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Dupixent - Regeneron
Dupixent - Regeneron

... Safety and efficacy of DUPIXENT have not been established in the treatment of asthma. Advise patients with comorbid asthma not to adjust or stop their asthma treatments without consultation with their physicians. ...
Pulmozyme® (dornase alfa) Inhalation Solution
Pulmozyme® (dornase alfa) Inhalation Solution

... In a randomized, placebo-controlled clinical trial in patients with FVC ≥40% of predicted, over 600 patients received Pulmozyme once or twice daily for six months; most adverse events were not more common on Pulmozyme than on placebo and probably reflected the sequelae of the underlying lung disease ...
FULL TEXT - Journal of Pre-Clinical and Clinical Research
FULL TEXT - Journal of Pre-Clinical and Clinical Research

... antagonism is not profitable from the clinical point of view. It is interesting that similar results were obtained with a ...
Neurology department Academic Half day Emergency Lecture
Neurology department Academic Half day Emergency Lecture

... paliperidone, perphenazine, and thioridazine. – ”Atypical" agents (less common) • Include aripiprazole, clozapine, olanzapine, quetiapine, risperidone, and ziprasidone. – Antiemetic drugs (eg, domperidone, metoclopramide, promethazine, prochlorperazine) – Usually develop during the first two weeks o ...
ccr5 antagonists in the treatment of treatment
ccr5 antagonists in the treatment of treatment

... infection. This is the first medication belonging to the new class of CCR5 antagonists, and the first approval of an oraly available drug in a new class since 1996. Yet another new class, the integrase inhibitors, are available in expanded access programs and are likely to become approved in 2007. T ...
kinetics.
kinetics.

... diazepam, amitriptyline). c) Activation of inactive drug. Few drugs (so called prodrugs) are inactive as such. They need conversion in the body to one or more active metabolites (e.g. levodopa, benfothiamine, enalapril, perindopril). The prodrug may offer advantages: their active forms may be more s ...
Update in Nephrology - American College of Physicians
Update in Nephrology - American College of Physicians

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Adverse reactions to drugs, BMJ 1998
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Carisoprodol (Soma) Finally Assigned DEA Scheduling (IV) and
Carisoprodol (Soma) Finally Assigned DEA Scheduling (IV) and

... into their final products. Nevertheless, a great deal of discussion has centered on the role of geranamine as primary constituent of Pump-It. Geranamine is also known as methylhexanamine, an old-time amphetamine-related stimulant and decongestant that is found naturally in the geranium plant, hence ...
Effects of Monotherapy and Combination Therapy with Inhibitors of
Effects of Monotherapy and Combination Therapy with Inhibitors of

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CoQ10 and Migraines By Lauren Griffiths
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Efficacy of Articaine over Lidocaine – A Review
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Diapositiva 1

... 2)Slatkin N. et al., 2009 – single dose, multicentric, doubleblind, randomized study; Advanced illness and opioid therapy, 154 patients Slatkin, N. et al., 2009. Methylnaltrexone for Treatment of Opioid-Induced Constipation in Advanced Illness Patients. The Journal of Supportive Oncology 7(1):39–46. ...
Prior Authorization Protocol ENTRESTO™ (sacubitril
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Protein Data Bank Advisory Committee
Protein Data Bank Advisory Committee

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Pharmaceutical care
Pharmaceutical care

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Drug disposition in pregnancy MEDSCI 722 Anna Ponnampalam
Drug disposition in pregnancy MEDSCI 722 Anna Ponnampalam

... Reviews, out of nearly 2,000 animal studies published in 2009, there was a bias toward the use of male animals in eight of 10 disciplines(Beery and Zucker 2011). Clinical trials are men-centric as well. Women made up less than one-quarter of all patients enrolled in 46 examined clinical trials compl ...
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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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