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Abnormal laboratory results Therapeutic drug monitoring: which
Abnormal laboratory results Therapeutic drug monitoring: which

Pharmacy Update on Dose Optimization Program
Pharmacy Update on Dose Optimization Program

... classified drugs to be added in this program, the majority of which have FDA approval for oncea-day dosing, have multiple strengths available in correlating increments at similar costs and are currently being utilized above the recommended dosing frequency. Prior authorization (PA) will be required ...
Samples of exam questions and answers
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... B) lower the incidence of adverse effects C) enhance activity against metabolically inactive mycobacteria D) delay the emergency of resistance 26. Concerning Isoniazid, all of the following statement are accurate, EXCEPT: A) it increase phenytoin plasma levels by inhibiting its liver metabolism B) ...
Antidepressant Drug Interactions - University of Iowa College of
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... such as tricyclic antidepressants, digoxin, warfarin, anticonvulsants, or theophylline. It is advised to observe clinically for side effects from such medications and to recheck serum blood levels of such medications as the dose of the antidepressant is titrated upwards. For example, patients who ar ...
Clinical pharmacology Academic year 2012/2013 Faculty of
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... presentations (in power point program) of the selected drug or process. Discussion about the presentation. The second of the classes: Lecture. Diversity of age and physiological condition of the patient, and its influence to the use of medication, due to the pharmacotherapy of newborns, pregnant wom ...
MEDICAL TREATMENT OF ALLERGIC RHINITIS
MEDICAL TREATMENT OF ALLERGIC RHINITIS

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... The antipsychotic drugs probably owe their therapeutic effects mainly to blockade of D2 receptors. The main groups, phenothiazines, thioxanthines and butyrophenones, show preference for D2 over D1 receptors; some newer agents (e.g. remoxipride) are highly selective for D2 receptors, whereas clozapin ...
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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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