the current development status of `444 and `802, we believe there is the potential to have definitive Phase 2b data for more than one compound prior to mid-2007 if the results of the ongoing Phase 2a work for these compounds are positive. We will not be providing any update at this point regarding overall program timing or the potential initiation of Phase 3 studies, as these plans remain under discussion pending the completion of the Phase 2b programs. While we're disappointed with the formulation issue that arose with `797 in late 2005, we believe that the subsequent work done by the project team has resulted in a stronger overall program. The Beyond Advakr collaboration between GSK and Theravance continues to be very solid, and continues to operate as initially envisioned, with multiple compounds advancing together through clinical development to increase the likelihood of bringing one medicine to the market around the end of the decade. I'm proud of the work completed by the GSK and Theravance team in quickly identifying a resolution to this issue, and I believe that the new development plan will enable us to reduce overall program risk and to provide definitive data on multiple compounds in a timely manner. I'd now like to turn the call over to the conference facilitator and open the call for questions. Operator: Thank you. If you would like to ask a question, please do so by pressing the star key followed by the digit one on your touch-tone telephone. If you are using a speakerphone, please make sure your mute function is turned off to allow your signal to reach our equipment. Once again, star one if you have a question. We'll take our first question from Dallas Webb with Stanford Group. Hey guys. Just real quick, in the press release it says multi-day administration. Is this an indication that the oncedaily may not be possible with `797? And would GSK want to continue development of a multi-day product? and aldactone.
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