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File - Lindsay Social Studies
File - Lindsay Social Studies

... information. Section 4 begins on page 506 of your textbook. ...
Pharmacokinetics of Chemotherapeutic Agents in Kidney Disease
Pharmacokinetics of Chemotherapeutic Agents in Kidney Disease

... is the dose-limiting side effect of this very effective chemotherapeutic agent (17–19). In the earliest reports of renal toxicity, incidence rates of 28%–36% were reported in patients receiving a single dose of 50 mg/m2 (Bristol Meyer Packaging), but the severity of renal toxicity decreased followin ...
Diamide, Capsule
Diamide, Capsule

... effects as measured by psychomotor tests (i.e. subjective drowsiness and the Digit Symbol Substitution Test). The concomitant administration of loperamide (16 mg single dose) and ketoconazole, an inhibitor of CYP3A4 and P-glycoprotein, resulted in a 5-fold increase in loperamide plasma concentration ...
Number: PL 00006/0195
Number: PL 00006/0195

... adolescents aged 8 to 18 years for the treatment of moderate to severe major depressive episodes and it should not be used in other indications. If, based on clinical need, a decision to treat is nevertheless taken, the patient should be carefully monitored for the appearance of suicidal symptoms. I ...
News Oklahoma State Board of Pharmacy
News Oklahoma State Board of Pharmacy

... tool. A pharmacist shall administer this exam as a prerequisite for approving an Oklahoma State Board of Pharmacy technician application. The pharmacist shall correct the exam, review incorrect answers with the technician applicant, and keep the original exam in the technician’s training file for re ...
If Long-term Outcomes Are Considered, Is This An
If Long-term Outcomes Are Considered, Is This An

... evidence of deterioration in contemporaneous educational outcomes including grade repetition and mathematics scores.When we turn to an examination of long-term outcomes, we find that increases in medication use are associated with increases in the probability that boys dropped out of school and with ...
Dr. Kelley`s PowerPoint slides
Dr. Kelley`s PowerPoint slides

... partial-onset seizures: results of randomized global phase III study 305. Epilepsia. 2013;54:117–125. 14. Krauss GL, Serratosa JM, Villanueva V, et al. Randomized phase III study 306: adjunctive perampanel for refractory partial-onset seizures. Neurology. 2012;78:1408–1415. 15. Bullman J, Nicholls A ...
Safety, Tolerability and Pharmacokinetics of L
Safety, Tolerability and Pharmacokinetics of L

... ‐Safety: Patients with “normal” renal function (Cr ≤1.5mg/dl)  received 3.3g OPA/d as a constant infusion. Safety reviewed by  committee before approving incremental doses up to 10g/d. ‐Tolerability: Adverse events and PK reviewed by committee  before approving use in patients with impaired renal fu ...
Triple Diagnosis: HIV, Substance Abuse and Mental Illness
Triple Diagnosis: HIV, Substance Abuse and Mental Illness

What’s In this Urine?
What’s In this Urine?

... dependence, buprenorphine is monitored for compliance. It is recommended that patients taking buprenorphine should NOT be taking other opioids or methadone.  Metabolized to norbuprenorphine (pharmacologically active) 0 to 21 days after  Target analyte: 9COOH-THC, the primary psychoactive use comp ...
Treatment for uterine fibroids: Searching for effective drug therapies
Treatment for uterine fibroids: Searching for effective drug therapies

... therapy is the relief of the symptoms. As we learn more about the impact of fibroids on fertility, it becomes important for patients and their physicians to have a toolbox of therapeutic options with viable drug therapies being one of those tools. To this end, promising drug therapies, their chemist ...


... The dissolution rate of selected prepared formulations F2 and F8 were compared with that of marketed conventional tablet. The F8 formulation shown prolonged release (86%) up to 12 hrs, but the marketed tablet released 97% of drug within 2.5 hrs. Further, to confirm the mechanism of drug release, F2 ...
Nonspecific Medication Side Effects and the Nocebo Phenomenon
Nonspecific Medication Side Effects and the Nocebo Phenomenon

... outpatient settings in the United States, an increase of 50% since 1992.1 Although many side effects (generally defined as an action of a drug other than the one for which it is being used) result directly from these drugs’ pharmacological activity, many others cannot be attributed to their specific ...
glucagon - DavisPlus
glucagon - DavisPlus

... Assess for nausea and vomiting after administration of dose. Protect patients with depressed level of consciousness from aspiration by positioning on side; ensure that a suction unit is available. Notify health care professional if vomiting occurs; patient will require parenteral glucose to prevent ...
Rosuvastatin Stada 5 mg film-coated tablets Rosuvastatin
Rosuvastatin Stada 5 mg film-coated tablets Rosuvastatin

... If CK levels are significantly elevated at baseline (5 time the upper limit of normal) treatment should not be started. Stop taking the drug and talk to your doctor immediately if you have any unusual aches or pains in your muscles which go on for longer than you might expect. As with other statins, ...
anxiolytics2011-09
anxiolytics2011-09

... effects. The pharmacologic effects appear late only after two weeks from administration. Ipsapirone and gepirone are even more selective for the same receptor. It does not cause rebound anxiety or withdrawal signs. Buspirone does not affect driving skills or potentiate CNS depressant effects of othe ...
Herbal Remedies: Drug-Herb Interactions
Herbal Remedies: Drug-Herb Interactions

... Although most people in the United States believe that herbs are harmless plants, about one third of our drugs (including digitalis, morphine, atropine, and several chemotherapeutic agents) were developed from plants. So, indeed, herbs can be potent products. Herbs can affect body functions; therefo ...
Basic Pharmacokinetics
Basic Pharmacokinetics

... Most drugs are eliminated by a first-order process, and the concept of first-order elimination must be understood. With first-order elimination, the amount of drug eliminated in a set amount of time is directly proportional to the amount of drug in the body. The amount of drug eliminated over a cert ...
improving the thrombolysis regime for central venous catheters
improving the thrombolysis regime for central venous catheters

... supported by the specialist nurses and the pharmacist attending the unit to provide teaching to ensure that the nursing staff were fully aware of the changes. One of the main concerns about how the units were previously giving urokinase was that there had been an over-simplification in the “push loc ...
Salmeterol vs. Combination Therapy
Salmeterol vs. Combination Therapy

... A total of 15 studies of good methodological quality met the inclusion criteria by randomly assigning 7814 participants with predominantly poorly reversible, severe COPD. Data were most plentiful for the FPS combination. Exacerbation rates were significantly reduced with combination therapies (rate ...
nations unies
nations unies

... and reduced fecundity in fish. Chemosphere 135, 38-45. (Metformin is a very widely-prescribed antidiabetic drug) If HSAC was asked its opinion on whether or not it considered a pharmaceutical such as metformin to be of environmental concern, how would it go about answering that question? This brief ...
Recreational Drugs - Immunodeficiency Clinic
Recreational Drugs - Immunodeficiency Clinic

... Please note: This chart summarizes some of the major drug interactions identified to date, based on current available data; other drug interactions may exist. Please use caution whenever adding/modifying therapy. The information in this table is intended for use by experienced physicians and pharmac ...
12th Lecture 1435
12th Lecture 1435

DUEXIS® (ibuprofen 800mg/famotidine 26.6mg) oral tablet
DUEXIS® (ibuprofen 800mg/famotidine 26.6mg) oral tablet

... approval with documentation of use of optimal dose / duration of the generic product and meeting other criteria within the coverage guideline. When the drug in question is a combination product, there must be documentation of failure / ineffectiveness of concurrent use (each ingredient used at the s ...
Product Information: Dolutegravir (as sodium)
Product Information: Dolutegravir (as sodium)

... Antiretroviral Naïve Patients The efficacy of TIVICAY in HIV-infected, therapy naive patients is based on the analyses of 48-week data from two randomized, international, double-blind, active-controlled trials, SPRING-2 (ING113086) and SINGLE (ING114467). In SPRING-2, 822 adults were randomized and ...
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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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