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GREEN ZONE: In Control You have no symptoms; You are able to do normal activities and or sports without being short of breath; You are not waking up at night or early in the morning due to your asthma; You are using your normal amount of reliever medication. OR Peak Flow Above: 80% personal best, for example, metrogel and alcohol. Prevalence of catamenial epilepsy the reported prevalence of catamenial epilepsy varies from 10 to 72 % table 1. The First 18 months of Primary Care Groups: Pharmaceutical Implications. Pharm J. 2002; 268: 407-9. : pharmj pdf papers pj 20020323 18months, for example, metrogel pv. 8. Known or suspected pregnancy. There is no indication for EstroGel in pregnancy. There appears to be little or no increased risk of birth defects in children born to women who have used estrogens and progestins from oral contraceptives inadvertently during early pregnancy. See PRECAUTIONS. ; WARNINGS See BOXED WARNINGS. 1. Cardiovascular Disorders Estrogen and estrogen progestin therapy has been associated with an increased risk of cardiovascular events such as myocardial infarction and stroke, as well as venous thrombosis and pulmonary embolism venous thromboembolism or VTE ; . Should any of these occur or be suspected, estrogens should be discontinued immediately. Risk factors for arterial vascular disease e.g., hypertension, diabetes mellitus, tobacco use, hypercholesterolemia, and obesity ; and or thromboembolism e.g., personal history or family history of VTE, obesity, and systemic lupus erythematosus ; should be managed appropriately. a. Coronary Heart Disease and Stroke: In the Women's Health Initiative WHI ; study, an increase in the number of myocardial infarctions and strokes has been observed in women receiving CE compared to placebo. These observations are preliminary and the study is continuing. See CLINICAL PHARMACOLOGY, Clinical Studies. ; In the CE MPA substudy of WHI, an increased risk of coronary heart disease CHD ; events defined as non-fatal myocardial infarction and CHD death ; was observed in women receiving CE MPA compared to women receiving placebo 37 vs. 30 per 10, 000 womenyears ; . The increase in risk was observed in year one and persisted. In the same substudy of WHI, an increased risk of stroke was observed in women receiving CE MPA compared to women receiving placebo 29 vs. 21 per 10, 000 womenyears ; . The increase in risk was observed after the first year and persisted. In postmenopausal women with documented heart disease n 2, 763, average age 66.7 years ; , a controlled clinical trial of secondary prevention of cardiovascular disease Heart and Estrogen Progestin Replacement Study; HERS ; treatment with CE MPA-0.625 mg 2.5 mg per day demonstrated no cardiovascular benefit. During an average follow-up of 4.1 years, treatment with CE MPA did not reduce the overall rate of CHD events in postmenopausal women with established coronary heart disease. There were more CHD events in the CE MPA-treated group than in the placebo group in year 1, but not during the subsequent years. Two thousand three hundred and twenty-one women from the original HERS trial agreed to participate in an open label extension of HERS, HERS II. Average follow-up in HERS II was an additional 2.7 years, for a total of 6.8 years overall. Rates of CHD events. 2.5 mg 4112 LILLY 4112 5 mg 4115 LILLY 4115 TABLET STRENGTH 7.5 mg 10 mg 4116 4117 LILLY LILLY 4116 4117 NDC 00024116-30 NDC 00024116-33 NDC 00024116-04 NDC 00024117-30 NDC 00024117-33 NDC 00024117-04 15 mg 4415 LILLY 4415 NDC 00024415-30 NDC 00024415-33 NDC 00024415-04 20 mg 4420 LILLY 4420 NDC 00024420-30 NDC 00024420-33 NDC 00024420-04 and mobic.

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MENOSTAR 14 MCG DAY PATCH .44 meperidine.8 meprobamate.26 MEPRON SUSPENSION .23 mercaptopurine21 MERREM.14 MERUVAX II VACCINE DIL UENT.49 mesalamine .50 MESNEX.21 MESTINON 180 MG TIMESPAN .26 MESTINON 60 MG 5 SYRUP.26 METADATE CD 10 MG CAPSULE .34 metadate er .34 metaproterenol.55 metformin hcl.27 methadone.8 methadose.8 methamphetamin e .34 methazolamide 33 methimazole.47 methocarbamol 57 methotrexate .21 methotrexate vial .21 methyclothiazide .34 methyldopa.32 methyldopa hctz .32 METHYLIN .34 methylin er .34 methylphenidate .34 methylphenidate er .34 methylprednisolo ne .19, 50 metipranolol 0.3% eye drops .52 metoclopramide .41 metolazone.34 metoprolol.30, 33 metoprolol-hctz 33 METROGEL .35 METROLOTION .35. Other Respiratory Agents G INTAL SOLUTION G ATROVENT TILADE INHALER INTAL SPIRIVA PA for members 30 years old ; PA MUCOMYST PA PULMOZYME PA COMBIVENT PA ACCOLATE PA SINGULAIR PA ZYFLO Misc. Respiratory Devices PEAK FLOW METER One per year ; SPACER 1 per year ; Emergency Respiratory Agents EPIPEN, JR ANAKIT ANAGUARD SKIN AND MUCOUS MEMBRANE AGENTS Anti-Acne Products G DESQUAM G BENZAMYCIN G CLEOCIN T SOLN, GEL, LOTION G T-STAT G EMGEL, A T S G ERYCETTE G RETIN A, AVITA SULFOXYL METROGEL, METROCREAM, METROLOTION, NORITATE TOPICYCLINE DIFFERIN AZELEX Oral Anti-Acne Agents PA ACCUTANE Antifungals Topical and moduretic.
States code, section 2461 c ; , to seek forfeiture of any other property of said defendant up to the value of the forfeitable property described above.

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Substitution maintenance clotting profile combivent arent staging homology with metrogel away. ADVISORY BOARD How do you use azelaic acid? WEBSTER Azelaic acid is a weird drug. Although it's weak on its own, if you add it to benzoyl peroxide it works as well as a drug such as Benzamycin. Studies are going on now to determine whether azelaic acid is doing anything or if the benzoyl peroxide alone is as effective as Benzamycin and the azelaic acid is just riding along. I use it particularly in black patients and medium-pigmented patients because it's also a "melanocyte discourager" and makes the postinflammatory hyperpigmentation go away. If you talk to black patients and tease out what they hate most about acne, it's the fact that they get postinflammatory pigmentation that outlives the original acne lesion by many weeks. ADVISORY BOARD In patients with acne rosacea, how do you treat those patients with solely telangiectatic lesions? How do you treat patients with primarily pustular lesions arising from sebaceous hyperplasia? WEBSTER Telangiectatic lesions are fairly resistant to anything other than laser treatment. Since no medications will shrink telangiectases, I turn the pulse dye laser on them to make them go away. For sebaceous hyperplasia, a variety of topical and systemic agents are available. I typically initiate treatment with a topical metronidazole agent such as Noritate or MetroGel and prednisolone.

10. Jennett B, Bond M. Assessment of outcome after severe brain damage. Lancet 1975; 1: 480-4. Rao SL SD, Gopukumar K. NIMHANS Neuropsychology Battery-2004-Manual. First ed. Bangalore: National Institute of Mental Health and Neurosciences, 2004. 12. Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet 1974; 2: 81-4. Haboubi NH, Long J, Koshy M, Ward AB. Short-term sequelae of minor head injury 6 years experience of minor head injury clinic ; . Disabil Rehabil 2001; 23: 635-8, for example, metrogel no prescription.

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The medical terms for this inflammation are 'rhinitis' inflammation of the nasal passages ; , 'sinusitis' inflammation of the sinuses, which are cavities of air in the head ; , and 'rhinosinusitis' inflammation of both areas and protonix. Dosage dogs: cefa-drops and cefa-tabs 1 gram, 50 mg, 100 mg and 200 mg should be administered orally at a dosage of 10 mg lb of body weight twice daily. He described the test algorithms and panels he implemented since joining the institution several years ago. Tests were organized not only to streamline the ordering process but also to expand their test menu. "An expanded menu is possible today, " Johnson explained, "because on-board capabilities exist on newer routine coagulation instruments. MGH uses the ACLTM 3000 PLUS to perform what were formerly considered to be esoteric hemostasis tests. Our goal was to provide rapid results with interpretations for physicians. This would enable them to make a diagnosis on a patient with a coagulopathy more quickly. "Routine coagulation testing is available 24 hours a day, everyday, at MGH. Assays include prothrombin times PT ; , activated partial thromboplastin times aPTT ; , fibrinogen levels and semi-quantitative D-dimer assays using latex agglutination. A plasma-based FDP assay is also available. The plasma-based FDP assay replaces the traditional serum FDP because of the inherent problems of serum specimen collection. Johnson reminded the audience of the importance of determining and monitoring reagent sensitivity for PTs and aPTTs whenever a laboratory changes a reagent lot number, a reagent manufacturer and or instruments. Studies should include normal ranges determined by using normal, healthy individuals -- not patients -- and heparin response curves for aPTT and PT reagents, if the PT reagent does not contain polybrene. Johnson suggests factor sensitivities for both reagents as well and theo-dur. Reich BA. "Non-invasive treatment of vascular and muscle contraction headache: a comparative longitudinal clinical study." Headache 1989; 29 1 ; : 34-41. Sacks O. Migraine--Understanding A Common Disorder. Expanded and updated version. Berkeley and Los Angeles: University of California Press; 1986. Saper JR, Magee KR. Freedom From Headaches. Revised and Updated. New York: Simon & Schuster, Inc.; 1981. Sargent JD, Green EE, Walters ED. "The use of autogenic feedback training in a pilot study of migraine and tension headaches." Headache 1972; 12: 20-24. -, Solbach P, Coyne L, Spohn H, Segerson J. "Results of a controlled, experimental, outcome study of nondrug treatments for the control of migraine headaches." J Behav Med 1986; 9 3 ; : 291-323. Spinhoven P, Linssen AC, Van Dyck R, Zitman FG. "Autogenic training and self-hypnosis in the control of tension headache." General Hospital Psychiatry 1992; 14 6 ; : 408-15. Stang PE, Osterhaus JT. "Impact of migraine in the United States: data from the National Health Interview Survey." Headache 1993; 33 1 ; : 29-35. Stewart WF, Lipton RB, Celentano DD, Reed ML. "Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors. JAMA 1992; 267 1 ; : 64-9. Stromfeld J, Weil A. Free Yourself from Headaches. New York: New American Library; 1989. Turin A, Johnson WG. "Biofeedback therapy for migraine headaches." Arch Gen Psychiatry 1976; 33: 517-19. Webster's Ninth New Collegiate Dictionary. Springfield: Merriam Webster Inc.; 1987. THE AMPAKINE CX546 RESTORES THE PREPULSE INHIBITION AND LATENT INHIBITION DEFICITS IN mGluR5 MICE T LIPINA1, K WEISS1, J RODER1, 2 In order to test the possible role of mGluR5 in the behavioral endophenotypes shared with schizophrenia and other psychiatric disorders, we used genetic engineering to create mice carrying null mutations in this gene. We how here for the first time, that compared to their mGluR5 + + littermates, mGluR5 mice has disrupted latent inhibition LI ; , measured in a thirst-motivated conditioned emotional response procedure by comparing suppression of drinking in response to a noise in mice which previously received 0 nonpreexposed ; or 40 noise preexposures preexposed ; followed by 2 noise-foot shock pairings. Administration of the modulator of acid receptor AMPAR ; , CX546, during only the conditioning phase improved the disrupted LI in mGluR5 mice to normal level and facilitated LI in control C57BL 6J mice with extended number of conditioning trails 4 noise-shock pairings ; . We confirm the work of others that Prepulse Inhibition PPI ; is impaired in mGluR5 mice to a level that could not be further impaired by antagonist of N-methyl-d-asparate receptors NMDAR ; MK-801, and go on to show rescue with CX546, but not aniracetam. This provides evidence that direct modulators of AMPAR can elicit antipsychotic action and represent a new pathway for treatment of schizophrenia. 1Samuel Lunenfeld Research Institute, Toronto, CANADA, 2Program in Neuroscience University of Toronto, CANADA. This work was supported by the Ontario Mental Health Foundation OMHF ; . DISENTANGING BEHAVIORAL PHENOTYPES OF INBRED MOUSE STRAINS CORRELATED WITH SPECIFIC GENE CLUSTERS M LOOS, AB SMIT, S SPIJKER Various inbred mouse strains differ in anxiety and attention related behavior due to genetic polymorphisms. Hovatta Hovatta et. al., 2005 ; showed that strain differences in anxiety-related behavior can be functionally related to gene expression differences. Using a test-battery of anxiety and attention test, we dissected these multi-component behaviors into behavior parameters that probe the different underlying components e.g. motivation, locomotor activity ; . Subsequently we investigated whether these disentangled behavioral components have specific gene expression correlates. We measured the behavior of six inbred mouse strains 129S6 SvEvTac, A J, C3H HeJ, C57BL6 J, DBA 2J and FVB NJ ; in eight different ethologically relevant exploration and hypophagia anxiety tests, as well as in the 5-choice serial reaction time test 5CSRTT ; to measure attention. Interestingly, strains that show low levels of anxiety at one parameter e.g. C57BL6 J, time spend in middle of open field ; can show high levels of anxiety at other parameters e.g. C57BL6 J, time spend exploring a novel object ; . This signifies that multiple ethologically relevant tests are necessary to disentangle complex behaviors, and hence to determine their specific genetic encoding. From the tests, we clustered multiple behavioral parameters to retrieve similar behavioral components across different genetic backgrounds. In addition, we retrieved the GEO-dataset from these 6 strains Hovatta et. al., 2005 ; , and correlated gene expression with clusters of behavioral parameters. This may indicate that specific genetic polymorphisms, by virtue of distinct gene expression profiles, translate into different modalities of behavioral output. Reference: Hovatta I, Tennant RS, Helton R, Marr RA, Singer O, Redwine JM, Ellison JA, Schadt EE, Verma IM, Lockhart DJ, Barlow C. Glyoxalase 1 and glutathione reductase 1 regulate anxiety in mice. Nature, 2005 Dec 1; 438 7068 ; : 662-6. Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Vrije Universiteit, Amsterdam THE NETHERLANDS. COGNITIVE DEFICITS IN THE R6 2 MOUSE MODEL OF HUNTINGTON'S DISEASE E LUDVIG, H HERMAN, G DILLON, B ALLEN, J GOODMAN, J MURPHY, B ZAHASKY, M PECK, L MENALLED, D BRUNNER The R6 2 transgenic mouse is one of the most popular mouse models for Huntington's disease HD ; . This mouse model is transgenic for the human huntingtin htt ; gene with 120-150 CAG repeats. R6 2 mice show decreased survival and gross motor deficits beginning as early as 5 weeks of age and cognitive impairment in both spatial learning and visual discrimination tasks. In this study, mice were and ventolin and metrogel, for example, mwtrogel use.
Standard for appetite stimulation; their role, if any, in enhancing muscle function or global quality of life in combination with other approaches remains to be established.
A Medicare beneficiary who had GHP coverage was hospitalized for 20 days in 1994. The hospital's charges for covered services were $5000. The inpatient deductible had not been met. The gross amount payable by Medicare as defined in 263.11 ; would have been $4000 for the stay if there had been no GHP coverage. The GHP paid $4500 of which $696 was credited to the Medicare deductible ; . Medicare makes no payment, since the plan's payment was greater than Medicare's gross amount payable of $4000 would have been. No part of the $500 difference between the hospital's charges and the GHP's payment can be billed to the beneficiary since the beneficiary's obligation, the deductible, was met by the GHP payment. The hospital files a no-payment bill reflecting the $696 credited to the deductible and cimetidine.
It is important to note that few randomized, controlled clinical trials and even fewer comparison studies have been done to evaluate these drugs.

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The total value of ethical pharmaceuticals purchased through Canadian drug store and hospital channels reached a high of $11.2 billion in 2001, setting an annual growth record of 17.3%. This figure surpassed the market's unprecedented four-year compound average growth rate CAGR ; of 14%. Drug store purchases accounted for over 89% of total ethical purchases in 2001, nearing the $10 billion mark, Figure 3 ; . Hospital pharmaceutical purchases of $1.2 billion accounted for the remaining 10.9% of the total Canadian market volume in 2001. Incremental drug purchases through hospitals reached $217.8 million in 2001 compared with $48.1 million in 2000. This additional volume represents a remarkable 21.7% growth figure over the year 2000. The annual growth is more than double the 4-year compound average growth rate of 10% for hospitals. Three classes cancer immunomodulators, anti-infectives, and hematinics, contributed 59.3% of the hospital growth for the year. The hospital boom was furthered by increased provincial spending on hospitals in the 2000 2001 fiscal year as compared to the 1999 2000 fiscal year.1. DRUG nAme estradiol estrace ; estradiol transdermal Climara ; estratest, HS estring estropipate Ogen ; Femhrt fluconazole 150mg Diflucan ; Follistim Follistim AQ levonorgestrel ethinyl estradiol Seasonale, Triphasil ; Lunelle medroxyprogesterone acetate Provera ; medroxyprogesterone acetate 150mg ml Depo-Provera ; menopur methergine metronidazole vaginal gel 0.75% megrogel ; norethindrone norethindrone acetate Aygestin ; norethindrone ethinyl estradiol.

Generic: lovastatin rmation online metrogel order on metrogel metrogel ingredients top - patient handout. Control Number: 06-AB-138-ESMO Topic 1: Supportive care PresentationPreference: Publishing Title: Prophylaxis of chemotherapy-induced oral mucositis: Double blind placebo-controlled randomized study of chlorhexidine versus placebo and with nonblinded randomized comparison to oral cooling cryotherapy ; Abstract Body: Purpose: Oral mucositis is a frequent complication to many chemotherapy regimens in conventional doses. Chlorhexidine prophylaxis has been beneficial in some studies and suggested detrimental in others, but never compared to oral cooling cryotherapy ; . This 3arm randomized study compared all these prophylactic measures. Methods: Previously untreated patients pts ; with GI-cancer receiving bolus 5-FU 425 mg m2 with leucovorine 20 mg m2 daily in five days were randomized, pending informed consent, to either chlorhexidine 0.1% 15 ml mouthrinse one minut TID for 3 wks. regimen A ; , or to double blind placebo normal saline with same taste additive as in A ; with same dose and frequency reg. B ; , or to cryotherapy with crushed ice 10 min. before to 35 min. after chemotherapy start reg. C ; . Pts self-reported on severity CTC-grading ; and duration of oral mucositis. Results: Among 225 pts randomized, 206 answered the questionnaire 70, 64, and 63 pts in reg.A, reg.B, and reg.C ; There were no differences between the regimens with respect to diagnoses, stage, age, gender, smoking habits, or performance status. Mucositis grade 3-4 impaired oral nutrition need of artificial nutrition ; occurred in 13%, 33%, and 11% in regimens A, B, and C, respectively. Reg. B was significantly worse than A p 0.01 ; and C p 0.005 ; . Median mucositis durations were A: 3 days 0-17 ; , B: 5 0-20 ; , and C: 1 0-20 ; . Duration was significantly longer in B than in both A p 0.035 ; and C p 0.003 ; . Conclusions: Frequency and duration of oral mucositis may be significantly improved by either prophylactic chlorhexidine or by cryotherapy. The latter is easy and inexpensive but is drug- and schedule-dependent as it cannot be used with infusional 5-FU or with chemotherapy with substantially longer half-lifes than 5-FU and mobic.

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The fda also asked manufacturers of nonprescription over-the-counter ; nsaids to include information on the product label about the potential for cardiovascular events and gi bleeding, as well as skin reactions in patients taking these drugs. Using the forced dose escalation method, an initial starting dose of 5 mg d or prior dose level of the ir formulation was raised by 5 mg increments on a weekly basis until complete continence had been obtained or a satisfactory balance between efficacy and tolerability had been established. Mental Health The communication "style" varies from culture to culture e.g., opening exchanges, getting to the point, directness, bluntness, self-disclosure by the interviewer ; . It may be advisable for the counselor interviewer, therapist, nurse ; to explain his or her point of view, values and assumptions. The degree to which each client identifies with his or her culture must be assessed. The client's environment should be kept as the focus of the interview; attempt to address the problem and understand it from the client's perspective. The interviewer must be prepared to be flexible to meet the client's expectations of where the interview should lead. Interest and genuineness are traits of the interviewer that can be recognized readily by clients of almost any culture. Some of these items require an in-depth knowledge of the culture. Consult experienced healthcare and social service professionals and para-professionals, elders, cross-cultural workers, interpreters and other members of the community itself. Firsthand experience and knowledge are best, but do not overlook the anthropological and historical literature on your area and its people. USE OF AN INTERPRETER Communication is most effective when the participants share a common tongue and culture, so that verbal and nonverbal messages are congruent and cultural meanings are clear. The following guidelines can be expected to compensate only partially for the degrees of difference between speakers. Be respectful and polite. Maintain eye contact if it does not appear to make the interpreter uncomfortable. Use the person's name remember that self-esteem is in part tied to one's name ; . Speak slowly, but do not shout. Volume does not compensate for difficulty with vocabulary or syntax. Discuss confidentiality. Be sure that you understand the interpreter's relationship to the client and that it does not pose a problem. Ask the interpreter for feedback at each step to be sure that communication takes place. As appropriate, ask for brief summaries to ensure that all three parties have a mutual understanding of what has been discussed. Explain to the interpreter that impressions of feelings and emotions should be described, in addition to the client's verbalizations.

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Pharmacopeia Drug Discovery Pharmacopeia Drug Discovery Protox Therapeutics Inc. Protox Therapeutics Inc. Novartis Pharmaceuticals Corp. Neose Technologies, Inc. Axis Genetics plc Juvaris BioTherapeutics, Inc. Cytovax Biotechnologies Inc. InterMune Pharmaceuticals, Inc. KaloBios Pharmaceuticals Inc. InterMune Pharmaceuticals, Inc. Cortecs International Ltd ProStrakan OSI Pharmaceuticals, Inc. OSI Pharmaceuticals, Inc. Astralis Ltd. CellGate, Inc. AEterna Zentaris Inc. Procyon BioPharma, Inc. Psychiatric Genomics Inc, because metrogel vagina. DTCA cannot be justified on the basis of consumer demand or right to access information. Where DTCA is banned, this represents a legal restriction on the manufacturers' rights to promote sales of prescription-only products in certain ways. There is no legal restriction on public information rights - the public maintains the right to obtain any available information about medicines. Surveys have shown that there is widespread consumer mistrust of the quality and completeness of information contained in DTCA. Health professionals remain the preferred source of independent advice on medication. Most New Zealand and overseas independent consumer groups have taken positions opposing DTCA after reviewing the evidence. Some, including the UK Consumers Association and Health Action International HAI ; a non-profit.
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The atherogenic stimuli responsible for the formation and progression of the stable atherosclerotic plaque are numerous Figure 1 ; . The emphasis on lipid atherogenic stimuli in the last 2030 years is related to the evidence that raised blood cholesterol levels are associated with an increased risk of IHD4 and to the demonstration that the reduction of blood cholesterol levels results in the reduction of the risk.57 A similar emphasis has been given to mechanical atherogenic stimuli, such as arterial blood pressure: indeed, raised pressure levels are associated with an increased risk of IHD4 and reduction of pressure levels results in a reduction of the risk.8 Similar considerations apply to chemical and metabolic atherogenic stimuli such as smoking9, 10 and diabetes.11, 12 More recently, a growing body of evidence has shown that endothelial dysfunction is an early alteration produced by the various atherogenic stimuli.13 Of note, endothelial dysfunction in asymptomatic subjects is associated, in turn, with an increased risk of IHD.14 Finally, a number of studies have recently shown that inflammatory cell activation plays an important role in the transition from endothelial dysfunction to the formation of the atherosclerotic plaque.15. Arrests for trespassing are generally made at establishments where the offender has been previously warned not to tread. Often, the same offender is arrested multiple times. Two of the 11 trespassing incidents that occurred during the first quarter of 2003 were at Harvard University and three were for violations at MIT properties.

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