Their customers the terms Dura used to stuff the channel in meetings with defendants Newman, Spath and Garner . These high-level meetings preceded the meetings Weiherer had with the national accounts managers . Examples of the terms that were typically offered were a 6% or 12%o discount on the price depending on the volume of the order higher volume orders received the highe r percentage discount ; , payment terms of 60, 90 or 120 days rather than the standard 30-day term tha t Dura provided and allowance for returns anywhere from three months to three years after shipment for a full or half credit on the purchase price . Product quantities were sold by the case, and each case contained between 12 and 24 packs of Cecl0r CD . A typical deal might include two dozen cases for a discounted price plus another two or three dozen cases for free with unlimited rights of return and no payment due for a year . The distributors were willing to accept these terms because it allowe d - 34 99-CV-01517L WMC.
This group of drugs act to prevent the release of noradrenaline from nerves in the sympathetic nervous system, which is involved in controlling involuntary autonomic functions including blood pressure, heart rate, and the activity of muscles of internal organs e.g. blood vessels, gastrointestinal tract, urogenital tract ; . Noradrenaline is the main neurotransmitter of the sympathetic nervous system, so adrenergic neurone blocker drugs act like other antisympathetic agents to cause an overall fall in blood pressure. Their therapeutic action normally takes some weeks to develop, and their mechanisms of action result in some initial release of noradrenaline. The main use of such drugs is in antihypertensive therapy see ANTIHYPERTENSIVE AGENTS ; , but side-effects limit their use. Examples include: bethanidine, bretylium, debrisoquine, guanethidine, for instance, side affects.
Assessment had not been possible due to Mrs B being unrousable, "but in view of reduced level of alertness, nil by mouth is recommended". Later that afternoon, Dr E discussed Mrs B's antibiotic prescription with PNH's clinical pharmacist, specifically in relation to Mrs B's reduced renal function.17 Having done so, Dr E recorded in the clinical notes the pharmacist's recommended doses of IV cefotaxime and clarithromycin, based on Mrs B's estimated weight. These were to be administered 12hourly and 24-hourly, respectively. This information was also entered on "Regular Medications" sheet 2. Notes by Ms S immediately follow those of Dr E, and record that Mrs B received IV cefuroxime at 2.30pm drug chart 2 records administration at 2pm ; , and that "new IV Abs" had been charted as per the pharmacist's advice. Drug chart 2 shows that Ms G administered cefotaxime at 4.45pm and clarithromycin at 4.50pm. Dr E stated that when he entered the new antibiotic prescriptions on "Regular Medications" sheet 2, he also reviewed the medications listed on the first drug chart and questioned the prescription of MST 100mg twice a day. He advised that he "scanned the notes [including the hospital admission note] to see if there was any obvious past medical reason for [Mrs B] to be the morphine".18 He went to see Mrs B, to check whether any member of her family was present. As there was not, Dr E contacted Dr I and the rest home. Dr E stated that after "double checking" Mrs B's medication list with them, "it became apparent that the medications charted for her on admission were not the medications that she had been taking prior to admission". The rest home faxed Mrs B's "[rest home] Medication Sheet" to Dr E 6.10pm on 9 April. This recorded her usual prescription medication as: gliclazide, enalapril, Slow K, frusemide, doxycycline, aqueous cream, Betadine Cream and Timotol drops. The prescription for Cecl9r commenced on 2 April was included on a second sheet. Dr E stated that immediately upon discovering that an error had occurred, he re-charted Mrs B's medications. Horizontal lines were drawn through entries for Duride, Losec, Frumil, MST, warfarin, oxybutynin and aspirin on the first "Regular Medications" sheet, and initialled as "stopped"; two diagonal lines were scored across the sheet and "recharted" written between them; gliclazide, frusemide, Slow K, enalapril, doxycycline, lactulose and senna were entered on "Regular Medications" sheet 2. These were all to be administered orally.19.
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Compounds having a methoxyethoxy substituent at the 4-position of the pyridine ring, such as the ethyl homolog. On this basis, Eisai simply argued that "the prior art cited and applied in the outstanding Official Action is not pertinent to this particular group of compounds as now defined by applicants' claims." Id. at DRLRAB 2753. ; 118. With the claims no longer covering compounds having a methoxyethoxy substituent, on August 30, 1996, the '013 application examiner withdrew the rejections involving the methoxyethoxy compounds of Byk Gulden, stating: The rejection of old claims 6-18 and 23-25 now 26-34 ; under 35 U.S.C. 103 as being unpatentable over Junggren et al. and [Byk Gulden] has been overcome. Id. at DRLRAB 2754-59. ; 119. After withdrawing the rejection based on the methoxyethoxy compounds, the Examiner in the June 1996 office action entered a new rejection, citing, for the first time in the '013 application prosecution, the disclosure of "C1-C4-alkoxy-C1-C4-alkoxy" in Byk Gulden. Id. at DRLRAB 2756 ; . 120. Eisai appealed the examiner's reliance on this disclosure in Byk Gulden by directly challenging the prima facie rejection on February 28, 1997, and arguing that it was legal error to cite the generic disclosure in support of a rejection. Id. at DRLRAB 2760-71 ; . In response, on July 15, 1997, the '013 examiner agreed that the rejection based on the "C1-C4-alkoxy-C1-C4alkoxy" generic disclosure of Byk Gulden was improper, issuing a Notice of Allowability stating that "the instant compounds are patentable over the art of record because of the butoxy-ethoxy group at the 4-position of the pyridine compound, which was not taught by the prior art." Id. at DRLRAB 2773 and clomid!
Mar 28, 2006 in the quarter the company recorded pre-tax impairment charges totaling $3 9 million for sarafem r ; $1 8 million ; and duricef r ; $2 1 million ; - pr newswire brand names synonyms : duricef is also known by the following brand names and or synonymsancef; biofuroksym; ceclor; ceclor cd; cedax; cefditoren; cefizox; cefotan; ceftin; ceftizoxime sodium; cefurax; cefuril; cefuroxim; cefuroxime; cefuroxime axetil; cefuroxime free acid; cefuroxime sodium; cefuroxime sodium salt; cefuroxime ; cefuroxime and dextrose in duplex container; cefuroximo ; cefuroximum ; cefzil; cephuroxime; ceptaz; duricef; elobact; fortaz; keflex; keftab; kefurox; kefurox in plastic container; kerurox; mandol; maxipime; mefoxin; monocid; omnicef; oraxim; rocephin; sharox; tazicef; vantin; velosef; zinacef; zinacef danmark; zinacef in plastic container; zinat; zinnat drug category : duricef is categorized under the following by the fda: anti-bacterial agents; cephalosporins; atc: j01dc02 dosage forms : powder; powder for solution; tablet absorption : well absorbed from the gi tract bioavailability is 37-52% ; interactions : drugbank: interactions for cefuroxime interactions for cefuroxime: drug laboratory test interactions: a false-positive reaction for glucose in the urine may occur with copper reduction tests benedictí s or fehlingí s solution or with clinitest ò tablets ; but not with enzyme-based tests for glycosuria.
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Variable No. Employment status prior to CFS Full part time work Looking for work Retired Unable to work Caring for family Other CFS prevented continuation of main occupation Main occupation Director Before CFS After CFS Senior manager Before CFS After CFS Manager Before CFS After CFS Administrative Before CFS After CFS Skilled manual Before CFS After CFS Unskilled manual Before CFS After CFS Student Before CFS After CFS None Before CFS After CFS Not specified Before CFS After CFS Time spent in main occupation Full time 4 days week 3 days week 2 days week Not applicable Required help because of CFS Help provided byd Partner Immediate family Friends Social services Health services Other Transport usage before CFS % usage ; c Driving car Passenger in car Public transport Taxi Bicycle Walking 45 0 0 and doxycycline!
No recommendations are made based on limited and controversial data. A substantial number of children, adolescents, and their parents use nonprescription cold medicines or simple home-based remedies such as soups, fruit juices, or teas as alternatives or complements to conventional therapy for the treatment of upper respiratory infections including rhinosinusitis.63, 64 Others use herbal remedies and nutritional supplements or seek care from acupuncturists, chiropractors, homeopaths, naturopaths, aromatherapists, massage and therapeutic touch practitioners, and a variety of other healing modalities.64 67 Few of these therapies for upper respiratory tract infection or rhinosinusitis have been validated in randomized controlled trials. Claims that homeopathic medicines, 68 70 vitamin C preparations, 71 or zinc lozenges72 prevent upper respiratory infections or hasten their resolution are controversial. A recently published study provides evidence that zinc nasal gel is effective in shortening the duration of symptoms of the common cold when taken within 24 hours of their onset.73 Studies performed among adults indicating efficacy of Echinacea preparations in stimulating the immune system, thereby reducing the incidence, duration, or severity of respiratory infections, are debated74, 75; however, a recent metaanalysis suggested a predominance of generally positive effects.76 Physicians treating children and young adults should be aware that many of their patients are using complementary therapies, often without informing them. Most of these remedies are harmless and, whether through pharmacologic or placebo effect, a perception of efficacy in providing relief from symptoms has stood the test of time. Nevertheless, many herbal medicines sold in the United States are of uncertain efficacy, content, and toxicity and carry a potential for serious adverse effects.77 Of particular concern is the ability of the botanicals, either by direct interaction or by altering excretion mechanisms, to magnify or oppose the effect of conventional medicines that patients may be using concurrently.78 Physicians should inquire about the use of complementary medicine for upper respiratory tract infections among their patients, particularly those on long-term medication for chronic conditions. Information on dietary supplements is available on a regularly updated Internet site.79, for example, drug interactions.
Results Descriptive Statistics In the blast lesion of the eardrum, conduction hearing loss was not always present in all the frequencies. Low frequencies of 1, 000 Hz were affected in 8086%, and frequencies of 2, 0006, 000 Hz in 97 99% of the cases Fig. 3 ; . High frequencies were more severely damaged than low frequencies Fig. 4 ; . Tympanoplasty Success According to the Material Used After tympanoplasty with any of the three materials temporal fascia, perichondrium, or heterograft ; , eardrum rupture closure was successful in 89-92% of eardrums. There was no significant difference in the values of postoperative air-bone gap conductive component of hearing loss ; among the patient groups analyzed according to the used material Table 1 and erythromycin.
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The diagrams of cervical neck ; lymph nodes were interesting I didn't realize they form chains in the neck. Also, I didn't know that Follicular tumours are more likely to be unifocal, and less likely to metastasize to lymph nodes; whereas, Papillary cancer is often multi-focal and less likely to metastasize to lung and bones. If you'd like to view the CD, it is available for loan or can be accessed on the corporate Intranet of Princess Margaret Hospital, Toronto. It is also available for purchase for $200 for the Clinical level version ; or $120 for the general level version ; from oncologyinteractive and floxin.
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FROM PAGE 2 Unlike other drugs that have already been approved for treating MS, Tysabri is a monoclonal antibody that is given by a monthly infusion into a vein. It is designed to interfere with movement of potentially damaging immune cells from the bloodstream, across the "blood-brain barrier, " and into the brain and spinal cord. Tysabri blocks this movement by attaching to alpha 4integrin, a protein on the surface of immune T cells that normally enables them to pass through the blood-brain barrier. This approach was initially studied in animal models, including studies supported by the National MS Society, which showed that monoclonal antibodies could block such immune cell movement and ameliorate disease. These animal studies led to the human studies that are currently underway. First-Year Results from AFFIRM Study The AFFIRM study of Tysabri alone is a placebo-controlled study involving 942 participants worldwide. Participants were randomly assigned to receive either 300 mg IV infusion of Tysabri or inactive placebo every four weeks. Those on active therapy showed a statistically significant 66 percent reduction in relapse rate. The annual rate of relapses in the Tysabri group was 25 percent versus 74 percent in the placebo group. The secondary outcomes of the study were also significantly different for the treatment versus placebo groups. Sixty percent of those on Tysabri developed either no new MRI lesions or no newly 6 Toll-Free Number: 1.800.FIGHT MS.
| Online PharmacyMake such subject-matter patentable would take effect. While India informed the Panel of the provisions under which such applications were being received and stored under the Patents Act of 1970, no record of this decision or of any administrative guidelines issued to or within the patent offices of India to this effect was made available to the Panel. 2.6 No public notice was given at that time of this administrative decision and no notification concerning it was made to the Council for TRIPS. However, on 2 August 1996, the Indian Minister of Industry responded to a question asked by a member of the Lok Sabha concerning whether applications for product patents in the pharmaceutical, food and agricultural chemical areas had been received in anticipation of changes in the Indian Patents Act of 1970 in accordance with the requirements of the World Trade Organization; the Minister responded by stating that the patent offices had received 893 patent applications in the field of drug or medicine from Indian as well as foreign companies institutions up to 15 July 1996 and that applications for patents would be taken up for examination after 1 January 2005 as per the WTO Agreement.4 2.7 Under Indian patent law, patent applications for pharmaceutical or agricultural chemical products made by any person entitled to apply under Section 6 of the Patents Act of 1970 are subject to the same fee as any other patent application being received and allotted a filing date and advertised, on a weekly basis, in the Gazette of India with serial number, filing date, name of applicant and title of invention. Under the administrative arrangements of the Indian patent offices pursuant to the decision taken in April 1995, such applications5 are, however, unlike other patent applications, being allotted a special identification number internally, stored separately and not referred by the Controller to an examiner as specified in Section 12 of the Act. The notification in the Gazette does not distinguish between applications that are the subject of these administrative arrangements and other patent applications. 2.8 The legal authority for these administrative arrangements that has been cited by India is Article 73 1 ; a ; the Indian Constitution in conjunction with the Indian Patents Act of 1970. 2.9 For the purposes of the case in hand, the main aspects of the provisions of the Patents Act of 1970 which are of relevance to the case in hand are as follows6: Chapter III Sections 6 through 11 ; deals with applications for patents. These provisions do not require that applications for patents must be limited to patentable subject-matter. In respect of the subject-matter of the claims, they only require that such applications should be for inventions. Inventions are defined in Section 2 1 ; j ; as, inter alia, any new and useful substance produced by manufacture, including any new and useful improvement of such a substance. Section 5 makes it clear that inventions claiming substances intended for use, or capable of being used, as a food, medicine or drug or relating to substances prepared or produced by chemical processes are not in themselves patentable, but methods or and fluoxetine and ceclor, for instance, ceclor medicine.
For hcpcs codes a4619, e0565, e0572: 01 50 - 01 tuberculous bronchiectasis unspecified examination - tuberculous bronchiectasis tubercle bacilli not found by bacteriological or histological examination but tuberculosis confirmed by other methods inoculation of animals ; 042 human immunodeficiency virus hiv ; disease 13 3 pneumocystosis 27 02 cystic fibrosis with pulmonary manifestations 49 0 bronchiectasis without acute exacerbation 49 1 bronchiectasis with acute exacerbation 51 19 other diseases of trachea and bronchus 74 61 congenital bronchiectasis 99 80 - 99 complications of unspecified transplanted organ - complications of other specified transplanted organ v4 0 tracheostomy status v5 0 attention to tracheostomy for hcpcs codes a7013, a7014, a7015, a7525: 01 50 - 01 tuberculous bronchiectasis unspecified examination - tuberculous bronchiectasis tubercle bacilli not found by bacteriological or histological examination but tuberculosis confirmed by other methods inoculation of animals ; 042 human immunodeficiency virus hiv ; disease 13 3 pneumocystosis 27 02 cystic fibrosis with pulmonary manifestations 48 0 - 50 pneumonia due to adenovirus - respiratory conditions due to unspecified external agent 51 19 other diseases of trachea and bronchus 74 61 congenital bronchiectasis 78 4 abnormal sputum 99 80 - 99 complications of unspecified transplanted organ - complications of other specified transplanted organ v4 0 tracheostomy status v5 0 attention to tracheostomy for hcpcs codes a7003, a7004, e0570, e0571, e0574: 01 50 - 01 tuberculous bronchiectasis unspecified examination - tuberculous bronchiectasis tubercle bacilli not found by bacteriological or histological examination but tuberculosis confirmed by other methods inoculation of animals ; 042 human immunodeficiency virus hiv ; disease 13 3 pneumocystosis 27 02 cystic fibrosis with pulmonary manifestations 48 0 - 50 pneumonia due to adenovirus - respiratory conditions due to unspecified external agent 74 61 congenital bronchiectasis 78 4 abnormal sputum 99 80 - 99 complications of unspecified transplanted organ - complications of other specified transplanted organ for hcpcs codes a7006, j2545: 042 human immunodeficiency virus hiv ; disease 13 3 pneumocystosis 99 80 - 99 complications of unspecified transplanted organ - complications of other specified transplanted organ for hcpcs codes a4217, a7007, a7010, a7011, a7012, a7017, a7018, e0585, e1372: 01 50 - 01 tuberculous bronchiectasis unspecified examination - tuberculous bronchiectasis tubercle bacilli not found by bacteriological or histological examination but tuberculosis confirmed by other methods inoculation of animals ; 27 02 cystic fibrosis with pulmonary manifestations 49 0 bronchiectasis without acute exacerbation 49 1 bronchiectasis with acute exacerbation 51 19 other diseases of trachea and bronchus 74 61 congenital bronchiectasis v4 0 tracheostomy status v5 0 attention to tracheostomy for hcpcs code a4216: 042 human immunodeficiency virus hiv ; disease 13 3 pneumocystosis 49 0 - 50 simple chronic bronchitis - respiratory conditions due to unspecified external agent 99 80 - 99 complications of unspecified transplanted organ - complications of other specified transplanted organ for hcpcs codes j7608: 48 0 - 50 pneumonia due to adenovirus - respiratory conditions due to unspecified external agent 78 4 abnormal sputum for hcpcs codes j7620, j7626, j7631, j7644, j7669, q4093, q4094: 49 0 - 50 simple chronic bronchitis - respiratory conditions due to unspecified external agent for hcpcs code j7639: 27 02 cystic fibrosis with pulmonary manifestations for hcpcs code j7682: 01 50 - 01 tuberculous bronchiectasis unspecified examination - tuberculous bronchiectasis tubercle bacilli not found by bacteriological or histological examination but tuberculosis confirmed by other methods inoculation of animals ; 27 02 cystic fibrosis with pulmonary manifestations 49 0 bronchiectasis without acute exacerbation 49 1 bronchiectasis with acute exacerbation 74 61 congenital bronchiectasis for hcpcs codes k0730, q4080 41 0 primary pulmonary hypertension 41 8 other chronic pulmonary heart diseases for hcpcs code a7005: 01 50 - 01 tuberculous bronchiectasis unspecified examination - tuberculous bronchiectasis tubercle bacilli not found by bacteriological or histological examination but tuberculosis confirmed by other methods inoculation of animals ; 042 human immunodeficiency virus hiv ; disease 13 3 pneumocystosis 27 02 cystic fibrosis with pulmonary manifestations 41 0 primary pulmonary hypertension 41 8 other chronic pulmonary heart diseases 48 0 - 50 pneumonia due to adenovirus - respiratory conditions due to unspecified external agent 74 61 congenital bronchiectasis 78 4 abnormal sputum 99 80 - 99 complications of unspecified transplanted organ - complications of other specified transplanted organ for arformoterol hcpcs code j7699ko ; : 49 0 - simple chronic bronchitis - other emphysema 496 chronic airway obstruction not elsewhere classified diagnoses that support medical necessity refer to the previous section for the specific hcpcs code indicated!
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FDA Approval: Amoxicillan clavulanate Augmentin ; , cefuroxime Ceftin ; , loracarbef Lorabid ; , clarithromycin Biaxin ; , and levofloxacin Levaquin ; are FDA-approved for the treatment of acute sinusitis. Azithromycin Zithromax ; , cefaclor Ceclo ; , cefpodoxime Vantin ; , and TMP SMX Septra ; are not approved by the FDA for acute sinusitis treatment as of the approval of this document in December 1999.
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The USA Government. As an educator, he was conscious of the function and responsibility of academic medicine in providing society with qualified physicians and medical scientists, and played a key role in promoting a controversial reform that revolutionized the entire curriculum of medical schools in Italy. He actively participated in a joint effort to coordinate national pre- and postgraduate medical curricula within the European Union. With regard to iodine deficiency, he recognized the obligation of the medical and academic sector to promote the health of the community. He was a champion of iodine prophylaxis as a means for improving health conditions as well as for promoting social and economic development in depressed endemic areas of Italy and elsewhere. He was a founder and Co-President of the National Committee for the Prevention of Endemic Goiter in Italy and a Senior Advisor in ICCIDD. Recently he launched a major project for extensive iodine prophylaxis in the most severely affected regions of southern and insular Italy. Nino had an ebullient and warm personality. His remarkable talent for leadership generated enthusiasm and inspired immediate alliance. He had a strong character and strong opinions, and defended and imposed his views with vehemence and determination, but was also ready to admit and correct his errors. He liked power, but used his eminent positions for promoting culture rather than for personal advantage. He was a man of passion and curiosity; he liked science, but also was attracted to music, history, cookery, games and any new electronic gadget. He liked to discuss and to communicate orally rather than by writing, a propensity that was greatly facilitated by the advent of cellular phones, to which he was a virtual addict. He was generous, almost up to prodigality, as hundreds of taxi drivers and waiters in Naples and elsewhere were well aware. He was a hyperactive man with an enormous capacity for work and no distinction between night and daytime. He equally liked to give appointments at noon or at midnight. His home was an open house all yearround; students, scientists, friends, and relatives would be found at any time in his sitting room, mixed with senators and ministers. He had a long and happy marriage to Marisa, a physician and scientist herself, who gave up her personal career to share his ebullient life. Although they had no children, any student or young scientist was sure to find in him a father who cared.
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This summer, the old provincial drug schedules in Nova Scotia were repealed and replaced with all new schedules. A comprehensive guide to these schedules was mailed to every licensed pharmacist and certified dispenser in the province. The drugs listed in the three provincial schedules Schedules I, II and III ; changed considerably and members were provided with the time needed to "rearrange" their pharmacies to accommodate these major changes. It is expected that each licensed, for example, cecclor serum.
Work Flow for Nurse Medical Assistant: Opening patient's chart and updating or placing Summary information. Creating a New SOAPnote and placing a Docuplate appropriate for the Patient's Chief Complaint. Taking Vital Signs and placing them into the SOAPnote. Dragging and Dropping in any labs, reports, etc. Pertaining to the clinic visit. Checking the Task List this needs to be a protocol within the clinic on how often the Task List should be checked throughout the day ; . Work Flow for Provider: Opening the patient's chart, inserting the appropriate Docuplate or if one has already been placed in the note, proceeding to the Objective for the exam. Using Smartext documenting, free text typing, or speech recognition. 41 and celecoxib.
Problematic drug use in Britain is now marked by an extensive polydrug repertoire, in which both heroin and crack play a central part. This is distinctively different from the US crack epidemic of the 1980s and early 1990s. And though we have used the term crack houses as a shorthand, our recent market studies have shown that most dealers, whether based on the street, on a mobile phone or in houses, sell both crack cocaine and heroin.
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Drug Name NIMOTOP NORVASC PLENDIL PROCARDIA XL SULAR taztia xt TIAZAC verapamil hcl VERELAN CARDIOTONICS digitek digoxin LANOXICAPS LANOXIN CARDIOVASCULAR AGENTS - MISC. BIDIL CADUET REVATIO TRACLEER CEPHALOSPORINS CECLOR CEDAX cefaclor cefadroxil cefdinir cefprozil CEFTIN ceftriaxone sodium cefuroxime axetil CEFZIL cephalexin MAXIPIME OMNICEF ROCEPHIN SPECTRACEF SUPRAX VANTIN 27.
Some women have mild and temporary side effects with EC. Side effects are less common with Plan B than they are with birth control pills. Plan B contains only progestin, while many birth control pills contain progestin and estrogen, a combination that is more likely to cause side effects. ; Side effects can include: Upset stomach or vomiting Headache or dizziness Sore breasts Spotting drops of blood in your underwear ; or irregular bleeding You may have less trouble with nausea if you take EC with food and liquids. If you have vomited the pills, get another dose and take it with an anti-nausea medication recommended by your health care provider, for example, penicillin ceclor.
U.S. Specialty Pharmaceuticals 31 July 2003.
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In 1986, the European Union established the European Home and Leisure Accident Surveillance System EHLASS ; . Since then, data on Home and Leisure Accidents HLA ; have been collected on a yearly basis from many countries of the European Union. The purpose of EHLASS was to provide a systematic description of the occurrence of accidents aimed to identify potential risk behaviours and dangerous products, and to implement prevention measures at various levels. The decision to include EHLASS in the Health Information Exchange and Monitoring System HIEMS ; , which is part of the European Public Health Information Network EUPHIN ; , meant the standardisation of the available individual databases sent by the participating countries for conversion into an aggregated form. The ultimate objective was to provide the general public with aggregated data on HLA for subsequent analyses. The Institute of Public Health North Rhine-Westphalia, lgd ; , Germany, was the responsible authority to lead this effort. According to the Agreement No. SI2.134037 99CVF3-311 ; the Institute of Public Health of North-Rhine Westphalia was given also the task to conducting the macro-accidentologic analysis Project 1999 IPP 1041 ; of the EHLASS data contained in the EUPHIN-HIEMS database. This analysis was aimed at assessing the quality and comparability of the EHLASS data, to present epidemiological indicators of the HLA data for the Participant Countries PC ; , and to show the possibilities and limitations of such a surveillance system. The analyses were focused exclusively on four, out of the twenty-one accident classes available, namely: type of injury, mechanism of injury, place of accident occurrence, and body part affected. Major concerns regarding the comparability of the databases within and between countries, lead to a pragmatic approach for analysing the data, which was basically of descriptive nature. However, some explorative analyses were also attempted.
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