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Major collections of type cultures: 1. American Type Culture Collection ATCC ; , 12301 Parkland Drive, Rockville, MD 20852, USA 2. National Collection of Type Cultures NCTC ; , Central Public Health Laboratory, Colindale Avenue, London NW9 5HT, United Kingdom.
1. Flurazepam HCl, Capsule, 15mg, 30mg Dalmane and generics ; Chlordiazepoxide HCl, Capsule, 5mg, 10mg, 25mg generics ; Clorazepate Dipotassium, Capsule, 3.75mg, 7.5mg, 15mg Generics ; Effective September 1, 2007, flurazepam, chlordiazepoxide and clorazepate will no longer be provided as benefits under the NIHB program. Patients receiving flurazepam, chlordiazepoxide or clorazepate prior to July 1, 2007 will be grandfathered. NOT ADDED TO FORMULARY The following drug products will not be added to the NIHB Drug Benefit List: 1. Adefovir Dipivoxil, Tablet, 10mg Hepsera - Gilead Sciences Canada Inc. ; 2. Alendronate Sodium and Cholecalciferol, Tablet, 70mg 70mcg FosavanceTM - Merck Frosst Canada Ltd. ; 3. Amlosipine Besylate and Atorvastatin Calcium, Tablet, 5 10mg, 5 CaduetTM - Pfizer Canada Inc. ; 4. Darifenacin Hydrobromide, Tablet, 7.5mg, 15mg Enablex - Novartis Pharmaceuticals Canada Inc. ; 5. Escitalopram Oxalate, Tablet, 10mg, 20mg Cipralex - Lundbeck Canada Inc. ; 6. Lansoprazole, Delayed-Release Tablet, 15mg, 30mg Prevacid FasTab - Abbott Laboratories Ltd.
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41. Laso W: Neurochemical and pharmacological aspects of cocaine-induced seizures. Pol J Pharmacol, 2000, 53, 5760 Loiseu P: Intractable epilepsy, prognostic evaluation. In: Intractable Epilepsy, Experimental and Clinical Aspects Ed. Schmidt D, Morseli PL, Raven Press, New York, 1986. 43. Meredith PA, Elliott HL: Clinical pharmacokinetics of amlodipine. Clin Pharmacokinet, 1992, 22, 2231. Meyer FB, Andreson RE, Sundt TM Jr: Selective central nervous system calcium channel blockers a new class of anticonvulsant agents. Mayo Clin Proc, 1986, 61, 239247. Meyer FB, Cascino GD, Whisnant JP, Sharbrough FW, Ivnik RJ, Gorman DA, Windschitl WL et al.: Nimodipine as an add-on therapy for intractable epilepsy Mayo Clin Proc, 1995, 70, 623627. Michalets EL: Update, clinically significant cytochrome P-450 drug interactions. Pharmacotherapy, 1998, 18, 84112. Nakane Y, Seino M, Yagi A, Kaji S, Yamauchi T: Effects of flunarizine therapy on intractable epilepsy. Arzneimittelforschung, 1989, 39, 793798. Overweg J, Binnie CD: Flunarizine. In: Comprehensive Epileptology. Ed. Dam M, Gram L, Raven Press, New York, 1990, 655664. 49. Overweg J, Binnie CD, Meijer JW, Meinardi H, Nuijten ST, Schmaltz S, Wanquier A: Double-blind placebo-controlled trial of flunarizine as add-on therapy in epilepsy. Epilepsia, 1984, 25, 217222. Pelliccia A, Sciaretta A, Matricardi M: Nimodipine treatment for drug-resistant childhood epilepsy letter ; . Dev Med Child Neurol, 1990, 32, 1114. Pickard JD, Murray GD, Illingworth R, Shaw MD, Teasdale GM, Foy PM, Humphrey PR et al.: Effect of oral nimodipine on cerebral infarction and outcome after subarachnoid heamorrhage. Brish aneurysm nimodipine trial. Br Med J, 1989, 298, 636642. Raemsch KD, Ahr D, Tettenborn D, Auer LM: Overview on pharmacokinetics of nimodipine in healthy volunteers and in patients with subarachnoid hemorrhage. Neurochirurgia, 1985, 28, 7478. Roy M, Sapolsky R: Neuronal apoptosis in acute necrotic insults, why is this subject such a mess? Trends Neurosci, 1999, 22, 419422. Ryan SG: Ion channels and the genetic contribution to epilepsy. J Child Neurol, 1999, 14, 5866. Schumacher TB, Beck H, Steinhaiser C, Schramm J, Elger CE: Effects of phenytoin, carbamazepine and gabapentin on calcium channels in hippocampal granule cells from patients with temporal lobe epilepsy. Epilepsia, 1998, 39, 355363. Scriabine A, Schuurman T, Traber J: Pharmacological basis for use of nimodipine in central nervous system disorders. FASEB J, 1989, 3, 17991806. Siesjo BK, Elmer E, Janelidze S, Keep M, Kristian T, Ouyang YB, Uchino H: Role and mechanisms of secondary mitochondrial failure. Acta Neurochir Suppl, 1999, 73, 713. Sobaniec W, Kuak W: Influence of flunarizine and clobazam on the electrically induced seizures in rats. Neurosci Jpn, 1990, 16, 541546. Speckmann EJ, Straub H, Kohling R: Contribution of calcium ions to the generation of epileptic activity and antiepileptic calcium antagonism. Neuropsychobiology, 1993, 27, 122126. Stefani A, Spadoni F, Bernardi G: Voltage-activated calcium channels, targets of antiepileptic drug therapy? Epilepsia, 1997, 38, 959965. Stephen CC: Voltage-gated ion channelopathies of the nervous system. Clin Neurosci Res, 2001, 1, 104117. OEwider M, Borowicz KK, Porbiak J, Kleinrok Z, Czuczwar SJ: Influence of agents affecting voltagedependent calcium channels and dantrolene on the anticonvulsant action of the AMPA kainate receptor antagonist LY 300164 in mice. Eur Neuropsychopharmacol, 2002, 12, 311319. Teasdale G, Mendelow AD, Graham DI, Harper AM, McCulloch J: Efficacy of nimodipine in cerebral ischemia or hemorrhage. Stroke, 1990, 21, 123125. Trojnar MK, Maek R, Chrooeciska M, Nowak S, Baszczyk B, Czuczwar SJ: Neuroprotective effects of antiepileptic drugs. Pol J Pharmacol, 2002, 54, 557566.
Restrictive lung disease in one subject. There was no significant difference in MIP and MEP values between AS and control group p 0.05 ; . Six minutes walking distance and PCI were found significantly lower in AS patients than controls p 0.05 ; . DISCUSSION Although our AS patients had markedly limited movement of the chest wall and restrictive lung disease, their respiratory muscle strength was not influenced by this restriction. We found that exercise capacities and energy costs of AS patients were lower than healthy subjects similarly the previous studies. This reduction was not related to respiratory muscle performance but it may be consequences of general muscle deconditioning. As a result, rehabilitation programmes should be directed not only to improve spinal mobility but also to increase cardio-respiratory fitness in AS patients.
Table 5: Summary of the median MPRs of three types of medicines in the private pharmacies. Brand Vs Most sold Statistics and amoxycillin.
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Apart from other chemically similar antagonists developed so far. Radioligand binding studies [17] have clearly established that the primary site of action of amlodipine is within the dihydropyridine binding domain of the Ca2 + -channel complex, where it slowly associates with one particular region of the channel complex. This relatively slow rate of association or "binding" to the channel complex is clinically relevant because it explains, in part Figure 1 ; , why the onset of action of amlodipine is so slow relevant to that of other drugs of this type [13]. Radioligand binding studies also showed that amlodipine dissociates from its specific binding sites extraordinarily slowly [17] a factor which must contribute to its prolonged effectiveness [18]. In this respect amlodipine differs from all of its predecessors, including felodipine and isradipine even when these are used as slow-release formulations. There is one other peculiarity relating to the chemistry of amlodipine which warrants mention at this stage and it relates to the fact that the presence of the basic amino group on.
Hospitalization and cost efficacy benefits, Diovan became the first and only drug of its kind to receive approval for treatment in heart failure patients. To complement the broad choice and flexibility for patients and physicians, a new higher dose 160 25 ; formulation of Co-Diovan was launched in the US. Lotrel 35% US: + 35%; hypertension ; , also extended its share of new prescriptions. A new formulation 10 mg amlodipine + 20 mg benazepril HCl ; was launched in July and has been well received by physicians and patients, reflecting the fact that 90% of Lotrel patients achieve their blood pressure goal with the additional benefits of an ACE inhibitor. Lescol + 18%, US: + 13%; cholesterol reduction ; sales grew strongly in Europe and in other regions, reflecting the drug's particularly favorable risk benefit profile and convenient XL extended-release formulation. Following the publication of data showing that Lescol reduced the risk of serious cardiac events after surgery to unblock coronary arteries, a new indication in angioplasty patients was filed in August for regulatory approval in the US. Lamisil + 4%, US: -3%; fungal infections ; sales picked up towards the end of the year mainly in the US. Whilst the onychomycosis market segment has been declining, Lamisil has extended its commanding share of both total and new prescriptions in the US to more than 80%. Elidel eczema ; was launched in 13 countries, including the US, and completed the mutual recognition procedure in Europe. Sales in 2002 reached CHF 148 million. Within just six months, this highly effective, non-steroid cream has become the numberone branded topical treatment for eczema in the US, where it has captured over 8% of new prescriptions. In Denmark, the first country in Europe where it has been launched, Elidel captured a 9% share of its segment within 10 weeks of launch. Exelon + 26%, US: + 28%; Alzheimer's disease ; posted good sales growth and captured a further share both of new and total prescriptions in the US. New marketing initiatives are under way to counter increased competition in its fast-growing segment. Studies revealed that Exelon inhibits an additional enzyme butyrylcholinesterase ; that contributes to neurological dysfunction in Alzheimer's disease. As a result, an expanded labeling was approved in Europe to include the product's unique dual inhibition properties. Zelnorm Zelmac constipation prone irritable bowel syndrome ; has now gained approval in 28 countries including the US where it was launched in September. With progress being made on reimbursement, 2002 sales totaled CHF 70 million and ampicillin.
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Alert produced? Test 1 2 3 All Prescribing scenario tested Aspirin prescribed for child of 8 years Methotrexate prescribed in pregnancy Penicillin prescribed in patient with penicillin allergy Oxytetracycline prescribed in a patient with renal impairment Enalapril prescribed in patient with renal impairment Microgynon 30 combined contraceptive pill ; prescribed in patient with history of deep vein thrombosis Oxytetracycline prescribed in patient with serum creatinine of 160 mol l Propranolol prescribed in patient with history of heart failure Sumatriptan prescribed in patient with history of coronary heart disease Naproxen prescribed in patient with history of peptic ulcer disease Propranolol prescribed in patient with history of asthma Sildenafil prescribed to patient already taking isosorbide mononitrate Methotrexate prescribed on a daily basis When patient requests salbutamol inhaler it should be clear whether this has been authorised as a repeat item Repeat prescription of salbutamol inhaler issued before it is scheduled Atenolol prescribed to patient taking amlodipine * Amoxicillin prescribed to patient taking hormone replacement therapy * The 10 most frequently used drug pairs with similar names No of appropriate alerts System A No No Yes No Yes Yes Yes No * No 4 System B No Yes Yes Yes No No No Yes Yes Yes No Yes No * No 7 System C No No Yes No No No Yes No No No System D No No Yes No No No Yes No No No Yes No 3.
High Blood Pressure 181. Gibson RS, Boden WE. Calcium channel antagonists: friend or foe in postinfarction patients? J Hypertens 9: 172S176S; 1996. Koren MJ, Devereux RB, Casale PN, Savage DD, Laragh JH. Relation of left ventricular mass and geometry to morbidity and mortality in uncomplicated essential hypertension. Ann Intern Med 114: 345 352; Liao Y, Cooper RS, McGee DL, Mensah GA, Ghali JK. The relative effects of left ventricular hypertrophy, coronary artery disease, and ventricular dysfunction on survival among black adults. JAMA 273: 1592 1597; Devereux RB. Do antihypertensive drugs differ in their ability to regress left ventricular hypertrophy? Circulation 95: 19831985; 1997. Gottdiener JS, Reda DJ, Massie BM, Materson BJ, Williams DW, Anderson RJ, for the VA Cooperative Study Group on Antihypertensive Agents. Effect of single-drug therapy on reduction of left ventricular mass in mild to moderate hypertension: comparison of six antihypertensive agents; the Department of Veterans Affairs Cooperative Study Group on Anti-hypertensive Agents. Circulation 95: 20072014; 1997. Levy D, Salomon M, D'Agostino RB, Belanger AJ, Kannel WB. Prognostic implications of baseline electrocardiographic features and their serial changes in subjects with left ventricular hypertrophy. Circulation 90: 17861793; 1994. Devereux RB, Agabiti-Rosei E, Dahlf B. Regression of left ventricular hypertrophy as a surrogate endpoint for morbid events in hypertension treatment trials. J Hypertens 14 suppl 2 : S95S102; 1996. 188. Frohlich ED. Pathophysiology of systemic arterial hypertension. In: Schlant RC, Alexander RW, O'Rourke RA, Roberts R, Sonnenblick EH eds. ; . Hurst's The Heart, eighth edition. New York, NY: McGraw-Hill; 1993: 13911401. Pr 189. Sheps SG, Frohlich ED. Limited echocardiography for hypertensive left ventricular hypertrophy. Hypertension 29: 560563; 1997. Vasan RS, Levy D. The role of hypertension in the pathogenesis of heart failure: a clinical mechanistic overview. Arch Intern Med 156: 17891796; 1996. Pfeffer MA, Braunwald E, Moy LA, for the SAVE Investigators. Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction: results of the Survival and Ventricular Enlargement Trials. N Engl J Med 327: 669677; 1992. Garg R, Yusuf S, for the Collaborative Group on ACE Inhibitor Trials. Overview of randomized trials of angiotensin-converting enzyme inhibitors on mortality and morbidity in patients with heart failure. JAMA 273: 14501456; 1995. Cohn JN, Archibald DG, Ziesche S. Effect of vasodilator therapy on mortality in chronic congestive heart failure. Results of a Veterans Administra-tion Cooperative Study. New Engl J Med 314: 15471542; 1986. Packer M, Bristow MR, Cohn JN, for the U.S. Carvedilol Heart Failure Study Group. The effect of carvedilol on morbidity and mortality in patients with chronic heart failure. N Engl J Med 334: 13491355; 1996. Australia New Zealand Heart Failure Research Collaborative Group. Randomised, placebocontrolled trial of carvedilol in patients with congestive heart failure due to ischaemic heart disease. Lancet 349: 375 380; Pitt B, Segal R, Martinez FA, for the ELITE Study Investigators. Randomised trial of losartan versus captopril in patients over 65 with heart failure Evaluation of Losartan in the Elderly Study, ELITE ; . Lancet 349: 747752; 1997. Packer M, O'Connor CM, Ghali JK, for the Prospective Randomized Amlodipune Survival Evaluation Study Group. Effect of amlodipine on morbidity and mortality in severe chronic heart failure. New Engl J Med 335: 11071114; 1996. Cohn JN, Ziesche S, Smith R, for the Vasodilator-Heart Failure Trial. Effect of the calcium antagonist felodipine as supplementary vasodilator therapy in patients with chronic heart failure treated with enalapril: V-HeFT III. Circulation 96: 856863; 1997. pdf App-10 and anastrozole.
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First, it should be remembered that urinary infections are a frequent, benign and easily treatable cause of hematuria, and that menstruation is a frequent cause of false positive results. The causes of hematuria are either glomerular or nonglomerular urological ; in nature. If there is proteinuria or renal failure, one must first look for a glomerular etiology that treatment might prevent from progressing to terminal renal failure. If there is no pro and arava.
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Record, because it was not submitted to the MRU at the time of review. There is no evidence in the record that the MRU relied on, showing that he previously submitted co-pay records to MRU, in addition to the prescription records reviewed in the Orders of Dismissal. Claimant was given the opportunity to submit additional records regarding the disputed medical services. He submitted the unpaid prescription and a schedule with circled items that he alleged remained unpaid. Consequently, I conclude that he had the opportunity to complete the record at the time of the review and provided MRU with those bills and prescriptions that claimant contended remained unpaid. Therefore, I decline to remand for consideration of these alleged unpaid copays. In WCB Case No. 06-00057H DMS 05-1176 ; , the record contains 15 exhibits which include, among other things, claimant's prescriptions, claimant's letters to Liberty requesting reimbursement, claimant's September 22, 2005 letter submitting a listing of all the medical providers with circled entries representing the outstanding bills that remained un-reimbursed. Liberty responded to MRU's Specification of Disputed Medical Issues with information regarding these specific prescriptions Exs. 11; 12; 13 ; . Based on Liberty's information, the MRU issued an Order of Dismissal after finding that there was no dispute to review Ex. 14 ; . Likewise, in WCB Case No. 06-00059H DMS 05-1200 ; the MRU requested additional information from Liberty regarding specific billings regarding bills that claimant submitted on November 29, 2005. Liberty responded by letter dated December 23, 2005 that the newly submitted prescriptions that were not duplicates of prescriptions addressed in Liberty's December 9, 2005 letter, had been sent for payment and would be paid within the allotted 30 days Ex. 36 ; . The MRU considered this information in issuing its December 30, 2005 Order of Dismissal Ex. 37 ; . After reviewing the individual Orders, and the exhibits supporting these Orders, I conclude that there was substantial evidence to support MRU's findings. The individual Orders listed the specific disputed medical services and prescriptions and the medical reviewer concluded, based on information provided by Liberty, that these services and prescriptions had either been paid or had not been received. Consequently, the MRU issued the Orders of Dismissal. Because I have found that there is substantial evidence to support the Orders of Dismissal, I decline to remand to MRU for further action. ORDER IT IS HEREBY ORDERED that claimant's Motion for Remand is denied, for example, olmesartan and amlodipine.
The Pharmacy 170 The Prescription Shoppe 158 Theuma, Pierre, MD .111 Thieman, Kent C, MD .122 Thiessen, Wendy K, MD .60 Thoen, Tyler C, MD .74 Thomas, David L, MD .60 Thomas, Paul C, DO .57 Thomas, Sarah, MD 54 Thompson, Andrea, PA 61 Thompson, Craig B, DO .47, 49 Thompson, Robert O, MD .112 Thompson, Stacy L, MD .92 Thompson, Stephen C, MD .106 Thompson, Stephen M, DO .72 Thompson, Tricia L, ARNP 75 Thomsen, Thomas, OD 183 Thorgaard, Bradley A, MD .138 Thrifty White Drug 157, 159 Thrower, Abby R, MD .98 Thurm, Terrie, ARNP 81, 83 Tieszen, Dennis D, OD .182 Timmerman, Shannon R, NP .49 Timmons, Janis A, ARNP 112 Tingleff Pharmacy Inc .165 Tipton Pharmacy 156 Todd, Katheryne J, ARNP 59 Todd, Rebecca A, NP .104 Toms Family Pharmacy 157 Toms Parkway Foods Pharmacy .164 Tong, Linda J, MD .125, 131 Toriello, Dante R, DO .65 Torsney, Michael, DC 179 Tortoriello, William A, MD .62 Towncrest X-Ray .93 Towner, Paul W, MD .77 Trachtenbarg, David, MD 62 Trad, Michael J, OD .184 Traina, Jeffrey F, MD .90 Trane, R N, MD .120 Treanor, Michael R, MD .104 Trecker, Ruth E, ARNP 116 Treiber, Karl D, DO .72 Tremont Pharmacy .169 Tremont Village Pharamcy 169 Tri State Dialysis 146 Trible, John R, MD .181 Trimble, Richard B, MD .47 Trinity At Terrace Park 143 Trinity Medical Center 143 Trinity Medical Center Terrace Park Campus 143 Trinity Medical Center West 143 Trinity Retail Pharmacy .167 Troll, Todd C, MD .119 Troxell, J L, DC .172 True, Cheryl A, MD .72 Truhlar, Scott M, MD .93 Truszkowski, Joseph A, MD .91 Tryon, Laura M, NP .59 Tuazon, Paulito D, MD .71 Tubaugh, Jaren R, DC .171 Tuchek, J Michael, MD 128 Tucker-Sanfellipo, Elizabeth L, MD 95 and atorvastatin.
Fig. 1. DT A ; and peak systolic [Ca2 ]i B ; in response to ISO stimulation in papillary muscles from sham-operated and MI rats at 6 weeks post-MI. Sham, sham-operated group; placebo-MI, MI group with placebo treatment; mibefradil-MI, MI group with mibefradil treatment; verapamil-MI, MI group with amlodiline treatment n 6 in each group. * p .05, * p .01 versus sham-operated group at ISO 10 6, 10 versus mibefradil-MI group at ISO 10 6, 10 and 10 4 M.
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Purpose for which personal information may be collected 74. No registrant may collect personal information regarding a client unless: a ; the information relates directly to and is necessary for providing health care services to the client or for related administrative purposes, or the collection of that information is expressly authorised by or under an enactment and azelaic and amlodipine, for example, picture of amlodipine.
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Pharmacokinetic information f 64-90 % f food does not effect bioavailability c max 30-50 min t max 6-12 hours vd 21 l protein binding 93-98% hepatic metabolism 90 % to inactive metabolite t 1 2 30-50 hours-increased with hepatic dysfunction urine 10% as parent, 60% as metabolite ; contents 1 brand name trade name 2 generic name of drug 3 description 4 mechanism of action 5 time required for therapeutic response 6 pharmacokinetic 1 absorption 2 distribution 3 metabolism 4 elimination 7 special populations 8 indications 1 fda approved indications 2 non-fda approved indications 9 dosage 10 administration 11 monitoring parameters 12 contraindications precautions 1 contraindications 1 2 precautions 1 3 pregnancy indications 1 4 breast-feeding indications 13 drug-drug interactions 14 drug-food-herb interactions 15 pharmacogenetics 16 adverse reactions side effects 17 overdose measures 18 product information and distribution 19 references 20 pubmed references 2 1 efficancy 2 therapeutic class comparison articles 2 3 pharmcokinetics articles 2 4 drug interaction 21 external links brand name trade name norvasc generic name of drug amlodipine loe di peen ; click here back to top description amlodipine besylate is an oral long acting dihydropyridine calcium channel blocker.
DISCUSSION The reduction in systolic and diastolic blood pressure showed that amlodipine was an effective antihypertensive agent in the treatment of hypertension in Japanese patients. The effectiveness of.
Practitioners may advise of or refer to any of a range of non-pharmacological therapies to treat conditions that benzodiazepines, opioid analgesics and stimulants are often prescribed for. These include pain and sleep clinics, counselling, behavioural therapies, relaxation techniques and dietary and exercise programs. Alternative therapies such as acupuncture and vitamin, mineral or herbal supplements may also provide relief. For some individuals these therapies may actually treat the underlying problem rather than simply ameliorating symptoms such as stress and sleeplessness. Other initiatives which can be used by prescribers to minimise the harms associated with prescription drug misuse include being vigilant in identifying substance misuse or dependence, assisting the individual to recognise misuse or dependence where it exists, setting goals for recovery and assisting the individual to seek appropriate treatment National Institute on Drug Abuse 2001 ; . Pharmacists and pharmacy staff initiatives Pharmacists may also play an important role in addressing the harm arising from prescription shopping and the misuse of prescription drugs. Pharmacists and their staff are encouraged to be aware of products that may be misused and should not supply these products where they reasonably suspect misuse Adcock 2001 ; . They should also be vigilant and proactive in identifying possible forged or altered prescriptions. Further, pharmacists can help to prevent prescription drug misuse by providing clear information on how a medication is to be taken, any effects the medication may have and any possible drug interactions National Institute on Drug Abuse 2001 ; . Initiatives to reduce prescription shopping The federal government established a project to reduce the harms arising from prescription shopping following an allocation of funding in the 1996-97 Budget. According to the Health Insurance Commission HIC ; , the Doctor Shopping Project aimed to significantly improve the health outcomes of individuals at risk from doctor shopping activity by reducing the number of people visiting more GPs than necessary to obtain more prescription medicines than are clinically required. For the purposes of the project the HIC defined a `doctor shopper' as an individual who saw 15 or more different GPs or had 30 or more Medicare consultations in a year or obtained more Pharmaceutical Benefits Scheme PBS ; prescriptions than appeared to be clinically necessary. In 1999-2000, the number of people who met the agency's criteria for a doctor shopper was 8780, which fell from 13 240 in 1995-96. Of the total PBS medicines obtained by individuals defined as doctor shoppers, 35.5% are benzodiazepines, 14.6% are codeine compounds and 8.4% are narcotic analgesics Health Insurance Commission 2002 ; . While no evaluation of the project has been made publicly available to date, it is ADCA's understanding that the Doctor Shopping Project was suspended in August 2002. Additional federal funding to decrease prescription shopping was announced in a package of 2002-03 budget measures to improve the quality use of PBS, for example, amlodipine besylate and benazepril.
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