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West Palm Beach, FL PRWeb ; January 9, 2007 -- This four-story landmark federal building was abruptly closed as result of mold growing in and outside of the building's walls. The mold was spawned from water leaking into the building spurred on by Florida hurricanes Frances and Jeanne. Forensic investigations revealed water that had seeped in around the windows. The resultant mold and bacteria growth was visibly noticeable as well as creating a musty "unhealthy" odor offensive to all. Ultimately, all the governmental employees of this federal courthouse including judges, court employees, federal marshals and countless clerical staff members had to relocated to new facilities as well as truckloads of court records. The mold had literally taken over forcing people and important hardbound legal records to flee. Left unabated, the mold could create a serious health concern for all inhabits as well as a catalyst for documentation delay and damage. The doors were locked and the problem circumvented re-occupation until the facility were clean, mold free, and certified safe for people and documents to come home. THE SOLUTION The General Services Administration GSA ; researched the industry and found Pure Air Control Services to be one of the most qualified, competent, interdisciplinary indoor environmental quality IEQ ; firms in the country. Pure Air Control Services a 22 year old interdisciplinary indoor environmental firm of four diverse divisions has over 10 million square feet of building environmental experience. Pure Air Control Services building sciences division has backgrounds in industrial hygiene, microbiology, mechanical engineering, building sciences and medical along with a state-o-the-art American Industrial Hygiene Association AIHA ; accredited microbiology laboratory and building remediation division to compliment high profile turn-key environmental projects. GSA requested Pure Air Control Services to develop a protocol of identifying baseline IEQ conditions and remediation necessary to heal this federal courthouse, in West Palm Beach Florida. Recommendations considered the removal of all outer walls and the adjacent flooring and ceilings in infected rooms located on several floors. Inspections evaluated remediation work in air handlers and ductwork as well. Pure Air Control Services comprehensive plan consisted of six 6 ; timely steps: 1. Establish all IEQ baseline conditions including containment and microbial contaminant concerns.

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25 ; En 26 ; 99944371.6 22 ; 11.08.1999 84 ; AT BE 13.06.2001 86 ; EP 1999 005876 11.08.1999 ; WO 2000 009098 2000 ; 13.08.1998 US 133855 54 ; VERFAHREN ZUR BEHANDLUNG VON OKULAREN NEOVASKULAREN ERKRANKUNGEN METHOD FOR TREATING OCULAR NEOVASCULAR DISEASES METHODE DE TRAITEMENT DE MALADIES OCULAIRES NEOVASCULAIRES 73 ; Novartis AG, Lichtstrasse 35, 4056 Basel, CH 84 ; BE CH Novartis Pharma GmbH, Brunner Strasse 59, 1230 Wien, AT 84 ; AT 72 ; BRAZZELL, Romulus, Kimbro, Alpharetta, GA 30201, US WOOD, Jeanette, Marjorie, CH-4105 BielBenken, CH CAMPOCHIARO, Peter, Anthony, Baltimore, MD 21210, US KANE, Frances, Elizabeth, Gainesville, GA 30504, US 74 ; de Weerd, Petrus G.W., et al, Novartis International AG Corporate Intellectual Property, 4002 Basel, CH and ceclor, for example, voltaren overdose.

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Summary of health professional and consumer advisories posted from May 31 to Aug. 31, 2003 advisories are available at hc-sc.gc hpfb-dgpsa tpd-dpt index advisories e ; Date. Conjoint Endocrine Laboratory B.M., H.L., K.R., R.M. ; , Clinical Research Centre, Royal Brisbane and Women's Hospital and Queensland Health Pathology Services, Herston, Queensland 4029, Australia; and the Department of Obstetrics and Gynaecology R.M. ; , The University of Queensland, St. Lucia, Queensland 4072, Australia and celecoxib.
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Conclusion Taking the above into account, we currently believe that the restatement of the 2005 results under IFRS will show a modest increase of approximately 2% to 3% in adjusted pre-tax profit before goodwill amortisation ; compared to these results reported under UK GAAP. Reported shareholders' funds will also increase under IFRS due to the write back of goodwill, the proposed dividend and an increase in the deferred tax asset. It should be emphasised that these are accounting adjustments only and have no impact on the economic conditions facing the Group, nor on its cash flows, distributable reserves or prospects and cleocin.
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Combination patent in the US until 2017. Generic manufacturers have challenged this patent, and Novartis has sued them. Our actions against two of these manufacturers are currently stayed. Lamisil. The active ingredient in Lamisil is covered by a compound patent family which expires in June 2007 in the US; in August 2007 in France; and has expired elsewhere. The US patent had been challenged by a generic manufacturer in the US. The generic manufacturer has since withdrawn its suit and conceded that this patent is valid and enforceable. Neoral. Patent protection exists for the Neoral micro-emulsion formulation and other cyclosporin formulations through 2009 and beyond in major markets. Despite this protection, generic cyclosporin products competing with Neoral have entered the transplantation market segment in the US, Germany, Japan, Canada and elsewhere. Patent infringement actions are pending against manufacturers of some of these generic products. At present, there are no injunctions in place against any of the manufacturers that we have sued. Sandostatin. Basic patent protection for the active ingredient of Sandostatin SC has expired in the US, Japan, Germany, France and the UK, and it will expire in May 2007 in Italy. Generic versions of Sandostatin SC have been approved in the US and elsewhere. Patent protection for the Sandostatin LAR formulation extending to 2010 and 2013 and beyond in the US ; continues in major markets. Sandostatin LAR is a long-acting version of Sandostatin which represents a majority of our sales in this product family. Trileptal. Patent protection for Trileptal's active ingredient has expired in major countries. However, a patent has been granted in the US directed to a method of treating seizures with our marketed formulations of Trileptal, which will expire in 2018, and corresponding patent filings are granted or pending in other major countries with the same expiration date. A number of parties have filed applications to market a generic version of Trileptal in the US. Of these, lawsuits have recently been initiated against certain of the generic manufacturers. In Europe, the corresponding granted patent is currently being opposed by certain other generic manufacturers. Femara. The active ingredient in Femara is covered by a compound patent which expires in 2011 in the US. A generic manufacturer has challenged this patent and has filed an application for a generic version of Femara in the US. Novartis has filed a lawsuit against the generic manufacturer for patent infringement. Voltaren. Voltaten is off-patent. As a result, revenue from Voltarn has declined, and may decline significantly further in the future. Exelon. The active ingredient in Exelon is covered by a compound patent granted to Proterra and licensed to us ; , which expires in the US in 2012 as a result of a patent term extension ; , and which expires in 2011-13 in other major markets. In addition, we hold an isomer patent on Exelon which expires in 2012-14. Three generic manufacturers have filed applications to market a generic version of Exelon in the US. Together with Proterra, we have sued all three parties for patent infringement. Visudyne. Basic patent protection for the active ingredient in Visudyne expires in 2011 in the US and in 2014 in other major countries. An academic institution has obtained granted patents for a method of use involving photodynamic therapy and subsequently filed a patent infringement suit against us and our licensor, QLT Phototherapeutics. Miacalcin Miacalcic. The specific Novartis formulation of this product is covered by patents which will expire in the US in 2015. However, patents on the Novartis formulation have expired in most other countries. One generic manufacturer has applied to the FDA for the right to sell a generic version of Miacalcin in the US using the Novartis formulation. We have sued that manufacturer for patent infringement. Two other companies have applied to the FDA for the right to sell a generic version of Miacalcin in the US based on a different formulation. We have not sued these companies. Another company's recombinant salmon calcitonin product is approved in the US, but would not be automatically substitutable in the US for Miacalcin. 56 and colchicine. Using Non-Massachusetts Providers The following information is added as Appendix D: What You Should Know When You Use Non-Massachusetts Providers This appendix contains important information about how the Commonwealth Indemnity Plan pays for services you receive from health care providers located outside of Massachusetts. Reimbursement to Non-Massachusetts Providers If you use a non-Massachusetts provider for any reason including emergency care you could be subject to balance billing. Balance billing is the practice by health care providers of billing patients for charges that exceed the amount paid by a patient's health plan for services rendered. For example, if your doctor bills your health plan $90 for your office visit and your health plan allows $75 for the office visit, some physicians may balance bill you for the difference of $15. The following information explains how the Plan reimburses non-Massachusetts providers and how you may be able to manage or avoid balance billing by these providers. The Plan pays non-Massachusetts providers according to fee schedules that establish the reasonable and customary allowed rates for payment of services. The payments in the fee schedules are consistent with what other plans pay providers. Charges in excess of the fee schedule amounts will not be considered for payment, as they will exceed these allowed amounts. A provider might balance bill you for the difference between the payment made by the Plan according to the fee schedules and the amount the provider charged. Ways to Avoid Balance Billing Here are two ways you can manage or even avoid balance billing: Use Massachusetts Providers for Your Health Care Whenever Possible If you are planning any elective health care services, or need to schedule a medical or surgical procedure, you should consider using Massachusetts providers for that care whenever possible. These providers are prohibited by Massachusetts law from balance billing members of the Commonwealth Indemnity Plan for amounts above the allowed amounts established in the fee schedules. The Plan encourages you to plan ahead, scheduling medical care in Massachusetts before you go away, or upon your return. This will guarantee that you don't get balance billed. Discuss the Balance Bill with Your Non-Massachusetts Provider Ask your provider to consider accepting the allowed amount from the Plan as payment in full for his or her services. The Commonwealth Indemnity Plan's fee schedules for out-of-state providers are intended to provide adequate compensation for services, usually at a level similar to and sometimes higher than what providers are receiving from many other health insurance plans in the area. Additionally, the Plan pays providers promptly; nearly 100 percent of provider claims are paid within 14 days of their receipt, because voltwren emulgel cream.
N.B. Measurement of glycosylated haemoglobin HbA1c ; is the preferred method of monitoring overall diabetic control Guidelines for Blood Glucose Monitoring Patients should be appropriately advised on the correct place and use of blood glucose monitoring products. If these products are required, patients should be trained to use the system correctly. The frequency of use as well as the costs of prescribing e.g. diagnostic strips ; should also be considered. Meters are not available on prescription and it is recommended that patients seek advice from their GP prior to purchasing a meter. Type 2 diabetes There is no need for the majority of patients with type 2 diabetes to monitor their blood glucose. Patients who are poorly controlled and being considered for insulin treatment may benefit from doing their own capillary blood glucose monitoring prior to starting insulin. Insulin-treated patients Blood glucose monitoring should be performed to assist the patient and or their diabetes carer in diabetes management and insulin dose adjustments. Measurements should be immediately before or after meals, or both, either on a daily basis or one day chosen per week random days ; . A high frequency daily rate of monitoring, i.e. qds, should be reserved for: newly diagnosed type 1 patients; people who are unwell; pregnancy; pre-surgery; frequent hypoglycaemic episodes; loss of hypoglycaemia warning signs. For products available please see section 19.1 and doxycycline.

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Lamisil, Nicotinell Habitrol, Otrivin and Voltaren. Alongside the brand team is a research & development team that will be looking to grow the brand through switches, line extensions and new forms of product delivery. These global brands increased sales by 10% during 2002 as shown in table 1. They represent one-third of the total OTC turnover. The five global brands are not only the growth drivers of the OTC unit but also offer Novartis the best margins. At the moment only one brand, Lamisil, is a truly global brand. However, the increased investment in these brands is expected to build critical mass and they have the ambition and potential to increase their geographic coverage. The whole Novartis organisation will be able to focus on these five global brands.

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