49. Sharma BC, Saraswat VA, Choudhuri G, Das A, Ghoshal UC, Pande R. Primary biliary cirrhosis without pruritus: an Indian variant. Trop Gastroenterol 1996; 17: 176-7. Naik SR, Ghoshal UC. Low grade pyrexia: is chronic fatigue syndrome a safe and justified diagnosis? letter ; J Assoc Physicians India. 1995; 43: 725-6. Ghoshal UC, Mukherjee S, De BK, Das P, Sarkar S, Guha Mazumder DN. Subacute hepatic failure in viral hepatitis A. Indian J Gastroenterol 1997; 16: 109. Puri AS, Poddar U, Ghoshal UC, Khan EM, Saraswat VA. Rapid reversal of manifestations of acquired zinc deficiency in alcoholic cirrhosis with diet therapy. Tropical Gastroenterol 1995; 17: 119-22. Sinha P, Ghoshal UC, Choudhuri G, Naik S, Ayyagari A, Niak SR. Does Entamoeba histolytica cause irritable bowel syndrome? Indian J Gastroenterol 1997; 16: 130-3. Ghosh A, Ghoshal UC, Kochhar R, Ghoshal P, Banerjee PK. Infectious mononucleosis hepatitis: report of two patients. Indian J Gastroenterol 1997; 16: 113-4 Ghoshal UC, Gupta R, Aggarwal R, Puri AS, Naik SR. Intestinal lymphangiectasia: Presentation in pregnancy and association with Herpes zoster and alopecia. Indian J Gastroenterol 1997; 16: 159-60. De BK, Ghoshal UC, Das AS, Nandi S, Guha Mazumder DN. Portal hypertensive gastropathy and gastric varices before esophageal variceal sclerotherapy and after obliteration. Indian J Gastroenterol 1998; 17: 5-7. Ghoshal UC, Das Gupta J, Datta A, Chatterjee B, Acharya A, Banerjee PK, Choudhuri TK. Isolated myoepithelial duodenal hamartoma presenting with massive upper gastrointestinal bleed. Indian J Gastroenterol 1998; 17: 109. Guha Mazumder DN, Ghoshal UC. Epidemiology of Helicobacter pylori in Indian scenario. Indian J Gastroenterol 1997; 16 Suppl 1 ; : S3. 59. Guha Mazumder DN, Ghoshal UC. Dental plaque as reservoir and determinants of pathogenic potential of Helicobacter pylori: The controversy remains. Indian J Gastroenterol 1998; 17: 123-5. Ghoshal UC, Ghosh TK, Chatterjee U, Mukherjee S, Das P, Banerjee P, De BK. Role of Helicobacter pylori in peptic ulcer in patients with hepatic cirrhosis. Indian J Gastroenterol 1999; 18: 90.
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A study conducted by researchers at Brown University examined the connection between state nursing home policies and resident hospitalization rates and found that state policies create financial incentives for nursing homes to hospitalize residents. According to the study authors, the lower the Medicaid reimbursement rate in a state, the more likely nursing homes in that state are to hospitalize residents. In addition, the odds of hospitalization were found to be 36% higher in states that reimbursed facilities for holding beds of hospitalized residents. In reference to the link between the size of Medicaid payments and the number of hospital admissions, study leader Vincent Mor stated, "We think the reason we see this relationship is that in states with higher payment rates, nursing home operators can afford to keep more medical professionals, such as nurse practitioners, on staff. With more staff, and more skilled staff, homes are better able to treat residents on site and they're better able to practice preventive care to head off problems such as pneumonia, bed sores or urinary tract infections." Regarding bedhold policies, Mor stated, "Because homes get some money from the state for holding a bed, the financial penalty for hospitalizing residents is reduced." For more information about the research and for statistics about hospitalization rates, bed-hold policies and Medicaid reimbursement rates for each state, go to: : brown Administration News Bureau 2006-07 06-067 . Source: : myziva , December 19, 2006.
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ISA Wagner and I traveled to the Ferrets 2000 Symposium together. We arrived Thursday, after innumerable airport snafus they lost our luggage on a direct flight! ; , and settled into the Novotel in Mississauga, Canada. The hotel was connected to a nearby office building with restaurants. After Lisa vetoed sushi, our hunt for food took us to Dick's Bar and Grill. Though the official "Meet and Greet" wasn't scheduled until 8: 30 PM, a large talbe was filled with many notables, including Bill Gruber, Bob Church, Randy Belair, our lovely hostess, and more continued to trickle in as we ordered from the very put-upon waitress. This began a nonstop, four day talkfest, grudgingly interrupted for sleep, food, and the actual lectures. So many ferret owners, shelter operators, experts, etc., just cannot stay in one place without talking ferrets. I'm sure we ruined the appetites of the poor folk seated around us as all topics were fair game. Due to the loud music and smoke at the bar, I became hoarse the first night, and a week later still trying to get my voice back. After the first of several late nights, the entire crowd piled on a school bus for the hour trip to the Toronto Zoo. The Zoo gave us an excellent presentation on the history and current status of the Black-Footed Ferret Mustela nigripes ; breeding program. As of this year, over 1300 BlackFooted ferrets have been released back into the wild, and at most sites are surviving and reproducing on their own. So far, this has been one of the most successful breeding programs in the Species Survival Program, aiding 195 endangered species through captive breeding programs at zoos throughout the world. After the presentation and some excellent pizza, the group scattered to check out the Zoo's exhibits.
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1. Figueredo E, Canosa L. Prophylactic ondansetron for postoperative emesis. Meta-analysis of its effectiveness in patients with previous history of postoperative nausea and vomiting. Acta Anaesthesiol Scand 1999 ; 43 : 637-44. 2. Domino KB, Anderson EA, Polissar NL, Posner KL. Comparative efficacy and safety of ondansetron, droperidol, and metoclopramide for preventing postoperative nausea and vomiting : a meta-analysis. Anesth Analg 1999 ; 88 : 1370-9. 3. Malins AF, Field JM, Nesling PM, Cooper GM. Nausea and vomiting after gynaecological laparoscopy : comparison of premedication with oral ondansetron, metoclopramide and placebo. Br J Anaesth 1994 ; 72 : 231-3. 4. Rose JB, Brenn BR, Corddry DH, Thomas PC. Preoperative oral ondansetron for pediatric tonsillectomy. Anesth Analg 1996 ; 82 : 558-62. 5. Splinter WM, Baxter MR, Gould HM, Hall LE, MacNeill HB, Roberts DJ, et al. Oral ondansetron decreases vomiting after tonsillectomy in children. Can J Anaesth 1995 ; 42 : 277-80. 6. Vongvatcharanon S, Kittijirawong T, Chanchayanon T, Lim A. Comparison of droperidol, Dexamethasone and saline in the Prevention of Postoperative Nausea and Vomiting after Gynecological Laparoscopic surgery in Outpatients. A Randomized, Double Blind, Placebo-Controlled Trial. Thai Journal of Anesthesiology 2000 ; 26 : 211-9. 7. Splinter WM, Rhine EJ. Prophylaxis for vomiting by children after tonsillectomy : ondansetron compared with perphenazine. Br J Anaesth 1998 ; 80 : 155-8. 8. Paxton LD, McKay AC, Mirakhur RK. Prevention of nausea and vomiting after day case gynaecological laparoscopy. A comparison of ondansetron, droperidol, metoclopramide and placebo. Anaesthesia 1995 ; 50 : 403-6. 9. Bugedo G, Gonzalez J, Asenjo C, De la Cuadra JC, Gajardo A, Castillo L, et al. Ondansetron and droperidol in the prevention of postoperative nausea and vomiting. Br J Anaesth 1999 ; 83 : 813-4. 10. Helmy SA. Prophylactic anti-emetic efficacy of ondansetron in laparoscopic cholecystectomy under total intravenous anaesthesia. A randomised, double-blind comparison with droperidol, metoclopramide and placebo. Anaesthesia 1999 ; 54 : 266-71. 11. Kothari SN, Boyd WC, Bottcher ML, Lambert PJ. Antiemetic efficacy of prophylactic dimenhydrinate Dramamine ; vs ondansetron Zofran ; : a randomized, prospective trial inpatients undergoing laparoscopic cholecy-stectomy. Surg Endosc 2000 ; 14 : 926-9 and
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Oral Health Improvement Program Caring for Colorado performed an assessment of oral health needs in the state, in response to public input and discussion with oral health experts and providers. The result was the finding that the unmet needs for prevention and treatment are substantial. During 2001 Caring for Colorado began the development of a five-year Oral Health Improvement Program. During the next five years the Foundation plans to invest in several projects intended to promote oral health in children and enhance the safety net for treatment of the underserved population.
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Our overall program is interested in the fundamental issues regarding the evolution and chemotherapeutic potential of polyketide natural products. Using the power of organic synthesis, we seek to learn about the specific structural features found in polyketides, their effect on conformation, and the importance of conformation on biological activity. Several years ago, we proposed that the myriaporones, a structurally truncated congener of the potently cytotoxic tedanolides, may possess useful and related biological activity. In fact, after successfully completing the first total synthesis, we utilized the material for a full biological study and found that the myriaporones are potent cytostatic agents which reversibly inhibit eukaryotic protein synthesis. Concurrently, Fusetani demonstrated that 13-desoxytedanolide inhibits protein synthesis through competitive binding of the 60S subunit of the ribosome with the structurally distinct pederin class of polyketides. Thus, our original hypothesis was indeed correct. Interestingly, structural aspects of the myxobacteria-derived gephyronic acid resemble portions of both the myriaporones and pederin. Gephyronic acid may be a structural link between the tedanolides and pederin classes of polyketide. Our efforts to probe the structural relationship between gephyronic acid, the myriaporones and pederin, and formulate a common pharmacophore for structures with eukaryotic protein synthesis inhibitory activity will be presented and esomeprazole.
Dose selection, and it may be useful to monitor renal function see PRECAUTIONS, General and DOSAGE and ADMINISTRATION ; . ADVERSE REACTIONS The following reactions have been reported: Gastrointestinal Diarrhea, oral candidiasis oral thrush ; , vomiting, nausea, stomach cramps, anorexia and pseudomembranous colitis. Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment see WARNINGS ; . Nausea and vomiting have been reported rarely. Allergic Anaphylaxis, eosinophilia, itching, drug fever, skin rash, Stevens-Johnson syndrome. Hematologic Neutropenia, leukopenia, thrombocytopenia, thrombocythemia. Hepatic Transient rise in SGOT, SGPT, and alkaline phosphatase levels has been observed. As with other cephalosporins, reports of hepatitis have been received. Renal As with other cephalosporins, reports of increased BUN and creatinine levels, as well as renal failure, have been received. Local Reactions Rare instances of phlebitis have been reported at site of injection. Pain at the site of injection after intramuscular administration has occurred infrequently. Some induration has occurred. Other Reactions Genital and anal pruritus including vulvar pruritus, genital moniliasis, and vaginitis ; . Cephalosporin-class Adverse Reactions: In addition to the adverse reactions listed above that have been observed in patients treated with cefazolin, the following adverse reactions and altered laboratory tests have been reported for cephalosporin-class antibiotics: Adverse Reactions: Allergic reactions, urticaria, serum sickness-like reaction, erythema multiforme, toxic epidermal necrolysis, colitis, renal dysfunction, toxic nephropathy, abdominal pain, reversible hyperactivity, hypertonia, hepatic dysfunction including cholestasis, aplastic anemia, hemolytic anemia, hemorrhage, and superinfection. Altered Laboratory Tests: Prolonged prothrombin time, positive direct Coombs' test, false-positive test for urinary glucose, elevated bilirubin, elevated LDH, increased creatinine, pancytopenia, and agranulocytosis. Several cephalosporins have been implicated in triggering seizures, particularly in patients with renal impairment when the dosage was not reduced see DOSAGE AND ADMINISTRATION ; . If seizures associated with drug therapy occur, the drug should be discontinued. Anticonvulsant therapy can be given if clinically indicated. DOSAGE AND ADMINISTRATION Usual Adult Dosage 1g Type of Infection Moderate to severe infections Mild infections caused by susceptible gram-positive cocci Acute, uncomplicated urinary tract infections Pneumococcal pneumonia Severe, life-threatening infections e.g., endocarditis, septicemia ; * Dose 500 mg to 1 gram 250 mg to 500 mg Frequency every 6 to 8 hrs. every 8 hours 2.5 mL Weight, for example, dimenhyrdinate high.
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12D-16.080 Procedures for Transfer. 1 ; An acknowledgment will be issued at the conclusion of the successful transfer of EDI return information or extension request for each return or extension request filed. This number provides a means of verifying receipt of the successful transmission and serves as receipt for the delivery of the return or extension request. The property appraiser shall maintain either this number or a trace number as a record of the transfer, for later retrieval. 2 ; Electronic transfers which are not received by the property appraiser on or before the due date of the return will constitute late returns and the applicable late filing penalties shall apply. 3 ; If a taxpayer does not receive an acknowledgment, the return information or extension request shall not be considered filed. Cross Reference: Rule 12D-8.005, F.A.C.
HCPCS J1170 J1180 J1190 J1200 J1205 J1212 J1230 J1240 J1245 J1250 J1260 J1270 J1320 J1325 J1327 J1330 J1364 J1380 J1390 J1410 J1435 J1436 J1438 J1440 J1441 J1450 J1452 J1455 J1460 J1470 J1480 J1490 J1500 J1510 J1520 J1530 J1540 J1550 J1563 J1564 J1565 J1570 J1580 J1590 J1600 J1610 J1620 J1626 J1630 J1631 J1642 J1644 DESCRIPTION Hydromorphone, up to 4 mg Dyphylline, up to 500 mg Dexrazoxane Hydrochloride, per 250 mg Diphenhydramine HCL, up to 50 mg Chlorodiazide Sodium, per 500 mg DMSO, Dimethyl Sulfoxide, 50%, ml Methadone HCL, up to 10 mg Dimenhydrinate, up to 50 mg Dipyridamole, per 10 mg Dobutamine Hydrochloride, per 250 mg Dolasetron Mesylate, 10 mg Doxercalciferol, 1 mcg Amitriptyline HCL, up to 20 mg Epoprostenol, 0.5 mg Eptifibatide, 5mg Ergonovine Maleate, up to 0.2 mg Erythromycin Lactobionate, per 500 mg Estradiol Valerate, up to 10 mg Estradiol Valerate, up to 20 mg Estrogen Conjugated, per 25 mg Estrone, per 1 mg Etidronate Disodium, per 300 mg Etanercept, 25 mg Filgrastim G-CSF ; , 300 mcg Filgrastim G-CSF ; , 480 mcg Fluconazole, 200 mg Fomivirsen Sodium, intraocular, 1.65 mg Foscarnet Sodium, per 1, 000 mg Gamma Globulin, intramuscular, 1 cc Gamma Globulin, intramuscular, 2 cc Gamma Globulin, intramuscular, 3 cc Gamma Globulin, intramuscular, 4 cc Gamma Globulin, intramuscular, 5 cc Gamma Globulin, intramuscular, 6 cc Gamma Globulin, intramuscular, 7 cc Gamma Globulin, intramuscular, 8 cc Gamma Globulin, intramuscular, 9 cc Gamma Globulin, intramuscular, 10 cc Immune Globulin, intravenous, 1 g Immune Globulin, 10 mg Respiratory Syncytial Virus Immune Globulin, 50 mg Ganciclovir Sodium, 500 mg Garamycin, Gentamicin, up to 80 mg Gatifloxacin, 10 mg Gold Sodium Thiomalate, up to 50 mg Glucagon Hydrochloride, per 1 mg Gonadorelin Hydrochloride, per 100 mcg Granisetron Hydrochloride, 100 mcg Haloperidol, up to 5 mg Haloperidol Decanoate, per 50 mg Heparin Sodium, Heparin Lock Flush, per 10 units Heparin Sodium, per 1, 000 units and famotidine.
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