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What do you propose or what are the reforms necessary to bring about if necessary ; a change to upgrade our profession? Pharmacists are the last professionals to be in touch with the prescription and in giving the medicament to a patient, and as such he shoulders the biggest the responsibility. Proposal: Pharmacists and doctors should work alongside one anothr. In the public sector, doctors shoul diagnose the patient while the pharmacist being drug experts, should advise on the medicaments. It must a team work and a two way flow of ideas. In the private doctors and pharmacists should consult one another without animosity. The pharmacist should be consulted and should participate in any reforms made in the governmental level MOH & QL ; . Their proposals and suggestions must be taken into consideration. The public must be made more aware of the role of the pharmacists and come to him her for proper advice and queries and their choice of medication and general health. The pharmacist should have a free hand in changing a medicament and replacing it with a generic, if he feels the need, or if he thinks it will be more beneficial to the patient. Do you think that permit should be given to "Non Phamacist proprietors" ? Before in Mauritius, there was not sufficient pharmacist so permits were issued to "Non Phamacist proprietors" but nowadays with a good panel of pharmacists permits should be issued only to pharmacist themselves. In a pharmacy, the responsible person is undoubtedly the pharmacist and he will definitely prime the etiquette of his profession above all. To him the welfare of the patient will be a great concern, he will advise , counsel and give more time to the patient. On the other hand a "Non Phamacist proprietor" will not have the same way of thinking. To him it will more of a business venture and the goal might differ as compared to the pharmacist, for instance, mexitil 200 mg.
14. Hamawaki, M., T. M. Coffman, A. Lashus, M. Koide, M. R. Zile, M. I. Oliverio, G. DeFreyte, G. Cooper IV, and B. A. Carabello. 1998. Pressureoverload hypertrophy is unabated in mice devoid of AT1A receptors. Am. J. Physiol. 274: H868H873. 15. Harada, K., I. Komuro, I. Shiojima, D. Hayashi, S. Kudoh, T. Mizuno, K. Kijima, H. Matsubara, T. Sugaya, K. Murakami, and Y. Yazaki. 1998. Pressure overload induces hypertrophy in angiotensin II type 1A receptor knockout mice. Circulation 97: 19521959. 16. Herizi, A., B. Jover, N. Bouriquet, and A. Mimran. 1998. Prevention of cardiovascular and renal effects of angiotensin II by endothelin blockade. Hypertension 31: 1014. 17. Ishikawa, T., M. Yanagisawa, S. Kimura, K. Goto, and T. Masaki. 1988. Positive chronotropic effects of endothelin, a novel endothelium-derived vasoconstrictor peptide. Pfluegers Arch. 413: 108110. 18. Ito, H., Y. Hirata, S. Adachi, M. Tanaka, M. Tsujino, A. Koike, A. Nogami, F. Murumo, and M. Hiroe. 1993. Endothelin-1 is an autocrine paracrine factor in the mechanism of angiotensin II-induced hypertrophy in cultured rat cardiomyocytes. J. Clin. Investig. 92: 398403. 19. Kasai, H., M. Takanashi, C. Takasaki, and M. Endoh. 1994. Pharmacological properties of endothelin receptor subtypes mediating positive inotropic effects in rabbit heart. Am. J. Physiol. 266: H2220H2228. 20. Kedzierski, R. M., T. Ohuchi, E. Isotani, Y. Y. Kisanuki, S. C. Williams, R. E. Hammer, J. A. Richardson, C. P. Reagan, G. K. Owens, K. E. Kamm, and M. Yanagisawa. Endothelin-A receptor gene knockout in smooth muscle causes hypotension and reveals an endothelin-B-mediated compensation in mice. In press. 21. Kedzierski, R. M., and M. Yanagisawa. 2001. Endothelin system: the doubleedged sword in health and disease. Annu. Rev. Pharmacol. Toxicol. 41: 851876. 22. Kisanuki, Y. Y., R. E. Hammer, J. Miyazaki, S. C. Williams., J. A. Richardson, and M. Yanagisawa. 2001. Tie2-cre transgenic mice: a new model for endothelial cell lineage analysis in vivo. Dev. Biol. 230: 230242. 23. Kurihara, Y., H. Kurihara, H. Suzuki, T. Kodama, K. Maemura, R. Nagai, H. Oda, T. Kuwaki, W. H. Cao, N. Kamada, et al. 1994. Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1. Nature 368: 703710. 24. Morimoto, T., K. Hasegawa, H. Wada, T. Kakita, and S. Kaburagi. 2001. Calcineurin-GATA4 pathway is involved in beta-adrenergic agonist-responsive endothelin-1 transcription in cardiac myocytes. J. Biol. Chem. 276: 3498334989. 25. Mulder, P., V. Richard, G. Derumeaux, M. Hogie, J. P. Henry, F. Lallemand, P. Compagnon, B. Mace, E. Comoy, B. Letac, and C. Thuillez. 1997. Role of endogenous endothelin in chronic heart failure: effects of long-term treatment with an endothelin antagonist on survival, haemodynamics, and cardiac remodeling. Circulation 96: 19761982. 26. Nicoletti, A., and J.-B. Michel. 1999. Cardiac fibrosis and inflammation: interaction with hemodynamic and hormonal factors. Cardiovasc. Res. 41: 532543. 27. Saetrum Opgaard, O., S. Moller, R. de Vries, L. Edvinsson, and P. R. Saxena. 2000. Positive inotropic responses mediated by endothelin ETA and ETB receptors in human myocardial trabeculae. Clin. Sci. 99: 161168. 28. Sakai, S., T. Miyauchi, M. Kobayashi, I. Yamaguchi, K. Goto, and Y. Sugishita. 1996. Inhibition of myocardial endothelin pathway improves longterm survival in heart failure. Nature 384: 353355. 29. Sakai, S., T. Miyauchi, T. Sakurai, Y. Kasuya, M. Ihara, I. Yamaguchi, K. Goto, and Y. Sugishita. 1996. Endogenous endothelin-1 participates in the maintenance of cardiac function in rats with congestive heart failure. Marked increase in endothelin-1 production in the failing heart. Circulation 93: 12141222. 30. Sakurai, T., M. Yanagisawa, Y. Takuwa, H. Miyazaki, S. Kimura, K. Goto, and T. Masaki. 1990. Cloning of a cDNA encoding a non-isopeptide-selective subtype of an endothelin receptor. Nature 348: 732735. 31. Soonpaa, M. H., K. K. Kim, L. Pajak, M. Franklin, and L. J. Field. 1996. Cardiomyocyte DNA synthesis and binucleation during murine development. Am. J. Physiol. 271: H2183H2189. 32. Tanaka, N., N. Dalton, L. Mao, H. A. Rockman, K. L. Peterson, K. R. Gottshall, J. J. Hunter, K. R. Chien, and J. Ross, Jr. 1996. Transthoracic echocardiography in models of cardiac disease in the mouse. Circulation 94: 11091170. 33. Yamauchi-Kohno, R., T. Miyauchi, T. Hoshino, T. Kobayashi, H. Aihara, S. Sakai, H. Yabana, K. Goto, Y. Sugishita, and S. Murata. 1999. Role of endothelin in deterioration of heart failure due to cardiomyopathy in hamsters: increase in endothelin-1 production in the heart and the beneficial effects of endothelin-A receptor antagonist on survival and cardiac function. Circulation 99: 21712176. 34. Yanagisawa, M., H. Kurihara, S. Kimura, Y. Tomobe, M. Kobayashi, Y. Mitsui, Y. Yazaki, K. Goto, and T. Masaki. 1988. A novel vasoconstrictor peptide produced by vascular endothelial cells. Nature 332: 411415. 35. Yorikane, R., S. Sakai, T. Miyauchi, T. Sakurai, Y. Sugishita, and K. Goto. 1993. Increased production of endothelin-1 in the hypertrophied rat heart due to pressure overload. FEBS Lett. 332: 3134. 36. Zolk, O., J. Quattek, G. Sitzler, T. Schrader, G. Nickenig, P. Schnabel, K. Shimada, M. Takahashi, and M. Bohm. 1999. Expression of endothelin-1, endothelin-converting enzyme, and endothelin receptors in chronic heart failure. Circulation 99: 21182123. Received September 29, 2003; first decision November 15, 2003; revision accepted November 25, 2003. From the Departments of Pharmacology W.W.B., I.M.G., P.R.S., A.H.J.D. ; and Thoracic Surgery and Heart Valve Bank J.P.v.K. ; , Erasmus Medical Center, Rotterdam, The Netherlands. Correspondence to Prof Dr A.H.J. Danser, Department of Pharmacology, Room EE1418b, Erasmus MC, Dr Molewaterplein 50, 3015 GE Rotterdam, Netherlands. E-mail a.danser erasmusmc.nl 2004 American Heart Association, Inc. Hypertension is available at : hypertensionaha DOI: 10.1161 01.HYP.0000110904.95771.26, because amiodarone.

Therapy usually is initiated with 10 20 mg daily, tags: blood pressure cholesterol drug by admin no comments » mexitil mexiletine ; blood pressure cholesterol drug mexitil mexiletine ; drug uses this medication is used to treat irregular heart rhythms arrhythmias ; and maintain a normal heart rate.

Methyltestosterone . METANDREN Methyltestosterone . TESTRED Methyltestosterone . VIRILON Metipranolol . OPTIPRANOLOL Metoclopramide . REGLAN Metolazone . DIULO Metolazone . ZAROXOLYN Metoprolol Succinate, extended-release TOPROL-XL Metoprolol Tartrate . LOPRESSOR Metoprolol + Hydrochlorothiazide . LOPRESSOR HCT Metronidazole . FLAGYL Metronidazole . METROCREAM Metronidazole . METROLOTION Metronidazole . NORITATE Metronidazole . PROTOSTAT Metronidazole Gel . METROGEL Metronidazole Gel Vaginal . METROGEL-VAGINAL Metronidazole, vaginal . VANDAZOLE Metyrosine . DEMSER Mexiletine . MEXITIL Micafungin MYCAMINE Miconazole . LOTRIMIN AF SPRAY POWDER Miconazole . MONISTAT Miconazole + Zinc oxide . VUSION Midazolam VERSED Midodrine . PROAMATINE Mifepristone . MIFEPREX Miglitol GLYSET Minocycline . DYNACIN Minocycline . MINOCIN Minocycline . MYRAC Minocycline . SOLODYN Minoxidil . LONITEN Minoxidil . ROGAINE Mirtazapine . REMERON Misoprostol . CYTOTEC Mitotane . LYSODREN Mitoxantrone . NOVANTRONE Modafinil . PROVIGIL Moexipril . UNIVASC Moexipril + Hydrochlorothiazide . UNIRETIC Molindone . MOBAN Mometasone ASMANEX TWISTHALER Mometasone . NASONEX Mometasone Furoate . ELOCON Montelukast . SINGULAIR Morphine, extended-release AVINZA and mexiletine.

Ask your health care provider any questions you may have about how to use mexitil. Or health care provider inertia about changing, altering, adding, or substituting medications. We cannot be certain whether this is related to consideration of "side effects" or lack of appreciation of treatment benefits. With combinations, which can include a diuretic and a blocker, diuretic ACE, diuretic ARB, diuretic CCB, an ACE inhibitor CCB or, in some cases, two different CCBs, a DHP and a non-DHP drug, goal pressures of 140 mm Hg can probably be achieved in many "resistant" patients. This assumes that causes of resistance have been ruled out, i.e., secondary causes, interfering substances, sleep apnea, etc. Goals pressures are most difficult to achieve in elderly patients, even if and micardis, for instance, atenolol.

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Consider changing the therapeutic regimen, including possibly discontinuing the medication in patients whose depression is persistently worse or includes symptoms of anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia psychomotor restlessness ; , hypomania, mania, or suicidality that are severe, abrupt in onset, or were not part of the patient's presenting symptoms.
Navarro, J. 2002 ; . Utilizacin de vacunas para el tratamiento de cocana y nicotina. Psiquiatria biolgica, 9, 175-177. Navarro, M. & Rodriguez De Fonseca, F. 2000 ; . Nuevas estrategas en el tratamiento de la cocana. Proyecto Hombre, 34, 5-9. Nistal de Paz, F., Ordiales Fernandez, J. J., Allende Gonzalez, J. & Colubi Colubi, L. 1999 ; . Pulmonary complications related to cocaine consumption. An Med Interna, 16 7 ; , 371-379. Nogu, S., Picn, M., Mestre, G., Devesa, R. & Corcuera, R. 2002 ; . Urgencias en ususarios de cocana. medicina Integral, 39, 249-259. Noguera, I., Medina, P., Segarra, G., Martinez, M. C., Aldasoro, M., Vila, J. M. & Lluch, S. 1997 ; . Potentiation by vasopressin of adrenergic vasoconstriction in the rat isolated mesenteric artery. Br J Pharmacol, 122 3 ; , 431-438. Nolla Salas, J. 1998 ; . Complicaciones derivadas del uso de la cocana. JANO Med Humanid, 55 1263 ; , 350. Ochoa, E. 1999a ; . Anxiety disorders and substance-related disorders. Actas Esp Psiquiatr. Ochoa, E. 1999b ; . Cocaina y cormobilidad psiquiatrica. Zaguan, 14, 4-5. Ochoa, E. 2000a ; . Cocaina y cormobilidad psiquiatrica Cocaine and psychiatric comorbidity ; . Actas Esp Psiquiatr, 28 1 ; , 40-52. Ochoa, E. 2000b ; . Cocana, la gran desconocida. Zagun, 14. Ochoa, E., Baca, E., Garca, V., Daz, C. & Vicente, N. 1999 ; . Predictores de trastornos de conducta e interconsulta psiquiatrica en hospitalizados por trastornos-VIH Predictors of behavioural disorders and consultation-liaison psychiatry in patients with HIV disorders ; . Actas Esp Psiquiatr, 27 2 ; , 97-102. Ochoa, E., Salvador, E., Alfonso, M. & Arranz, M. 2002 ; . Consumo de cocana en adictos a opiceos. Medicina clinica, 118, 597-598. Ortega, M., Perea M, Trejo O & S., N. 2000 ; . Intoxication aguda por cocaina en un body-stuffer Acute cocaine intoxication in a body-stuffer ; . Med Clin Barc ; , 114 7 ; , 279. Osorio, J., Farreras, N., Ortiz De Zarate, L. & Bachs, E. 2000 ; . Cocaine induced mesenteric ischaemia. Dig Surg, 17 6 ; , 648-651. Paraiso, P., Rivares Esteban, J. & Martin Martin, J. 2003 ; . An Otorrinolaringol Ibero Am., 30 4 ; , 389-396. Pascual, F., Torres, T. & Calafat, A. 2001 ; . Cocaine monograph. Adicciones, 13 2 ; , 247. Pascual Pastor, F. 2001 ; . Aproximacin histrica a la cocana. De la coca a la cocana. Adicciones, 13 2 ; , 7-22. Pavon Jimenez, R., Garcia Rubira, J. C. & Calderon Leal, J. 1999 ; . Total occlusion of the left main coronary artery in a young cocaine user. Int J Cardiol, 70 1 ; , 87-90 and minipress.
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MERUVAX II VACCINE W DILUENT mesalamine enema MESNA MESNEX MESTINON 60MG TABLET MESTINON INJECTION MESTINON Syrup and 180mg Tablet SA METADATE ER AND CD METAGLIP metaproterenol sulfate solution and syrup METAPROTERENOL SULFATE Tablets metformin hcl and metformin er METHADONE HCL INJECTION METHADONE HCL SOLUTION methadone tablets and oral concentrate METHAMPHETAMINE HCL methazolamide methenamine hippurate methenamine mandelate METHERGINE METHIMAZOLE 20mg methimazole 5mg and 10mg METHITEST methocarbamol methotrexate sodium methotrexate sodium pf methotrexate tablets METHYCLOTHIAZIDE methyldopa methyldopa hydrochlorothiazide 250-25mg METHYLDOPA HYDROCHLOROTHIAZIDE 250-15mg METHYLIN methylphenidate methylprednisolone METHYLPREDNISOLONE ACETATE INJECTION METHYLPREDNISOLONE SOD SUCC INJECTION metipranolol metoclopramide hcl METOCLOPRAMIDE INJECTION metolazone metoprolol hydrochlorothiazide metoprolol tartrate METROGEL AND METROCREAM METROGEL-VAGINAL METROLOTION metronidazole metronidazole 0.75% cream, gel, and lotion METRONIDAZOLE IV metronidazole vaginal gel MEVACOR mexiletine hcl MEXITIL MIACALCIN MICARDIS MICARDIS HCT miconazole nitrate vaginal microgestin microgestin fe MICRO-K MICRO-K 10 MICRONASE MICROZIDE MIDAMOR midodrine hcl MIGERGOT MIGRANAL MIMYX MINDAL MINIPRESS MINIRIN Tier 2 Tier 1 Tier 4 Tier 4 Tier 3 Tier 1 Tier 2 Tier 2 Tier 3 Tier 1 Tier 2 Tier 1 Tier 3 Tier 2 Tier 1 Tier 3 Tier 1 Tier 1 Tier 1 Tier 2 Tier 2 Tier 1 Tier 3 Tier 1 Tier 1 Tier 1 Tier 1 Tier 2 Tier 1 Tier 1 Tier 2 Tier 3 Tier 1 Tier 1 Tier 3 Tier 3 Tier 1 Tier 1 Tier 3 Tier 1 Tier 1 Tier 1 Tier 3 Tier 3 Tier 2 Tier 1 Tier 1 Tier 3 Tier 1 Tier 3 Tier 1 Tier 3 Tier 3 Tier 3 Tier 3 Tier 1 Tier 1 Tier 1 Tier 2 Tier 3 Tier 3 Tier 3 Tier 2 Tier 1 Tier 2 Tier 2 Tier 3 Tier 2 Tier 3 Tier 3 32 33.
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Susan L Hickenbottom, Univ of Michigan, Ann Arbor, MI; Gretchen Birbeck, Michigan State Univ, East Lansing, MI; Brad Jacobs, Wayne State Univ Detroit Med Cntr, Detroit, MI; Rashmi Kothari, Borgess Rsch Institute, Kalamazoo, MI; Mathew Reeves, Michigan State Univ, East Lansing, MI; for the MASCOTS Study Group Objective: In-hospital stroke IHS ; has not been studied extensively. We sought to describe the occurrence and characteristics of IHS in a pilot statewide stroke registry in Michigan. Methods: A representative sample of 16 Michigan hospitals was obtained by stratified random sampling. At each hospital, a trained coordinator prospectively identified all hospitalized acute stroke cases over a 6-month period. Eligible cases had to present with signs and symptoms of acute stroke and meet stroke sub-type case definitions. Relevant patient level data was abstracted using a 135-item data collection instrument. Descriptive univariate and Chi-square analyses were conducted using unweighted data. Results: Of 2742 stroke cases identified, 177 6.5% ; occurred while patients were already in-hospital. 62 patients 35% ; had been admitted with a cardiac diagnosis, 24 14% ; with a neurologic diagnosis, 12 7% ; for surgery, and 78 44% ; for other medical reasons. There was no difference in demographic characteristics between those with IHS and non-IHS. Those with IHS were less likely to have investigation of the cerebrovasculature performed 58% versus 78%, P 0.01 ; and less likely to have lipid screening 28% versus 43%, p 0.01 ; , but more likely to have a neurologist neurosurgeon involved in their care 90% versus 80%, p 0.01 ; . There were no differences in rates of those discharged on antithrombotic, lipid lowering or antihypertensive medications, smoking cessation counseling provided, or dysphagia screening or DVT prophylaxis. Mean time to first radiologic imaging was 144 minutes for IHS and 78 minutes for non-IHS p 0.01 ; . Mean length of stay was 14.5 days for IHS and 6.7 days for non-IHS p 0.01 ; . Those with IHS were less likely to be discharged home 24% versus 51%, p 0.01 ; and more likely to have DNR comfort care status during hospitalization 40% versus 25%, p 0.01 ; . Mortality rate was higher for IHS 17% versus 8.7%, p 0.01 ; . Stroke was listed as a primary ICD-9 code 430 436 and 997 ; for 41 23% ; of IHS and as a secondary code for 127 72% ; . Conclusions: IHS is a relatively common occurrence, and patients with IHS have worse outcome than those with non-IHS. There may be opportunity to improve imaging times and secondary prevention measures for patients with IHS and prazosin.

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Revenues of $694, 000 in the quarter ended December 31, 2004 increased by $394, 000 compared to revenues of $300, 000 in the same quarter of 2003 and consist of royalty fees from the sale of Memantine in the U.S. and in certain European countries. Revenues of $300, 000 in the quarter ended December 30, 2003 consist of $281, 000 of license fees relating to the approval for sale of Memantine and $19, 000 of royalty fees from the sale of Memantine in certain European countries. Research and development expenses of $2, 269, 000 in the quarter ended December 31, 2004 increased by $1, 756, 000 compared to expenses of $513, 000 in the same quarter of 2003. The increase resulted from expenses incurred to prepare for Phase III clinical trials of ViprinexTM, which are anticipated to commence within the next nine months, and for continuing the Phase III clinical trials for XERECEPT, the first of which was initiated during April 2004. General and administrative expenses of $1, 090, 000 in the quarter ended December 31, 2004 increased by $235, 000 compared to $855, 000 for the same quarter in 2003, and resulted primarily from expense for the administrative operations of the New Jersey office established for the development of ViprinexTM subsequent to NTII's acquisition of Empire in July 2004, together with professional fees related to public reporting and compliance with the Sarbanes-Oxley Act of 2002 and minocycline.

In the next five years, then, will India's pharma companies pursue a course of closer cooperation, or sharper competition with global pharma firms? "The answer is both, " says Ashish Singh, managing director of Bain & Company India Pvt. Ltd. "But generics will continue to be a strong driving force for the Indian pharma industry, even as it brings them into direct competition with global players in the major markets of North America, Europe and Japan." Singh sees a rapidly growing awareness of the Indian market both as a commercial market and a source of capability. Even three years ago, that was not the case, he adds. The general trend toward price consciousness in the developed markets is one important factor in the rising prospects of India's pharmaceutical sector, he believes. Patients, physicians and healthcare payers are increasingly willing to consider generics as a lower-cost alternative to branded medicines, says Singh. Equally important, he adds, big pharma companies recognize the need to look outside their traditional business models for new capabilities, even in areas that are strategic such as drug development and production. Pfizer's deal with Nicholas Piramal, for instance, would have the Indian health care and pharmaceutical company providing process development and scale-up services to Pfizer's animal health division. As a market, India also holds appeal to global pharma companies, particularly as they confront slowing growth and pricing constraints in maturing markets of North America, Europe and Japan. Of course, the increasing visibility of companies like Ranbaxy has also raised awareness of Indian pharma capabilities even though the company's tactics are regarded as a direct challenge to some leading global brands. With low-cost manufacturing and abundant scientific talent as historical strengths, and a lack of strong patent laws and bureaucracy as the legacy of a developing nation, India was traditionally viewed by global drug firms as a base for manufacturing and a vast commercial market rather than as a center for research and development and drug discovery. Indian companies had the reputation of being copycats, which, while not a very flattering label, enabled them to supply the domestic market as well as other low-income countries with inexpensive drugs that were copied from innovator companies. Indian companies could do that because they had to observe foreign patents on the manufacturing process, but not on the, for example, usp. Page 1, line 3, delete everything after the semicolon Page 1, line 4, delete everything before the period and insert "appropriating money" And when so amended the bill do pass and be re-referred to the Committee on Finance. Amendments adopted. Report adopted. Senator Krentz from the Committee on Environment and Natural Resources, to which was referred S.F. No. 812: A bill for an act relating to natural resources; appropriating money for a Civilian Conservation Corps worker statue. Reports the same back with the recommendation that the bill do pass and be re-referred to the Committee on Finance. Report adopted. Senator Krentz from the Committee on Environment and Natural Resources, to which was referred S.F. No. 70: A bill for an act relating to the environment; banning the sale and manufacture of fever or basal thermometers containing mercury; amending Minnesota Statutes 2000, section 116.92, subdivision 6. Reports the same back with the recommendation that the bill be amended as follows: Delete everything after the enacting clause and insert: "Section 1. Minnesota Statutes 2000, section 116.92, subdivision 6, is amended to read: Subd. 6. [MERCURY THERMOMETERS PROHIBITED.] a ; A medical facility may not routinely distribute thermometers manufacturer, wholesaler, or retailer may not sell or distribute at no cost a thermometer containing mercury that was manufactured after the effective date of this section. b ; Paragraph a ; does not apply to: 1 ; an electronic thermometer with a battery containing mercury if the battery is in compliance with section 325E.125; 2 ; a mercury thermometer used for food research and development or food processing, including meat, dairy products, and pet food processing; 3 ; a mercury thermometer that is a component of an animal agriculture climate control system or industrial measurement system until such time as the system is replaced or a nonmercury component for the system is available; or 4 ; a mercury thermometer used for calibration of other thermometers, apparatus, or equipment, unless a nonmercury calibration standard is approved for the application by the National Institute of Standards and Technology. Sec. 2. [EFFECTIVE DATE.] Section 1 is effective January 1, 2002." Delete the title and insert: "A bill for an act relating to the environment; restricting the sale of mercury thermometers; amending Minnesota Statutes 2000, section 116.92, subdivision 6." And when so amended the bill do pass. Amendments adopted. Report adopted and meloxicam.

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