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Antitussives and substance abuse Substance Abuse and Rehabilitation Dove press
Antitussives and substance abuse Substance Abuse and Rehabilitation Dove press

... Health report, which revealed that in 2006 around 3.1 million people in the United States aged 12–25 stated that they had used OTC cough and cold medicine to “get high.”2 Since the early 1990s, there have been numerous reports of codeine cough syrup abuse from India, Japan, People’s Republic of Chin ...
Myoclonus and seizures in progressive myoclonus epilepsies
Myoclonus and seizures in progressive myoclonus epilepsies

... PME are primarily anecdotal or observational, based on individual responses in very small groups of patients. In the present review, we summarize the results of the treatment of PMEs using a number of drugs (including AEDs) and procedures. The issues of designing and performing controlled clinical t ...
DOBUTamine
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... Treatment: To obtain up-to-date information about the treatment of overdose, a good resource is your certified Regional Poison Control Center. Telephone numbers of certified poison control centers are listed in the Physicians’ Desk Reference (PDR). In managing overdosage, consider the possibility of ...
Wrath Thor UNSIN
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New oral anticoagulants for stroke prevention in atrial fibrillation
New oral anticoagulants for stroke prevention in atrial fibrillation

... 15 to 30 ml/min despite the fact that such patients were excluded from the RE-LY trial, and that the efficacy and safety of this dose regimen has never been e­valuated in patients with atrial fibrillation. The approval of dabigatran etexilate as an alter­native to warfarin for stroke prevention in a ...
Valtrex - GlaxoSmithKline
Valtrex - GlaxoSmithKline

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Abuse Liability & Drug Scheduling: Role of FDA
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EFFECT OF THE GLOBAL VARIATION OF THEGENETIC BIOMARKER URIDINE DIPHOSPHATE
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... that prolong the QT interval independently of serum potassium concentration (eg, sotalol, dronedarone, ibutilide, propafenone). Therefore, combinations of drugs that can cause hypokalemia (eg, diuretics) and antiarrhythmic agents require vigilant monitoring of potassium and appropriate replenishment ...
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... namely bronchial smooth muscle and the inflammatory cells characteristic of bronchial infiltrates ¹ would allow the beneficial effects of theophylline to be obtained in the absence of cardiovascular, gastrointestinal, and central nervous system side-effects. Many such family-selective or ‘second-gen ...
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... chronic). The differentiation between acute (a single use event or occasional use) versus chronic (persistent, long-term, continued usage) is important to establishing reliable detection benchmarks. As a result, drug court practitioners should attempt to gather as much information as they can about ...
GLUCOVANCE (Glyburide and Metformin HCl) - Products
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Tips and Tricks for SG Procedures and GTL for Clinical Graphs
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... the sample mentioned above is a sophisticated multi-cell graph created using GTL. Here we will explore how you can create such a graph using the SGPLOT procedure. The primary motivation for the SGPLOT procedure is the easy creation of sophisticated single-cell graphs. As we have seen for the surviva ...
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AusPAR: Glycopyrronium (as bromide)

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An Epidemic of Clandestine Labs and Health Risk

... depression, sea sickness, sexual dysfunction, myasthenia gravis and asthma. In WWII, amphetamines were part of each soldier’s kit bag in the form of nasal sprays and Benzedrine tablets (Tripod.net). This kit was used by the Allied and Axis troops to improve soldiers’ performance. Japan was the first ...
Benzodiazepine usage in the North Eastern Health Board
Benzodiazepine usage in the North Eastern Health Board

... the benzodiazepine-related drugs zolpidem and zopiclone. The total average number of Defined Daily Doses (DDDs) per prescription items for all included drugs was for the period for 22 days supply. All the hypnotics had average number of DDDs per prescription higher than the recommend, for 14 days su ...
a review on sarpagandha
a review on sarpagandha

... view, dravya / rasa / vipaka / veerya could These hypothesis is proved to be be considered to be contextually important true in case of Sarpagandha as Reserpine than others, but in therapeutic application has reported many ADRs and also human all of them combinedly bring about the population have de ...
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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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