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Do THE BENEFITS OUTWEIGH THE RISKS?
Do THE BENEFITS OUTWEIGH THE RISKS?

... also been plagued with problems in recent years. Presently, more drugs are being pulled off the market than ever before because of safety concerns. This has been followed by a wave oflawsuits aimed at correcting the error of allowing such drugs on the market in the first place. As a result, the phar ...
Pharmacology PowerPoint
Pharmacology PowerPoint

... complaint is a headache. What, if any, medication do you recommend? ...
Research Involving Investigational Drugs
Research Involving Investigational Drugs

... investigator may provide a plan to ensure that the investigational drug or biologic will be used according to the IRB-approved protocol, under the direction of the approved investigator(s), and in compliance with FDA and university requirements. 8. Additional Responsibilities of Sponsor-Investigator ...
clinical services for substance misusers
clinical services for substance misusers

... This PSO introduces a new standard for Clinical Services for Substance Misusers and replaces Health Care Standard 8. The new clinical standard concerns the effective clinical practice and management of the substance misuse treatment service provided by staff working in prisons. It is in line with th ...
SW_QA257.4_LMWH_in_renal_impairment _PROPHYLAXIS _Final
SW_QA257.4_LMWH_in_renal_impairment _PROPHYLAXIS _Final

... (7,8,11). The risk of hyperkalaemia seems to increase with duration of therapy but is usually reversible (7,8). Monitoring of plasma potassium is advised in patients at risk before starting heparin therapy and regularly thereafter particularly if treatment is prolonged beyond about 7 days (7,8). Gui ...
Guidance for Industry Acne Vulgaris:  Developing Drugs for Treatment DRAFT GUIDANCE
Guidance for Industry Acne Vulgaris: Developing Drugs for Treatment DRAFT GUIDANCE

... The Agency recommends that phase 2 clinical studies provide sufficient information to optimize dose and duration of treatment chosen for phase 3 evaluation (with adequate consideration given to both safety and efficacy before end-of-phase 2 discussion). In general, a minimum treatment duration of 12 ...
032797 The Effects of Ibuprofen on the Physiology
032797 The Effects of Ibuprofen on the Physiology

... Seven medical centers in the United States and Canada participated in this trial, which was approved by the institutional review board at each center. Consent was obtained from all the patients or their next of kin before enrollment. Patients were recruited from intensive care units if they had a kn ...
PowerPoint - 埼玉医科大学総合医療センター 内分泌・糖尿病内科
PowerPoint - 埼玉医科大学総合医療センター 内分泌・糖尿病内科

... The key components of lifestyle therapy include medical nutrition therapy, regular physical activity, sufficient amounts of sleep, behavioral support, and smoking cessation and avoidance of all tobacco products (see Comprehensive Type 2 Diabetes Management Algorithm—Lifestyle Therapy). In the algori ...
Omnicare Diabetes Health Management Program
Omnicare Diabetes Health Management Program

... medication that substantially duplicates a particular effect of another medication that the individual is taking.”  “Duplicate therapy is generally not indicated, unless current clinical standards of practice and documented clinical rationale confirm the benefits of multiple medications from the sa ...
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Document

... Hydralazine… • Its original clinical use was in hypertension. • It is still used for short-term treatment of severe hypertension in pregnancy but can cause an immune disorder resembling systemic lupus erythematosus, so alternative agents are now usually preferred for long-term treatment of hyperten ...
The Effect of Changes in Co-payment and Premium Policies
The Effect of Changes in Co-payment and Premium Policies

... provincial drug programs, they see cost-sharing policies, including co-payments, as vital to program sustainability. In the absence of effective measures to control the growth in prescription drug use and overall costs (for example, by promoting more cost-effective prescribing), sufficient growth in ...
Acetylcholinesterase Inhibitors for the Treatment of Mild to Moderate
Acetylcholinesterase Inhibitors for the Treatment of Mild to Moderate

... Memantine is licensed and approved for the treatment of moderate to severe Alzheimer’s disease. Dosage and Administration Donepezil is available as tablets or orodispersible tablets. It should be initiated at 5mg once daily at bedtime and increased to 10mg once daily at bedtime after at least one mo ...
set a smooth recovery in motion
set a smooth recovery in motion

... References: 1. Data on file. Parsippany, NJ: Pacira Pharmaceuticals, Inc.; February 2015. 2. Kessler ER, Shah M, Gruschkus SK, Raju A. Cost and quality implications of opioid-based postsurgical pain control using administrative claims data from a large health system: opioid-related adverse events a ...
COLONIC DRUG DELIVERY SYSTEM OF TRIMETAZIDINE HYDROCHLORIDE FOR ANGINA  PECTORIS    Research Article 
COLONIC DRUG DELIVERY SYSTEM OF TRIMETAZIDINE HYDROCHLORIDE FOR ANGINA  PECTORIS    Research Article 

Prinivil - Merck.com
Prinivil - Merck.com

... PRINIVIL is indicated for the treatment of hypertension in adult patients and pediatric patients 6 years of age and older to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have b ...
Treatment Guidelines HTN, DM, Hyperlipidemia
Treatment Guidelines HTN, DM, Hyperlipidemia

... If goal BP cannot be reached with 2 drugs, add and titrate a third drug from the list provided. Do not use an ACEI and an ARB together in the same patient. If goal BP cannot be reached using only the drugs in recommendation 7 because of a contraindication or the need to use more than 3 drugs to reac ...
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... drug is indicated only for women with severe diarrheapredominant IBS who have chronic symptoms for at least 6 months and who have failed conventional therapy. The safety and efficacy of the drug in men was not shown in the initial pivotal phase III clinical trials.26 However a recent analysis of the ...
Sodium-Glucose Co-transporter 2 Inhibitor: A Perspective on
Sodium-Glucose Co-transporter 2 Inhibitor: A Perspective on

... inhibitors include BP, weight, visceral adiposity, hyperinsulinemia arterial stiffness, albuminuria, uric acid levels, and oxidative stress.4 These clinical findings suggest that it is now time to recognize that SGLT2 inhibitors may well be more than just another class of drugs to decrease blood glu ...
Fluoroquinolone resistance in mycobacterium tuberculosis strains
Fluoroquinolone resistance in mycobacterium tuberculosis strains

... resistant to one or more drugs, and randomly selected 138 susceptible to all four drugs. Of the 78 resistant strains, 25 were MDR-TB. The strains were subjected to drug susceptibility testing to Gat among other second-line drugs. Results: Of the 216 strains tested, 32 [32/216 (14.8%)] showed resista ...
Slides - Paradigm Outcomes
Slides - Paradigm Outcomes

... ■ Inaccurate pain diagnosis, and reliance on subjective pain report over objective measures, will begin a treatment trajectory that may be based on trial and error procedural care, and often leads to emphasis on polypharmacy and narcotic escalation. ■ The term “substance use disorders” encompasses a ...
and B
and B

... DVS: summary of regulatory history ...
important drug warning
important drug warning

... 12-20 hours postdose. INVIRASE/ritonavir 1500/100 mg twice daily resulted in a Day 3 mean Cmax of INVIRASE approximately 1.4-fold higher than the mean Cmax observed on Day 3 with the approved therapeutic dose in healthy volunteers (within the same study). QTcS in this study was QT/RR0.319 for males ...
Cholesterol-lowering medications in myositis
Cholesterol-lowering medications in myositis

...  Most widely prescribed drugs worldwide  Still underused – only 50% of those who would benefit are prescribed.  25% taking statins stop them within 6 mo  60% taking statins stop them within 2 yrs  Main reason for stopping – patient and physician fear of myopathy ...
View Acrobat PDF
View Acrobat PDF

... conversion of 7-dehydrocholesterol in the skin to vitamin D3 (cholecalciferol) and (2) dietary intake of either vitamin D2 (ergocalciferol) or vitamin D3. Vitamin D2 and vitamin D3 must be metabolically activated in the liver and the kidney before becoming fully active on target tissues. The initial ...
IN SITU IMPLANTS FOR PARENTERAL ADMINISTRATION    Research Article
IN SITU IMPLANTS FOR PARENTERAL ADMINISTRATION    Research Article

... The  efficiency  of  any  drug  therapy  can  be  described  by  achieving  desired  concentration  of  the  drug  in  blood  or  tissue,  which  is  therapeutically effective and  non toxic  for a  prolonged period. This  goal  can  be  achieved  on  the  basis  of  proper  design  of  the  dosage  ...
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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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