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CRS Newsletter. Volume 25, Number 2. 2008
CRS Newsletter. Volume 25, Number 2. 2008

... thus leading to potential under- or overdosing. In addition, the excipients employed in order to act, for example, as preservatives or to enhance organoleptic properties—notably ethanol, benzyl alcohols, and certain flavourings and sweeteners—may also pose potentially fatal toxicity and health-relat ...
phentermine informed consent - Ultimate Weight Loss Solutions
phentermine informed consent - Ultimate Weight Loss Solutions

... dexfenfluramine (Redux) can cause a rare fatal lung disorder called pulmonary hypertension. Do not  take this medicine with any other diet medications without your doctor's advice.  ...
Drug Master Files
Drug Master Files

... The applicant must be supplied by the ASM with sufficient information to be able to take responsibility for an evaluation of the suitability of the active substance specification to control the quality of the substance. This normally includes a brief outline of the manufacturing method, information ...
DEVELOPMENT OF A NEW RP-HPLC METHOD FOR THE ESTIMATION OF... TABLET DOSAGE FORM  Research Article
DEVELOPMENT OF A NEW RP-HPLC METHOD FOR THE ESTIMATION OF... TABLET DOSAGE FORM Research Article

... Results and discussion: The retention time for nevirapine was found to be 3.660 min. The method was validated for Linearity, Accuracy, and Precision. Linearity for nevirapine was in the range of 2-10 µg/ml with correlation coefficient values 0.9999. The %RSD reported was found to be less than 2% ind ...
Prescription Drug Cost Sharing - Associations With Medication and
Prescription Drug Cost Sharing - Associations With Medication and

Selected Operating and Administrative Practices of the Bureau of
Selected Operating and Administrative Practices of the Bureau of

... greater deterrent to prescription drug diversion. Our initial analysis of this prescription data for just a 15-month period identified several hundred thousand prescription records containing inaccurate or inconsistent information. These prescriptions were reportedly filled over a halfmillion times ...
Dosage Patenting in Personalized Medicine
Dosage Patenting in Personalized Medicine

... medicinal effects or improve patient compliance.5 Patient compliance can be crucial for optimal treatment of various conditions. The more doses required or the more difficult the treatment plan, the less likely a patient is to comply. Although medical agents have the ability to enhance patients’ qua ...
New CMS Guidance to Surveyors: Pharmacy Services and
New CMS Guidance to Surveyors: Pharmacy Services and

... abuse, except when the facility uses single unit package medication distribution systems in which the quantity stored is minimal and a missing dose can be readily detected ...
DERIVATIVE SPECTROPHOTOMETRIC DETERMINATION OF ROSIGLITAZONE MALEATE IN
DERIVATIVE SPECTROPHOTOMETRIC DETERMINATION OF ROSIGLITAZONE MALEATE IN

... measurement of absorbance at 245nm and second method is the derivative spectrophotometric method in which derivative amplitude was measured at 218nm. The correlation coefficient for first and second method were 0.99992 and 0.99995 respectively.%Recovery from pharmaceutical formulation were 99.577 an ...


International Journal of Innovative Pharmaceutical Sciences and
International Journal of Innovative Pharmaceutical Sciences and

... Acetaminophen commonly known as paracetamol, belonging to non-steroidal anti-inflammatory drugs (NSAIDs), widely used over the counter medicine [3].Chemically, it is 4-hydroxy acetanilide, its structure shown in Figure 1. [1] .Paracetamol is approved for reducing fever in people of all ages [2]. It ...
LSD, mushrooms and other hallucinogenic drugs
LSD, mushrooms and other hallucinogenic drugs

... experimented with LSD, hallucinogenic mushrooms or poppers than the others [8]. Among students, age and gender (the fact of being a boy) are associated with experimentation with LSD and hallucinogenic mushrooms or poppers. At school, the fact of being in a professional channel is only associated wit ...
Entrenching the KNH Formulary to Clinical Practice
Entrenching the KNH Formulary to Clinical Practice

... • Used to be drug- list based • Now it’s a comprehensive system of medication use policies to ensure safe, appropriate use of pharmaceuticals • MTCs now have broader functions – ADR reporting, development of STGs , Mx of drug product shortage ...
9. precursor trends and manufacturing methods
9. precursor trends and manufacturing methods

... Coincident with the increased use of phenylacetic acid in recent years, there has been a significant rise in the use of non-controlled precursor chemicals in the manufacture of amphetamine, methamphetamine and ecstasy-group substances. This development can also be attributed in part to increased con ...
What is Nanocrystal Technology
What is Nanocrystal Technology

... Education program for health care providers and patients Safety surveillance of PML, serious opportunistic infections, and deaths Program evaluation of health outcomes, process compliance, and assessment of knowledge ...
Elan Drug Technology
Elan Drug Technology

DEVELOPMENT, CHARACTERIZATION AND EVALUATION OF SOLID DISPERSIONS OF
DEVELOPMENT, CHARACTERIZATION AND EVALUATION OF SOLID DISPERSIONS OF

... poorly soluble in water with bioavailability of 1.18ug/ml and 0.44ug/ml respectively. Artemether has rapid onset of action and is rapidly eliminated from the body. It is thus thought to provide rapid symptomatic relief by reducing the number of malarial parasites whereas Lumefantrine has a much long ...
National Conference on “Recent Advances in Herbal Drug Technology”
National Conference on “Recent Advances in Herbal Drug Technology”

... Abstract: Tectona grandis Linn. (Verbenaceae) is an important medicinal plant commonly known as sagwan. The bark of this plant is acrid and useful in the treatment of bronchitis. Aim of the present study is to validate traditional asthmatic action of the bark. Dried powdered bark was extracted using ...
Ravimid laste jaoks
Ravimid laste jaoks

... FDA: 127 changes in drug information • New dose or changes in exsisting dose (n = 25) • New data on tolerability (n = 35) • “No data in children” added into label (n = 28) • New dosing recommendations for infants or neonates (n = 83) ...
Adrenergic_antagonis..
Adrenergic_antagonis..

... It produces arterial & venous dilation. So it decreases BP, so it is used for the treatment of hypertension It causes less tachycardia than non–selective vasodilators (because it doesn’t act on α2 receptors) It precipitates less angina & cardiac arrhythmia It may increase HDL / cholesterol ratio. HD ...
Analytical method development for pharmaceutical
Analytical method development for pharmaceutical

... Chibroxin (ophthalmic) is approved for use in children older than one year of age. Norfloxacin was first patented in 1979. Kyorin granted Merck & Company, Inc., an exclusive license, to import and distribute norfloxacin under the brand name Noroxin. The U.S. Food and Drug Administration (FDA) appro ...
In the scientific literature, which countries first appeared term
In the scientific literature, which countries first appeared term

... In the scientific literature, which countries first appeared term "biopharmacy"? A. USSR B. Russia C. USA D. Ukraine E. England ANSWER: C Which of the twentieth century appeared in the scientific literature the term "biopharmacy"? A. 50-s B. 60's C. 80th D. 90th E. 40-s ANSWER: B In what year were d ...
Trends in Retail Prices of Brand Name Prescription Drugs
Trends in Retail Prices of Brand Name Prescription Drugs

... 54 prescriptions every year—or 4.5 prescriptions per month.3 Consequently, older adults who use brand name prescription drugs are likely to have experienced an average annual retail cost of drug therapy totaling more than $26,000 in 2015. This annual retail cost of brand name prescription drugs exce ...
Registration process of API - International Journal of Pharma
Registration process of API - International Journal of Pharma

... API materials that are the active for new drugs are covered by NDA documentation. Innovator companies would use their IND or NDA filings to provide the expected details covering an API, while all others would establish and submit a DMF with the FDA or other appropriate country authority, such as EMA ...
Validated RP-HPLC Method for Concurrent Determination of
Validated RP-HPLC Method for Concurrent Determination of

... and all parameter are tested. The method is free from interference from other ingredients and additives used in formulation. The method showed linearity in the range 10200µg/ml with regression coefficient of phenytoin sodium and clopidogrel bisulphate is 0.9992 and 0.9993. The recovery is nearly 100 ...
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Pharmaceutical marketing

Pharmaceutical marketing, sometimes called medico-marketing or pharma marketing in some countries, is the business of advertising or otherwise promoting the sale of pharmaceuticals or drugs.Many countries have measures in place to limit advertising by pharmaceutical companies.Pharmaceutical company spending on marketing far exceeds that of its research budget. In Canada, $1.7 billion was spent in 2004 to market drugs to physicians; in the United States, $21 billion was spent in 2002. In 2005, money spent on pharmaceutical marketing in the United States was estimated at $29.9 billion with one estimate as high as $57 billion. When the U.S. numbers are broken down, 56% was free samples, 25% was pharmaceutical sales representative ""detailing"" (promoting drugs directly to) physicians, 12.5% was direct to user advertising, 4% on detailing to hospitals, and 2% on journal ads. There is some evidence that marketing practices can negatively affect both patients and the health care profession.
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