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Type here
Type here

... extended release tablets, which will be introduced on the market this week. VoSpire ER is indicated for the relief of bronchospasm in adults and in children 6 years of age and older who have reversible obstructive airway disease. VoSpire ER's advantage over other therapeutically equivalent drugs is ...
The legality and ethics of self-prescribing
The legality and ethics of self-prescribing

... review by the FDA for the treatment of metastatic melanoma. Temozolomide has an orphan drug designation for the treatment of malignant gliomas and advanced metastatic melanoma. There are 4 strengths of temozolomide available (5 mg, 20 mg, 100 mg, and 250 mg) permitting appropriate dosing for brain t ...
Présentation PowerPoint
Présentation PowerPoint

Luitpold Pharmaceuticals, Inc. Submits Injectafer® NDA to the U.S.
Luitpold Pharmaceuticals, Inc. Submits Injectafer® NDA to the U.S.

Tier 0 (zero) prescription drug benefit program
Tier 0 (zero) prescription drug benefit program

... generic drugs with a cost of $0— that’s right, no copayment, no cost to you! Many of these generic drugs are used to treat chronic, high-cost conditions like diabetes, high blood pressure and heart disease. Tier 0 generic drugs, which are safe and effective, are often considered the best therapies—a ...
Position Paper on the Importation of Foreign Prescription Drugs
Position Paper on the Importation of Foreign Prescription Drugs

... The potential for harm exists even with medications obtained from Canada. Canadian drugs, like all foreign drugs, are outside the realm of the US Food and Drug Administration (FDA) approval process and oversight systems, including those manufactured here in the US and exported. FDA officials mainta ...
iv-po stepdown program
iv-po stepdown program

... Pharmacy: 1. A clinical pharmacist will assess patients receiving the drugs listed below to determine if oral therapy is feasible. 2. If patients meet the criteria for oral conversion: • continues to need medication • is clinically stable • is capable of tolerating the oral dosage from and • has no ...
Not For Human Consumption - North Inner City Drugs Task Force
Not For Human Consumption - North Inner City Drugs Task Force

... These drugs are only being produced for sale in the last number of years In the short-term, there are not a lot of hard facts about them and their side effects and little is known about the longer term effects on people’s health These new products have not been tested or approved for ...
Drug Resistance through the Back Door: How the Pharmaceutical
Drug Resistance through the Back Door: How the Pharmaceutical

... Economics and Policy (CDDEP) recorded a 30 per cent increase in total human antibiotic consumption between 2000 and 2010, from approximately 50 billion to 70 billion standard units.13 Under current scenarios, this figure is set to rise over the coming decades as population levels increase and people ...
History
History

... • There was a disregard for the need to observe proper laboratory, animal care, and data management procedures. • Sponsors failed to adequately monitor the studies performed by contract testing laboratories. • Firms failed to systematically verify the accuracy and completeness of scientific data in ...
NMUPD - MassTAPP
NMUPD - MassTAPP

... 2008; Subramaniam & Stitzer, 2009); however it is unknown if this indicates a directional relationship, or whether another factor might account for both conditions. Research has found an association between illicit drug use and increased risk of suicide, however, however this has not been directly l ...
Rational prescribing in the older adult
Rational prescribing in the older adult

Pharmaceuticals and Medical Devices Safety Information
Pharmaceuticals and Medical Devices Safety Information

Botanix Secures Commercial-Scale Synthetic
Botanix Secures Commercial-Scale Synthetic

... processes that must be used to separate natural cannabidiol from the hundreds of other chemicals found in the plant. This represents a significant advantage for Botanix products, as the Company will not be required to comply with the extensive testing and controls in the US Food and Drug Administrat ...
Document
Document

... 2008; Subramaniam & Stitzer, 2009); however it is unknown if this indicates a directional relationship, or whether another factor might account for both conditions. Research has found an association between illicit drug use and increased risk of suicide, however, however this has not been directly l ...
Food Drug and Cosmetic Act (Federal)
Food Drug and Cosmetic Act (Federal)

... Drug Price Competition and PatentTerm Restoration Act 1984 • Also called Waxman-Hatch Amendment • Streamlined generic drug approval process to make them more readily available • Brand-name manufacturers have become increasingly creative at delaying generics • Bush limits automatic 30-month patent e ...
Stop Drugging Our Elders!
Stop Drugging Our Elders!

...  Biological needs – food, shelter, activity  Psychological needs – choice, control, connection ...
class 20
class 20

... ◦ Remind customers of positive experience with ad copy, specialty items, thank you gifts ...
An informative guide to the most commonly used drugs in youth
An informative guide to the most commonly used drugs in youth

... Boost Mobile conducted a survey of 500 males and females between the ages of 16-25 : 68% confessed to checking their feeds a staggering 10 times a day. 67% admitted to being addicted to social media, 67% of which were female. 37% admitted that social media updates more important than listening in cl ...
Drug Products That Have Been Withdrawn from the US Market
Drug Products That Have Been Withdrawn from the US Market

... for new molecular entities. In the same time period, a few new drugs were withdrawn from the market by the manufacturers, typically in close consultation with FDA. The table below lists many of the approved new drugs that were withdrawn from the U.S. market from 2000 to present and as to which there ...
DEVELOPMENT AND VALIDATION OF UV SPECTROSCOPIC METHOD FOR DETERMINATION
DEVELOPMENT AND VALIDATION OF UV SPECTROSCOPIC METHOD FOR DETERMINATION

... transferred to 100ml volumetric flask. Drug was dissolved and diluted up to the mark with 0.1N HCl solution to obtain final con centration of 1000 mcg/ml, then the solution was ultrasonicated for few minutes and the resulting Solution was used as working standard solution. ...
Glossary of Terms
Glossary of Terms

... An ideal of therapeutic practice in which drugs are prescribed and used in exact accordance with the best understanding of their appropriateness for the indication and the particular patient, and of their benefit, harm effectiveness and risk. Rechallenge The point at which a drug is again given to a ...
how a Cmo Can help wIth InvestIgatIonal new drug applICatIons
how a Cmo Can help wIth InvestIgatIonal new drug applICatIons

... candidate progresses through further phases of clinical testing, additional CMC data are required.3 As a result of the changing dynamics in the pharmaceutical industry, including the shift of growth to emerging markets that prefer lower-cost drugs and away from blockbusters to therapies designed f ...
Generic Drugs - CN Pensioners` Association
Generic Drugs - CN Pensioners` Association

... therapeutic effect and can be safely interchanged with typically higher priced brand medications. All drugs sold in Canada must be approved by Health Canada. Each product must meet strict regulations and both generic and brand name drugs are subjected to the very same rigorous standards. Ea ...
Unsafe Drugs: Congressional Silence is Deadly
Unsafe Drugs: Congressional Silence is Deadly

... And the pre-market safety of new drugs is not even addressed. To the extent that recent drug withdrawals raise questions about FDA's premarket consideration of drug risks or its will to prevent the marketing of distinctly and highly toxic but questionably necessary drugs, the changes mandated by tha ...
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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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