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Brand-Name vs Generic Finasteride Jan-Feb 2016
Brand-Name vs Generic Finasteride Jan-Feb 2016

... is the central ingredient. The second is known as the excipient, which is the inactive substance that serves as the vehicle for the API itself. If the drug is in a syrup form, then the excipient is the liquid that has been used to make it as such.² APIs are commonly referred to as “bulk pharmaceutic ...
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Chris`s Handouts - American Sociological Association
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... First, “Did anyone figure out what drug this is? What do you think it is? Did your idea of what you thought the drug was affect your classification of it? Then I tell them what the drug really was. Then we analyze how the class classified the drug on the chart. I go through this one drug at a time, ...
Me-too drugs: is there a problem
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SUSTAINED DRUG DELIVERY TO THE POSTERIOR SEGMENTS
SUSTAINED DRUG DELIVERY TO THE POSTERIOR SEGMENTS

... etc, and a strategy for disease management developed. For example, an intravitreous injection of the drug every six months may be considered minimally invasive and feasible, if such sustained-release options exist and have been validated. Likewise, treatment of retinoblastoma should likely be addres ...
I.V. bolus injection
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Introduction to Pharmacology
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15. Drug-Induced Torsade de Pointes
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biliary excretion
biliary excretion

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Glaucoma Treatment Market Value Projected to Hit $3 Billion by 2023
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Medications Requiring Prior Authorization for Medical
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optimising drug and device together for novel
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Effects of different drugs of different - Sun Yat
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... attachment caused by many reasons. Now the clinical treatments usually use two kinds of medicines: the H2 receptor antagonist and the proton pump inhibitor. Being the H2 receptor antagonist,Cimetidine can compete the H2receptors with histamine.Thereby,it can block the histamine’s function of promoti ...
SYLABUS
SYLABUS

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Stimulants Drug Information
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IJPhS_Mar_Aprl 07.pmd - Indian Journal of Pharmaceutical Sciences
IJPhS_Mar_Aprl 07.pmd - Indian Journal of Pharmaceutical Sciences

... prepared containing Avicel PH 102 as a diluent and Ac-Di-sol as a superdisintegrant by wet granulation process. All the formulations were evaluated for characteristics such as hardness, friability, weight variation, wetting ability, disintegration time and dissolution rate. A modified disintegration ...
Зразок для теоретичних кафедр
Зразок для теоретичних кафедр

... During exacerbation of duodenal and gastric ulcer omeprazole administered at a dose of 20-40 mg/day. For the prevention of relapse of peptic ulcer omeprazole administered in a dose of 20 mg (lansoprazole - 30 mg) three times a week for 4 weeks. In Zollinger-Ellison syndrome omeprazole first appoint ...
Pharmacology
Pharmacology

... eliminate pathogenic organisms within body. ...
Revisão - Química Nova
Revisão - Química Nova

... Besides plant species (Angiosperms and Gymnosperms), there are several other organisms to be studied on Earth. Terrestrial biodiversity includes many biomes that remain largely underexplored or entirely unexplored, even though they represent potentially rich sources of new molecular models for synth ...
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Orphan drug

An orphan drug is a pharmaceutical agent that has been developed specifically to treat a rare medical condition, the condition itself being referred to as an orphan disease.In the US and EU it is easier to gain marketing approval for an orphan drug, and there may be other financial incentives, such as extended exclusivity periods, all intended to encourage the development of drugs which might otherwise lack a sufficient profit motive. The assignment of orphan status to a disease and to any drugs developed to treat it is a matter of public policy in many countries, and has resulted in medical breakthroughs that may not have otherwise been achieved due to the economics of drug research and development.According to Thomson Reuters in their 2012 publication ""The Economic Power of Orphan Drugs"", there has been increased investing in orphan drug Research and Development partly due to the U. S. Orphan Drug Act (ODA) 1983 and similar Acts in other regions of the world and also driven by ""high-profile philanthropic funding."" The period between 2001 to 2011 was the ""most productive period in the history of orphan drug development, in terms of average annual orphan drug designations and orphan drug approvals."" For the same decade the compound annual growth rate (CAGR) of the orphan drugs was an ""impressive 25.8 percent, compared to only 20.1 percent for a matched control group of non-orphan drugs."" By 2012 the market for orphan drugs was worth USD$637 million compared to the USD$638 million matched control group of non-orphan drugs, Thomson Reuters.By 2012, ""the revenue-generating potential of orphan drugs [was] as great as for non-orphan drugs, even though patient populations for rare diseases are significantly smaller. Moreover, we suggest that orphan drugs have greater profitability when considered in the full context of developmental drivers including government financial incentives, smaller clinical trial sizes, shorter clinical trial times and higher rates of regulatory success.""
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