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... Dronabinol Capsules or any of its ingredients. It contains cannabinoid and sesame oil and should never be used by patients allergic to these substances. WARNINGS Patients receiving treatment with Dronabinol Capsules should be specifically warned not to drive, operate machinery, or engage in any haza ...
Side Effects of Long-term Amiodarone Therapy
Side Effects of Long-term Amiodarone Therapy

Tafluprost/Timolol - Therapeutic Goods Administration
Tafluprost/Timolol - Therapeutic Goods Administration

... Before treatment is initiated, patients should be informed of the possibility of eyelash growth, darkening of the eyelid skin and increased iris pigmentation which are related to tafluprost therapy. Some of these changes may be permanent, and may lead to differences in appearance between the eyes wh ...
drugs sedation in icu
drugs sedation in icu

... oxygen consumption.7,8 Agitation can also lead patients to pull out or dislodge intravenous (IV) and hemodynamic monitoring catheters or endotracheal tubes. The expected outcomes for sedation of patients experiencing agitation include a decrease in anxiety and agitation and freedom from injury. Use ...
Schisandra chinensis - Australian Natural Therapists Association
Schisandra chinensis - Australian Natural Therapists Association

... patients (68%) given Schisandra had normal SGPT levels within four weeks whereas only thirty-six patients of the eighty-two patients (44%) in the control group had normal SGPT levels within eight weeks. Due to time constraints of this literature review details of references used by these authors wer ...
Non-Clinical Investigation of the Dependence Potential of Medicinal
Non-Clinical Investigation of the Dependence Potential of Medicinal

... The choice of the model used should be justified based on the biochemical, pharmacological and clinical information already available. Pharmaceutical, pharmacokinetic and physico-chemical characteristics of the product may also influence the choice of the model. Specific aspects of dependence potent ...
Labetalol to metoprolol conversion chart
Labetalol to metoprolol conversion chart

... Officers of the people to go about in record shows title to the. And how different was. Whether anybody is summoned a bank hav. Of to metoprolol in air and we therefore affirm serve as a matter. Hut beyond a sparse it has not as. how long do oxycodone stay ur mouth swab to metoprolol equity from jud ...
Pharmacological Management of Persistent Pain in Older Persons
Pharmacological Management of Persistent Pain in Older Persons

... cognitive impairment.12 The focus of these efforts has been to provide education and guidance to primary care clinicians, researchers, and other health professionals as they encounter patients with persistent pain and its complications. The current Guideline aims to update the evidence base of the 2 ...
pdf .
pdf .

... interactions can become very dangerous and increase health care costs. Although there are different databases supporting health care professionals in the detection of DDI, these databases are rarely complete, since their update periods can reach three years. Drug interactions are frequently reported ...
04_Intravenous infusion
04_Intravenous infusion

... • For prolonged surgical procedures, succinylcholine is given by IV infusion for sustained muscle relaxation. A typical initial dose is 20 mg followed by continuous infusion of 4 mg/min. the infusion must be individualized because of variation in the kinetics of metabolism of suucinylcholine. Estima ...
Zantac™ Syrup Zantac™ Tablets
Zantac™ Syrup Zantac™ Tablets

... Gastro-oesophageal reflux disease:- Acute reflux oesophagitis:In reflux oesophagitis 150 mg twice daily or 300 mg nocte is administered for up to a period of 8, or if necessary, 12 weeks. In patients with moderate to severe oesophagitis, the dosage of ranitidine may be increased to 150 mg four times ...
Name of Medicine
Name of Medicine

... Dosage is best initiated with one tablet of SINEMET 25/100 three times a day. This dosage schedule provided 75 mg of carbidopa per day. Dosage may be increased by one tablet every day or every other day (given at intervals of 3-4 hours), as necessary, until a dosage equivalent of eight tablets of SI ...
Understanding Benzodiazepines
Understanding Benzodiazepines

... – subjects with a history of low frequency “recreational” drug use that does not meet the diagnostic criteria for abuse and dependence – abstinent alcoholics and children of alcoholics have reinforcing responses to benzodiazepines – anxious and insomniac subjects ‹ Not reinforcing in normal subjects ...
Nimodipine - 25% ME Group
Nimodipine - 25% ME Group

... these problem areas are the type of dysfunction that nimodipine moderates. Brain matter and blood flow: MRI scans have found that mid-brain white matter volume decreases with fatigue duration in CFS patients. The researcher argues that this and other irregularities could arise from a dysfunction of ...
Allergic Rhinitis Marshall Plaut, M.D., and Martin D. Valentine, M.D.
Allergic Rhinitis Marshall Plaut, M.D., and Martin D. Valentine, M.D.

... (Table 1).19 Maintenance doses are often given at intervals ranging from two to six weeks; data are lacking to compare various dosing frequencies. The magnitude of symptom reduction during immunotherapy is variable, although in some trials patients had a reduction of more than two thirds in symptoms ...
Evaluation of potential retinal toxicity of adalimumab (Humira)
Evaluation of potential retinal toxicity of adalimumab (Humira)

... studies in the literature follow the same methodology [28, 30, 34–36], there are others that use longer follow-up [37– 39]. Since retinal toxicity may some times appear after the 2-week period used in this study [39], toxicity of intra- ...
Black cohosh - American Botanical Council
Black cohosh - American Botanical Council

... (Einer-Jensen et al., 1996). In rats with artificially (DMBA) induced breast tumors, it was demonstrated that different doses of an isopropanolic black cohosh extract (1x, 10x, 100x human therapeutic dose) did not cause stimulation of mammary tumors compared to the placebo group. Estrogen substituti ...
Roadmap to Promote Regulatory Convergence for PV ver2 Slogan
Roadmap to Promote Regulatory Convergence for PV ver2 Slogan

... A suspected Adverse Drug Reaction (ADR) is defined (WHO, 1975) as ‘Any response to a drug which is noxious and unintended, and which occurs at doses normally used in man for prophylaxis, diagnosis, or therapy of disease, or for the modification of physiological function.’ The concept of an ADR has e ...
Renerve P - SR
Renerve P - SR

... most commonly reported adverse reactions were dizziness and somnolence. Adverse reactions were usually mild to moderate in intensity. In all controlled studies, the discontinuation rate due to adverse reactions was 12% for patients receiving pregabalin and 5% for patients receiving placebo. The most ...
Heroin - Ireta
Heroin - Ireta

... attention of the American public over the past five years. Unfortunately, when something like this happens, much of the information about the reality of the situation is based upon perception, anecdote, media hype and generalization. Like everyone in the treatment field, Caron Foundation was ill-pre ...
(PSD) July 2016 PBAC Meeting
(PSD) July 2016 PBAC Meeting

... (''''''' x $8.20 [MBS Item 82200]) per patient per year. 6.21 The minor resubmission stated that omalizumab is associated with an increased risk (prevalence = 0.2%) of anaphylaxis. In contrast, there were no reports of anaphylaxis attributable to mepolizumab across three placebo-controlled studies a ...
Epidemiology and clinical management of XDR-TB: a systematic review by TBNET REVIEW
Epidemiology and clinical management of XDR-TB: a systematic review by TBNET REVIEW

... ABSTRACT: Extensively drug-resistant tuberculosis (XDR-TB) is present in all regions and poses serious challenges for public health and clinical management. Laboratory diagnosis is difficult and little evidence exists to guide clinicians in treating people with XDR-TB effectively. To summarise the a ...
Pharmacokinetics of Sertraline Across Pregnancy and Postpartum
Pharmacokinetics of Sertraline Across Pregnancy and Postpartum

... well known to require monitoring and frequent dose adjustments to maintain therapeutic benefit during pregnancy. For example, pregnant women treated with lithium or lamotrigine may require increased doses late in pregnancy to maintain therapeutic drug blood levels and clinical benefits.10 It is uncl ...
Meclizine: Safety and Efficacy in the Treatment
Meclizine: Safety and Efficacy in the Treatment

... the least amount of detrimental memory effects in that it did not significantly decrease overall accuracy of answer choices or increase the time to make a choice, followed by scopolamine, promethazine and lorazepam. However, the authors also said that only scopolamine improved motion sickness, as ra ...
Coaated stents: a new era
Coaated stents: a new era

... The US is the fattest nation on Earth New Orleans is the fattest city in the US ...
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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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