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Full Prescribing Information
Full Prescribing Information

... base exhibited evidence of maternal toxicity including decreased body weight gain and/or body weight loss and a concomitant decrease in food consumption during the first week of dosing. No teratogenic or embryo-fetal effects were observed at doses equivalent to up to 22.5 mg/kg per day rolapitant f ...
Treating Respiratory Tract Infections In The Era Of Antibiotic
Treating Respiratory Tract Infections In The Era Of Antibiotic

... Table 2.3,18,19,22,31,32 Increasing support for the “no antibiotic alternative” or “delayed antibiotic prescribing” is appearing in the literature. For example, recently published guidelines for the treatment of acute otitis media identify an “observation option” in patients 2 years of age and older ...
Vitex agnus
Vitex agnus

... syndrome (PMS) and especially breast swelling and pain, due to its dopaminergic effect. Although approximately 50% or more of young women suffer from PMS, there is no generally accepted therapy and only a few preparations for that purpose are available on the Swiss market. Therefore the extract prep ...
NEUROCHEMICAL SELVES
NEUROCHEMICAL SELVES

... antihistamines by company scientists at the pharmaceutical firm Rhone-Poulenc in the years after the Second World War. Two French psychiatrists, Pierre Deniker and Jean Delay, who administered it to a group of psychotically agitated patients at the Hôpital Sainte-Anne in Paris in 1952, are credited ...
SHEET L.13 SLIDE 5 (IV drug preparation guidelines)
SHEET L.13 SLIDE 5 (IV drug preparation guidelines)

... paracetamol can be used as an alternative for NSAID's but it does not have an antiinflammatory effect, it only has an analgesic effect, so in the inflammatory conditions paracetamol cannot be used. NSAID's are given with PPI's to decrease the risk of developing peptic ulcers. Skeletal muscle relaxan ...
Memorandum of  Meeting  Minutes Meeting  Date: February  15,2002
Memorandum of Meeting Minutes Meeting Date: February 15,2002

... the data were sufficient for monograph status. The Agency replied that it had not fully resolved the material time and extent issues or what would constitute an adequate safety profile because the ingredient had not been marketed in the U.S. for over 25 years. The Agency stated that inclusion in the ...
Expanded Role Training for Support Staff
Expanded Role Training for Support Staff

... 2. check that all medication administration records or protocols are available, up to date and legible 3. report any discrepancies or omissions you might find to the person in control of the administration and to relevant staff as appropriate 4. read the medication administration record or medicatio ...
Document
Document

... Introduction • The discovery of pharmacologic agents by modern pharmaceutical companies and universities often involves the use of receptor-ligand binding techniques. Following the synthesis of a series of new chemically related compounds, which can constitute hundreds to thousands of compounds, th ...
汤慧芳
汤慧芳

... inhibitor, and cross-resistance between rifampin and rifapentine is complete. Rifapentine is a potent inducer of cytochrome P450 enzymes, and it has the same drug interaction profile. Toxicity is similar to that of rifampin. Rifapentine 600 mg (10 mg/kg) once weekly is indicated for treatment of tub ...
Pharmacy Prior Authorization Form: Dispense as Written (DAW)
Pharmacy Prior Authorization Form: Dispense as Written (DAW)

... Brand medications with A-equivalent generics are not covered for Medicaid Certain self-funded groups do not apply the MPD to brand medications Brand name medications with “authorized generics” available are not eligible for DAW authorization. Authorized generics are prescription drugs produced by th ...
1427967058PR Aptar Pharma Twister Sine Promod 040215LV
1427967058PR Aptar Pharma Twister Sine Promod 040215LV

... Key benefits of Aptar Pharma’s Twister® Twister® is a new capsule-based DPI, designed and developed by a multidisciplinary technical team based at Aptar Pharma’s Centre of Excellence in Le Vaudreuil, France to specifically address unmet medical needs in fast-growing markets. Twister® has a simple an ...
Diapositive 1 - Moodle Lille 2
Diapositive 1 - Moodle Lille 2

... Partnership since 2002 for development of Trofile test Trofile used in all Selzentry Clinical trials Trofile used before Prescription Currently the only CLIA-validated tropism assay available ...
otezla - Celgene
otezla - Celgene

... No significant interactions were observed when 30 mg oral apremilast was administered with ketoconazole (CYP3A4 inhibitor), methotrexate and oral contraceptives (CYP3A4 substrate) containing ethinyl estradiol and norgestimate. Combination with: Strong CYP3A4 Inducers: Apremilast exposure (AUC) and m ...
Pharmcokinetics in Critical Care
Pharmcokinetics in Critical Care

... support on Day 4, his 02 requirements increased, along with increased suction passes, & he developed a new consolidation on CXR antibiotics broadened to Tazocin 3.375 g IV q6h & vancomycin 1 g IV q12h to cover VAP ...
ranolazine - Physicians Academy
ranolazine - Physicians Academy

... mechanism of action different from that of currently available pharmacological therapies. • Do not affect HR & BP. Ranolazine was approved on January 27, 2006, in the United States for use in patients with chronic angina who continue to be symptomatic on ß-blockers, calcium antagonists, or nitrates. ...
Avapro - Sanofi Canada
Avapro - Sanofi Canada

... AVAPRO (irbesartan) should be discontinued as soon as possible. The use of ARB is contraindicated during pregnancy. Epidemiological evidence regarding the risk of teratogenicity following exposure to ACE inhibitors (another class of therapeutic products interfering with the RAAS) during the first tr ...
Pharmacokinetics and Pharmacodynamics for Medical Students: A
Pharmacokinetics and Pharmacodynamics for Medical Students: A

... not have the desired activity but may exert toxic effects. Simultaneously, the drug undergoes clearance by metabolism and excretion. After oral administration, the situation is more complex, since the drug must undergo dissolution and absorption, then survive firstpass metabolism in the liver, befor ...
SANTEN RECEIVES FDA APPROVAL OF IQUIX
SANTEN RECEIVES FDA APPROVAL OF IQUIX

... fluoroquinolone active against a broad spectrum of Gram-positive and Gram-negative ocular pathogens. Levofloxacin's high solubility, at neutral pH, allows the solution to be formulated with a concentration of active drug (1.5%), three times higher than any other ophthalmic fluoroquinolone on the mar ...
AZOPT ® Suspension
AZOPT ® Suspension

... regular routine. Do not use a double dose to make up for a missed dose. AZOPT® Product Monograph ...
Nitrates in Heart Failure with Preserved Ejection Fraction
Nitrates in Heart Failure with Preserved Ejection Fraction

... failure and a preserved ejection fraction have been well described.3,4 Owing to the insensitivity of BNP assays to hemodynamic abnormalities in patients with heart failure and a preserved ejection fraction, patients were permitted to enter the trial without elevated BNP assay levels if they had othe ...
Injectable Soft-Tissue Fillers: Clinical Overview
Injectable Soft-Tissue Fillers: Clinical Overview

... materials of differing compositions for injection treatments either are now available or will soon be available for clinical use. Methods: A review of the medical literature was performed to provide chemical compositions, methods of preparation, biological behavior, and clinical outcomes for every k ...
TRIPLEFLEX RAPID RELIEF
TRIPLEFLEX RAPID RELIEF

... Glucosamine: Daily intake of 1500 mg/day consistently effective;1-4 two 3-year trials showed slowing of cartilage loss compared to placebo.5.6 MSM: Three clinical trials report that MSM at doses of 2250 mg/day7 and 1500 mg/day8 and 6000 mg/day9 reduced joint discomfort. White Willow Bark: Four clini ...
The Translational Research Cycle – Example in Infectious Diseases
The Translational Research Cycle – Example in Infectious Diseases

... also called SXR or NR1I2). SFN appeared to tightly, perhaps irreversibly, bind to the ligand binding site of the receptor, thus preventing other ligands from binding and activating the receptor. Ligand activation of PXR was known to be a major contributor to both ‘constitutive’ (basal) and inducible ...
DDD107498: A novel clinical candidate for malaria
DDD107498: A novel clinical candidate for malaria

... No cross-resistance to current antimalarial drugs ...
An Example Case Study
An Example Case Study

... mass production of heroin due to addiction and abuse by both patients and physicians. It was hoped that a thebaine-derived drug would retain the analgesic effects of morphine and heroin with less of the euphoric effect which led to addiction and over-use. To some extent this was achieved, as oxycodo ...
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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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