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NIDA Research Report - Heroin
NIDA Research Report - Heroin

... to receive pharmacotherapy for their heroin addiction, detoxification from opiates during pregnancy can be accomplished with relative safety, although the likelihood of relapse to heroin use should be considered. Why are heroin users at special risk for contracting HIV/AIDS and hepatitis B and C? er ...
3% annual mortality rate
3% annual mortality rate

... CSA who have reduced LV systolic function, provided that such patients are on background treatment with ACEI.  Practice guidelines recommend that ß-blockers are the first choice of therapy for uncomplicated CSA. (N Engl J Med. 2005; 352: 2524–2533) ...
Slides - Clinical Trial Results
Slides - Clinical Trial Results

... After a 600mg clopidogrel LD, poor responders (PRI ≥ 50%) received additional 600mg bolus (max 2400 mg) until reaching therapeutic target. ...
5-HIV-Pharmacotherapy-Update-2016-no
5-HIV-Pharmacotherapy-Update-2016-no

... I have no conflicts of interest. • However, I will be using brand names extensively ...
VT PowerPoint Template5
VT PowerPoint Template5

... Tissue Residues At 5 x T1/2 (after you stop dosing) 97% has been eliminated.  Make sure you use the longest half-life  Metabolites MAY be more important than the drug  Absorption may have the longest half-life. ...
Avances en el desarrollo de productos biológicos para
Avances en el desarrollo de productos biológicos para

... Pseudomonas aeruginosa exoprotein, which was made nontoxic by deletion of an amino acid. This vaccine showed good immunogenicity and appeared safe and effective, particularly among individuals who produced high antibody titers. A randomized, double-blinded, placebo-controlled multicenter clinical tr ...
Acute Mental Status Changes, Hypotension, and
Acute Mental Status Changes, Hypotension, and

D I NEW DRUGS - Ontario Pharmacists Association
D I NEW DRUGS - Ontario Pharmacists Association

... * The primary efficacy variable(s). † Before being randomized to treatment, all patients were weaned from existing antihypertensive medications and underwent a 4-week single-blind placebo lead-in period. ‡ The starting dose was left to the clinical discretion of the investigator; titration to 360 mg ...
How should ankle oedema caused by calcium channel blockers be
How should ankle oedema caused by calcium channel blockers be

... reducing ankle oedema caused by amlodipine in a similarly designed study. Both ARBs reduced foot volume, but valsartan reduced oedema significantly more than olmesartan9. Nitrates Nitrates, due to their venodilating action, may be offer some useful effects in treating CCB induced ankle oedema, but t ...
ENCLOSURE- I 6.1. BRIEF RESUME OF INTENDED WORK NEED
ENCLOSURE- I 6.1. BRIEF RESUME OF INTENDED WORK NEED

... indomethacin. The prepared spherical crystals with used polymers exhibited excellent physicochemical properties like flowability, packability, and wettability compared with the pure raw crystals of indomethacin. Ram Mohan G et al20 prepared celecoxib spherical agglomerates with polyvinylpyrrolidone ...


... Marc S Weinburg, Adam J. einburg, ion H Zap – effectively targeting the rennin angiotensin – aldosterone system in cardiovascular and renal disease; rationale for using angiotensin II receptor blockers in combination with angiotensin – converting enzyme inhibitors ...
calibration - Beckman Coulter
calibration - Beckman Coulter

... BARB reagent, in conjunction with UniCel® DxC 600/800 System(s) and SYNCHRON® Systems Drugs of Abuse Testing (DAT) Urine Calibrators, is intended for the qualitative determination of barbiturates in human urine at a cutoff value of 200 ng/mL. The BARB assay provides a rapid screening procedure for d ...
Treating Anxiety with either Beta Blockers or Antiemetic
Treating Anxiety with either Beta Blockers or Antiemetic

... Inderal® is available in oral doses ranging from 10 to 80 mg per dose for the treatment of hypertension. Multiple doses per day may be permitted. This drug can also be absorbed mucosally, as demonstrated by sublingual delivery [12], and its bioavailability is higher when absorbed by this route rathe ...
Prescription Must contain all of the following Except : name of
Prescription Must contain all of the following Except : name of

... -151 1deciliter = ………liter a)10 b)100 c)0.1* d)0.01 152- The concentration of one drug is 1:100, if the patient takes 900 ml at the morning and 600 ml in the evening, How much drug will the patient take in 15 days? 15 mg 15 gm ...
Pharmacologic insights into the future of trastuzumab
Pharmacologic insights into the future of trastuzumab

... upon pharmacokinetic considerations, current studies are examining whether trastuzumab can be administered i.v. every three weeks or by the s.c. route. These regimens would have advantages for patients and medical staff in terms of acceptability, ease of administration and, potentially, cost effecti ...
Comparative bioavailability and pharmacokinetic study of Cefadroxil
Comparative bioavailability and pharmacokinetic study of Cefadroxil

... guided by FDA guidelines. Another objective was to conduct pharmacokinetic evaluation in Pakistani population. A single-dose, randomized, cross-over pharmacokinetic study was conducted during the month of May’2013 to August’2013. Washout period was one week. Fourteen healthy male adult volunteers we ...
The BC Public Health Opioid Overdose Emergency
The BC Public Health Opioid Overdose Emergency

... Mapping rates of Illicit Drug Overdose Deaths by Health Services Delivery Area (HSDA)* or Local Health Area (LHA)* assists in local and regional overdose prevention activities and resource allocation. The BC Coroners reports are updated and release publicly on monthly basis and include mortality ma ...
Potentially Harmful Drugs in the Elderly: Beers List
Potentially Harmful Drugs in the Elderly: Beers List

... In 1991, Dr. Mark Beers and colleagues published a methods paper describing the development of a consensus list of medicines considered to be inappropriate for long-term care facility residents.12 The American Geriatrics Society Beers Criteria or “Beers list” is now in its fifth permutation.1 It is ...
Fall 2003 Bulletin - College of Pharmacy - Home
Fall 2003 Bulletin - College of Pharmacy - Home

... politicians, students and anyone else with whom we interact. We can support efforts to promote the profession by volunteering our time, by being active in our professional organizations, by mentoring upcoming pharmacists and by providing financial support. We are proud of the high regard in which ou ...
Antiretroviral effect of MK-0518, a novel HIV
Antiretroviral effect of MK-0518, a novel HIV

... – Not a potent inhibitor or inducer of CYP3A4 • Does not require “ritonavir boosting” – No substantive issues from preclinical studies • Phase I – Data support dosing 100 - 800 mg po bid without regard to food • At 100mg b.i.d, mean C12hr > IC95 – Drug interaction studies support dosing of MK-0518 w ...
Oral Therapies for Cancer - Oncology Nursing Society
Oral Therapies for Cancer - Oncology Nursing Society

... Copyright © 2011 by the Oncology Nursing Society. All rights reserved.     ...
Use of Herbal Products and Potential
Use of Herbal Products and Potential

... before the release of an herbal product and from any post-marketing surveillance. Although herbal remedies are perceived as being natural and therefore safe, many have adverse effects that can sometimes produce life-threatening consequences. Despite the paucity of scientific evidence about the safet ...
GPIIb - IIIa - ICU education
GPIIb - IIIa - ICU education

... clinicians consider the risk of HIT to be > 1%, we suggest that platelet count monitoring be performed every 2 or 3 days from day 4 to day 1For patients receiving heparin in whom clinicians consider the risk of HIT to be > 1%, we suggest that platelet count monitoring be performed every 2 or 3 days ...
rimadyl once-a-day dosing chart for chewables and caplets
rimadyl once-a-day dosing chart for chewables and caplets

... which maintain normal homeostatic function. These anti-prostaglandin effects may result in clinically significant disease in patients with underlying or pre-existing disease more often than in healthy patients.12,14 NSAID therapy could unmask occult disease which has previously been undiagnosed due ...
β-Lactam Antibiotics
β-Lactam Antibiotics

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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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