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1 Lanoxi b 0.13 mg 2 Prilosec 20.0 mg 3 Norvasc 5 mg 4 K-Dur 20 meq 5 Pepcid 20 mg 6 Laanoxin b 0.25 mg 7 Imdur b 60 mg 8 Synthroid b 0.1 mg 9 Vasotec 5 mg 10 Procardia XL 30 mg 11 Glucophage 500 mg 12 Lipitor 10 mg 13 Fosamax 10 mg 14 Synthroid b 0.05 mg 15 Zoloft 50 mg 16 Vasotec 10 mg 17 Xalatan 0.01 % 18 Premarin 0.63 mg 19 Cardizem CD b 240 mg 24 hr 20 Humulin N b 100 IU 21 APAP propoxyphene b 650 mg 22 Cozaar 50 mg 23 Cardizem CD b 180 mg 24 hr 24 Norvasc 10 mg 25 albuterol b 90 mcg 26 Coumadin b 5 mg 27 Zocor 10 mg 28 Zocor 20 mg 29 Synthroid b 0.08 mg 30 Imdur b 30 mg 31 Atrovent 0.02 mg ac 32 Procardia XL 60 mg 33 Miacalcin 200 IU ac 34 ranitidine HCl b 150 mg 35 Zestril b 10 mg 36 Toprol XL 50 mg 37 Pravachol 20 mg 38 Coumadin b 2 mg 39 Klor-Con 10 b 10 meq 40 Ultram 50 mg 41 Mevacor 20 mg 42 Paxil 20 mg 43 furosemide b 40 mg 44 Propulsid 10 mg 45 Relafen 500 mg 46 Cardizem CD b 120 mg 24 hr 47 metoprolol b 50 mg 48 Nitrostat b 0.4 mg 49 lorazepam b 0.5 mg 50 Demadex 20 mg Top 50 Drugs, Average Weighted by Salesc CPI - All Items, Cumulative Percent Change.
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ENTONOX SIDE EFFECTS ANY NEW PYREXIA 37.5 38 ; 38 ; SHIVERING VOMITING NAUSEA DIARRHOEA COMPLICATIONS THICK MECONIUM ABRUPTIO OTHER TACHYSYSTOLE WAS TACHYSYSTOLE ASSOCIATED WITH FETAL DISTRESS? MODE OF DELIVERY NVD CESAREAN INSTUMENTAL Y N Y.
These diagnostic tools are not available or the results are not conclusive, a diagnosis should be based on the clinical information at hand. If the initial investigation is not suggestive of active TB but the contact remains symptomatic, repeat physical examinations, smears and cultures should be performed monthly with repeat chest X-ray as needed.
In early 2002, Hartlepool's first smoking cessation Dropin Clinic was established at Greatham, a small village on the outskirts of the town. The success of this initiative led to the subsequent expansion of these communitybased clinics across Hartlepool. Dropin Clinics, staffed by Smoking Cessation Advisers working alongside Nurse Prescribers, offer clients an informal environment with easy access. They provide a holistic package of assessment, advice, information and a prescription of NRT with followup support and reviews. Dropin Clinics are run across Hartlepool. Perhaps one of the most unusual venues is the Fens Pub, where support is available on a weekly basis between 6pm and 8pm. The Fens Pub is within short walking distance of an area of the town which not only has a disproportionately high number of smokers 70% of adults in some pockets ; , but also some relatively profound levels of deprivation and health inequality IMD national rank 25 in Owton ward ; . Up to smokers wishing to stop have attended this clinic in a twohour session. The Dropin Clinics create an atmosphere of understanding and nonjudgmental support, which encourages those who fail to quit to ultimately return and try again. The target set by the DH for Hartlepool was to achieve 1, 680 fourweek quitters over a threeyear period. The threeyear target has almost been met within two years. Over 60% of those setting a quit date are smoke free at four weeks.
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O Resident Condition.--The resident's condition is an important factor to take into consideration. For example, a fluid pill erroneously administered to a dehydrated resident may have serious consequences, but if administered to a resident with a normal fluid balance may not. If the resident's condition requires rigid control, a single missed or wrong dose can be highly significant. o Drug Category.--If the drug is from a category that usually requires the resident to be titrated to a specific blood level, a single medication error could alter that level and precipitate a reoccurrence of symptoms or toxicity. This is especially important with a drug that has a Narrow Therapeutic Index NTI ; i.e., a drug in which the therapeutic dose is very close to the toxic dose ; . Examples of drugs with NTI are as follows: Anticonvulsant: phenytoin Dilantin ; , carbamazepine Tegretol ; , Anticoagulants: warfarin Coumadin ; Antiarrhythmic digoxin ; Lanoxih ; Antiasthmatics: theophylline TheoDur ; Antimanic Drigs: lithium salts Eskalith, Lithobid and triamterene.
1. Anaesthetics 1.1 General anaesthetics and oxygen halothane ketamine nitrous oxide oxygen thiopental 1.2 Local anaesthetics bupivacaine injection, 0.25%, 0.5% hydrochloride ; in vial injection for spinal anaesthesia, 0.5% hydrochloride ; in 4-ml ampoule to be mixed with 7.5% glucose solution lidocaine injection, 1%, 2% hydrochloride ; in vial injection for spinal anaesthesia, 5% hydrochloride ; in 2-ml ampoule to be mixed with 7.5% glucose solution topical forms, 24% hydrochloride ; lidocaine + epinephrine adrenaline ; injection 1%, 2% hydrochloride ; + epinephrine 1 : 200 000 in vial dental cartridge 2% hydrochloride ; + epinephrine 1 : 80 000 inhalation injection, 50 mg as hydrochloride ; ml in 10-ml vial inhalation inhalation medicinal gas ; powder for injection, 0.5 g, 1.0 g sodium salt ; in ampoule.
Infants and Children: In general, divided daily dosing is recommended for infants and young children under age 10 ; . In these patients, where dosage adjustment is frequent and outside the fixed dosages available, LANOXICAPS may not be the formulation of choice. In the newborn period, renal clearance of digoxin is diminished and suitable dosage adjustments must be observed. This is especially pronounced in the premature infant. Beyond the immediate newborn period, children generally require proportionally larger doses than adults on the basis of body weight or body surface area. Children over 10 years of age require adult dosages in proportion to their body weight. Some researchers have suggested that infants and young children tolerate slightly higher serum concentrations than do adults. Daily maintenance doses for each age group are given in Table 6 and should provide therapeutic effects with minimum risk of toxicity in most patients with heart failure and normal sinus rhythm. These recommendations assume the presence of normal renal function: Table 6. Usual Digitalizing and Maintenance Dosages for LANOXICAPS in Children With Normal Renal Function Based on Lean Body Weight Digitalizing * Dose Daily Maintenance Dose Age mcg kg ; mcg kg ; 2 to Years 25 to 35 25% to 35% of 5 to 10 Years 15 to 30 the oral or I.V. Over 10 Years 8 to 12 digitalizing dose * IV digitalizing doses are the same as digitalizing doses of LANOXICAPS. Divided daily dosing is recommended for children under 10 years of age. Projected or actual digitalizing dose providing desired clinical response. In children with renal disease, digoxin must be carefully titrated based upon clinical response. It cannot be overemphasized that both the adult and pediatric dosage guidelines provided are based upon average patient response and substantial individual variation can be expected. Accordingly, ultimate dosage selection must be based upon clinical assessment of the patient. Atrial Fibrillation: Peak digoxin body stores larger than the 8 to 12 mcg kg required for most patients with heart failure and normal sinus rhythm have been used for control of ventricular rate in patients with atrial fibrillation. Doses of digoxin used for the treatment of chronic atrial fibrillation should be titrated to the minimum dose that achieves the desired ventricular rate control without causing undesirable side effects. Data are not available to establish the appropriate resting or exercise target rates that should be achieved. Dosage Adjustment When Changing Preparations: The absolute bioavailability of the capsule formulation is greater than that of the standard tablets and very near that of the intravenous dosage form. As a result, the doses recommended for LANOXICAPS Capsules are the same as those for LANOXIN Injection see Table 1 in CLINICAL PHARMACOLOGY and dipyridamole.
Instructions: Check with your doctor or pharmacist before you start taking any new drugs. Other drugs such as Phenytoin DILANTIN ; , Warfarin COUMADIN ; , and Digoxin LANOXIN ; may interact with BRAJTR. You may drink small amounts of alcohol, as it will not affect the safety or usefulness of your treatment. Tell other doctors that you are being treated with BRAJTR before you receive any treatment from them. If you were having menstrual periods before chemotherapy, these may have stopped temporarily or permanently during or after chemotherapy. Even if you have stopped having periods after treatment, if you were fertile prior to chemotherapy, you may be able to conceive a pregnancy. Use birth control but not birth control pills ; if you could become pregnant, even if you have stopped menstruating because of chemotherapy. Do not breast feed during treatment. Talk to your doctor if you have questions about fertility and birth control after treatment.
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For years, researchers have sought to understand and mitigate flooding, especially in urban areas where floods cause the most damage. The development of our cities and towns is a primary cause of flooding. In urban areas, stream channels are truncated and replaced by storm drain pipes and natural vegetation is paved over. Thus, storm runoff is delivered to the surface channel network faster and in greater quantity than in pre-development conditions. The processes that control flooding in urban environments, however, are very complex and still not well understood. This paper explores one important control on flooding -- urban drainage network patterns and structure. The drainage network is defined here as the many different pathways that drops of rainwater may take once they hit the ground and flow over the land surface, into storm pipes, and through the surface channels that make up a watershed. Each unique raindrop pathway is determined by drainage network structure: the natural and built spatial patterns and form of our cities and towns, and where and how development occurs. Because drainage network and methyldopa.
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Hudghton Verts ALE ; , in writing. - Karin Junker's own-initiative report seeks to tackle one of the world's most difficult challenges, of achieving more of the stated outcomes of the UN International Conference on Population and Development, held in 1994. The report starkly highlights some of the statistics which clearly demonstrate that more action is required. Globally, one woman dies each minute from pregnancy-related causes, about 200 000 maternal deaths per year result from the lack or the failure of contraceptive services, at least 75 million of the 175 million pregnancies each year are unwanted, and rape and other forms of sexual violence are increasing, including in Europe. These, and a whole host of other facts contained in the report, clearly point to a need for increased action and assistance to be given by developed countries to combating poverty and encouraging economic growth, with a corresponding increase in educational opportunities, particularly lacking in some countries, for women and girls. On the basis of the latest figures, the indicators for the Cairo conference objectives are still showing shocking inequalities between the world's wealthy and poor countries and regions. The EU governments can and should take a lead in improving the situation and zetia.
What else might it be? Other causes of low back pain besides simple mechanical damage include: Degenerative changes Structural changes, e.g. spinal stenosis ; Inflammatory changes, e.g. ankylosing spondylitis, rheumatoid arthritis rare ; Infections, e.g. pyelonephritis, bacterial osteomyelitis, tuberculous osteomyelitis, epidural abscess, brucellosis Neoplasms, e.g. multiple myeloma, lymphoma, secondary metastases, primary cancer rare ; Metabolic bone disease, e.g. osteoporotic collapse, osteomalacia, Paget's disease Other, e.g. gynaecological problems, sickle cell disease, vascular claudication Complications and prognosis Pain can become chronic People with back pain may develop depression Some low back pain initially diagnosed as 'simple mechanical' may be due to sinister causes General issues Diagnostic triage should distinguish between simple backache, nerve root pain and serious spinal pathologies. It forms the basis for referral, investigation, and management. Early treatment of acute non-serious back problems, specifically mobilization and exercise, is considered to be VERY IMPORTANT in the prevention of chronic low back pain. Risk factors for chronicity include: [Waddell, 2004]. Previous history of low back pain Regular work loss due to low back pain ; in past 12 months Radiating leg pain Reduced straight leg raising Signs of nerve root involvement Reduced trunk muscle strength and endurance Poor physical fitness Self-rated poor health Heavy smoking Psychological distress and depressive symptoms Disproportionate illness behaviour Low job satisfaction Personal problems - alcohol, marital, financial Adversarial medico-legal proceedings Refer patient to GP if risk factors for chronicity apparent. This section continued on next page Go to the MAIN INDEX or DRUG INDEX or INDICATION INDEX or REFERENCES.
EARTH MOUND - A mound of rubble, dirt and or rocks used to obstruct automobile use. - Ain Arik Beitunia Ramallah and cordarone.
INDOCIN SR See indomethacin eR indomethacin . indomethacin eR INFLAMASe See prednisolone sodium phosphate INTAL INHALeR INTRON-A isoniazid . ISORDIL . See isosorbide dinitrate isosorbide dinitrate . isosorbide mononitrate eR K-DUR See potassium chloride eR tabs K-LOR See potassium chloride for oral solution 20 meq K-LYTe See potassium bicarbonate K-LYTe CL . See potassium bicarbonate and chloride K-PHOS KADIAN . KeFLeX . See cephalexin KeNALOG . See triamcinolone acetonide KePPRA . KeRLONe . betaxolol ketoconazole labetalol lactulose . LAMICTAL LAMISIL . LANOXIN . See digoxin LANTUS . LARIUM . See mefloquine LASIX See furosemide LeSCOL . LeSCOL XL leucovorin . LeUKeRAN . LevAQUIN LevITRA . levothyroxine sodium . LevSIN . See hyoscyamine sulfate LevULAN LeXAPRO.
Coronary artery LAD ; as compared with expected population norms.96, 97 A z score 2.5 ie, a coronary dimension that is 2.5 SDs above the mean for body surface area ; in 1 of these arterial segments would be expected to occur in 0.6% of the population without Kawasaki disease, and a z score 3.0 in 1 of these segments would be expected to occur in 0.1% of the population without Kawasaki disease. Having a coronary artery z score 2.5 in both the proximal RCA and LAD would be uncommon in the general population. Because of anatomic variation in the left main coronary artery LMCA ; , its z score must be interpreted with caution. Occasional cases of coronary prominence in patients with other disorders have been noted. Clinical experience, however, suggests that coronary enlargement in other febrile illnesses is rare, whereas coronary enlargement in Kawasaki disease is relatively common. Thus, coronary artery z scores should be incorporated into the recommendations for the evaluation and treatment of Kawasaki disease. The present writing group proposes a scheme to aid the clinician in deciding which patients with fever and 4 classic criteria should undergo echocardiography or receive IVIG treatment or both for Kawasaki disease Fig 1 ; . In the absence of a gold standard for diagnosis, this algorithm cannot be evidence based but rather represents the informed opinion of a committee of experts evidence level C ; . We offer this opinion as guidance to clinicians until an evidence-based algorithm or a specific diagnostic test for Kawasaki disease becomes available and hyzaar.
Eddy CA. "The fallopian tube: physiology and pathology." In Infertility diagnosis and management. Aiman J, ed. Springer, 1984: 161-76. Class R ; Schlaff WD, Hassiakos DK, Damewood MD, et al. "Neosalpingostomy for distal tubal obstruction: prognostic factors and impact of surgical technique." Fertil Steril 54: 984-90, 1990. Class B.
URECHOLINE METABOLIC MODIFIER ORFADIN ANTIHYPERTENSIVES CARDIAC DIGITEK TABS DIGOXIN LANOXICAPS LANOXIN Use PA Form # 20420 Approved for Type 1 hereditary tyrosinemia patients. Must include laboratory evidence of dx at first PA and tricor.
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But must pay for the additional costs of higher-priced drugs. RP requires that officials determine a drug to be equivalent to another in order to be a reference for it. As in the case of PA, it is problematic to judge drugs as equivalent given drug and patient heterogeneity. Furthermore, if poor and elderly patients are particularly sensitive to price then RP can have unintended consequences for consumption and health. For further analysis of RP, see Danzon and Ketcham 2003 ; reviewed in PEPC Brief 4. ; Sabastian Schneeweiss and colleagues 2002 ; studied the impact of RP for ACE inhibitors to treat hypertension ; on 120, 000 elderly patients in British Columbia's Pharmacare program. The policy cut drug costs because per-unit costs and volume fell. Hospitalization did not increase, but physician visits increased temporarily. No blood pressure data were collected so it was not possible to determine potential long run health risks. Future Research According to Soumerai, research on the health impact of Medicaid policy has not kept pace with policy implementation. "It is sobering to realize that if such policies were considered for a clinical study, the possible risks of reduced access to essential medications would likely result in a failure to obtain human-subject approval from most institutional review boards IRBs ; . These policies can be viewed as massive experiments on vulnerable populations" p.141.
Average time between patent expiration and entry of the first generic to less than three months, from more than three years previously. Sandoz believes that rigorous scientific criteria should be consistently applied to the approval process for all follow-on biotechnology medicines. Unnecessary duplication of animal studies and human clinical trials should be avoided, however, so that resources are not wasted that could otherwise be invested in innovation. Biotechnology medicines are produced in living organisms, altered by recombinant technology. But by using advanced product development, analytical methodologies and manufacturing processes, Sandoz can manufacture biosimilars designed to have the same quality, efficacy and safety characteristics as the reference product. Sophisticated analytical tools used today are more powerful than those available at the time when reference products were approved. "Characterizations of molecules that weren't possible scientifically a decade ago are commonplace today, " Dr. Windisch says. "And Sandoz and Novartis have been part of that advance of science all the way." Patient Safety Is Paramount The manufacturer of a biosimilar eliminates some requirements of a conventional new drug application by establishing the bridge between the reference medicine and its own product. Streamlined requirements for clinical trials and the opportunity for competition once the originator drug has lost patent protection translate into lower prices for biosimilar products. Above all, patient safety remains paramount for Sandoz and Novartis. From the outset of Omnitrope development in 1997 and imdur and Buy lanoxin.
Example 2 Doctor's order: Lahoxin 0.5 mg po Medication label: Laboxin 0.25 mg per tablet How many tablets should you give? The starting factor is 0.5 mg, the conversion factor is 0.25 mg 1 tablet, and the answer unit is the number of tablets you would give. Starting factor 0.5 mg conversion factor 1 tablet 0.25 mg answer unit.
The MU-JHU site benefits greatly from their relationship with the hospital, as all of their participants are recruited there, and they rely on the hospital as a referral site for many of their participants. Proximity MU-JHU Research House is located on hospital grounds, in walking distance to the outpatient and inpatient sections of the hospital. The close proximity makes recruitment, referral and collaboration easier than in places where the sites are more spread out. Shared Goals The researchers and the hospital staff have a common cause of improving participants' health. Many hospital staff view research participation as beneficial for their patients, a way to improve their patients' health, so they are happy to refer participants to the research site. Two doctors at PIDC said that they know their patients will receive good care, and extra things, like social support. Partnerships with other organizations MU-JHU refers participants to other organizations in Kampala besides Mulago Hospital after a study ends. However, these relationships are not as developed as with the hospital. There is little regular communication, no shared staff, and no identifiable mutually beneficial aspects of the relationships. The study has partnered with the MOH to disseminate the findings of the HIVNET 012 study. Staff have conducted trainings at hospitals throughout Uganda on PMTCT. The CAB has also worked to disseminate information on PMTCT to the community. Committed Staff MU-JHU staff have a strong commitment to participants. They do not view the people as merely study participants, but as people who need their help. This view translates into staff taking action to make sure participants' needs are met, whether it means finding a way to provide the care themselves e.g., by writing grants ; , providing resources to their partner organizations where participants go for care, or volunteering their time. Staff have great empathy and compassion for their study participants. There is a lot of energy, commitment and desire from research staff to improve the community in which they work and live. The site also has very committed volunteers. Not to deal with these other issues-- why are we doing this? It is solely for the research so we can write papers and say this is effective? Or are we also looking at, on a more micro level, and saying these are actually human beings, and how can I benefit them, you know? study coordinator 1 and avapro.
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This publication was prepared with support from the United States Agency for International Development USAID ; . The author's views expressed in this publication do not necessarily reflect the views of USAID or the United States Government.
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This notice is being sent to summarize the upcoming PDL changes for the TennCare pharmacy program. We encourage you to read this notice thoroughly and contact First Health's Technical Call Center 866-434-5520 ; should you have additional questions. PREFERRED DRUG LIST PDL ; FOR TENNCARE EFFECTIVE 10 03 07 TennCare is continuing the process of reviewing all covered drug classes. Changes to the PDL may occur as new classes are reviewed and previously reviewed classes are revisited. As a result of these changes, some medications your patients are now taking may be considered non-preferred agents in the future. Please inform your patients who are on these medications that switching to preferred products will decrease delays in receiving their medications. For medications with existing prior authorizations in place, each PA will remain active through the current expiration date. A copy of the new PDL will be posted October 3, 2007 to: : tennessee.fhsc . We encourage you to share this information with other TennCare providers. The individual changes to the PDL are listed below. For more details on clinical criteria, please visit: s: tennessee.fhsc Downloads provider TNRx PDL CC ST QLL . Below is a summary of the PDL changes that will be effective October 3, 2007. Cardiovascular: Anti-Anginal Agents, Miscellaneous Class CC o Ranexa CC will become non-preferred Cardiovascular: Agents for Pulmonary Arterial Hypertension Class CC o Revatio CC, QL, Tracleer CC, and Ventavis CC will become preferred o Letairis CC will become non-preferred Cardiovascular: Vasopressors o Midodrine will become preferred o ProAmatine will become non-preferred Cardiovascular: Cardiac Glycosides o Digoxin will become preferred o Digitek, Lanoxicaps, and Lanoxin will become non-preferred * Current Lanoxicaps users will be grandfathered indefinitely.
Eli Lilly 2006 ; . ADHD . URL: : ADHD Evidence Based Medicine Working Group 1992 ; . Evidence-Based Medicine: A New Approach to Teaching the Practice of Medicine, Journal of the American Medical Association 268 17 ; : 24202425. Foucault, M. 1978 ; . The History of Sexuality. Volume 1: An Introduction, New York: Vintage Books. Foucault, M. 1994 ; . The Order of Things. An Archaeology of the Human Sciences, New York: Vintage Books. Foucault, M. 2001 ; . Discipline, Toezicht en Straf, Dutch translation of French original: Surveiller et punir ; , Groningen: Historische Uitgeverij. Foucault, M. 2003 ; . Abnormal. Lectures at the Collge de France 1974-1975, New York: Picador. Goodyer, I. & Klaassen, P. 2007 ; . Interview with Professor Ian Goodyer, 09.05.2007, Appendix D below. Green, H., McGinnity, ., Meltzer, H., Ford, T. & Goodman, R. 2005 ; . Mental health of children and young people in Great Britain, 2004, Office for national statistics. Hampshire: Palgrave Macmillan. Hacking, I. 1986 ; . Making Up People, in T. Heller, M. Sosna & D. Wellbery eds ; , Reconstructing Individualism. Autonomy, Individuality, and the Self in Western Thought, Stanford: Stanford UP. Hacking, I. 1998 ; . Mad Travellers. Reflections on the Reality of Transient Mental Illnesses, Cambridge MA: Harvard UP. Healy, D. 1996 ; . The History of British Psychopharmacology, in G. Berrios & H. Freeman eds ; , 150 Years of British Psychiatry. Volume II: the Aftermath, London: Athlone, pp. 61 88. Healy, D. 2002 ; . The Creation of Psychopharmacology, Cambridge MA: Harvard UP. Holmes, J., Payton, A., Barrett, J., Harrington, R., McGuffin, P., Owen, M., Ollier, W., Worthington, J., Gill, M., Kirley, A., Hawi, Z., Fitzgerald, M., Asherson, P., Curran, S., Mill, J., Gould, A., Taylor, E., Kent, L., Craddock, N. & Thapar, A. 2002 ; . Association of DRD4 in children with ADHD and comorbid conduct problems, American Journal of Medical Genetics 114 2 ; : 150153. URL: : dx.doi 10.1002 ajmg.10149 Janssen-Cilag 2005 ; . In the community. URL: : janssen-cilag bgdisplay.jhtml?itemname community Kendall, T. & Klaassen, P. 2007 ; . Interview with Dr. Tim Kendall, 23.05.2007, Appendix F below. Kendall, T. & McGoey, L. 2007 ; . Truth, Disclosure and the Influence of Industry on the Development of NICE Guidelines: An Interview with Tim Kendall, BioSocieties 2 1 ; : 129140. Kendall, T., Pilling, S., Pettinari, C. & Whittington, C. 2004 ; . Clinical Guidelines in Mental Health I: The National Collaborating Centre for Mental Health, Psychiatric Bulletin 28: 156159. Kendall, T., Pilling, S., Whittington, C., Pettinari, C. & Burbeck, R. 2005 ; . Clinical Guidelines in Mental Health II: a guide to making NICE Guidelines, Psychiatric Bulletin 29: 38. Kent, L. & Klaassen, P. 2007 ; . Interview with Dr. Lindsey Kent, 08.05.2007, Appendix C below. Kuhse, H. & Singer, P. eds ; 2006 ; . Bioethics: An Anthology, Malden MA: Blackwell.
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