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Improving survival in pulmonary arterial hypertension EDITORIAL M. Humbert
Improving survival in pulmonary arterial hypertension EDITORIAL M. Humbert

... collect data from 32 centres on patients diagnosed by uniform criteria as having so-called primary pulmonary hypertension [7, 8]. Between July 1, 1981 and September 30, 1985, 194 patients were entered into the NIH registry, providing the first multicentre, detailed clinical and haemodynamic descript ...
Positron Emission Tomography Imaging: A Quantitative Biomarker in
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... Welcome to the New American Pharmaceutical Review Website - the Review of American Pharmaceutical Business and ...
ProCare HospiceCare Medicare Part D and the Hospice Patient
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... Preventing Part D Payment for Hospice Drugs Hospice programs, as specified in section 1861(dd) of the Social Security Act and in Federal regulations at Part 418, must provide individuals under hospice care with drugs and biologicals related to the palliation and symptom management of the terminal il ...
glucovision - Canadian Association of Nuclear Medicine
glucovision - Canadian Association of Nuclear Medicine

... lung neoplasms.A total of 99 patients evaluated were visually observed during PET scan for evidence of adverse events. No adverse events were observed. A single-centre prospective study was conducted in oncology patients to evaluate the safety of fludeoxyglucose F-18. Three hundred and twelve adult ...
Dabigatran
Dabigatran

... Comparison of Oral Antithrombotics. Pharmacist's Letter. 2012; 28(1):280102. Dentali F, Riva N, Crowther M, et al. Efficacy and safety of the novel oral anticoagulants in atrial fibrillation: a systematic review and meta-analysis of the literature. Circulation 2012; 126:2381. Guyatt GH , Akl EA, Cro ...
The Seventh Report of the Joint National Committee on
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enrofloxacin - Ballston Spa Veterinary Clinic
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Enhancing adherence in clinical research
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01/27/2012 - The Medical University of South Carolina
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... presence of cardiac or extracardiac events or when compliance to medical therapy is inadequate. These conditions represent a cause of increasing hospital admissions and readmissions as well as of a high mortality. Patients presenting with an acute decompensation of chronic congestive heart failure f ...
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Milk Thistle: Hepatoprotection at its Best
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gefitinib - Cancer Care Ontario
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... Dosage with Hepatic Impairment: Increased gefitinib exposure has been reported in patients with moderate and severe hepatic impairment due to cirrhosis.  Dose adjustment is not required, but use with caution and monitor closely. Exercise caution in patients with mild to moderate changes in liver fun ...
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... almitrine also stimulates external ventilation through stimulation of peripheral chemoreceptors [1, 3]. Our study shows that almitrine causes a submaximal Pao~ improvement 2 and 3 h after a single lOO mg oral dose in COPD patients, but also that there are large inter-individual variations in the res ...
Rodos Biotarget moves into larger laboratory and production facility
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... Rodos Biotarget GmbH is a biopharmaceutical company that joins the ranks of industry leadership in nanocarriers for drug delivery. Rodos has developed the versatile TargoSphere® platform technology comprising biocompatible and biodegradable nanocarriers. These are designed to achieve enhanced prophy ...
New Drugs and Formulations: Effect on Therapeutic Paradigms
New Drugs and Formulations: Effect on Therapeutic Paradigms

Article: Managing Arthritis and Joint Inflammation, Naturally
Article: Managing Arthritis and Joint Inflammation, Naturally

... users (1). In the U.S., side effects from these drugs are associated with 10,000 – 20,000 deaths per year (2). Even the new COX-2 inhibitor drugs may only reduce intestinal tract damage by 50% (3). NSAIDS also encourages erosion of joint cartilage, which accelerates the arthritic process (4). They a ...
Application and Utility of Pharmacogenetics in the Clinical Laboratory
Application and Utility of Pharmacogenetics in the Clinical Laboratory

... acids in the normal protein sequence, which may lead to altered or abrogated protein function. These events that may also cause a shift in the reading frame of a DNA sequence, thereby altering the transcribed codon sequence. Therefore, when a frameshift occurs during protein translation, the end pro ...
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Bad Pharma



Bad Pharma: How Drug Companies Mislead Doctors and Harm Patients is a book by British physician and academic Ben Goldacre about the pharmaceutical industry, its relationship with the medical profession, and the extent to which it controls academic research into its own products. The book was published in September 2012 in the UK by the Fourth Estate imprint of HarperCollins, and in February 2013 in the United States by Faber and Faber.Goldacre argues in the book that ""the whole edifice of medicine is broken"" because the evidence on which it is based is systematically distorted by the pharmaceutical industry. He writes that the industry finances most of the clinical trials into its own products and much of doctors' continuing education, that clinical trials are often conducted on small groups of unrepresentative subjects and negative data is routinely withheld, and that apparently independent academic papers may be planned and even ghostwritten by pharmaceutical companies or their contractors, without disclosure. Goldacre calls the situation a ""murderous disaster,"" and makes suggestions for action by patients' groups, physicians, academics and the industry itself.Responding to the book's publication, the Association of the British Pharmaceutical Industry issued a statement arguing that the examples the book offers are historical, that the concerns have been addressed, that the industry is among the most regulated in the world, and that it discloses all data in accordance with international standards.In January 2013 Goldacre joined the Cochrane Collaboration, British Medical Journal and others in setting up AllTrials, a campaign calling for the results of all past and current clinical trials to be reported. The British House of Commons Public Accounts Committee expressed concern in January 2014 that drug companies were still only publishing around 50 percent of clinical-trial results.
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