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March 06, 2014 Meeting Summary - Posted 03/24/2014
March 06, 2014 Meeting Summary - Posted 03/24/2014

... specifically the area concerning this medication used in the treatment of pseudobulbar affect (PBA). Adverse events and contraindications were considered, and a comprehensive breakdown of utilization by diagnosis was presented. The DUR Board recommended the following: ...
3. Antiproliferative and antimetabolic drugs
3. Antiproliferative and antimetabolic drugs

... and B and T lymphocytes are highly dependent on this pathway for cell proliferation ...
潒慳楬a - WebMedFamily.org
潒慳楬a - WebMedFamily.org

... (ESC/EAS) published in July 2011 considerably broadened the range of very high CV risk patients, thus necessitating the more widespread use of modern statin products in order to achieve the target values (20). The ACC/AHA protocol issued in November 2013 resulted in a paradigm shift. The main messag ...
Lecture 7 Bio3124 - University of Ottawa
Lecture 7 Bio3124 - University of Ottawa

... that relate zone diameter to degree of microbial resistance table values plotted and used to determine if concentration of drug reached in body will be ...
FIXED DOSE COMBINATION PRODUCTSOF ANTI-HYPERTENSIVE’SAND ANTI-DIABETIC’S -
FIXED DOSE COMBINATION PRODUCTSOF ANTI-HYPERTENSIVE’SAND ANTI-DIABETIC’S -

... will continue to be there in the market benefiting the pharmaceutical companies, physicians and the patients. The only possible bottleneck in the way of FDC is the unclear guidelines by the respective authorities which would definitely be clarified in near ...
Treating Allergies
Treating Allergies

... For drugs available by prescription only, monthly costs reflect nationwide retail average prices for February 2013, rounded to the nearest dollar. Data is provided by Symphony Health Solutions, which is not involved in our analysis or recommendations. For drugs available OTC, prices were obtained by ...
3. Antiproliferative and antimetabolic drugs
3. Antiproliferative and antimetabolic drugs

... and B and T lymphocytes are highly dependent on this pathway for cell proliferation ...


... several diseases. According to WHO, 80% of the world’s population depend directly on medicinal plants for their basic preventive and curative healthcare. Over 9000 plants have known medicinal applications in various cultures and countries. Medicinal plants synthesize and accumulate a variety of comp ...
Introduction to Pharmacology 2 General Principles: Absorption
Introduction to Pharmacology 2 General Principles: Absorption

... o Base: proton acceptor; in aqueous solution, can pick up proton to become ionized (less well-absorbed; usually have an amino group) o Quaternary ammonium compounds- charge is not dependent on pH; permanent positive charge o NOTE: most important clinical point is they should be given by injection, n ...
Dose translation from animal to human studies revisited
Dose translation from animal to human studies revisited

... However, scientific evidence does not favor one alternative formula over another (16 –18). While the reliability of the Du Bois formula has been contested, the resultant approximation should be accepted not as a method of precise measurement but as a means of achieving more correct comparisons among ...
alprostadil
alprostadil

... insertion. Topical delivery of alprostadil offers an improved alternative. AIM: To evaluate the long-term safety and efficacy of topical alprostadil cream. METHODS: This was a multicenter, open-label, long-term study in 1,161 patients (998 double-blind rollover; 163 naïve) with ED. For the first 4 w ...
Guidance on CMC for Phase 1 and Phases 2/3 Investigational New
Guidance on CMC for Phase 1 and Phases 2/3 Investigational New

... Safety is the main concern which is addressed with pharm/tox data Drug substance has been tested, thus impurity profile and potency are known in animals before given to human Generally a small number of patients in Phase 1 Trial duration is normally short for Phase 1 Clinical trials are conducted un ...
Visudyne™ (Verteporfin) Therapy
Visudyne™ (Verteporfin) Therapy

... Protect from light for at least 5 days or as long as skin is swollen or discolored Consult burns specialist or dermatologist if needed If venous access was not obtained after several attempts, treatment can be attempted again after 24 hours ...
Neul – Clinical trials family
Neul – Clinical trials family

... clinical trial (NCT01253317) ...
- Biology of Blood and Marrow Transplantation
- Biology of Blood and Marrow Transplantation

... from brand-name to generic tacrolimus showed a significant drop in tacrolimus trough levels in one patient and acute rejection in another patient without a meaningful change in serum levels [12]. More important is a large multicenter study of generic tacrolimus conversion in solid organ recipients. ...
Case Study from Thailand - World Trade Organization
Case Study from Thailand - World Trade Organization

... some kind of insurance, they have to pay a subsidized level of user fees, according to their ability to pay. However, if they do not have insurance and have no (or not enough) money, they can also receive free medical care from public facilities. User fee system was started in Thailand for more than ...
How to begin treatment in chronic heart failure? * Ronnie Willenheimer
How to begin treatment in chronic heart failure? * Ronnie Willenheimer

... LVEF, there was a significant interaction regarding the primary endpoint (P ¼ 0.001) (Figure 5). Among patients with LVEF ,28%, those receiving bisoprolol-first were significantly less likely to die or be hospitalized than those receiving enalapril-first (HR, 0.61; 95% CI, 0.44–0.85; P ¼ 0.003), whe ...
Sedative - Hypnotics
Sedative - Hypnotics

... • anterograde amnesia – cannot recall events happening during the drug’s action (benzodaazepines) 2. Hypnosis • time to fall asleep is , duration of stage 2 NREM sleep is ; duration of REM sleep is  • use of sedative-hypnotics for > 1 – 2 weeks may lead to some tolerance to their effects on sleep ...
Enhancement of Dissolution rate of Rifabutin by preparation of
Enhancement of Dissolution rate of Rifabutin by preparation of

... Commercial RFB used in the study was characterized with low solubility. Microcrystals of RFB were prepared by solvent change method. Addition of organic phase to the aqueous phase results in precipitation of drug particles. The manufacturing of a microcrystals implies the creation of additional surf ...
Theories of addiction: Causes and maintenance of addiction
Theories of addiction: Causes and maintenance of addiction

... Behaviourist models of addiction focus on directly observable behaviour. One group concentrates on the fact that behaviour is maintained (or made more likely) by the consequences (reinforcers) of such behaviour (West, 1989). Drug self-administration is then an example of instrumental behaviour becau ...
February 2008, Number 2
February 2008, Number 2

... manufacturer would likely have no legal recourse. If a manufacturer marketed their product for this off-label use, there could be patent-infringement issues. Therefore, Totect® was designated nonformulary and not available. Peppermint oil has been used as a room deodorizer. It routinely appeared on ...
Herb-drug interactions
Herb-drug interactions

... or dental procedures, i.e., herbal anticoagulants (cause bleeding), sedative or stimulant herbs (modify anesthesia). Know principles for clinical coping with herb-drug interactions ...
Empirical Bayes Model to Combine Signals of Adverse Drug
Empirical Bayes Model to Combine Signals of Adverse Drug

... INTRODUCTION ...
FY M.Pharm - ICT Mumbai
FY M.Pharm - ICT Mumbai

...  Genetic basis of variation of pharmacokinetics  Methods for pharmacogenomic profiling & study Pharmacokinetic Introduction to ADME and basic pharmacokinetic parameters like Volume of distribution, Elimination half life, Elimination rate constant, Clearance, Area under curve, Bioavailability, calc ...
Safety monitoring and reporting
Safety monitoring and reporting

... Medicines Control Council (MCC) A regulatory authority that was established in terms of the Medicines and Related Substances Act, 1965 (Act No. 101 Of 1965) to oversee the regulation of medicines in South Africa. Its main purpose is to safeguard and protect the public by making sure that all medicin ...
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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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