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Mortal Wkly Rep 1996; 45: 365-70. Fujiwara PI, Frieden TR. Tuberculosis epidemiology and control in the inner city. In: Rom WN, Garay SM, eds. Tuberculosis. Boston, MA: Little Brown, 1996: 99-111. 37. Tuberculosis statistics in the United States--1992. Atlanta, GA: Centers for Disease Control and Prevention, 1994. 38. Doster B, Caras GJ, Snider DE. A continuing survey of primary drug resistance in tuberculosis, 1961 to 1968. A United States Public Health Service cooperative study. Rev Respir Dis 1976; 113: 419-25. Kopanoff DE, Kilburn JO, Glassroth JL, et al. A continuing survey of tuberculosis primary drug resistance in the United States: March 1975 to November 1977. A United States Public Health Service cooperative study. Rev Respir Dis 1978; 118: 835-42. Outbreak of multidrug-resistant tuberculosis--Texas, California, and Pennsylvania. MMWR Morb Mortal Wkly Rep 1990; 39: 369-72. Interstate outbreak of multidrug-resistant tuberculosis involving children--California, Montana, Nevada, Utah. MMWR Morb Mortal Wkly Rep 1983; 32: 516-18. Transmission of multidrug-resistant tuberculosis from an HIV-positive client in a residential substance-abuse treatment facility--Michigan. MMWR Morb Mortal Wkly Rep 1991; 40: 129-31. Nosocomial transmission of multidrug-resistant tuberculosis among HIV-infected persons--Florida and New York, 1988-1991. MMWR Morb Mortal Wkly Rep 1991; 40: 585-91. Pearson ML, Jereb JA, Frieden TR, et al. Nosocomial transmission of multidrug-resistant Mycobacterium tuberculosis: a risk to patients and health care workers. Ann Intern Med 1992; 117: 191-6. Edlin BR, Tokars JI, Grieco MH, et al. An outbreak of multidrug-resistant tuberculosis among hospitalized patients with the acquired immunodeficiency syndrome. N Engl J Med 1992; 326: 1514-21. Snider DE Jr, Dooley SW. Nosocomial tuberculosis in the AIDS era with an emphasis on multidrug-resistant disease. Heart Lung 1993; 22: 365-9. Telzac EE, Sepkowitz K, Alpert P, et al. Multidrug-resistant tuberculosis in patients without HIV infection. N Engl J Med 1995; 333: 907-ll. Park MM, Davis AL, Schluger NW, et al. Outcome of MDR-TB patients, 1983-1993: prolonged survival with appropriate therapy. J Respir Crit Care Med 1996; 153: 317-24. National action plan to combat multidrug-resistant tuberculosis. MMWR Morb Mortal Wkly Rep 1992; 41 RR-ll ; : 5-48. 50. Raviglione MC, Sudre P, Rieder HL, et al. Secular trends of tuberculosis in western Europe. Bull World Health Organ 1993; 71: 297-306. Hargreaves J. Tuberculosis notifications in Australia, 1992. Commun Dis Intell 1994; 18: 330-7. Raviglione MC, Rieder HL, Styblo K, et al. Tuberculosis trends in eastern Europe and the former USSR. Tuber Lung Dis 1994; 75: 400-16. Sudre P, ten Dam HG, Kochi A. Tuberculosis: a global overview of the situation today. Bull World Health Organ 1992; 70; 149-59. Tuberculosis, HIV on collision course in Asia. World Health Organization, Office of Information, press release, August 10, 1994. WHO 63 ; . 55. Kleeborg HH, Olivier MS, eds. A world atlas of initial drug resistance. 2nd rev ed. Atlanta, GA: Centers for Disease Control, 1984. 56. Bloom BR, Murray CJL. Tuberculosis: commentary on a reemergent killer. Science 1992; 257: 1055-64. Arno PS, Murray CJL, Bonuck K, et al. The economic impact of tuberculosis in hospitals in New York City: a preliminary analysis. J Law Med Ethics 1993; 21: 317-23. The global burden of disease, 1990. In: World development Epidemiol Rev Vol. 18, No. 1, 1996, for example, mexitil drug. Medication for anxiety 24th october 2004.
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BCNA's Project Manager, Anne-Maree Polimeni, conducted individual interviews with women from Queensland, New South Wales, Victoria and Tasmania, and facilitated two focus groups in Victoria and in Queensland to explore women's experiences, especially when they were newly diagnosed with secondary breast cancer. She found that consistent themes emerged, including the need for: women to hear messages of hope and stories of survival women to speak to others living with secondaries emotional support and to freely discuss worries with counsellors or in support groups ; information about how women can contribute to their own health and wellbeing such as nutrition, relaxation, coping with side effects ; a good working relationship with health professionals information about financial assistance Women living with secondary breast cancer have said there is a lack of accessible information, including medical information and information about where to get practical, emotional and financial support. They also cite a lack of appropriate, accessible and affordable emotional support options, including individual or group support. There are very few support groups or peer support programs for women with secondary breast cancer in Australia. Using the services of psychologists or psychiatrists can be very costly, and often women are not well enough to attend services that might exist. We are currently asking women to identify the information, resources, services, and supports that they found useful and not so useful during their experience with secondary breast cancer. A survey to women, distributed through BCNA's database, will enable us to consult with a wider range of women of different ages, locations and situations around Australia so that the final product will result from extensive consultations with a diverse range of women. As with the My Journey Kit, we will draft the resource, seek comment from a range of women and breast cancer clinicians, and request endorsement from professional associations to ensure currency, validity and quality and mexiletine.

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25 ; p 0.001 for the Sheffield table compared with each of the other two guidelines for both doctors and nurses ; . Similar results were. GILEAD SCIENCES Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need.The company's unique portfolio of therapeutics is designed to advance the care of patients suffering from life-threatening infectious diseases. How we help them: advertising, strategic planning, Web design, interactive animation, e-mail marketing, patient relationship marketing, product collateral, outdoor advertising and advocacy Web sites for the company's HIV and hepatitis B brands and telmisartan. UPMC Open Access PPO option: The Open Access PPO plan is similar to the Advantage PPO plan except that the highest level of benefits are provided when using a UPMC Health Plan network provider for covered services. Facilities are not limited to the UPMC Advantage network.
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SP - Specialty Pharmacy - These medications can not be filled at a regular retail pharmacy. QL - Quantity Limit - These medications have a limit to the amount that the plan will cover. PA - Prior Authorization - These medications require approval by the plan. 23, for instance, dizziness. Polpharma S.A. Starogardzkie 30 10 05 Zaklady Farmaceutyczne Warszawskie Zaklady Farmaceutyczne POLFA Zaklady Farmaceutyczne Polpharma SA, Starogard Gdanski A.C.E.F., Wlochy Pharma Cosmetic, Krakw Pharma Zentrale PPH Galfarm Sp. z o.o., Krakw Zaklady Farmaceutyczne Polpharma SA, Starogard Gdanski Zaklady Farmaceutyczne Polpharma SA, Starogard Gdanski 30 11 05 Labor, Wroclaw BUFA b.v. Pharmaceutical Products Pharma Cosmetic, Krakw Pharma Zentrale PPH Galfarm Sp. z o.o., Krakw Ldzkie Przedsiebiorstwo Farmaceutyczne POLON Sp. z o.o. Pharma Zentrale PPH Galfarm Sp. z o.o., Krakw Tablets Tablets Lehning Laboratoires Heel GmbH Pfizer Polska Sp. z o.o and meloxicam.
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There is a very active drug discovery program supported by the National Institute on Drug Abuse to develop medications for cocaine addiction, but there are still no FDAapproved medications for this indication. Animal models have generally not replicated the bingeing pattern displayed by human addicts. Low, intermittent doses in rodents have demonstrated behavioral sensitization. This means that the same dose produces progressively increasing motor activity instead of decreased activity or tolerance. This sensitization is hypothesized to play a major role in compulsive drug seeking in humans 58 ; . In human addicts, there is subjective evidence of tolerance and no clear signs of sensitization, although some have speculated that stimulant psychosis represents a form of sensitization. Since only 16% of those who try cocaine develop addiction 59 ; , perhaps the majority of users experience sensitization as unpleasant and stop using cocaine. Recently, however, five different medications already approved for other purposes have been found in randomized, controlled trials to be effective among cocaine addicts. Disulfiram was initially tested by Carroll and colleagues 60 ; in patients suffering from alcohol abuse and dependence coexisting with cocaine dependence. They discovered, however, that the medication was also helpful to those who met criteria for cocaine addiction alone, with no significant accompanying alcohol problem. The mechanism whereby disulfiram reduces the frequency of cocaine use is unknown, but it does not appear to be related to the prevention of alcohol use. Rather, abusers of cocaine--but not alcohol--showed more benefits from disulfiram than those with a history of combined alcohol cocaine abuse or dependence. The mechanism for this effect is unknown, but disulfiram is known to increase plasma concentrations of cocaine three- to sixfold 61 ; and to inhibit dopamine beta hydroxylase 62 ; , thus increasing the effects of cocaine and possibly making cocaine use aversive. Modafinil, approved for the treatment of narcolepsy, has been found by two groups to reduce the high from cocaine and to reduce cocaine craving 63 ; . After positive results from an open trial, the results from a randomized, controlled trial were also positive 64 ; , and a multiclinic trial is in progress. The mechanism of action of modafinil is unknown, but it does increase glutamate levels in the brain, thus reversing the effect of chronic cocaine use, as measured in animal models 65 ; . Modafinil is very well accepted by patients, who report a reduction of cocaine withdrawal symptoms and a blunting of the effects of cocaine if they begin to relapse while taking the medication. The medication has not been reported to produce euphoria, and there has been no indication of excessive use or abuse in clinical trials 64.
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