Retail pharmacies carry a co-payment of $9.00 or 20 percent of the allowable charge, whichever is greater see Table 1.2 ; . The overwhelming majority of drug store chains are in-network: thus, most seniors pay a maximum co-payment of $9.00 per prescription. As noted above, the implementation of the TSRx program was followed by a substantial increase in DoD pharmacy expenditures. This increase was particularly dramatic within the retail sector. In FY 2000, the last full fiscal year before the TSRx program was implemented, DoD spent $455 million on retail prescriptions almost entirely on non-elderly military beneficiaries; elderly military beneficiaries were for the most part excluded from the retail benefit5 ; . Just two years later, in FY 2002, spending on retail prescriptions was $1.28 billion--nearly triple the amount spent in FY 2000. By comparison, spending on MTF prescriptions increased by just one-third during the same two-year period Remund, 2003 ; . The DoD Formulary System Although TSRx enrollees can obtain TRICARE-covered drugs through all four dispensing locations described above, not all TRICARE-covered medications are readily available at each dispensing location. On April.
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About 10% of children born short for gestational age will not catch up and will remain short at adult age. Indeed shortness at birth is an important cause of short stature in children. Investigations that have been performed in the last 10 years have clearly demonstrated that Growth Hormone GH ; treatment induces a rapid and important catch up when administrated in short children born SGA. Fjellestad et al. Acta Paediatrica 1998 ; have treated a group of short children -3, 3 SDS ; born SGA in their 5th year with 1.4 u O, 47 mg ; kg week of GH Saizen ; for 3 years. These children have gained 2 SD during this period without significant side effects. Similar results have been obtained by other investigators. The short-term efficacy of GH on height velocity has been established, however, several questions remained unanswered. Duration of treatment: In the study by Fjellestad et al., the same group of GH treated patients have been followed for another 5 years without GH treatment. A dramatic catchdown was observed and, after 5 years, they have lost 1 SD jeopardizing the effect of GH on height. These results clearly demonstrate that GH treatment should be maintained throughout childhood. Whether the treatment should continue during puberty remained questionable since the GH treatment during puberty have shown a positive effect on height velocity although minimal. Age at initiation of GH treatment: Since it has been shown that in infants born SGA catch up occurs immediately after birth and may continue until the end of the 2nd year of life, it seems reasonable to initiate GH treatment after 2 years of age. After this age an early treatment is probably more efficient. Dosage: Most short-term studies have shown that a dosage twice the replacement dose given for GH deficiency is efficient and induces pronounced height gain. More recently Hokken-Koelega et al. have published the long-term results of a randomized study using 2 dosages : 1 GH dosage close to the replacement dose used in the treatment of GHD and a dosage twice this amount. After 5 years the results obtained on height SDS were similar with these two dosages. It is also shown in this study that after 3 years the results obtained with the higher dosage are superior to the lower dosage. The higher dosage is therefore recommended for initial treatment and the lower dose could be considered for maintenance therapy. Side effects: All studies published so far have shown that no significant side effects were observed including effects on carbohydrate metabolism. In conclusion: GH treatment of short children born SGA is efficient and safe. Although, the exact therapeutic strategy remains to be defined in more detail, we have enough convincing evidence that short children born SGA should benefit from GH treatment, because temovate.
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Mr. Prasad holds a Masters Degrees in Science and Business Administration and enjoys more than 20 years of industry experience. Mr. Prasad possesses a successful track record of turning around a number of acquired loss making companies. Under his leadership, Matrix has emerged as a major player in the Indian pharma industry within only four years. Mr. Prasad was previously the Managing Director and CEO of Vorin Laboratories, the erstwhile subsidiary of Ranbaxy. Mr. Prasad started his career in 1984 as a Management Trainee in Indian Molasses Company associate of United Molasses Co. U.K ; and was associated with Rhone Poulenc Chemicals India ; Limited renamed Aventis.
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The Office of Chief Scientists OCSs ; of both the Ministry of Industry and Trade and the Ministry of Science. Recently, the Israeli government decided to establish an intergovernmental steering committee to promote the biotechnology area as a national project. The Israeli government, through the OCS, evaluates the viability of innovative ideas and, where appropriate, offers financial incentives through matching funds that share in the high risks intrinsic in the earliest stages of new projects. The OCS also enhances international strategic co-operation between Israeli and overseas communications companies by negotiating bi-national international R&D frameworks and funds. In addition, the OCS and this is especially crucial for the future of biotechnology places great emphasis on promoting the broadening of high-tech know-how accumulating in Israel by closer co-operation between industry and academia. This is accomplished through such programmes as Magnet, which encourages universities and private companies to work together on the development of generic pre-competitive technologies and
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Tic effect of NSAlDs for musculoskeletal disorders the most common indication ; is limited to the reduction of symptoms and is only moderate19.20 Thus, there is little risk in an empirical trial of a different drug or even of a period away from the drug. Indeed, the limited emcacy of NSAIDs may partly ex, for instance, side effects.
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ANTIEPILEPTIC THERAPY An acute symptomatic seizure with an obvious precipitating cause does not require AED therapy to prevent further seizures. Rectifying the underlying etiology is the appropriate management for such cases. For older patients with an isolated idiopathic seizure, the question of therapy becomes more complex. Older persons who present with an initial seizure are more likely than younger individuals to have recurrent seizures.37 The risk factors that are associated with an increased risk for seizure recurrence in younger patients--known symptomatic cause, partial seizures, a family history of epilepsy, epileptiform EEG, and abnormal neurologic findings--may predict seizure recurrence in the elderly as well.38 At present, there are few studies to guide us in counseling older patients about future risk following an unprovoked seizure. AED therapy should be initiated for patients with epilepsy, and it should be considered for those with an unprovoked seizure and high risk of recurrence. AED pharmacokinetics and the elderly The pharmacokinetics of AEDs are more complex in the elderly than in younger patients because of lower protein binding, impaired hepatic metabolism, altered volume of distribution, decreased renal elimination, and decreased enzyme inducibility. Because polypharmacy is more prevalent in the elderly, AED therapy carries a greater risk of adverse effects Table 3 ; 39, 40 and drug interactions Table 4 ; in elderly patients. The optimal AED for use in this population would be fully absorbed and demonstrate linear pharmacokinetics, with clearance unaffected by renal impairment. It would neither induce nor inhibit hepatic enzymes. It would be inexpensive and well tolerated and would not interact with other medications. Unfortunately, there is no medication that completely fulfills these ideal characteristics. AED use in the elderly is widespread AEDs are widely prescribed for the elderly: 7.7% of nursing home residents are receiving AEDs upon admission to a nursing home, and AED therapy is initiated in another 2.7% within the first 3 months of nursing home admission.41 AEDs account for almost 10% of adverse drug reactions in the elderly and are the fourth leading cause of adverse drug reactions in nursing home residents.42 Despite these statistics and the dramatic increase in treatment options for epilepsy over the past decade, few studies have specifically addressed the clinical use of AEDs in the elderly. Recent guidelines from the and
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Received November 14, 2001; accepted after revision February 13, 2003. From the Division of Neurosurgery N.A.-M., M.A.C.-L. ; , Division of Neuroimaging J.H.-C. ; , and Division of Medical Education T.C.-V. ; , Instituto Nacional de Neurologi y Neurocirugi Mexa a, ico City, Mexico. Address correspondence to Nicasio Arriada-Mendicoa, M.D., San Francisco 657-1201, Colonia del Valle, Mexico City, CP 03100, Mexico and
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