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a study of prescription pattern of non steroidal anti
a study of prescription pattern of non steroidal anti

... High frequency of non-selective NSAID prescription in this study points towards the changing trends observed in the prescriber‘s preference for NSAID prescription after the withdrawal of rofecoxib22. This trend is quite evident in a study conducted in New York, which showed that selective COX-2 inhi ...
When Childhood Gets Commercialized, Can Children
When Childhood Gets Commercialized, Can Children

... The view that ads are inherently unfair and exploitative comes from a series of research studies begun in the 1970s whose aim was to assess what children can understand about ads and how they receive them. The studies ask questions such as: At what age can children discriminate between advertising a ...
Chapter 5 Drugs for Neoplastic Disorders
Chapter 5 Drugs for Neoplastic Disorders

... Discuss OTC products that could have drug interactions with prescriptions and the important role technicians have in identifying problem OTC purchases. The technician is often in a position to prevent many potentially serious complications from inappropriate OTC drug use. Often the patient will brin ...
Quality Assessment of the Commonly Prescribed Antimicrobial Drug
Quality Assessment of the Commonly Prescribed Antimicrobial Drug

Adulteration and Evaluation of Crude drugs
Adulteration and Evaluation of Crude drugs

View PPT - Indian Drug Manufacturers` Association
View PPT - Indian Drug Manufacturers` Association

... • Today India has nearly 117 Million people over 60 years ...
Slide 1
Slide 1

... (2) Curriculum vitae. (3) Clinical protocol. (4) Financial disclosure information. ...
FDA`s Acetaminophen Notice: A Snapshot of the Current Regulatory
FDA`s Acetaminophen Notice: A Snapshot of the Current Regulatory

... by Merck and Pfizer, respectively. In each case, the sponsor voluntarily withdrew the product following communications with FDA regarding new postmarketing clinical trial data. Thus, while FDA has long had the authority to withdraw drug approvals, the preferred path appears to be suggesting voluntar ...
Slide 1
Slide 1

... has been approved by FDA in any other application submitted under section 505(b) of the act. • Active moiety means the molecule or ion, excluding those appended portions of the molecule that cause the drug to be an ester, salt (including a salt with hydrogen or coordination bonds), or other noncoval ...
11_Bioequivalence
11_Bioequivalence

... another product if it contains the same active substance or therapeutic moiety and, clinically, shows the same efficacy and safety as that product, whose efficacy and safety has been established. • In practice, demonstration of bioequivalence is generally the most appropriate method of substantiatin ...
6. 7. 8. BRIEF RESUME OF THE INTENDED WORK ENCLOSURE
6. 7. 8. BRIEF RESUME OF THE INTENDED WORK ENCLOSURE

... aqueous solubility of poorly aqueous soluble drug molecules in the gastrointestinal fluid often causes unsatisfactory bioavailability. Poorly aqueous soluble drugs often require high doses in order to reach therapeutic plasma concentrations after oral administration of any drug to be absorbed must b ...
GenDrux: A guided supervised biomedical
GenDrux: A guided supervised biomedical

... domain and cannot be discerned from this tool. GenDrux, however, retrieves information in an automated fashion saving the user time; it makes results available on-line and freely. It has been shown that the gene-drug relations will help physicians make more informed decisions while prescribing treat ...
Prescribing Practices in 24-hour Supervised Community Residences
Prescribing Practices in 24-hour Supervised Community Residences

... This figure is higher than the rate of benzodiazepine use in the general population in Ireland of 11.6%3 in 2000 but much lower than a psychiatric inpatient population in Ireland in 2008 of 64%4.In 1989, Dunbar et al5 found a rate of benzodiazepine prescribing of 10.8% in the general population, and ...
Confusion regarding the generic name of the HER2
Confusion regarding the generic name of the HER2

... IV infusion every 3 weeks (21-day cycle) as a SINGLE AGENT until disease progression or unacceptable toxicity. Doses higher than that should not be given. However, trastuzumab (Herceptin) is prescribed in doses up to 8 mg/kg per loading dose, followed by a maintenance dose of 6 mg/kg every 3 weeks—a ...
Small Is Beautiful: Issues in Nanomedicine
Small Is Beautiful: Issues in Nanomedicine

... potentially  serious  and  inhibitory  consequences  if  nanomedicine  is  overregulated.  A  balanced  approach  is  required  here,  at  least  on  a  case‐by‐case  basis,  which  addresses  the  needs  of  commercialization  against  mitigation  of  inadvertent  harm  to  patients  or  the  envir ...
Chapater 12 - IND/NDA/ANDA/AADA
Chapater 12 - IND/NDA/ANDA/AADA

... disease, or if there is no comparable alternative drug or therapy available to treat that stage of the disease in the intended patient population. In addition, these patients are not eligible to be in the definitive clinical trials, which must be well underway, if not almost finished. An immediately ...
Regulatory Aspects of Ophthalmic Drug
Regulatory Aspects of Ophthalmic Drug

... execution of a broad array of regulatory and other services to drug, biologics and medical device/diagnostic clients seeking to market products in the United States. His expertise includes product development strategies, compliance and enforcement initiatives, recalls and crisis management, submissi ...
ACUROX TABLETS NEW DRUG APPLICATION ACCEPTED FOR
ACUROX TABLETS NEW DRUG APPLICATION ACCEPTED FOR

... Inc. (King) that King’s New Drug Application (NDA) for Acurox® (oxycodone HCl) Tablets was accepted for filing by the US Food and Drug Administration (FDA) with a Priority review classification and a Prescription Drug User Fee Act (PDUFA) date of June 17, 2011. In addition to filing acceptance and a ...
DEVELOPMENT AND VALIDATION OF UV SPECTROSCOPIC METHOD FOR DETERMINATION
DEVELOPMENT AND VALIDATION OF UV SPECTROSCOPIC METHOD FOR DETERMINATION

... The present study describes a simple, accurate, precise and cost effective UV-Spectrophotometric method for the estimation of Atazanavir sulphate, an Anti-HIV drug, in bulk and pharmaceutical dosage form. The drug was first dissolved in 20% glacial acetic acid and final volume was made up with disti ...
Do THE BENEFITS OUTWEIGH THE RISKS?
Do THE BENEFITS OUTWEIGH THE RISKS?

... companies, federal regulatory agencies, and patients who use the drugs. This Note will discuss the significant ramifications of withdrawing a blockbuster drug from the market and how such a decision may impact particular persons or entities. Part II will define a blockbuster drug and a subsequent wi ...
Metabolism of drugs
Metabolism of drugs

... Drug-Drug Interactions during Metabolism Allopurinol both prolongs the duration and enhances the chemotherapeutic action of mercaptopurine by competitive inhibition of xanthine oxidase. Consequently, to avoid bone marrow toxicity, the dose of mercaptopurine is usually reduced in patients receiving ...
Click Here - Suresh Gyan Vihar University
Click Here - Suresh Gyan Vihar University

... communication skills, awareness of ethical and social responsibilities, and lifelong self-learning ability. Possibility,motivational & scope for self learning Pharmaceutical science helps identify preferred of optimal methods to deliver or dose a drug and reliably ensure therapeutic benefit with min ...
DIPHENHYDRAMINE HYDROCHLORIDE CAPSULES, USP 25mg
DIPHENHYDRAMINE HYDROCHLORIDE CAPSULES, USP 25mg

DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR
DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR

... Probe Software was employed for this work. Shimadzu AX200 (Japan) digital balance and Spectra lab UCB 40 (Germany) ultrasonicator, were also used. Preparation of Standard Solutions The standard stock solution of S (-) MET was prepared by transferring, accurately weighed, 100 mg of API to 100 mL of v ...
Traditional Chinese Medicine And New Drug Development
Traditional Chinese Medicine And New Drug Development

... – Part of Asian American (especially Chinese American) culture – The Chinese railroad workers used TCM for routine medical needs since the early 1850s (CPRR) ...
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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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