PHOSPHORYLATIONINK + -INDUCEDSUSTAINEDARTERIAL MUSCLE CONTRACIION BY PHORBOL DIBUTYRATE. K Barany, A. Rokolya, T.S. Guzeman, and M. Barany. Departments of Physiology and Biophysics and Biochemistry, College of Medicine, University of Illinois, Chicago, IL 60612. It is known that phosphorylation of the 20 kDa myosin light chain LC ; decreases during sustained K + -contraction of arterial smooth muscle. We have found that this dephosphorylation of LC can be prevented by addition of phorbol dibutyrate PDBu ; into the bath of the K + -contracted muscle at 2 min. This phenomenon was investigated by phosphopeptide analysis in order to identify the enzymes involved in the phosphorylation of LC. Recently, we observed Barany et al., BBA 1035. 165, 1990 ; that in a 1 2-min K + contracted muscle, about 95% of the peptides were phosphorylated by myosin light chain kinase MLCK ; and about 90% of the phosphate was incorporated into a serine residue. Essentially, the same phosphopeptide pattern was found in 60-min K + -contracted muscle. On the other hand, in 60-min PDBu-contracted muscle 25-40% of the phosphopeptides were attributed to protein kinase C PKC ; phosphorylation and 60-75% to MLCK phosphorylation. When the muscle was treated with K + for 2 min and subsequently with K + and PDBu for 60 min, LC phosphorylation was much higher than in muscles treated with K + alone for 62 min or with PDBu alone for 60 min. Both MLCK- and PKC-induced phosphorylations contributed to this higher level. Furthermore, the pattern of MLCK-catalyzed phosphorylation changed so that instead of a selective serine phosphorylation, considerable threonine phosphorylation occurred as well. Such a switch from serine to threonine phosphorylation in K + PDBu treated muscle could be reproduced in vitro: LC was first phosphorylated by PKC and subsequently by MLCK. The results indicate an interrelationship between PKC and MLCK phosphorylated sites of LC in intact arterial smooth muscle. Supported by AHA and NIH, AR 34602.
In many ways pharmaceutical crime can be viewed as a natural extension or `business diversification' ; of illicit narcotic and psychotropic drug manufacturing and distribution. Experience with illicit narcotic and psychotropic production lends itself to increasing sophistication in clandestine manufacture of medicinal products. With respect to illicit API production, a strong indicator of API counterfeiting is the existence of very small companies with around fifty employees ; that claim to manufacture hundreds of different APIs and sell them under their own label as if being manufactured by that company. Where do counterfeit medicines placed on the European market originate from? Organised criminal gangs from the former Soviet Union and Balkans are known to be involved in the pharmaceutical crime business and manufacturing sites are either within these regions or outside Europe, sited in countries such as China and India that have weak pharmaceutical regulatory and enforcement structures. As Box 5 shows see p. 11 ; , pharmaceutical crime is a creative business. Pharmaceutical criminals take maximum advantage of the deficiencies and loopholes in the international pharmaceutical trading, regulatory, legislative and administrative systems. Pharmaceutical crime is assisted by increasing sophistication in clandestine manufacture and a lack of knowledge and understanding by authorities of the `pharmaceutical crime business model'. As stated in the essay `Europe needs an FBI', `if details of organised crime operations in Europe are vague it is because they are so by definition organised gangs keep themselves hidden, hence information about them is scarce. Many base, for example, medications.
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Abacavir, acyclovir, Adriamycin, aerosolized pentamidine, Agenerase, aminosalicylic acid, amprenavir, Aptivus, atazanavir sulfate, atovaquone * , Atripla, azithromycin, AZT Bactrim, Biaxin, cidofovir, clarithromycin, Cleocin, Clinda-Derm, clindamycin, clotrimazole, Combivir, Cotrim, Crixivan, cyloserine, Cytovene * d4T, dapsone, Daraprim, darunavir, daunorubicin citrate, DaunoXome, ddC, ddI, delavirdine, didanosine, Diflucan, Doxil, doxorubicin HCI, efavirenz, Emtriva, emtricitabine, enfuvirtide * , Epivir, epoetin alfa * , Epogen * , Epzicom, ethambutol, ethionamide famciclovir, Famvir, Fansidar, filgrastim * , fluconazole, fomivirsen sodium intravitreal injectable * , Fortovase, fosamprenavir calciumH, foscarnet * , Foscavir * , Fuzeon * ganciclovir * Hivid indinavir, interferon alfa-2b, 2a, intraconazole, Intron A, Invirase, isoniazid Kaletra, ketoconazole lamivudine, leucovorin, levofloxacin, Levoquin, Lexiva, lopinavir Mepron * , Microsulfon, Myambutol, Mycelex, Mycobutin Nebupent, nelfinavir , Neupogen * , Neutrexin, nevirapine, Nizoral Norvir, Nydrazid PASER, Prezista, Procrit * , pyrazinamide, pyrimethamine Rescriptor, Retrovir, Reyataz, rifabutin, Rifadin, Rifamate, rifampin, Rifater, Rimactane, ritonavir, Roferon A, Rubex saquinavir, Septra, Seromycin, Sporanox, stavudine, streptomycin, sulfa trimethoprim, sulfadiazine, Sustiva 3TC, T20 * , tenofovir, tipranavir, Trecator, trimetrexate glucuronate, Trizivir, Truvada valacyclovir, Valcyte, valganciclovir HCl, Valtrex, Videx, Viracept, Viramune, Viread, Vistide, Vitravene * , zalcitibine, Zerit, Ziagen, zidovudine, Zithromax, Zovirax Notes: * Prior authorization required. * Very expensive drug. Please use only as last resort. Use may generate a utilization review contact from CAREAssist Provider Panel. Generic substitution will occur whenever available. All drugs must be transmitted through CAREAssist s on-line claims processor. CAREAssist cannot pay for drugs that are eligible for reimbursement from another source such as Medicare or Medicaid. CAREAssist provides prescription drugs only, over-the-counter medications are not covered and nicotine.
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Large groups of people found that those with higher vitamin D levels also had lower rates of cancer. For some of these studies, doctors had blood samples to measure vitamin D, making the findings particularly strong. Even so, these studies aren't the gold standard of medical research - a comparison over many years of a large group of people who were given the vitamin with a large group who didn't take it. In the past, the best research has deflated health claims involving other nutrients, including vitamin E and beta carotene. Lab and animal studies show that vitamin D stifles abnormal cell growth, helps cells die when they are supposed to, and curbs formation of blood vessels that feed tumors. Cancer is more common in the elderly, and the skin makes less vitamin D as people age. Blacks have higher rates of cancer than whites and more pigment in their skin, which prevents them from making much vitamin D. Vitamin D gets trapped in fat, so obese people have lower blood levels of D. They also have higher rates of cancer. Diabetics, too, are prone to cancer, and their damaged kidneys have trouble converting vitamin D into a form the body can use and nortriptyline, because boehringer ingelheim.
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Source: Wong D, Shumack S. HIV and skin disease. In: Stewart G ed. ; . Managing HIV. Sydney: Australasian Medical Publishing Company, 1997: 105 and pamelor.
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CERTIFICATE To the members of GlaxoSmithKline Pharmaceuticals Limited We have examined the compliance of the conditions of Corporate Governance by GlaxoSmithKline Pharmaceuticals Limited for the year ended 31st December 2003 as stipulated in clause 49 of the Listing Agreements of the said Company with stock exchanges in India. The compliance of conditions of Corporate Governance is the responsibility of the Companys Management. Our examination was limited to the procedures and implementation thereof, adopted by the Company for ensuring the compliance of the conditions of Corporate Governance. It is neither an audit nor an expression of an opinion on the financial statements of the Company. In our opinion and to the best of our information and according to the explanations given to us, the Company has complied with the conditions of Corporate Governance as stipulated in the above mentioned Listing Agreements. We state that in respect of investor grievances received during the year ended 31st December 2003, no investor and orap.
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Cd4 counts increased by an average of 34 cells among those who remained on sustiva, compared to an average decrease of 8 cells among those who switched to viramune.
Medical accuracy. Although Boehringer Ingelheim had similarly had no direct influence as to who should receive the review it had agreed to the quantity to be mailed. The guest editor had had no contact with anyone from Boehringer Ingelheim. The review had not been used by Boehringer Ingelheim for promotional purposes it had only been mailed by the agency to health professionals. The Panel noted the content of emails sent between Boehringer Ingelheim and the agency when the two were discussing potential sponsorship of the abstract review. Reference was made by the agency to `educational clinical communications to support your objectives with Viramume and Tipranavir' and by Boehringer Ingelheim to `abstract books etc for both Vi4amune and Tipranavir'. A copy of the brief, which appeared to have been given to the guest editor, was provided. The brief stated that `In addition to subsidising the production of a text that honestly and usefully reports the latest news on the Sponsor's products, the Sponsor expects to see negative as well as positive information reported concerning its products'. The Panel considered that Boehringer Ingelheim would thus have expected some information on its products to appear in the abstract review in return for its sponsorship. The brief further stated that `The Sponsor also expects to see relevant news concerning other therapies of interest that and orinase.
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VAGISTAT - 1 valacyclovir . VALCYTE . valproate . valproic acid . vancomycin . vasopressin VELCADE VEPESID . verapamil . verapmil ER VESANOID . VFEND . VIDEX . VIOKASE . VIRACEPT . VIRAMUNE . VIREAD . VIVACTIL . VYTORIN.
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Bactrim Bactrim DS Biaxin Biaxin Xl Biaxin Xl Pac Bicillin C-R Bicillin L-A Cedax Cefaclor Cefaclor ER Cefadroxil Cefazolin Sodium Cefazolin Sodium-Dextrose Cefizox Cefizox in Dextrose Cefotaxime Sodium Cefoxitin Cefoxitin Sodium Cefpodoxime Proxetil Cefprozil Ceftazidime Ceftin Ceftriaxone in Iso-Osmotic D Ceftriaxone Sodium Ceftriaxone Dextrose Cefuroxime Axetil Cefuroxime Sodium Cefuroxime Dextrose Cefzil Cephalexin Cephalexin Cephalexin Monohydrate Chloramphenicol Sodium Succinate Chloromycetin Cipro Cipro I.V. 200mg, 1200mg ; Cipro I.V. 400mg ; Cipro I.V. in D5W Cipro XR Ciprofloxacin Tablets, 400 mg Injection ; Claforan Claforan D5W Clarithromycin Cleocin Capsule, Cream ; Cleocin Injection, Suppository ; Cleocin Pediatric Granule B B B Cleocin Phosphate Clindamax Clindamycin HCl Clindamycin Phosphate Clindesse Colistimethate Sodium Coly-Mycin S Coly-Mycin-M Cubicin Declomycin Demeclocycline HCl Dicloxacillin Sodium Dispermox Doryx Doxy-Caps Doxycycline Hyclate Doxycycline Monohydrate Duricef Dynabac D5-Pak Dynacin 100mg Capsule ; Dynacin 75mg Capsule, Tablet ; E.E.S. Suspension for Reconstitution ; E.E.S. Suspension, Tablet ; E-Mycin Eryc Eryped Eryped 200 Eryped 400 Ery-Tab Erythrocin Erythrocin Lactobionate Erythrocin Stearate Erythromycin Erythromycin Base Erythromycin DR Erythromycin Ethylsuccinate Erythromycin Lactobionate Erythromycin Stearate Erythromycin Sulfisoxazole Factive Flagyl Flagyl ER Floxin Fortaz 1gm Injection, 2gm Injection, 6gm Injection ; Fortaz 2gm 50mL Injection, 500mg Injection ; Fortaz Galaxy B G G Fortaz Infusion Pack Furadantin Gantrisin Pediatric Garamycin Gentamicin Sulfate Gentamicin Sulfate Sodium 60mg Injection, 80mg Injection, 100mg Injection ; Gentamicin Sulfate Sodium 70mg Injection, 90mg Injection ; Geocillin Hiprex Humatin Invanz Isotonic Gentamicin Kanamycin Sulfate Keflex 250mg Capsule, 500mg Capsule, Suspension for Reconstitution ; Keflex 750mg Capsule ; Ketek Ketek Pak Levaquin Injection ; Levaquin Tablet ; Levaquin Leva-Pak Levaquin Premix Lincocin Lorabid Macrobid Macrodantin Mandelamine Mandol D5W Maxipime Mefoxin Mefoxin Add-Vantage Mefoxin in Dextrose Merrem Methenamine Hippurate Methenamine Mandelate Metro I.V. Metrogel Vaginal Metronidazole Metronidazole in NaCl MHP-A Minocin Minocycline HCl Monodox Monurol Myrac Nafcillin Sodium 1gm Injection, 2gm Injection, 10gm Injection ; B B B Nafcillin Sodium 200gm Injection ; Nallpen Iso-Osmotic in Dextrose Nallpen Dextrose Nebcin Nebcin MDV Neggram Neo-Fradin Neomycin Sulfate Neutrexin Nitrofurantoin Nitrofurantoin Macrocrystalline Nitrofurantoin Monohydrate Noroxin Ofloxacin Omnicef 125mg 5mL Suspension for Reconstitution ; Omnicef 250mg 5mL Suspension for Reconstitution, Capsule ; Omni-Pac Oracea Oxacillin Sodium Panixine Disperdose Paromomycin Sulfate PCE Pediazole Penicillin G Potassium Penicillin G Procaine Penicillin G Sodium Penicillin V Potassium Pentam 300 Pentamidine Isethionate Periostat Pfizerpen-G Piperacillin Sodium Pipracil D5W Polymyxin B Sulfate Primaxin I.M. Primaxin I.V. Primaxin I.V. Add-Vantage Primsol Proloprim Proquin XR Prosed EC Prosed Ds Atropine Free ; Raniclor Rocephin 10gm Injection, 250mg Injection, 500mg Injection ; Rocephin 1gm Injection, 2gm Injection ; Rocephin in Iso-Osmotic D B B B Septra Septra DS SMZ-TMP DS Solodyn Spectracef Streptomycin Sulfate Sulfadiazine Sulfamethoxazole Trimethoprim Sulfatrim Sulfisoxazole Sumycin Syrup ; Sumycin Tablet ; Suprax Synercid Tazicef 1gm Injection, 2gm Injection, 6gm Injection ; Tazicef 1gm 50mL Injection, 2gm 50mL Injection ; Tetracycline HCl Timentin Tobi Tobramycin Sulfate Tobramycin Sulfate ADD-Vantage Tobramycin Sulfate Flipto Tobramycin Sulfate Sodium Trac Trimethoprim Trimethoprim Sulfamethoxazole Trimox Tygacil Unasyn Unasyn Add-Vantage Unasyn Bulk Pack Unasyn Piggyback Unit Urelle Uretron D S Urex Urimar-T Urin D S Urinary Antiseptic #2 Urinary Antiseptic F.C. Urised Uriseptic Urisym Uritact DS Uritact-EC Uro Blue Urogesic-Blue B B G B Uroqid #2 Usept Uta Utira Utrona Vancocin HCl Capsule ; Vancocin HCl Injection ; Vancocin HCl Iso-Osmotic Vancomycin HCl Vandazole Vantin Veetids Velosef Vibramycin Vibratab Xifaxan Zinacef 1.5gm Injection, 750mg Injection ; Zinacef 7.5gm Injection ; Zinacef D5W Zithromax Injection, Packet ; Zithromax Suspension for Reconstitution, Tablet ; Zithromax Tri-Pak Zithromax Z-Pak Zmax Zosyn Zyvox B G B Fluconazole in NaCl Fungizone Grifulvin V Suspension ; Grifulvin V Tablet ; Griseofulvin Microsize Griseofulvin Ultramicrosize Gris-Peg Gynazole-1 Itraconazole Ketoconazole Lamisil Miconazole 3 Monistat 3 Monistat 7 Combination PA Mycamine Mycelex Nizoral Nystatin RA Clotrimazole 3 SB Miconazole 3-Day Combo Sporanox Capsule ; Sporanox Kit ; Sporanox Solution ; Sporanox Pulsepak Terazol 3 Cream ; Terazol 3 Suppository ; Terazol 3 w Applicator Cream ; Terazol 7 Terconazole Terconazole Vaginal Vagistat-1 Vagistat-3 Vfend Vfend I.V. Zazole G B B Agenerase Capsule ; Agenerase Solution ; Aptivus Atripla Combivir Crixivan Didanosine Emtriva Epivir Epivir HBV Epzicom Fuzeon Hivid Invirase Kaletra Lexiva Norvir Prezista Rescriptor Retrovir Capsule ; Retrovir Syrup, Tablet ; Retrovir I.V. Infusion Reyataz Sustiva Trizivir Truvada Videx Solution for Reconstitution ; Videx EC Viracept Viramun4 Viread Zerit.
UNIRETIC . 20 unithroid . 45 UNIVASC. 20 URINARY ANTI-INFECTIVES . 46 URINARY ANTISPASMODICS . 46 URISPAS . 46 UROCIT-K . 37 UROXATRAL . 37 ursodiol . 36 VACCINES . 46 VAGIFEM. 47 VAGINAL PRODUCTS. 47 VALCYTE . 24 valproic acid . 13 VALTREX . 25 VANCOCIN . 20 vancomycin. 20 VANTIN. 27 VARIVAX . 47 VASERETIC . 20 VASOTEC. 20 veetids . 44 VELOSEF . 27 VENTOLIN HFA. 12 verapamil hcl. 27 VERMOX . 11 VESANOID . 22 VESICARE. 46 VFEND. 17 VICODIN. 10 VICOPROFEN . 10 VIDEX . 25 VIGAMOX . 43 VIOKASE . 34 VIRACEPT . 25 VIRAMUNE . 25 VIREAD . 25 VIROPTIC. 43 VISTARIL. 11 VITAMINS-THERAPEUTIC . 47 VIVELLE . 36 VOLTAREN . 9, 43 VOLTAREN-XR . 9 VYTONE . 33 VYTORIN. 18 warfarin sodium. 13 and
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The complete text of the jnc vi report will be published in the november 25 issue of the archives of internal medicine, a journal of the american medical association.
In the case of these two drugs, people are about as likely to experience some kind of side effect on one as the other 22 percent on sustiva; 27 percent on vidamune and ondansetron.
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The problem of these `misconnection' errors where a drug intended to be given by one route is erroneously given by another ; can be conceptualised in different ways. In this scenario, the focus is on ineffective labelling and packaging and the incident was categorised by risk managers as `mixed'. In the tablets scenario, the focus was on the lack of knowledge demonstrated by the nurse and the incident was categorised by risk managers as `human error.' Clearly, human factors issues need addressing in current NHS risk initiatives.
RADIATION SAFETY MANUAL V. 1.3 ; Date: 5 30 2007 MUHC Licenses for Nuclear Substances and Devices 3.2.1. There are four CNSC licenses for Nuclear Substances and Radiation Devices at the MUHC. These are: 1- Consolidated use of nuclear substances Group 3.1 ; , license No. 01185-13-08.X, valid until November 30, 2008 2- Therapeutic Nuclear Medicine Group 2.4 ; , license No. 01185-3-11.X, valid until November 30, 2011 3- Diagnostic Nuclear Medicine Group 2.4 ; , license No. 01185-2-11.X, valid until November 30, 2011 4- Irradiation: self-shielded type Group 2.3 ; , license No. 01185-18-08.X, valid until to August 31, 2008 The licenses are valid for the period indicated above unless otherwise suspended, amended, revoked or replaced. Each license includes a list of conditions that shall be met by the licensee and subject to inspections or audits by the Commission on a periodic basis. Also, the licensee shall submit to the CNSC a written annual compliance report in a form acceptable to the Commission. Failure to comply with the all the regulations might result in the licenses being suspended or revoked by the Commission. 3.2.2. Copies of the MUHC licenses are given in Appendix 1 and include all the conditions that need to be met for compliance with the CNSC regulations. These conditions serve as a basis for the policies developed in this manual for the consolidated use of nuclear substances. This manual also includes policies that meet or exceed the conditions for all licenses listed above. Copies of the licenses are available from the RPS at the MUHC.
Interactions Between Opioids and Protease Inhibitors Non-Nucleoside Reverse Transcriptase Inhibitors NNRTI's ; Narcotic Route of Metabolism1 Mild-Moderate Enzyme Inhibitors Atazanavir-Reyataz2; Delavirdine-Rescriptor3; Fosamprenavir-Telzir4; Indinavir-Crixivan5; Nelfinavir-Viracept6; Saquinavir-Invirase7; Efavirenz-Sustiva * 8 concentrations.21 Interaction not clinically significant. Potent Enzyme Inhibitors Ritonavir - Norvir9; Lopinavir Ritonavir Kaletra10 Enzyme Inducers Nevirapine Viramune11 Efavirenz-Sustiva * 8 Tipranavir-Aptivus12.
Boehringer ingelheim further intensifies fight against aids - may 19, 2007 medical news today press release ; , in order to further improve access to its anti-hiv drug viram8ne nevirapine ; in developing countries boehringer ingelheim has amended its policy of boehringer ingelheim initiates international head-to-head hiv aids and
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Viramune directly inhibits the activity of reverse transcriptase and blocks the production of dna and new viruses.
Children will take Fortovase, Zerit, Videx, Epivir, Viramune, Viracept, Norvir and hydroxyurea. Children stay in the hospital for 2 weeks and have multiple blood tests done. Then, a study nurse will come to the child's home twice a day for 6 weeks to give the child the study medications.
2003 oct; 13 10 ; : 459, 463-4, 468-9, virxmune [ nevirapine] is not approved for multiple-dose postexposure prophylaxis.
S1 S2 S3 S10 S11 S12 S13 S14 S15 S16 S17 S18 S19 S20 S21 S22 "ANGINA PECTORIS" "ANGIOPLASTY, TRANSLUMINAL, PERCUTANEOUS CORONA" "CORONARY ARTERY BYPASS" S1 OR S2 "COSTS AND COST ANALYSIS" "COST-BENEFIT ANALYSIS" ECONOMIC ; EVALUATION OR ANALYSIS ; TI COST ; EFFECTIVE? TI "HOSPITAL COSTS" HEALTH RESOURCES "HEALTH RESOURCES" S5-S9, S10 S5-S9, S11 S4 AND S13 S14 HUMAN, ENG S3-S11 DT "LETTER" DT "EDITORIAL" S16-S18 S15 NOT S19 S20 1985-1991 S21 unique items.
Whether you've just started therapy or have been on therapy for several months or years, side effects are a major reason for switching therapies. If you recently started anti-hiv combination therapy and are experiencing a severe side effect uncontrollable and persistent diarrhea, for example ; you can talk with your doctor about switching the offending drug for another drug that is similar in potency strength ; and associated with fewer or different side effects. The same holds true if you've been receiving therapy for a while, have an undetectable viral load, but are experiencing a debilitating long-term side effect. A perfect example is lipodystrophy, a possible sideeffect of anti-hiv therapy that can lead to disfiguring body-shape changes, along with increased levels of fats triglycerides and cholesterol ; and sugar glucose ; in the blood. While the jury is still out regarding the exact cause of this problem, many researchers believe that it is a common side effect of most of the pis, with the possible exception of Reyataz atazanavir ; . Some research has shown that switching the protease inhibitor for an nnrti e.g., Virxmune nevirapine ; or Sustiva efavirenz might help reduce the severity of lipodystrophy. It is also believed that some of the nucleoside reverse transcriptase inhibitors nrtis ; -- particularly Zerit d4T ; --are responsible for the loss of fat in the arms, legs, and face of some people with hiv, a condition known as lipoatrophy. Some reports suggest that switching Zerit for another nrti, most notably Epivir 3TC ; , Ziagen abacavir ; , or Viread tenofovir df ; , may help prevent further loss of fat, but may not necessarily help restore the fat that was lost.
Reimbursed under the durable medical equipment "DME" ; provisions of Medicare Part B. See 42 U.S.C. 1395 et. seq. ; Because the.
Phrma publications policy 2002-04-19.391 16 ; G.D. Lundberg, A. Flanagin, New requirements for authors: signed statements of authorship responsibility and financial disclosure, "JAMA", n. 262, 1989, p. 2003-2004 17 ; E. Wager, How to dance with porcupines: rules and guidelines on doctors' relations with drug companies, "BMJ", n. 326, 2003, p. 1196-8 18 ; R. Smith, Medical journals and pharmaceutical companies: uneasy bedfellows, "BMJ", n.326, 2003, p. 1202 19 ; S. Gottlieb, Congress criticises drugs industry for misleading advertising, "BMJ", n. 325, 2002, p. 137 20 ; M.S. Wilkes, B.H. Doblin, M.F. Shapiro, Pharmaceutical advertisements in leading medical journals: experts' assessments, "Ann Intern Med", n. 116, 1992, p. 912-9 21 ; P. Villanueva, S. Peiro, J. Librero, I. Pereiro, Accuracy of pharmaceutical advertisements in medical journals, "Lancet", n. 361, 2003, p. 27-32 22 ; M. Egger, C. Bartlett, P. Jni, Are randomised controlled trials in the BMJ different?, "BMJ", n. 323, 2001, p. 1253 23 ; P.A. Rochon, J.H. Gurwitz, M. Cheung, J.A. Hayes, T.C. Chalmers, Evaluating the quality of articles published in journal supplements compared with the 9.
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Newt : hello joel until recently, many studies were done using sustiva, but not viramune, as first-line therapy, which secured its status as the preferred starter nnrti.
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