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Know your patient`s renal function
Know your patient`s renal function

... is provided as part of standard pathology reporting and is based on the Modification of Diet in Renal Disease (MDRD) equation. This equation uses the serum creatinine results, adjusts for specific patient factors but assumes a person is of average body size (body surface area of 1.73m2).9 The eGFR c ...
Taxotere® product monograph
Taxotere® product monograph

... physician immediately should this occur. Should TAXOTERE be used during pregnancy, or if the patient becomes pregnant while receiving this drug, the patient should be apprised of the potential hazard to the fetus. Nursing Women: It is not known whether TAXOTERE is excreted in human milk. Because man ...
10158-28698-1
10158-28698-1

... Currently, a limited number of studies have been conducted to investigate the relation between CYP2C9 gene polymorphisms and lipid-lowering response to stains. Kirchheiner et al. [21, 22] reported that the pharmacokinetics of fluvastatin (e.g. AUC) differed significantly in CYP2C9 genotype in 24 pat ...
4 2. LITERATURE REVIEW: Ariyana, et al (2014), developed
4 2. LITERATURE REVIEW: Ariyana, et al (2014), developed

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Histamine and Antihistaminic Agents

... This is most evident among the first generation agents many of which function as antagonists at muscarinic receptors and, to a lesser extent, adrenergic, serotonergic and dopamine receptors. While some of these non-target receptor interactions may be of some therapeutic value (as discussed above), m ...
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Case 5 - Tripod.com

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Appendix 5 - Cancer Care Ontario

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Peri-operative Management of Patients on Strong

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... The purpose of this review was to describe the potential influence of childhood obesity on pharmacosedation in pediatric dentistry and provide specific recommendations for managing obese patients. Increasingly common in the United States, childhood obesity poses specific challenges to the dentist. The ...
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(Avastin) in treatment of diabetic macular edema

... rization and very high intraocular levels in patients  with proliferative diabetic retinopathy decline after  successful laser  photocoagulation.[2]  These  observa‐ tions have led to the hypothesis that antiangiogenic  agents could be used to inhibit the development of  proliferative  retinopathy,  ...
SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF
SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF

... Care should be taken when treating acute asthma attacks or exacerbation of severe asthma as increased serum lactate levels, and rarely, lactic acidosis have been reported after the use of high doses of salbutamol have been used in emergency situations this is reversible on reducing the dose of salbu ...
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Calcium-Channel Blocker–Clarithromycin Drug Interactions and

... We used the Ontario Drug Benefit Program database to identify prescription drug use. This database contains highly accurate records of all outpatient prescriptions dispensed to patients aged 65 years or older, with an error rate of less than 1%.18 We identified diagnostic and procedural information ...
DEVELOPMENT AND CHARACTERIZATION OF TRANSDERMAL PATCHES OF ONDANSETRON HYDROCHLORIDE  Research Article
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... hydrochloride has been used by oral and injectable administration. Ondansetron hydrochloride is rapidly absorbed orally, but extensively metabolized by the liver. It should be administered 30 min before chemotherapy, and the orally administered antiemetic drug tends to be discharged by vomiting. On ...
NON-CLINICAL SAFETY IN DRUG DEVELOPMENT LA SÉCURITÉ NON-CLINIQUE S
NON-CLINICAL SAFETY IN DRUG DEVELOPMENT LA SÉCURITÉ NON-CLINIQUE S

... experimental toxicology studies focus on their adverse effects in selected laboratory animal species, before extrapolating the findings and predict potential adverse effects in man. As the non-clinical safety file is based on stringent global regulatory constraints, core studies are very well define ...
Simvastatin
Simvastatin

... levels and in such patients measurements should be repeated promptly and then performed more frequently. If the transaminase levels show evidence of progression, particularly if they rise to three times the upper limit of normal and are persistent, the drug should be discontinued. Liver biopsy shoul ...
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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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