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Purpose of the Fund and its Realization The purpose of the Investors' Compensation Fund is to safeguard claims of investors covered by the Fund, in its member companies providing investment services and member credit institutions, as provided in the Act on Companies Rendering Investment Services and in the Rules of the Fund. In 2004, the Fund did neither compensate investors on any receivables from the member companies nor was any compensation claims made to the Fund. The Fund's compensation liability would require the member company to be bankrupt or otherwise insolvent. Rules of the Fund According to the Act on Companies Rendering Investment Services, the Fund has rules ratified by the State Treasury. The Rules were amended in 2004, because the amended legislation concerning companies rendering financial services required certain changes of a minor nature. The Delegation of the Fund approved the amended rules on 5 May 2004 and the Ministry of Finance ratified the amendment on 14 July 2004. Members of the Fund Membership of the Fund is mandatory for all Finnish investment service companies, credit institutions providing investment services as well as Finnish funds holding licence for rendering investment services. At the end of the year, the Fund had 377 members. 47 of the members were investment service companies and the rest were credit institutions. The consortium of co-operative banks has been deemed as one member in the determination of the Fund's administrative charge. Administration of the Fund Each member of the Fund appoints one member to the Delegation of the Fund. The Chairman of the Delegation is Ilona Ervasti-Vaintola. The Delegation has convened once in 2004. The Fund has a Board of Directors elected by the Delegation. In 2004, the members of the Board of Directors were Jukka Huotari Chairman ; , Harri Nummela Vice Chairman ; , Heikki Alanen, Izmo Kaaronen, Timo T. Laitinen and Markku Savikko. Until May 2004, the deputy members were Erkki Kontkanen and Timo Mkel and from May 2004 Erkki Kontkanen and Kristian Warras. The Board of Directors convened 10 times in 2004.
A. B. Authority. The Director of Public Services is assigned the responsibility and authority to interpret the requirements of this Zoning Code. Language. 1. Abbreviations. For the purpose of brevity, the following phrases, personnel and document titles are shortened hereafter in this Zoning Code. The City of Pismo Beach is referred to hereafter as the "City." The City of Pismo Beach Zoning Code is referred to hereafter as "this Zoning Code." The Director of Public Services is referred to hereafter as "Director, " the City Council is referred to as the "Council, " the Planning Commission is referred to as the "Commission." "Buildings and structures" are referred to hereafter as "structures." Terminology. When used in this Zoning Code, the words "shall, " "must, " "will, " "is to, " and "are to" are always mandatory. "Should" is not mandatory but is strongly recommended; and "may" is permissive. The present tense includes the past and future tenses; and the future tense includes the present. The singular number includes the plural number, and the plural the singular, unless the natural construction of the word indicates otherwise. The words "includes" and "including" shall mean "including but not limited to .". Number of days. Whenever a number of days is specified in this Zoning Code, or in any permit, condition of approval, or notice issued or given as provided in this Zoning Code, the number of days shall be construed as calendar days. Time limits will extend to the next working day where the last of the specified number of days falls on a weekend or holiday.
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Labeling of elements in the plasma. They observed that circulating drugs might become labeled as well. In our study however, we are unable to correlate interpatient variability of the in vivo half-time with our patients' medications, which are listed in Table 1. The complex kinetics of the concentration of Tc-99m bound to RBCs is still without a model. Possibly a major oecompartment this model is that related to renal of excretion. In patients whose cells label poorly, high bladder counts are seen after 30 mm 17 ; Eckelman et al. feel that the oeexpandedlood pool obtained by Tc b 99m-labeled red blood cells after 30 mm in vivo is the result of urinary excretion and not of uptake by any organ10 ; . Labeled molecules of a size falling between and monoket.
It should be noted that the deadline 31 March 2004 ; for submission of applications to register single mineral homeopathic products has now passed. Single mineral products, for which a registration application has not been received by the IMB, can no longer remain lawfully on the market. H E R APPOINTMENT TO THE NEW EMEA COMMITTEE ON HERBAL MEDICINAL PRODUCTS Following agreement on the EU Council Directive on Traditional Herbal Medicinal Products in March 2004, a new Committee on Herbal Medicinal Products HMPC ; has been established at the European Medicines Agency. This committee will be responsible for issues relating to traditional herbal medicinal products registered in accordance with this Directive. The IMB is pleased to announce that Dr. Dairine Dempsey has been appointed as the Irish representative to the HMPC, with Dr. Elaine Breslin as her alternate.
Figure 2. Proportion of sputum cultures negative at Weeks 2, 4, 6, and 8 of treatment by study drug A ; and dosing frequency B and imdur, for example, el ismo.
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In the 2002 FDA survey, 18% of those recalling ads said DTC ads had at some time caused them to talk to their doctor about a specific medical condition or illness for the first time. This is a remarkable result, suggesting that approximately one-sixth of the adult population who have seen doctors in the past three months have been motivated by advertising to discuss a new topic. The number in the 1999 survey was higher, 27%, whereas the 1999 Prevention survey, which unlike the FDA survey did not oversample persons who had recently seen a doctor, found 14%. ; The 1999 FDA survey also asked whether respondents were likely to ask their doctor about a drug that was advertised to treat a condition that was "bothering you." A very large proportion 80% ; said they were somewhat or very likely to ask.
Why did you try that? I knew a lot about cardiac pacing because of my experiments in the engineering approaches to cardiac rhythm management and similar experiments. I knew the heart could be paced from the esophagus and I had seen in the literature that it had been done once or twice. The esophagus was also used as a site for defibrillation in classic experiments by Paul Zoll. I knew the esophagus was close enough to the heart to pace from it, but didn't know much more. After obtaining some data on esophageal pacing, I recognized that this was a really hot item. Instead of merely recording from the pill electrode, I also could pace from it. I worked on a small business proposal to the NIH for the next several years to support the clinical testing of this technique for esophageal pacing. I got Phase I and Phase II SBIR grants for my small company, Arzco Medical Systems. With those grants I was able to recruit 140 patients to do clinical studies in five different centers. We proved that esophageal pacing was both safe and effective and got pre-market approval. No longer a substantial equivalence thing, this required the full FDA pre-market route. It was necessary to perform experiments and prove there would be no damage to the esophagus. It also had to be proved that this device was effective in pacing the heart. Following all those studies we appeared before the FDA Cardiology Advisory Board at the end of 1986 and got the PMA approved. I developed a small battery-operated electronic external and sorbitrate.
Cumulation as observed 24 h postchallenge Table 2 ; . As illustrated in Figure 2, both exuded volume and cellular influx observed 4 h after the i.t. injection of ovalbumin 12 pg cavity ; were inhibited in PAF-desensitized animals. Administered 1 h before PAF itself, BN 52021, WEB 2086, and WEB 2170 20 mg kg ; reduced the exudation by the lipid from 840 29 h' mean SEM ; to 273 21 h1 P .001 ; , 306 48 h1 P .001 ; , and 273 31 h1 P .001 ; , respectively. BN 52021 and WEB 2086 were also effective against the late pleural eosinophil accumulation caused by the antigenic challenge Fig. 3 ; but, as observed with WEB 2170, failed to modify either exudation or pleural leukocyte accumulation observed 4 h after allergen stimulation Table 3.
Regulations to enable all NRT products to be available on the NHS are currently in preparation and are expected to come into force in April, it was announced on 14 March 2001, National No-Smoking Day. Currently, the majority of NRT products are included in Schedule 10 to the NHS General Medical Services ; Scotland ; Regulations 1995, which lists drugs that may not be prescribed by GPs on the NHS. A number of other NRT preparations have been introduced since the last major Schedule 10 update. NRT preparations are already available from community pharmacies and now certain lower strength products will also be available from supermarkets and other retail outlets. We will update you again following official clarification and imipramine.
Bone, K. 1997 ; . Echinacea: what makes it work. Alternative Medicine Review. 2 ; Online ; . Redrawn 2006-06-27. Available at the Internet. : thorne pdf journal 2-2 echinaeca Jansson, E. 2006 ; . All photos of the plants. Letchamo, W., Livesey, J., Arnason, T.J., Bergeron, C., & Krutilina, V.S. 1999 ; . Cichoric acid and isobutylamide content in Echinacea purpurea as influenced by flower developmental stages. In: J. Janick ed. ; , Perspectives on new crops and new uses. ASHS Press, Alexandria, VA. p. 494498. Online ; . Redrawn 2006-06-27. Available at the Internet. : hort.purdue newcrop proceedings1999 v4-494 Mossberg, B. & Stenberg, L. 2003 ; . Den Nya Nordiska Floran, Wahlstrm & Widstrand, Stockholm. p. 540, 396 Lewis, W.H. & Elvin- Lewis, M.P.F. 2006 ; . Medical Botany- Plants affecting human health, 2nd edition, John Wiley & Sons INC, Hoboken, New Jersey, p. Sanchez, M.A. 2000 ; . Drug Action and Treatment. online ; , cited 2006-03-17. Available at the Internet: : chemweb lpoly chem bailey 377 PapersSp2000 Marlene drugact.
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Introduction The International Society for Mobile Youth Work ISMO ; and the National Council of Churches in Kenya NCCK ; organised from the 27th to 30th October 2003 at the Jumuia Conference and Country Home in Limuru Kenya with 198 participants from 35 countries around the world the 8th International Symposium on Mobile Youth Work with special focus on children at risk street children and youth ; in Africa. For this purpose there were invited field workers, scientists and stakeholders engaged as advocates for the rights and well being of endangered children and youths. The participants came mainly from African countries and of course especially from Kenya, but also from Asia, Latin America and from Europe. The organizers NCCK and ISMO Following the official launch, Rev. Mutava Musyimi, the General Secretary of NCCK, gave a brief background to the process that led to the 8th International ISMO symposium. He said in November 2001, with funding from Bread for the World, NCCK organised a national conference on children on the streets that that helped participants come to terms with the Kenyan scenario, and in addition prepared them fully to participate in the 8th ISMO symposium. It was at this forum that NCCK and other stakeholders agreed on the theme: Street Children and Mobile Youth Work In Solidarity With Youth at Risk. Rev. Musyimi revealed that NCCK for a long time had been involved in work that contributed to the welfare of children, so the symposium was just part of their contribution. He noted that the government of Kenya had indeed put some measures in place to address issues the 2001 conference had raised as expressed by the Vice President. He welcomed all participants to the symposium in Kenya and urged them to deliberate on approaches that: can cate4r for the vast numbers of children in need; encourage collaboration between academia and children and youth serving organisations; address root causes that drive children to the street; promote networking among service providers; and finally come up with a framework for legislation in issues of children and youth. Prof. Dr. Walther Specht, the chairman of ISMO, hailed the 8th symposium as unique, and one of its own kind for three reasons: It was the first symposium held in Africa, the first one that actively involved youth participants during the programme and thirdly had three planning preconferences. Two of these were for adult participants, one held in Germany and the other in Kenya, and one also held in Kenya for youth participants preceding the actual event.1 and tofranil.
SORE THROAT 1. Take temperature. 2. If temperature is elevated schedule for clinic. 3. Do throat culture, if ordered. 4. Give salt water gargle 1 2 tsp. salt to 8 oz. warm water ; 5. For fever and or as an analgesic give oral acetaminophen: 1 tab 325 mg ; , if under 43 kg 95 lbs. ; 2 tabs 650 mg ; , if over 43 kg 95 lbs. ; STOMACH UPSET NAUSEA ; 1. Take temperature 2. If temperature is elevated, schedule for clinic. 3. Give antacid or Pepto-Bismol, or Milk of Magnesia ; 4. Consider medication toxicity and call to physician's attention. SUNBURN 1. Apply cool compresses to all affected areas 2. IF large body area is affected, use aloe or Silvadene to reduce severity of thermo injury to skin 3. Give water room temperature to prevent nausea related to heat exhaustion ; 4. Give analgesic and instruct to keep area out of sun or covered until healed.
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Towards evidence based medicine for paediatricians ADCH, 2002; 87: 258-262 : adc.bmjjournals cgi reprint archdischild%3b87 3 258 2 ; Ontogeny of hepatic and renal systemic clearance pathways in infants. Part 1 Clinical Pharmacokinetics, 2002; 41: 959-998, because isno kallio.
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