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Exane BNP Paribas Pharma Conference
Exane BNP Paribas Pharma Conference

... The manager responsible for preparing the company’s financial reports Fritz Squindo declares, pursuant to paragraph 2 of Article 154-bis of the Consolidated Law on Finance, that the accounting information contained in this press release corresponds to the document results, books and accounting recor ...
THE SAFETY PHARMACOTHERAPY DURING PREGNANCY
THE SAFETY PHARMACOTHERAPY DURING PREGNANCY

... C- Either studies in animals have revealed adverse effects on the fetus ( teratogenic or embryocidal, or other ) and there are no controlled studies in women or studies in women and animals are not available. Drugs should be given only if the potential benefit justifies the potential risk to the fet ...
to view the slides
to view the slides

... intake of rescue or concomitant medication, inevaluable tumor assessment, switch to new antineoplastic therapy (ANP), death etc. Treatment discontinuation due to lack of efficacy ...
An Overview of the Pharmaceutical Development Process
An Overview of the Pharmaceutical Development Process

PPT - ACoP7
PPT - ACoP7

... Conc (ng/mL) ...
How everything began - Departamentos e GEs
How everything began - Departamentos e GEs

... respect, their results confirm indirect evidence, from a casecontrol study [24] and in secondary analysis of clinical trials [25,26] that has implicated short-acting calcium antagonists in an increased risk of MI. Similarly, a trial with African-American patients with hypertensive renal disease show ...
Is It Making a Difference? [PDF, 8.72MB]
Is It Making a Difference? [PDF, 8.72MB]

... recommended approval for parecoxib at a single dose only, because of concerns about the safety of multiple doses. ADRAC has, to date, received 20 reports of adverse reactions associated with parecoxib, and 13 of these involved renal impairment with elevated creatinine and/or oliguria, including four ...
Pharmacology 120
Pharmacology 120

... (antagonist) (i.e. SSRIs block removal of serotonin from receptor sites – more serotonin available to cell, less depression) Almost all drugs lack specific and selective effects; those which are specific (such as penicillin) are said to have selective toxicity. These other effects may be desirable o ...
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... 5. A brief summary of the study including the purpose, hypothesis, number of subjects, patient population, condition or disease (if applicable), dose, route, and duration of substance administration, and endpoint measures. 6. A copy of the protocol 7. A brief explanation of why you consider the subs ...
Dr. Sitar's presentation
Dr. Sitar's presentation

... disease y Please see your health care worker for ...
Common types of clinical trial design, study objectives
Common types of clinical trial design, study objectives

... • Statistics looks at design and analysis • Our exercise noted an example of a flawed design (single sample, uncontrolled, biased population selection, regression to the mean) • And statistical theory can be used to understand the reason for the results • Not a completely outrageous example ...
Conclusion - Shodhganga
Conclusion - Shodhganga

... guna. So in the trial drug, Sunthi siddha Godugdha as Anupana found very effective, as Sunthi is the best Ama pachaka. Here the Anupana adds the extra result with the trial drug. This work was done by keeping in view all the caution. In spite of that, there may be the chance of bios in research and ...
PowerPoint-esitys
PowerPoint-esitys

... For categories B and C, a detailled numerical information on the magnitude of dosage modification is provided whenever available. ...
US Results for End of Phase II Meeting Modified Endometriosis
US Results for End of Phase II Meeting Modified Endometriosis

... This presentation contains forward-looking statements and information regarding the future performance and actions of Repros Therapeutics Inc. (RPRX) that involve risks and uncertainties that could cause actual results and actions to differ materially. These risks include those discussed in this pre ...
Dr. Michael Sinz zpresentation
Dr. Michael Sinz zpresentation

... Don’t’ wait until your get boils the size of fondue pots.” Consumer: “Boy, that Varvacron sounds pretty good.” Then the TV announcer lists the potential side effects and drug interactions. TV announcer: “In some patients, Varvacron causes stomach discomfort and growth of an extra hand coming out of ...
Fact Sheet - BioMolecular Products
Fact Sheet - BioMolecular Products

... Lym-X-Sorb™ (Lymphatic Xenobiotic AbSorbability), winner of the 2004 Eurand Award, is a unique drug delivery with controlled release. Lym-X-Sorb™ was developed as an analogue to the basic products of fat digestion by David W. Yesair, PhD., founder of BioMolecular Products, Inc. Dr. Yesair first desc ...
TIMOPTOL
TIMOPTOL

... vision and night blindness produced by miotics are not evident. In addition, in patients with cataracts the inability to see around lenticular opacities when the pupil is constricted by miotics is avoided. When changing patients from miotics to TIMOPTOL a refraction might be necessary when these eff ...
lec#8 done by Ghaida`a Abuzahra and Nahla
lec#8 done by Ghaida`a Abuzahra and Nahla

Withdrawal from long-term benzodiazepine treatment
Withdrawal from long-term benzodiazepine treatment

... withdrawal was gradual, double-blind, and placebo-controlled. The patients were recruited over one year and allocated at random to two groups, A and B. Both groups continued with their drugs, at full dosage,for the first two weeks; group A was then reduced to halfthe dose for a further two weeks bef ...
article pdf - ONdrugDelivery
article pdf - ONdrugDelivery

... Surgery at the University of Kentucky, served on the faculty of Tufts University, and worked as a Pharmaceutical Scientist at Hoffman-La Roche. Dr Ashton received a BSc in Chemistry from Durham University (UK), and a PhD in Pharmaceutical Science from the University of Wales. ...
Lec 8
Lec 8

... II-optimizing access to the target • The compound with the best binding interaction is not necessarily the best drug to use in medicine. • The drug needs to pass through many barriers to reach its target in the body. • There are many ways to make drugs which can reach its target such as linking the ...
Delipid
Delipid

... Concomitant anticoagulant dosage may need to be reduced and frequent determinations of prothrombin carried out to confirm that the desired prothrombin level has been re-established. There have been reports of severe myositis with marked elevation of creatinine kinase and myoglobinuria when Delipid® ...
Drug Interactions Every Health Care Provider Should Know
Drug Interactions Every Health Care Provider Should Know

Safety in Small Populations
Safety in Small Populations

... • Adverse events (AEs),DA dosing, hemoglobin (Hb) concentrations, and transfusions were recorded. • Inclusion Criteria: children and adolescents age 0–16 years with anemia attributed to CKD receiving dialysis or have an eGFR of <60 ml/min × 1.73 m2 for at least 3 months, and receiving DA at the time ...
Addiction
Addiction

... – nicotinic receptors on the actual dopaminergic neuron when nicotine binds to that receptor, it turns the dopamine cell on – nicotine stimulates glutamatergic inputs, which are excitatory on the dopamine neuron which leads to more dopamine being released – nicotine stimulates GABAergic neurons • Wh ...
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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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