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3rd International Syncope Symposium 5 March, 2003; Stratford-upon-Avon, UK E. trudie stars EPTA Spring Scientific Meeting and AGM 6 March, 2004; Stafford, UK E. nigel.hudson phnt.swest.nhs Neurology Study Days 8-12 March, 2004; Institute of Child Health, London, UK E. courses ich.ucl.ac , Tel. 020 78298692 Neuro-Oncology Conference 9 March, 2004; VA, US Fax. 757-446-6146, E. cme evmsmail.evms 2nd NNI-NUS Neuroscience Symposium 12-14 March, Singapore, Singapore E. claire lee ttsh .sg Brain Awareness Week 15-21 March, 2004, UK E. enquiries edab , Tel. 020 7019 4914 Life Sustaining Treatments & Vegetative State: Scientific Advances & Ethical Dilemmas 17-20 March, 2004; Rome, Italy E. gigli.gianluigi aoud.sanita.fvg.it, Fax. 0039 0 432 552 719 Austrian Society of Neurology Meeting 18-20 March, 2003; Austria E. klaus.berek bkh-kufstein A Practical Approach to Epilepsy 19 March, 2004; Institute of Child Health, London, UK E. courses ich.ucl.ac , Tel. 020 78298692 BSCN Scientific Meeting 19 March, 2004; Newcastle, UK E. bscn secretariat eeserve 3rd European Eiscsa Congress, 'Current Concepts In Training And Therapy' 19-20 March, 2004; Freiburg, Germany E. EISinfo2004 msn1 l -freiburg Parkinson's Disease: An Essential Update for Healthcare Professionals 22 March, 2004; London, UK Tel. 020 7834 3181 Cambridge Workshop on Universal Access and Assistive Technology 22-24 March, 2--4; Cambridge, UK E. Aejaz.Zahid bdgh-tr.trent.nhs Electrophysiology in the Young and Adults: A New Frontier 23-25 March, 2004; Saudi Arabia E. web symposia kfshrc .sa 3rd Unterinntal-Neurological Congress 24 April, 2004; Kufstein, Austria E. Klaus.berek bkh-kufstein Update in Spinal Imaging 24 March, 2004; London, UK E. tamara.anderson bir Growth And Death In The Nervous System 24-28 March, St Moritz, Switzerland Fax. + 41 1 255 E. adriano pathol zh.ch 36th International Diagnostic Course: diseases of the Brain, Heart & Neck 27 March - 2 April, 2004; Davos, Switzerland Fax. 00-41 13 849 339, E. idkd congressorg.ch.
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Page 28 Drug Name PROCANBID PRONESTYL Rythmil ; Quinaglute ; QUINIDINE GLUCONATE Quinidex ; RYTHMOL SR TIKOSYN RANEXA Cardiotonic Agents digoxin Lanoxin ; LANOXICAPS LANOXIN PEDIATRIC Tier Notes * 2 1 tab.sr 12h; 1000mg, 500mg capsule, tablet; 375mg, 500mg tablet; 150mg, 225mg, 300mg tablet sa; 324mg vial; 80mg ml tablet, tablet sa cap.sr 12h; 225mg, 325mg, capsule PA; tab.sr 12h ampul, tablet; 125mcg, 250mcg, ml, 500mcg capsule; 100mcg, 200mcg ampul; 100mcg ml PA; capsule packet, powder soln recon soln recon vial cream gm ; , gel; 0.01%, 0.025%, 0.05%, capsule, syrup, tablet tablet dr tablet, tablet sa tablet patch td24 tablet tablet QL, PA; solution, tab ds pk, tablet tablet tablet tablet capsule, tablet tablet; 25-100-200 tablet; 37.5-150mg tablet; 12.5-50mg PA; capsule tablet solution capsule. Introduction: The most widely used methods for estimating the glomerular filtration rate GFR ; are the formulas of Cockcroft-Gault CG ; and abbreviated Modification of Diet in Renal Disease MDRD ; equations. But these formulas have some limitations because previous studies of Asian chronic kidney disease CKD ; patients suggests that the calculated GFR from these equations were significantly lower than the measured GFR and these equations have not been validated in patients with diabetes mellitus DM ; . The objective of this study was to evaluate the validity of these equations for calculating GFR in CKD patients with or without DM type 2, using 99mTc-DTPA renograpy GFR measurement as the gold standard method. Methods: Stable CKD patients whose conditions fulfilled the NKF-K DOQI definition of CKD were evaluated using the CG and MDRD equations for calculating GFR GFRcg and GFRmdrd ; compared with measured GFR from 99mTc-DTPA renograpy GFR measurement GFRscan ; . Results: One hundred and ninety stable CKD patients with or without DM type 2 were enrolled from July 2005 through Oct 2006. The common causes of underlying CKD were DM type 2 47.37% ; , glomerulonephritis 22.11% ; and hypertension 20.00% ; . The percentages of CKD patients in stages 1 to 5 were 3.18, 11.05, 27.89, and 28.42 respectively. The means of GFRcg, GFRmdrd and GFRscan were 55.5833.05, 54.1931.61 and 73.1439.24 ml min 1.73 m2 respectively. The Pearson R2 for GFRcg and GFRmdrd compared with GFRscan was 0.514 p 0.01 ; and 0.564 p 0.01 ; respectively. Regression analysis showed GFRscan equal to 1.195 x GFRcg R2 0.867, P 0.01 ; or 1.244 x GFRmdrd R2 0.884, P 0.01 ; . Among 90 patients with DM type 2, the means of GFRcg, GFRmdrd and GFRscan were 57.2135.85, 55.5335.15 and 72.0136.53 ml min 1.73 m2 respectively. The Pearson R2 for GFRcg and GFRmdrd compared with GFRscan was 0.498 p 0.01 ; and 0.546 p 0.01 ; respectively. Regression analysis showed GFRscan equal to 1.108 x GFRcg R2 0.857, P 0.01 ; or 1.147 x GFRmdrd R2 0.870, P 0.01 ; . Among 100 patients without DM, the means of GFRcg, GFRmdrd and GFRscan were 54.1130.42, 52.9928.18 and 74.1541.68 ml min 1.73 m2 respectively. The Pearson R2 for GFRcg and GFRmdrd compared with GFRscan was 0.559 p 0.01 ; and 0.624 p 0.01 ; respectively. Regression analysis showed GFRscan equal to 1.288 x GFRcg R2 0.883, P 0.01 ; or 1.349 x GFRmdrd R2 0.906, P 0.01, because medications. 23. Pritchett E L C, Page R L, Carlson M, Undesser K, and Fava G, for the Rhtyhmol Atrial Fibrillation Trial RAFT ; Investigators, "Efficacy and safety of sustained-release propafenone propafenone SR ; for patients with atrial fibrillation", Am. J. Cardiol. 2003; 92: 941946. Meinertz T, Lip G Y H, Lombardi F Sadowski Z P Kalsch B, Camez A, Hewkin A, and Eberle S, on behalf of the ERAFT Investigators, "Efficacy and safety of propafenone sustained release in the prophylaxis of symptomatic paroxysmal atrial fibrillation The European Rytjmol Rythmonorm Atrial Fibrillation Trial ERAFT ; Study ; ", Am. J. Cardiol. 2002; 90: 1, Pederson O D, Bagger H, Keller N, Marchant B, Kober L, and Torp-Pederson C, for the Danish Investigations of Arrhythmia and Morality ON Dofetilide Study Group, "Efficacy of dofetilide in the treatment of atrial fibrillation-flutter in patients with reduced left ventricular function: A Danish Investigations of Arrhythmia and Mortality ON Dofetilide DIAMOND ; substudy", Circulation 2001; 104; 292296. Singh S, Zoble R G, Yellen L, Brodsky M A, Feld G K, Berk M, and Billing C B, "Efficacy and safety of oral dofetilide in converting to and maintaining sinus rhythm in patients with chronic atrial fibrillation or flutter: the symptomatic atrial fibrillation investigative research on dofetilide SAFIRE-D ; study", Circulation 2000; 102: 2, Greenbaum R, Campbell T J, Channer K S, et al., "Conversion of atrial fibrillation and maintenance of sinus rhythm by dofetilide. The EMERALD study abstract ; ", Circulation 1998; I-633. 28. Prystowsky E N, Freeland S, Branyas N A, Rardon D P Fogel R I, Padanilam B J, and Rippy J S, "Clinical experience with , dofetilide in the treatment of patients with atrial fibrillation", J. Cardiovasc. Electrophysiol. 2003; 14: S287S290. 29. Kochiadakis G E, Igoumenidis N E, Marketou M E, Solomou M C, Kanoupakis E M, Vardas P E, "Low-dose amiodarone versus sotalol for suppression of recurrent symptomatic atrial fibrillation", Am. J. Cardiol. 1998; 81: 995998. Roy D, Talajic M, Dorian P et al. for the Canadian Trial of Atrial Fibrillation Investigators", "Amiodarone to prevent recurrence , of atrial fibrillation", N. Eng. J. Med. 2000; 342: 913920. Vorperian C R, Havighhurst T C, Miller S, January C T, "Adverse effects of low dose amiodarone: a meta-analysis", J.Am. Coll. Cardiol. 1997; 30: 791798. Maisel W H, Kuntz K M, Reimold S C, Lee T H, Antman E M, Friedman P L, and Stevenson W G, "Risk of initiating antiarrhythmic drug therapy for atrial fibrillation in patients admitted to a University Hospital", Ann. Intern. Med. 1997; 127: 281284. Naccarelli G V Wolbrette D L, Dell'Orfano J T, Patel H M, and Luck J C, "A decade of clinical trial developments in post, myocardial infarction, congestive heart failure and sustained ventricular tachyarrhythmia patients: From CAST to AVID and beyond", J. Cardiovasc. Electrophysiol. 1998; 9: 864889. Incidence rate was highest among IDUs who were patients of the STD clinic 2.85% per year ; and lowest among clients of the drug treatment center 0.15% per year ; . None of the studies exhibited a statistically significant temporal trend in HIV incidence, either for MSM-IDUs or non-MSM-IDUs or all subjects combined. Aggressive HIV prevention interventions targeted at needleborne transmission among IDUs were implemented in San Francisco in the late 1980s and sustained consistently during the 1990s, including street-based outreach education, free HIV counseling and testing, and needle exchange. The HIV incidence among IDUs in San Francisco during that decade was lower than in Baltimore and New York, although the incidence in those cities declined during that decade as those interventions were implemented there.810 The high incidence among MSM-IDUs and among STD clinic patients who use injection drugs suggests that further reductions in HIV incidence among IDUs in San Francisco may require targeting high-risk sexual behavior. Of note, the sexual networks of MSMIDUs are connected to other segments of the MSM community in San Francisco where the prevalence and incidence of HIV is higher than among non-MSMIDUs.2, 4, 11 The studies presented here have limitations. Clients in 3 of the studies were specifically accessing services, ie, STD screening, drug treatment, or HIV and pyrazinamide. Figure 15 Scenario diagram for CPS SP agreed completion date failure 1 ; 2 ; 3 ; The CPS SP identifies an unavoidable delay in fulfilling the ServiceRequestOrder and issues a SRO Delay Notification to the Agent with a proposed revised Date and Time The Agent issues a SRO Amend with new date and time to the CPS AP, optionally, may forward the delay notification to the Customer. The CPS AP responds with a SRO FirmConfirmation with the new CPS AP Date and Time. It may be different to the CPS SP's date and time because of 'cooling off' period constraints. The 'cooling off' period is not adjusted after it is started but the amendment cannot be used to bring the activation date forward into the Cooling-off period. The agent forwards the SRO FirmConfirmation CPS AP revised data and time ; to the Service Customer and the CPS SP The process completes as normally Should the CPS revised data and time be unacceptable the CPS SP can initiate another SRO Delay Notification CPS AP agreed completion Date Failure ORD-FAL 2. John's wort, garlic supplements lopinavir dihydroergotamine mesylate, ergotamine, ritonavir flecainide tambocor ; , lovastatin, kaletra ; 7 ; pimozide, propafenone rythmol ; , rifampin, simvastatin, triazolam, st and quetiapine. LABELER --MAJOR PHARM. MAJOR PHARM. PHARBEST PHARMA ADVANCE PHARM ADVANCE PHARM BERGEN BRUNSWIG BERGEN BRUNSWIG BERGEN BRUNSWIG LEADER LEADER --MCKESSON PACKAG MCKESSON PACKAG THE F. DOHMEN AKYMA PHARMACEU AKYMA PHARMACEU PADDOCK LABS. BERGEN BRUNSWIG UNITED RESEARCH LEADER THE F. DOHMEN --THE F. DOHMEN IVAX PHARMACEUT RUGBY QUALITEST PHARBEST PHARMA MCKESSON PACKAG MCKESSON PACKAG IVAX PHARMACEUT IVAX PHARMACEUT RUGBY --RUGBY QUALITEST QUALITEST QUALITEST QUALITEST PHARBEST PHARMA BERGEN BRUNSWIG BERGEN BRUNSWIG LEADER MCKESSON PACKAG --MCKESSON PACKAG MCKESSON PACKAG WYETH CONSUMER WYETH CONSUMER B.F ASCHER & CO.

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This activity has been planned and implemented in accordance with Essential Areas and Policies of the Accreditation Council for Continuing Medical Education ACCME ; through the joint sponsorship of Medical Education Collaborative and Medscape. Medical Education Collaborative, a nonprofit education organization, is accredited by the ACCME to provide continuing medical education for physicians and takes responsibility for the content, quality and scientific integrity of this CME activity. This activity is co-provided by Medical Education Collaborative MEC ; and Medscape. MEC is approved as a provider of continuing education in nursing by the Colorado Nurses Association, which is accredited as an approver of continuing education in nursing by the American Nurses Credentialing Center's Commission on Accreditation. CME in this activity indicates continuing education for medical professionals. Please click and quinine. And it was the most used behavioral modification component. None of the other specific lifestyle treatments were implemented in more than 5% of obesity drug trials. It was particularly interesting how infrequently lifestyle exercise and walking were incorporated into drug studies, even in the 1990s. These data suggest that the design of obesity drug trials are deficient and do not provide comprehensive treatments. This is despite organizational calls to approach obesity from a multidisciplinary perspective and provide multicomponent treatments 8, 11, 13, ; . Previous reports on lifestyle interventions found that most lifestyle obesity intervention trials had been conducted with middle-aged, overweight to moderately obese women 15, 16 ; . Our meta-analysis also found that many randomized obesity drug trials were conducted with patients who were moderately obese, women, and in their 40s. This trend of obesity trials using similar populations suggests that their outcomes may not be generalized to the larger population of obesity patients who seek treatment, particularly those with more severe obesity i.e., BMI 35 kg m2 ; One-third of the reviewed obesity-drug studies did not identify who provided the lifestyle treatment. Among those that did, the physician who also provided the drug delivered the lifestyle treatment s ; . Whereas this model is probably a more efficient and pragmatic way to provide treatment in primary care settings 28 ; , physicians often are not trained in nutrition, exercise, or behavior modification 29 33 ; . addition, this practice is contrary to the positions espoused by most obesity organizations calling for multidisciplinary treatment teams 13 ; . Thus, it is unclear how well the lifestyle interventions were implemented and whether or not outcomes would be improved if individuals with specific training and expertise in these areas provided the treatments. A substantial portion of weight loss experienced by patients in obesity drug trials was attributable to both "placebo effects" and to the lifestyle treatments, with dietary interventions plus, to some degree, placebo effects ; accounting.

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Since the effectiveness of many diuretics ultimately depends on establishing a negative Na balance to mobilize edema fluid, restriction of dietary Na intake is generally an essential part of diuretic therapy. Therefore, one cause of therapeutic failure or apparent patient refractoriness to diuretics could be the patient's continued ingestion of large quantities of NaC1. Some of the older diuretic drugs were self-limiting; that is, prolonged administration resulted in a gradual diminution of their effectiveness. This problem was corrected through the use of intermittent diuretic therapy. Such a program of several days of diuresis followed by several days of drug withdrawal delayed refractoriness to the drug by preventing excessive disturbances in body electrolyte composition, for instance, drug interactions. Allergies anti-depressants anti-infectives anti-psychotics anti-smoking antibiotics asthma cancer cardio & blood cholesterol diabetes epilepsy gastrointestinal hair loss herpes hiv hormonal men's health muscle relaxers other pain relief parkinson's rheumatic skin care weight loss women's health allegra atarax benadryl clarinex claritin clemastine periactin phenergan pheniramine zyrtec anafranil celexa cymbalta desyrel effexor elavil, endep luvox moclobemide pamelor paxil prozac reboxetine remeron sinequan tofranil wellbutrin zoloft albenza amantadine aralen flagyl grisactin isoniazid myambutol pyrazinamide sporanox tinidazole vermox abilify clozaril compazine flupenthixol geodon haldol lamictal lithobid loxitane mellaril risperdal seroquel nicotine zyban achromycin augmentin bactrim biaxin ceclor cefepime ceftin chloromycetin cipro, ciloxan cleocin duricef floxin, ocuflox gatifloxacin ilosone keftab levaquin minomycin noroxin omnicef omnipen-n oxytetracycline rifater rulide suprax tegopen trimox vantin vibramycin zithromax advair aerolate, theo-24 brethine, bricanyl ketotifen metaproterenol proventil, ventolin serevent singulair arimidex casodex decadron eulexin femara levothroid, synthroid nolvadex provera, cycrin ultram vepesid zofran acenocoumarol aceon adalat, procardia altace atenolol amlodipine avapro caduet calan, isoptin capoten captopril hctz cardizem cardura catapres cilexetil, atacand clonidine, hctz combipres cordarone coreg coumadin cozaar dibenzyline diovan fosinopril hydrochlorothiazide hytrin hyzaar inderal ismo, imdur isordil, sorbitrate lanoxin lasix lercanidipine lopressor lotensin lozol micardis minipress moduretic normadate norpace norvasc plavix plendil prinivil, zestril prinzide ruthmol tenoretic tenormin trental valsartan hctz vaseretic vasodilan vasotec zebeta crestor lipitor lopid mevacor pravachol tricor zocor accupril actos alpha-lipoic acid amaryl avandia diamicron mr gliclazide metformin glucophage glucotrol glucotrol xl glucovance lyrica micronase orinase prandin precose starlix depakote dilantin lamictal neurontin sodium valproate tegretol topamax trileptal valparin aciphex asacol bentyl cinnarizine colospa compazine cromolyn sodium cytotec imodium motilium nexium nexium fast pepcid ac pepcid complete prevacid prilosec propulsid protonix reglan stugil zantac zelnorm zofran propecia, proscar famvir rebetol valtrex zovirax combivir duovir-n epivir pyrazinamide retrovir sustiva videx viramune zerit ziagen aldactone calciferol danocrine decadron prednisone provera, cycrin synthroid avodart flomax hytrin levitra propecia, proscar viagra lioresal soma tizanidine ibuprofen zanaflex accupril alpha-lipoic acid amantadine aralen arcalion aricept ascorbic acid benadryl bentyl betahistine calciferol carbimazole compazine cyklokapron ddavp, stimate detrol dihydroergotoxine ditropan dramamine exelon florinef imitrex imuran isoniazid lasix melatonin myambutol nimotop orap persantine piracetam pletal quinine rifampin rifater rocaltrol strattera ticlid tiotropium urecholine urispas urso vermox zyloprim acetylsalicylic acid advil, medipren celebrex flunarizine imitrex ketorolac maxalt ponstel tylenol ultram benadryl ditropan eldepryl requip sinemet trivastal advil, medipren arava colchicine decadron feldene indocin sr mobic naprelan naprosyn zyloprim betamethasone differin nizoral oxsoralen prograf retin-a xenical advil, medipren allyloestrenol clomid, serophene diflucan evista folic acid fosamax isoflavone nexium parlodel ponstel prevacid prilosec progesterone provera, cycrin rocaltrol tibolone generic dibenzyline generic name: phenoxybenzamine hcl ; qty and requip.
At this time, ryhmol is sent through registered mail, which provides delivery confirmation but not real-time tracking. 2004 Expert Consensus Guidelines Keck et al. ; : psychguides ecgs15 ; Bipolar Disorder Core Modules : psychiatrist bauer ; Depression and Bipolar Support Alliance : dbsalliance ; Griswold & Pessar, AFP, 2000. Kaye, JABF, July-August 2005. Kupfer, Bipolar Depression, 2004. NIMH, Bipolar Disorder : nimh.nih.gov Publicat bipolar ; psychCME Reports : psychcme CME Reports ; Suppes & Keck, Bipolar Disorder, 2005. Texas Implementation of Medication Algorithms project : dshs ate.tx mhprograms TIMABDalgos2005 and ropinirole!

Clinical governance provides the framework through which Sedgefield PCT is accountable for safeguarding and continuously improving the quality of its services. The PCT's Chief Executive is accountable for clinical governance. The clinical governance agenda is driven by the Healthcare Governance Committee, which is responsible for reviewing clinical governance arrangements across the health care community in our area, not just across the PCT. It receives regular reports on progress on various pieces of work. City and employs a significant number of tenants to operate the buildings' front desk services. CUCS, a provider of mental health and social services, is partner to BHC at all six of its housing sites. Goals and philosophy: The Rio offers permanent, affordable housing with on-site support services. A strong emphasis on self-sufficiency is supported by numerous employment opportunities and a focus on self-help approaches. Tenancy profile: Seventy-five single individuals and seven families reside at the Rio. Tenants range in age from infants to the elderly. All of the tenants were formerly homeless or marginally housed. Approximately 35 percent of the units are reserved for individuals with a serious mental illness. Physical description: The Rio is a five-floor elevator building, and each studio unit has a private bath and kitchenette. The two-bedroom apartments each have a full kitchen, bath, and living room. A laundry room is located within the building, and common spaces include an entry lounge, a garden roof deck, a penthouse with offices, a public meeting space, and an art gallery. Services description: On-site supportive services are available to all tenants and are intended to be flexible and based on individual need. Accepting services is not required as a condition of tenancy. Services include case management, education and employment assistance, relapse prevention services, psychiatric and health care services, assistance with activities of daily living, crisis intervention, parenting groups, cultural awareness programs, and recreational groups. The Rio, located in a neighborhood plagued by high drug activity, has onsite recovery support groups and AA and NA meetings. The use of alcohol is discouraged, although it is not prohibited except in public spaces. Use of illegal substances is prohibited on-site. Education is provided to all tenants regarding substance use, mental illness, and HIV disease. The Rio staff includes three case managers with supervision provided by a master's level social worker. Staff are on-site during the day, Monday through Friday. During nonbusiness hours, supportive services staff are on call. Eligibility criteria lease and occupancy agreement rent: All tenants sign a one-year renewable lease and pay 30 percent of their income for rent, which is often subsidized by Section 8. Abstinence is not a condition of eligibility and tretinoin and rythmol, for instance, rythmol drug.
Diagnosis of heart failure in the community how does echocardiography compare with BNP? G A Whalley, S P Wright, G D Gamble, H J Walsh, A Pearl, N Sharpe, R N Doughty. Department of Medicine, University of Auckland, Auckland. Background Recently, we have demonstrated the high negative predictive value and usefulness of N-BNP as a `rule out' test for diagnosis of heart failure HF ; in the community. This study aimed to determine whether common echo measurements of systolic and diastolic function could be used in a similar discriminative manner as NBNP. Methods Patients were recruited as part of the Natriuretic Peptides in the Community Study who presented to their primary care physician with HF symptoms dyspnoea oedema ; . They underwent clinical evaluation, N-BNP assay and echocardiography. The gold standard diagnosis of HF was the decision of an expert panel using ESC criteria. Receiver operating characteristics ROC ; curves were used to assess the N-BNP assay and echo variables as diagnostic tests for HF, first in the whole group and then in the group of patients with abnormal N-BNP 50 pmol l ; . Results 305 patients were included: 65% female, mean age 72 years SD 11.4 ; . Seventy seven 25% ; met the case definition of HF. 161 patients had N-BNP 50 pmol l, of whom 70 met the case definition of HF. No echo variable was superior to the N-BNP for the HF diagnosis and left atrial area was the best single measurement from the echo variables for the whole group. In the patients with abnormal N-BNP, both fractional shortening FS ; and mitral annular systolic velocity SM ; performed as well as N-BNP.

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The adult dose for prophylaxis is 250 mg atovaquone 100 mg proguanil 1 adult tablet ; orally once daily. From the 1Leiden University Medical Center, Department of Ophthalmology, Leiden, The Netherlands; and the 2Department of Ophthalmology and Visual Sciences, Coimbra University, Coimbra, Portugal. Submitted for publication April 11, 2001; revised July 18, 2001; accepted August 14, 2001. Commercial relationships policy: N. The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. 1734 solely to indicate this fact. Corresponding author: Martine J. Jager, Department of Ophthalmology, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands; m.j.jager lumc.nl, for example, propafenone.
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