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Chapter 7 212 Seiler, M.P.; Stoll, A.; Closse, A.; Frick, W.; Jaton, A.; Vigouret, J.M. 1986 ; Structureactivity relationships of dopaminergic 5-hydroxy-2-aminotetralin derivatives with functionalized N-alkyl substituents. J. Med. Chem. 29, 912-917. 213 Damsma, G.; Bottema, T.; Westerink, B.H.C.; Tepper, P.G.; Dijkstra, D.; Pugsley, T.A.; MacKenzie, R.G.; Heffner, T.G.; Wikstrm, H. 1993 ; Parmacological aspects of R- + ; -7OH-DPAT, a putative dopamine D3 receptor ligand. Eur. J. Pharmacol. 249, R9-R10. 214 van Vliet, L.A.; Rodenhuis, N.; Wikstrm, H.; Pugsley, T.A.; Serpa, K.A.; Meltzer, L.T.; Heffner, T.G.; Wise, L.D.; Lajiness, M.E.; Huff, R.M.; Svensson, K.; Haenen, G.R.M.M.; Bast, A. 2000 ; Thiazoloindans and thiazolobenzopyrans: a novel class of orally active central dopamine partial ; agonists. J. Med. Chem. Submitted. 215 Rodenhuis, N.; Timmerman, W.; Wikstrm, H.; Dijkstra, D. 2000 ; Thiophene analogs of naphthoxazines and 2-aminotetralins: bioisosteres with improved relative oral bioavailability, as compared to 5-OH-DPAT. Eur. J. Pharmacol. 394, 255-263. 216 Thrift, R.I. 1967 ; Derivatives of 2-aminotetralin. J. Chem. Soc C ; , 288-293. 217 Chiemprasert, T.; Rimek, H.-J.; Zumalkowski, F. 1965 ; Zur stereospezifischen synthese von cis- und trans-aminotetralolen. Liebigs Ann. Chem. 685, 141-148. 218 Berg, K.J., van den and Leusen, A.M.v. 1993 ; Formation and [4 + 2] cycloaddition reactions of 2, 3-dimethylene-2, 3-dihydrothiophene. Recl. Trav. Chim. Pays-Bas 112, 7-14. 219 Miller, D.D.; Harrold, M.; Wallace, R.A.; Wallace, L.J.; Uretsky, N.J. 1988 ; Dopaminergic drugs in the cationic form interact with D2 dopamine receptors. TiPS 9, 282-284. 220 March, J. 1992 ; Bonding weaker than covalent. In: Advanced organic chemistry; reactions, mechanisms and structure. Wiley, New York, 75-79. 221 Zuika and Bankowskii. 1973 ; The hydrogen bond in sulphur-containing compounds. Russ. Chem. Rev 42, 22-36. 222 Pogorelyi. 1977 ; Weak hydrogen bonds. Russ. Chem. Rev 46, 316-336. 223 van Vliet, L.A.; Tepper, P.G.; Dijkstra, D.; Damsma, G.; Wikstrm, H.; Pugsley, T.A.; Akunne, H.C.; Heffner, T.G.; Glase, S.A.; Wise, L.D. 1996 ; Affinity for dopamine D2, D3 and D4 receptors of 2-aminotetralins. Relevance of D2 agonist binding for determination of receptor subtype selectivity. J. Med. Chem. 39, 4233-4237. 224 Pardo, L.; Campillo, M.; Giraldo, J. 1997 ; The effect of the molecular mechanism of G protein-coupled receptor activation on the process of signal transduction. Eur. J. Pharmacol. 335, 73-87. 225 Thornber, C.W. 1979 ; Isosterism and molecular modification in drug design. Chem. Soc. Rev. 8, 563-580. 226 Kloetzel, M.C.; Little, J.E., Jr; Frisch, D.M. 1953 ; Synthesis of 4-substituted thianaphthene derivatives. J. Org. Chem. 18, 1511-1515. 227 Nedelec, L.; Pierdet, A.; Fauveau, P.; Euvrard, C.; Proulx-Ferland, L.; Dumont, C.; Labrie, F.; Boissier, J.R. 1983 ; Synthesis and central dopaminergic activities of ; -hexahydro-7H-indolo[3, 4-gh][1, 4]benzoxazine derivatives [ ; -9-oxaergolines]. J. Med. Chem. 26, 522-527. 228 House, H.O. and Berkowitz, W.F. 1963 ; The stereochemistry of the Neber rearrangement. J. Org. Chem. 28, 2271-2276. 229 O'Brien, C. 1964 ; The rearrangement of ketoxime o-sulfonates to amino ketones. Chem. Rev. 64, 81-89 and levothroid.
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Pharmaceutical segment sales in 1998 were $8.90 billion, an increase of 12.7% over 1997 including 24.3% growth in domestic sales. International sales increased .6% as sales gains in local currency of 5.4% were offset by a negative currency impact of 4.8%. Worldwide growth reflected the strong performance of PROCRIT, RISPERDAL, DURAGESIC, LEVAQUIN, and the oral contraceptive line of products. At year-end 1998, the Company received approval from the FDA for LEVAQUIN levofloxacin ; for the indication of uncomplicated urinary tract infection. Additionally, the Company completed the acquisition of the U.S. and Canadian product rights for RETAVASE reteplase ; , an acute-care cardiovascular drug, from Roche Healthcare. The 1998 special pre-tax charge for the Pharmaceutical segment was $65 million. See Note 14 for detailed discussion on the Restructuring and IPR&D charges. Significant research activities continued in the Pharmaceutical segment, increasing to $1.9 billion in 2000, or an 18.6% increase over 1999. This represents 15.9% of 2000 Pharmaceutical sales and a compound annual growth rate of approximately 13.1% for the five-year period since 1995. Worldwide Pharmaceutical research organizations include Janssen Research Foundation, headquartered in Belgium, and the R.W. Johnson Pharmaceutical Research Institute, located in La Jolla, California and Raritan, New Jersey. Additional research is conducted by Centocor and through a collaboration with the James Black Foundation in London, England. Professional The Professional segment includes a broad range of products used by or under the direction of health care professionals. These would include suture and mechanical wound closure products, surgical equipment and devices, wound management and infection prevention products, interventional and diagnostic cardiology products, diagnostic equipment and supplies, joint replacements and disposable contact lenses. These products are used principally in the professional fields by physicians, nurses, therapists, hospitals, diagnostic laboratories and clinics. Acquisitions and divestitures in the Professional segment during recent years are part of an ongoing process to transform this segment from a medical supply business to one serving a range of higher technology medical specialties. Worldwide sales in 2000 of $10.3 billion in the Professional segment represented an increase of 3.7% over 1999. Domestic sales were up 4.0%, while international sales increased 3.4% as sales gains in local currency of 10.3% were offset by a negative currency impact of 6.9%. Worldwide sales gains in local currency of 6.9% were reduced by 3.2% due to the strength of the U.S. dollar. Strong sales growth from Cordis' coronary and endovascular stents, DePuy's spinal products, Ethicon's MITEK suture anchors and Gynecare's women's health products and lotrel.
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Antibiotic treatment of children with E coli O157-H7 increased risk of the hemolytic-uremic syndrome. NEJM June 29, 2000: 342: Original investigation, first author Craig S Wong, University of Washington School of Medicine, Seattle : nejm Comment: 1 If no antibiotics are given, and no symptomatic therapy in the form of antimotility drugs is indicated, only bismuth compounds Pepto-Bismol ; and supportive therapy with fluids remain. I doubt that adults who develop "traveler's diarrhea" will accept this. I believe most will demand antibiotics. See the review article this month in Practical Pointers 6-22 ; on advice to travelers for self treatment of acute traveler's diarrhea: A. Non-dysenteric diarrhea: a. Fluid replacement b. Loperamide Imodium; generic ; with or without an antimicrobial agent. Do not use for children under age 2. Do not use antimotility agents alone if either fever or blood in stool is present. Some experts would not use any antimotility drug at all if diarrhea was associated fever or blood in stool c. Antimicrobial agent. Eg, a single dose of ciprofloxacin Cipro - 750 mg ; or levofloxacin Llevaquin - 500 mg ; or, azithromycin Zithromax - 500 mg ; d. Bismuth subsalicylate Pepto-Bismol -- 2 tablets or 2 tablespoons 4 times daily ; has been used for prophylaxis B. Severe or dysenteric diarrhea: a. Antimicrobial agent eg, ciprofloxacin 500 mg twice daily for 3 days levofloxacin 500 mg once daily for 3 days, or azithromycin 500 mg once on day one then 250 mg daily for 4 days, or 1000 mg once only. ; REFERENCE ARTICLE 6-16 THE IMPORTANCE OF DIAGNOSING POLYCYSTIC OVARY SYNDROME Most women with hyperandrogenism show evidence of a disorder known as the polycystic ovary syndrome. PCOS ; 1 The syndrome is " .extremely common, but heterogeneous". It " considered the most frequently encountered endocrinopathic condition". Originally the diagnosis required pathognomonic ovarian findings and the clinical triad of hirsutism, ammenorrhea, and obesity. Later, abnormalities of the hypothalamic-pituitary axis were noted, focusing the diagnosis on endocrine criteria such as elevations of serum luteinizing hormone and increased luteinizing hormone folliclestimulating-hormone ratio. Most women with PCOS have some degree of insulin resistance, although it may be subtle.
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405. Parker, G. 1999 ; . Depression comorbid with physical illness. Current Opinion in Psychiatry, 12, 87-92. 406. Parker, G. 1999 ; . Bipolar depression: does its clinical expression inform us about the clinical features of melancholia? abstract ; . Bipolar Disorders, S1 1 ; , 93. 407. Parker, G. 1999 ; . Diagnostic line-drawing: How to pick an eagle from a turkey comment ; . Australian Psychologist, 34 1 ; , 30-34. 408. Parker, G. 1999 ; . The RADAR detection system for depression. Paper presented at the Directions in Psychiatry, Sydney, NSW. 409. Parker, G. 1999 ; . Defining depression as a movement disorder. Paper presented at the Fifth Lingard Symposium. 410. Parker, G. 1999 ; . Depression Management: No longer at all costs. In M. Maj Ed. ; , Evidence and Experience in Psychiatry Vol. 1, pp. 468-470 ; . Geneva: World Psychiatric Association. 411. Parker, G., Mahendran, R., Yeo, S. G., Loh, M. I., & Jorm, A. F. 1999 ; . Diagnosis and treatment of mental disorders: A survey of Singapore mental health professionals. Social Psychiatry & Psychiatric Epidemiology, 34 10 ; , 555-563. 412. Parker, G., Mitchell, P., Wilhelm, K., Menkes, D., Snowdon, J., Schweitzer, I., et al. 1999 ; . Are the newer antidepressant drugs as effective as established physical treatments? Results from an Australasian clinical panel review. Australian & New Zealand Journal of Psychiatry, 33 6 ; , 874881. 413. Parker, G., Roy, K., Wilhelm, K., Mitchell, P., Austin, M. P., & Hadzi-Pavlovic, D. 1999 ; . Subgrouping non-melancholic major depression using both clinical and aetiological features. Australian & New Zealand Journal of Psychiatry, 33 2 ; , 217-225. 414. Parker, G., Roy, K., Wilhelm, K., Mitchell, P., Austin, M. P., & Hadzi-Pavlovic, D. 1999 ; . An exploration of links between early parenting experiences and personality disorder type and disordered personality functioning. Journal of Personality Disorders, 13 4 ; , 361-374. 415. Parker, G., Roy, K., Wilhelm, K., Mitchell, P., Austin, M. P., Hadzi-Pavlovic, D., et al. 1999 ; . Subgrouping non-melancholic depression from manifest clinical features. Journal of Affective Disorders, 53 1 ; , 1-13. 416. Parker, G., Wilhelm, K., Mitchell, P., Austin, M.-P., Roussos, J., & Gladstone, G. 1999 ; . The influence of anxiety as a risk to early onset depression. Journal of Affective Disorders, 52 1-3 ; , 11-17. 417. Parker, G., Wilhelm, K., Mitchell, P., Roy, K., & Hadzi-Pavlovic, D. 1999 ; . Subtyping depression: Testing algorithms and identification of a tiered model. Journal of Nervous & Mental Disease, 187 10 ; , 610-617. 418. Schofield, P., Badenhop, R., Adams, L., Morris, J., Moses, M., Ma, L., et al. 1999 ; . Haplotype analysis of a bipolar affective disorder susceptibility locus on chromosome 4q35 abstract ; . Molecular Psychiatry, 4 1 ; , S20. 419. Van der Linden, G., Chalder, T., Hickie, I., Koschera, A., Sham, P., & Wessely, S. 1999 ; . : blackdoginstitute .au research publications index Updated 21 December 2006.
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