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Vitamin K Content in Common Foods
Vitamin K Content in Common Foods

... combination because calcium carbonate supplements can reduce the utilization of thyroid hormone, especially when a patient takes it in high doses and in the morning.11 Levothyroxine is best absorbed on an empty stomach, so it should be taken in the morning 1 hour prior to breakfast. To minimize the ...
HCV Nucleoside Prodrug Design and their Potencies
HCV Nucleoside Prodrug Design and their Potencies

... drop (88% RVR); GT2/3: 5.0 log drop (90% RVR) compared to 2.95 log drop for SOC (10% RVR) • Phase IIb: 408 patients 12 weeks 1000 mg bid with SOC >80% cEVR • Combination DAA studies: 1000 mg RG7128 with 900 mg of PI RG7227 (danoprevir) 14 days. Treatment naïve 5.1 log drop and IFN-null responders 4. ...
Safe Opioid Prescribing
Safe Opioid Prescribing

... (E.g. for oral morphine in adult patients – not normally more than 50% higher than the previous dose) ...
voltaren ophtha
voltaren ophtha

... Caution should be exercised when topical NSAIDS such as diclofenac are used concomitantly with topical steroids (see PRECAUTIONS Interactions with Other Drugs). Eye drops are not for injection. They should never be injected subconjunctivally, nor should they be directly introduced into the anterior ...
Reference ID: 3953274
Reference ID: 3953274

... authorized to receive POMALYST, and comply with REMS requirements. Further information about the POMALYST REMS program is available at www.CelgeneRiskManagement.com or by telephone at 1-888-423-5436. 5.3 Venous and Arterial Thromboembolism Venous thromboembolic events (deep venous thrombosis and pul ...
Interactions of herbs and food products with drugs
Interactions of herbs and food products with drugs

Herbal supplements and the geriatric population
Herbal supplements and the geriatric population

... This act was passed to make natural medicine available to the population at a faster rate then if they went through the rigorous testing of the FDA The act worked under the assumption that “natural” medicines were safe and did not need to be as regulated ...
Comparative effects of levosimendan and
Comparative effects of levosimendan and

... arrhythmias. Treatment with PDE inhibitors has been associated with increased nonsustained ventricular tachycardia (VT), sudden death, and overall mortality (11, 12). Since positive inotropes have been arrhythmogenic, it is important to determine the proarrhythmic potential of any new inotropic agen ...
Mixed reviews for a stage-fright remedy
Mixed reviews for a stage-fright remedy

... that they affect only physical, not cognitive, anxiety. "There's very little downside except whatever number you do on yourself about taking the drugs." But now that the drugs have established themselves as a seemingly permanent part of the classical music world, some musicians and physicians are be ...
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Morphine Sulphate MOR Drugs

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STADOL NS®

... Use of butorphanol in geriatric patients, patients with renal impairment, patients with hepatic impairment, and during labor requires extra caution (see below and the appropriate sections in PRECAUTIONS). STADOL Injection: For pain relief the recommended initial dosage regimen of STADOL Injection is ...
a to z guide of illicit and licit drugs
a to z guide of illicit and licit drugs

... Engage parents and families in schoolbased alcohol education programs as they can have a strong influence on young people’s use of alcohol, both positively and negatively. ...
Phase I and Pharmacokinetic Study of Farnesyl Protein Transferase
Phase I and Pharmacokinetic Study of Farnesyl Protein Transferase

... were available that would allow the detection of ras mutations and possibly the preselection of patients who would be the best candidates for this ras-targeted therapy.27 However, subsequent preclinical studies have shown the pharmacology of farnesyl protein transferase inhibitors to be more complex ...
Full Text  - Asian Journal of Sports Medicine
Full Text - Asian Journal of Sports Medicine

... inhibitors (except aspirin ≤ 325 mg/day for cardiovascular prophylaxis), or other medications such as neuroleptics, tricyclic antidepressants, and lithium that could potentially confound the assessment of analgesia within 24 hours of the first dose of study drugs; pregnancy; history of current or pa ...
Hutchison MediPharma R&D briefing Friday, 17 October 2014 9:30am to 1pm
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... - Clinical benefit beyond first generation • Greater inhibition of primary pharmacology / target • Inadequate inhibition of primary target typically limits efficacy (e.g. Crizotinib) • Lack of potency means many compounds have high dose and poor PK (e.g. Lapatanib) • Precise mechanism of action stil ...
Neuroleptics
Neuroleptics

... During intravenous introduction of the drug narcosis develops after 1530sec, lasts for 8-10 min, during intramuscular introduction – after 2-3 min, lasts for 20-30 min ...


... the patients had had multiple treatments with other drugs, all of them unsuccessful (a situation which explains the frequent use of "intractable hiccup" to designate CH in the literature). Coincidental improvement is more possible for the five cases whose hiccups, whilst severe and persistent, had a ...
The JNC 7 Report Prevention, Detection, Evaluation, and Treatment
The JNC 7 Report Prevention, Detection, Evaluation, and Treatment

... guideline for hypertension prevention and management. The following are the key messages: (1) In persons older than 50 years, systolic blood pressure (BP) of more than 140 mm Hg is a much more important cardiovascular disease (CVD) risk factor than diastolic BP; (2) The risk of CVD, beginning at 115 ...
Subdural hematoma cases identified through a Danish patient
Subdural hematoma cases identified through a Danish patient

... laterality (unilateral or bilateral), thickness of SDH in millimeter, and presence of displacement of midline structures. To collect this information, the study neurosurgeons inspected the original brain scan images and performed the aforementioned measurements. If brain scan images were unavailable ...
Research and Development at Sun Pharma
Research and Development at Sun Pharma

...  Key features of technology for cytotoxic substances  Avoids toxic excipients  Better safety index as proven in animal model  Increases circulation half life and improved efficacy  More drugs can be delivered at target site  Avoids hypersensitivity reaction to toxic excipients  Uses all appro ...
Slide 1
Slide 1

... – Does patient have a history of PUD? • Are they being treated with a PPI? – If not, did you start one today? ...
DEVELOPMENT AND VALIDATION OF A RAPID RP-HPLC METHOD FOR THE... ZIPRASIDONE HYDROCHLORIDE MONOHYDRATE IN DRUG SUBSTANCE AND ITS DOSAGE
DEVELOPMENT AND VALIDATION OF A RAPID RP-HPLC METHOD FOR THE... ZIPRASIDONE HYDROCHLORIDE MONOHYDRATE IN DRUG SUBSTANCE AND ITS DOSAGE

... The HPLC chromatograms recorded for the placebo showed almost no peaks at the retention time of ZHM. The peak for ZHM is clearly separated from other excipients of the formulations. As there is no blank interference is not observed at the retention time of ZHM, the HPLC method presented in this stud ...
In Vitro-In Vivo Correlation (IVIVC) and Determining
In Vitro-In Vivo Correlation (IVIVC) and Determining

... (active pharmaceutical ingredient, API) release characteristics of solid oral dosage products for both product development and quality control purposes. Dissolution tests are mostly conducted in vessel-based apparatuses, commonly known as the paddle and basket apparatuses [1] to demonstrate appropri ...
Natural products as starting points for future anti
Natural products as starting points for future anti

... Background: The discovery and development of new anti-malarials are at a crossroads. Fixed dose artemisinin combination therapy is now being used to treat a hundred million children each year, with a cost as low as 30 cents per child, with cure rates of over 95%. However, as with all anti-infective ...
Critical Care of the Morbidly obese Patient Louis Brusco Jr, MD, FCCM
Critical Care of the Morbidly obese Patient Louis Brusco Jr, MD, FCCM

... past 3 decades.7 Obesity in other countries presents different problems. Although the rates of obesity in Japan and Korea are far less than in the United States, comorbid conditions occur at lower weights so that obesity is a significant problem in these countries as well.13 Nearly one-third of pati ...
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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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