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A38 DUCHENNE MUSCULAR DYSTROPHY CLINICAL PATHWAY A Cormick, M.D., L. Martin, B .N, G. Bowes, P.T., E. Churcher, O.T., D. Demizio, R.T., L. Grandmaison-Dumond, R.N., S. Miles, O.T., The Neuromuscular Team CHEO Objective: To develop a tool that promotes comprehensive, coordinated, efficient and effective multidisciplinary care for individuals aged 0-18 years with Duchenne Muscular Dystrophy. Methods: An experienced, multidisciplinary, neuromuscular team developed a unique, comprehensive, clinical pathway spanning the ages 0-18 years. This was developed through consensus and an up-to-date literature review. The pathway subdivides the clinical condition into 4 functionally defined stages. The aspects of care required and expected outcomes for each stage are defined to ensure that team goals are achieved as care is provided. Results: The entire pathway, as currently utilized at the Children's Hospital of Eastern Ontario will be provided. Steps in development are outlined and the future plans for evaluation and database development are highlighted. Conclusion: In a progressive, multi-system disease such as Duchenne Muscular Dystrophy, complications can be life threatening and timely interventions life saving. There are also significant equipment needs, families need to plan carefully and family stress is enormous. Clinical pathways are becoming more common within pediatric health care centers. They provide important structure and assist to ensure a high quality standard of care for the children and families we serve. As well, pathways provide important information for resource planning and research data base development.

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Thc home article home contact us thc login articles, news & information search + just for parents : substance abuse rohypnol by nov 9, 2004, email this article printer friendly page add to favorites rohypnol drug classification: rohypnol is a brand name for flunitrazepam a benzodiazepine ; , a very potent tranquilizer similar in nature to valium diazepam ; , but many times stronger. Genetic Studies There is scientific evidence that a subset of fibromyalgia patients have genetic factors that predispose them to vulnerability to FM. These patients tend to have primary FM. Primary FM usually has been present since childhood though the symptoms may not be clinically apparent until the patient is exposed to a significant physical or emotional stressor. Secondary FM is usually secondary to an overwhelming infection, injury, or a predisposing rheumatic disease. Genetic abnormalities in the functional polymorphism in the promoter region of the serotonin transporter gene have been noted in FM. 7 Patients with adequate serotonin promoter genes seem to be less susceptible to the adverse effects of chronic stress and depressive events. Another gene, catecholamine-Omethyltransferase COMT ; has been shown to be associated with pain regulation and myofascial pain of the jaw, and there is an increased association of COMT in FM patients. 8 Myofascial Pain and Muscle Biopsy Studies Myofascial pain is a big problem for many FM patients. Patients with this condition get palpable "knots" in their muscles and soft tissues that look and feel like painful muscle spasms. Doctors of physical medicine and rehabilitation often describe myofascial pain as originating in painful tissue which contains nodules associated with "trigger points" * in palpable, tense, or taut bands that may produce a twitch response upon palpation. These trigger points are often so painful that the patient is very uncomfortable. There can also be latent trigger points that are only painful upon palpation. Trigger points are typically associated with a referred pain pattern, sometimes at distant sites in the body. See Figure 1 ; All trigger points are responsible for musculoskeletal stiffness, weakness, and limitation of motion. There is scientific evidence that myofascial tissue on muscle biopsy has reduced blood flow, reduced oxygen receptors, 9 increased levels of the pain neurotransmitter substance P, 10 and reduced ATP receptors.11 Muscle biopsies are not necessary for the diagnosis of myofascial pain, but they may be ordered if there is an abnormal EMG-nerve conduction study, and neuromuscular disease is suspected. Sympathetic nerve blockade reverses, for instance, ketamine. Administration of medication and provision of medical services by district school board personnel, " s; 1006.062, F.S., 2002. Retrieved February 14, 2005, from : flsenate.gov statutes index ?App mode Display Statute&Search Str ing &URL Ch1006 SEC062 &Title - 2004- Ch1006 Section%20062#1006.062 Agency for Health Care Administration. 2001 ; . Diabetes: Medical practice guidelines. Tallahassee Florida. American Academy of Pediatrics 1999 ; . "Pediatric asthma: Promoting best practice guide for managing asthma in children." Retrieved June 18, 2004, from : aaaai members resources initiatives pediatricasthmaguidelines defau lt m Americans with Disabilities Act. 1990 ; . 42 U.S.C. 12101 et seq. Retrieved June 14, 2004, from : usdoj.gov crt ada pubs ada.txt American School Health Association. 2003 ; . "Compendium of resolutions 2003: School-based asthma management." Retrieved February 14, 2005, from : ashaweb pdfs resolutions Schlbsdasthmamgmt Child with a disability, 34 C.F.R. Part 300 300.7 1999 ; . Retrieved February 14, 2005, from : framework c18 documents 34CFR300 0 100 300.007 a ; Delegation of tasks prohibited. 1996 ; . Chapter 64B9-14.003, F.A.C. Retrieved June 09, 2004, from : fac.dos ate.fl Florida Department of Health, School Health Services. 2004 ; Annual School Health Services Report. Florida Department of Health, School Health Services. 2003 ; . "Nursing guidelines for the delegation of care for students with diabetes in Florida schools." Hendeles, L., and Hansen C. 2003 ; . "Quick-relief asthma medications." Unpublished document, University of Florida at Gainesville, College of Pharmacy. Hendeles, L., and Hansen, C. 2003 ; . "Long- term control medications." Unpublished document, University of Florida at Gainesville, College of Pharmacy. Individuals with Disabilities Education Act, 1997, Public Law 105-17. 1997 ; . Retrieved February 14, 1005, from : ed.gov offices OSERS Policy IDEA regs K-12 student and parent rights, s. 1002.20 3 ; h ; , F.S. Retrieved February 14, 2005, from.

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Orbus Pharma Inc. Annual Report 2005 Page 15. Date: 04 14 04ISR Number: 4340537-7Report Type: Expedited 15-DaCompany Report #RENA-10959 Age: 57 YR Gender: Male I FU: I Outcome Dose Duration Hospitalization 2.4 G DAILY Initial or Prolonged PO PT Scleroderma Report Source Foreign Health Professional Company 300 MG QD Representative Other Phos-Ex Rphypnol Marcumar Restex Einsalpha C C C Beloc Zok Neurontin SS SS Product Renagel Role PS Manufacturer Route ORAL and singulair.
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Two patients had sleep events on first exposure to the drug, but in the others they occurred with recurrent exposures 2 weeks to 20 years. Computer modelled HIV protease inhibitors first went into clinical development, cryogenic reactions -a key technology for these complex molecules- was nowhere to be found except in Europe4. In Biotechnology, because we are loosing the race to the Americans, the EU spares no effort to stimulate and support European efforts, both state and private ones, in this area. Yet in pharmaceutical fine chemicals -an area where Europe is light years ahead of anyone else the EU is legislating a stifling environment that provides the Industry with the dilemma of locating elsewhere or disappearing. 2. Helpful legislation sits side-by-side with unwise and stifling regulation The competitive position of Europes' Pharmaceutical Fine Chemicals industry is subject to an extensive, dense, complex, rigorously supervised body of legislation in force at both National and EU levels, at international level WHO and ICH ; and at the export markets: the USA and Japan. Most of it is embraced by the industry as a necessary driver for a level playing field but others appear to be nothing more than a European idiosyncrasy that serves no other pratical purpose but to diminish the advantages of a European location. The legislation that is embraced as innovative, common sense and has the benefit of world harmonization is that connected with the registration and approval of new pharmaceutical products. The key examples are the ICH5 guidelines turned into law through Directives in the EU and into Guidelines to Industry published in the USA's Code of Federal Regulations, with similar solutions in other countries: Australia, Japan, Switzerland, etc ; . The basis for the ICH is the global standardization of best practices that have the double aim of 1 ; enabling the faster and quasi-simultaneous access to patients in all countries of new medicines and 2 ; the reduction of costs by avoiding duplication of tests and studies. ICH is notable by the degree of collaboration and consultation between authorities and industry. Additional components of these international harmonized legislative initiatives are the Mutual Recognition protocols between regulatory authorities and the Common Technical Document6. On the other hand the last 10 years have seen in Europe a plethora of legislation that markedly interferes with the international market and distinctly affects the competitive advantage of the European Pharmaceutical fine chemical industry. The impact in the market place is one of distortion, the actions of the players are to take measures to meet the new legislative demands in ways that are totally opposite to the intent of the legislator, the net effect is that Europe looses jobs, manufacturing capacity, exports and -worst- know-how. The legislation that most distorts the markets is that which is connected with the innovation process. The issues that must be addressed include: The SPC and the lack of Roche Bolar amendment type law The existing and proposed controls of registration, evaluation and authorization of Chemicals both existing and new ; Other areas of legislation that will be reviewed are: IPPC: Integrated Plan for Pollution Control, an industrial licensing process EPER: European Pollutant Emission Register We shall show how the application of this legislation is hurting the industry, having an effect opposite that that intended by the legislator and often that its application within the EU presents inexplicable inconsistencies and tamoxifen. These products are not the same as oil supplements that are recommended as food supplements to make a pet's coat shiny, instead these are true anti-inflammatory drugs capable of relieving joint pain, cramps, and itchy skin, for example, ghb side effects. In may 2000, the dea in conjunction with the united states border patrol seized approximately 900 rohypnol tablets concealed in a vehicle at a checkpoint in falfurrias , texas and temazepam. 2When we watch the condition of modern medicine and the unparalleled influence of pharmaceuticals, an interesting paradox arises. The drug companies claim that pharmaceuticals can do wonders for people: lower their cholesterol, end clinical depression, reverse osteoporosis, calm your children, put passion into your life and so on. However, if prescription drugs are so good for people, where are all the healthy medicated customers? As simple, a question as this may seem, to my ear the horrible truth is; it is a very complex and very convoluted question with no clear answer. The ultimate in selfdiscovery however, is to take charge of your own health, learning as much as you can about your condition and the many treatment options available. Find out about the drugs you have been prescribed and all their potential side effects. By doing this you will empower yourself and create within you, an attitude of healing. John G. Sherman DCH is a professional classical homeopath practicing in Kelowna B.C. He operates the Okanagan Centre for Homeopathy. Contact him by calling 764-2487 or by visiting okanaganhomeopathy or emailing him at homeopath okanaganhomeopathy, for example, drug rohypnol. Description: This report describes the specific market segment of the pharmaceutical market for diabetes and two of its related diseases, metabolic syndrome and cardiovascular disease. It begins with a textbook explanation of the biology underlying diabetes, and then it reviews and evaluates widely accepted pharmaceutical approaches to diabetes that are currently in use. Finally, market forecasts and an analysis of products in the worldwide prescriptions market will help the reader understand the significance of past developments and speculate on future possibilities about the market of diabetes therapies as an area of research and investment. The principal objectives of this report are to: 1 ; identify viable technology drivers through a comprehensive look at various platform technologies for diabetes, metabolic syndrome and cardiovascular disease; 2 ; provide a complete understanding of the leading diabetes tests that are used for disease prediction, screening, prognosis and monitoring, encompassing their basic principles and applications; 3 ; discover feasible market opportunities via an identification of high-growth applications in different therapeutic areas, with a focus on the largest and most rapidly expanding markets for diabetes, metabolic syndrome and cardiovascular disease; 4 ; focus on global industry development through an in-depth analysis of the major world markets for molecular diagnostics, including forecasts for growth; and 5 ; summarize the blood glucose testing market, including definitions, processes and trends. Market figures regarding the current value of the diabetes drug market are taken from the most recently available data of the global pharmaceutical industry. The following categories of diabetes drugs will be covered herein: 1 ; rapid-acting insulin; 2 ; short-activity insulin; 3 ; intermediate-acting insulin; 4 ; long-acting insulin; 5 ; ultra-long-acting insulin; 6 ; insulin mixtures; 7 ; sulfonylureas; 8 ; meglitinides; 9 ; biguanides; 10 ; thiazolidinediones; and 11 ; alpha-glucosidase inhibitors and terazosin. Although most descriptions of rohjpnol tout it as odorless and tasteless, both the new and original formulas do produce a bitter taste when mixed with alcohol. L. CAUCHI, A. AYORINDE , P. DIGGORY, D. GRIFFITH, V. JONES, E. LAWRENCE, J. MESSENGER, A. MEHTA, P. O'MAHONY AND G. THOMAS Department of Medicine for the Elderly, Mayday University Hospital, Croydon and tiazac.

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1 E~virO~ental Ad juatntant Factor" -imum Tbie table provides in the local cnmmunicy. when on such facili tiee are available in the local community ehnuld be coneiderad in juatificatione centars. 2 Youth population should be eetabliehed of the activeduty military enrollment iaete.llation and the authorized civilian school districte, eix to 19 in the lncal ineta2Lacion. 3 ~e batical eqtipmant roon areaa ahnwn when decennining fecility. 4 E. Accrmmndete in other epece as e eingle. Forty six infertile women with PCOS, aged between 22-39 years and mean BMI 38.1; range 28.149.0 kg m ; were recruited in the Division of Reproductive Medicine at the University Hospital Charit. Fifteen 32% ; patients revealed regular menstrual cyclicity, 24 52% ; patients had less than four cycles in the last six months and seven 16% ; women had chronic amenorrhoea. The polycistic ovaries were demonstrated by transvaginal ultrasound in all volunteers and tobradex and rohypnol, because alprazolam. Marijuana THC in marijuana changes the way in which sensory information gets into and is processed by the hippocampus, a part of the brain crucial for learning, memory, and the integration of sensory experiences with emotions and motivations. The short-term effects of marijuana use can include problems with memory and learning, distorted perception, difficulty in thinking and problem-solving, loss of coordination, increased heart rate, anxiety and panic attacks - even after discontinuing its use for 24 hours. Long-term use can result in lack of personal achievement in the real world. Effects of marijuana abuse can include frequent respiratory infections, impaired memory and learning, increased heart rate, anxiety, panic attacks and tolerance. Marijuana may cause psychological or even physical dependence in some users over time, and some people report withdrawal symptoms. The use of marijuana by a mother during the first month of breast-feeding can impair the infant's motor development. The levels of tar inhaled and carbon monoxide absorbed by marijuana smokers are three to five times greater than among tobacco smokers. Symptoms include daily cough and phlegm, symptoms of chronic bronchitis, and more frequent chest colds. Continuing to smoke marijuana can lead to abnormal functioning of lung tissue injured or destroyed by marijuana smoke. MDMA Ecstasy, Rohypnol, GHB and Ketamine MDMA Ecstasy is a synthetic, psychoactive mind-altering ; drug with hallucinogenic and amphetamine-like properties. Using MDMA may cause serious psychological and physical damage. The psychological effects can include confusion, depression, anxiety and paranoia, and may last weeks after ingesting the substance. Physically, a user may experience nausea, faintness, and significant increase in heart rate and blood pressure. MDMA use can cause hyperthermia, muscle breakdown, seizures, stroke, kidney and cardiovascular system failure, and may lead to death. Chronic use of MDMA may produce long-lasting, possibly permanent, damage to the sections of the brain critical to thought and memory. Rohypnol, GHB, and ketamine are all central nervous system depressants. Lower doses of Rohpynol can cause muscle relaxation and can produce general sedative and hypnotic effects. In higher doses, Rohypn0l causes a loss of muscle control, loss of consciousness, and partial amnesia. When combined with alcohol, the toxic effects of Rohypnlo can be aggravated. GHB has been shown to produce drowsiness, nausea, unconsciousness, seizures, severe respiratory depression and coma. Additionally, GHB is increasingly involved in poisonings, overdoses, date rapes and fatalities. The use of ketamine produces effects similar to PCP and LSD, causing distorted perceptions of sight and sound and making the user feel disconnected and out of control. The overt hallucinatory effects of ketamine are relatively short-acting, lasting approximately one hour or less. However, the user's senses, judgement and coordination may be affected for up to 24 hours after initial use of the drug. Use of this drug can also bring about respiratory depression, heart rate abnormalities, and a withdrawal syndrome. Methamphetamine "Speed" ; Effects of methamphetamine use include addiction, psychotic behaviour and brain damage. Methamphetamine is highly addictive. Users attempting to abstain may suffer withdrawal symptoms such as depression, anxiety, fatigue, paranoia, aggression and intense cravings for the drug. Date: november 14, 2002 by: s richard lane - richard lane chief executive officer principal executive officer ; date: november 14, 2002 by: s angelo malahias - angelo malahias senior vice president and chief financial officer principal financial and accounting officer ; 53 10-q 54th page of 55 toc 1st previous next bottom just 54th certifications i, richard lane , certify that: i have reviewed this quarterly report on form 10-q of andrx corporation; based on my knowledge, this quarterly report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this quarterly report; based on my knowledge, the financial statements, and other financial information included in this quarterly report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this quarterly report; the registrant 's other certifying officers and i responsible for establishing and maintaining disclosure controls and procedures as defined in exchange act rules 13a-14 and 15d-14 ; for the registrant and we have: a ; designed such disclosure controls and procedures to ensure that material information relating to the registrant , including its consolidated subsidiaries , is made known to us by others within those entities, particularly during the period in which this quarterly report is being prepared; b ; evaluated the effectiveness of the registrant 's disclosure controls and procedures as of a date within 90 days prior to the filing date of this quarterly report the evaluation date and c ; presented in this quarterly report our conclusions about the effectiveness of the disclosure controls and procedures based on our evaluation as of the evaluation date; the registrant 's other certifying officers and i have disclosed, based on our most recent evaluation, to the registrant 's auditors and the audit committee of registrant's board of directors or persons performing the equivalent function ; : a ; all significant deficiencies in the design or operation of internal controls which could adversely affect the registrant's ability to record, process, summarize and report financial data and have identified for the registrant 's auditors any material weaknesses in internal controls; and b ; any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant's internal controls; and the registrant 's other certifying officers and i have indicated in this quarterly report whether or not there were significant changes in internal controls or in other factors that could significantly affect internal controls subsequent to the date of our most recent evaluation, including any corrective actions with regard to significant deficiencies and material weaknesses and toprol.

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Edwin J.R. van Beek MD PhD FRCR, Section of Academic Radiology, Royal Hallamshire Hospital, Sheffield, United Kingdom Editor ; Bernard Charbonnier MD, FESC, Department of Cardiology, University Hospital Trousseau, Tours, France Guy Meyer, MD, Respiratory and Intensive Care, Hopital Laennec, Paris, France Mario Morpurgo MD, FESC, Ospedale San Carlo Borromeo, Milano, Italy Antonio Palla, MD, Dipartimento Cardio Toracico Universita di Pisa, Italy ` Arnaud Perrier, MD, PD, Medical Clinics 1 and 2, Department of Internal Medicine, Geneva University Hospital, Geneva, Switzerland Adam Torbicki MD, FESC, Department of Chest Medicine, Institute of Tuberculosis and Lung Diseases, Warszawa, Poland Chair, for example, drugs ghb.
He history of medicine and the history of psychiatry have always reflected, to a greater or lesser extent, the histories of the societies in which they evolved. Advances in both medicine and psychiatry have been shaped, interpreted and implemented by society, and the history of medical progress has, in many ways, reflected the development of peoples, societies and civilisations all around the globe. In the case of psychiatry, the social history of mental illness has been increasingly well documented and explored in recent years by a number of different authors, often writing from a range of different perspectives. One of the very finest writers in this field was undoubtedly the late Professor Roy Porter, whose book, `Madmen: A Social History of Madhouses, Mad-Doctors and Lunatics, ' was reissued last year Tempus, 2004 ; . Originally published as `Mind Forg'd Manacles' Athlone, 1987 ; , this excellent volume provides fascinating accounts of mental illness in Georgian England, the use of treatments such as opium and blood-letting, and the role of confinement, especially in the context of the well-known Bethlem Hospital in England and serevent.

A. Castillo et al. International Journal of Antimicrobial Agents 27 2006 ; 263266 Table 2 Concentration of antimicrobial and time corresponding to optical density values of 0.91 for the streptococcal bacterial strains tested. Identifies key differences in the use and types of schedules as they pertain to marijuana, cocaine, methamphetamine, rohypnol, ghb, ecstasy and ketamine!

3. Summary This Prescribing Incentive Scheme incorporates a range of interventions and, although they only cover specific parts of the prescribing spectrum, they are aimed at improving medicines management and the quality of care. The scoring emphasises the need to have a scheme that is flexible to meet the needs of individual practices localities. Improved medicines use and better care should be achieved with the levels of investment that have gone into primary care prescribing budgets over the last five years. Regular feedback will be given to practices quarterly ; - to notify them on standards reached in the Prescribing Incentive Scheme.

Cnn - us ; women who really do ask for it nov 19, 2006 a police study published last week found that alcohol is the main factor in most date rape sex attacks, and that those old tabloid favourite date rape drugs , rohypnol and gbh, feature so little that they are heading for urban myth territory.

Ndash; hill i used rohypnol as a kind of sleeping pill. Department of Biochemistry and Molecular Biology, and Neuroscience Center, Louisiana State University Health Sciences Center, New Orleans, LA 70112-2223; Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New JerseyRobert Wood Johnson Medical School, 675 Hoes Lane, Piscataway, NJ 08854; and Howard Hughes Medical Institute, University of Chicago, 5841 South Maryland Avenue, MC1028, Chicago, IL 60637 Contributed by D. F. Steiner, December 31, 2001. 00603254821 00603255021 00603255121 BUTALBITAL TAB CPD BUTALBITAL CAP CPD BUT APAP CAF TAB SALSALATE SALSALATE SALSALATE REPAN-CF QUALA-CET ACETAMIN ACETAMIN ACETAMIN ACETAMIN ASPIRIN ASPIRIN FORTABS ACETAMIN SALSALATE SALSALATE ASPIRIN TAB 500MG TAB 750MG TAB 750MG TAB 650-50MG TAB TAB 325MG CAP 500MG CAP 500MG SUP 120MG TAB 325MG EC TAB 325MG EC TAB SUP 650MG TAB 500MG TAB 750MG 2 $38.93 $27.07 $73.78 $97.08 $1, 697.18 $0.00 $65.25 $48.31 $20.76 $55.27 $1.64 $27.43 $11.02 $157.22 $58.95 $0.00 $44.58 $91.05 $36.83 $2, 631.50 $31.47 $32.55 $129.71 $58.27 $4.99 $55.56 $5.34 0.04% 0.05% 0.00% 0.02% 0.05% 0.04% 0.00% 0.04% 0.05% 0.09.

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L.L. Rourke, M.D Division of Surgical Oncology, The University of Tennessee Graduate School of Medicine, Knoxville, Tennessee Co-Authors: J.L. Bell, MD, E.C. Fitzhugh, PhD Introduction: Prophylactic mastectomy ; is gaining acceptance as a therapeutic option for women with a personal history or a familial risk of breast cancer. Currently, three management options exist for the at risk female patient: surveillance, prophylactic surgery mastectomy and or oophorectomy ; , and or chemoprevention.1 The purpose of the study was to investigate what factors motivate patient's choice of PM. Methods: All patients seen between 1992 and 2002 that underwent prophylactic mastectomy were mailed a survey inquiring about their experience with, and the factors most influential in their decision to have PM. Demographic as well as perioperative data were retrospectively collected. Results: 91 eligible patients were mailed surveys, and 50 responded. The Results indicate that 96% 48 ; of respondents had been diagnosed with breast cancer prior to contralateral PM. Among these patients, 93.9% 46 ; elected to have their "healthy" breast removed at the same time as the diseased breast. Also, 61.2% N 30 ; of the total sample reported a family history of breast cancer. When asked to rank the factors 1 strongest; 6 weakest ; that contributed to their decision to undergo PM, the order of influence was: 1- personal diagnosis, 2- phobia, 3- "other", 4- family history, 5- physician consultation, and 6- genetic test When asked about their decision to undergo PM, 85.7% 42 ; indicated they felt "very comfortable" or "comfortable" knowing and understanding their options. 85.1% 40 ; stated they had "total choice" in deciding to undergo PM. Conclusion: Though we anticipated personal diagnosis of breast cancer to significantly impact the decision to choose PM, we unexpectedly noted cancer phobia as the second most influential factor before family history in patients choosing PM. Despite diverse demographic backgrounds, these women, as a group, had a consistent bias of personal history and phobia when choosing to undergo PM. Page 3. Table III. MIL-T-81533 1, Trichloroethane, Methyl Chloroform ; Inhibited Vapor Degreasing ; and an Azeotrope of Trichlorotrifluoroethane and Methylene Chloride, Du Pont Freon TMC or Equivalent are Listed as Immersion Fluids on Table III. CFC 113 Trichlorotrifluoroethane CFC-113 ; MIL-T-81533 ODS CHEM 2: Comments: Methyl Chloroform.

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