Drug administration

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  • Drug Administration be very precise. (Standardized medicinal teaspoons and tablespoons are available.) Eye drops and nose drops (A) are designed for application to the mucosal surfaces of the eye (conjunctival sac) and nasal cavity, respectively. In order to prolong contact time, nasal drops are formulated as solutions of increased viscosity. Solid dosage forms include tablets, coated tablets, and capsules (B). Tablets have a disk-like shape, produced by mechanical compression of active substance, filler (e.g., lactose, calcium sulfate), binder, and auxiliary material (excipients).

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  • This Institute of Medicine/National Research Council report was written in response to a congressional request that the U.S. Food and Drug Administration (FDA) contract with the National Academies for a comprehensive study of gaps in public health protection provided by the food safety system in the United States. In particular, the study was to review the role of the FDA in ensuring the safety of the nation’s food supply.

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  • The publication Approved Drug Products with Therapeutic Equivalence Evaluations (the List, commonly known as the Orange Book) identifies drug products approved on the basis of safety and effectiveness by the Food and Drug Administration (FDA) under the Federal Food, Drug, and Cosmetic Act (the Act). (For more information, see the Orange Book Preface.)

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  • Tham khảo sách 'the acquisition of drugs and biologics for chemical and biological warfare defense', khoa học xã hội, lịch sử văn hoá phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả

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  • he bestselling and most useful aid available for finding all references to FDA and DEA regulations, Interpharm Master Keyword Guide: 21 CFR Regulations of the Food and Drug Administration, is used in hundreds of active pharmaceuticals, pharmaceutical, biotechnology, diagnostic, and device manufacturing companies. And it is in use by every FDA district in the United States to sort their way through their own regulations.

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  • Description: Identifies drug products approved on the basis of safety and effectiveness by the Food and Drug Administration under the Federal Food, Drug, and Cosmetic Act.

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  • Introduction: As coumarin rodenticides, warfarin, coumatetralyl, coumafuryl, coumachlor and bromadiolone are commercially available in Japan. The coumarin rodenticides do not show direct anticoagulant action causing bleeding, but inhibit the metabolic cycle of vitamin K; the inhibition causes the interference with protein biosynthesis of vitamin K-dependent coagulant factors (II, VII, IX and X factors) in the liver, which are very important for the blood coagulation system. The lowered coagulant factors cause the bleeding deaths of the rodents [1].

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  • Despite massive efforts in drug discovery fueled by combinatory chemistry, recombinant DNA technology, and highthroughput screening, surprisingly few molecules make it through the drug development process. While the reasons are debated, it is certain that many new chemical entities (NCEs) suffer from recurring problems that hinder development— low water solubility, instability, or inadequate pharmacokinetics. An estimated 43% of NCEs are poorly water-soluble.

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  • Introduction: Phenothiazine drugs, including chlorpromazine and levomepromazine, have been being widely used as neuroleptics (major tranquilizers), antiparkinsonian drugs and antihistaminics for a long time [1]. Table 1.1 shows chemical structures of representative phenothiazines. These drugs show blocking action on D2 receptors of dopaminergic neurons; there is close relationship between the receptor blocking and tranquilizing actions. The dopamine D2 receptor-blocking actions provoke extrapyramidal symptoms, such as muscular stiffness, tremor and ptyalism.

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  • This chapter describes the physiological role and pathophysical consequences of histamine release and provides a summary of the therapeutic use of histamine H1-receptor antagonists. H2-receptor antagonists are discussed in detail in Chapter 37: Agents Used for Control of Gastric Acidity and Treatment of Peptic Ulcers and Gastroesophageal Reflux Disease in the context of prevention and treatment of peptic ulcers, their principal therapeutic application.

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  • This Handbook of Police Administration, co-edited by Jim Ruiz and Don Hummer, provides a smorgasbord of topics that are at the coalface of policing: the difficulties police encounter dealing with drug problems, traffic issues, race and ethnicity challenges, and street gang problems. Cross-cutting themes such as leadership in policing, use of force, and understanding how the law shapes (or fails to shape) police practice are relevant to students of police studies, practitioners, and scholars alike.

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  • In one sense, pharmacology can be considered a “good news, bad news” scenario. The good news is that exciting and innovative changes in drug therapy continue to occur at lightning speed. The bad news is that it is often difficult for health care practitioners to stay abreast of this rapidly changing field. Oftentimes, drug therapies that were considered state-of-the-art only a few years ago are now outdated and replaced by more contemporary treatments.

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  • However, these events are but the immediate manifestation of a continuing dependent relationship that involves three types of interactions: licensing CBW drugs and biologics, especially vaccines; using Investigational New Drugs in military combat (and other special situations); and ensuring the compliance of producers with manufacturing requirements. DoD has not been well organized to respond to FDA. This report proposes various education and training programs that should be initiated for all defense personnel engaged in the development or acquisition of drugs and biologics for CBW defense.

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  • "In China, illicit drug use is an administrative offense and Chinese law dictates that drug users 'must be rehabilitated.' In reality, police raids on drug users often drive them underground, away from methadone clinics, needle exchange sites, and other proven HIV prevention services. And every year Chinese policy send tens of thousands of drug users to mandatory frug treatment centers, often for years, without trial or due process" -- p. [4] of cover.An Unbreakable CycleDrug Dependency Treatment, Mandatory Confinement, and HIV/AIDSin China’s Guangxi ProvinceI. Executive Summary ...........

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  • Purpose: Based on theoretical studies of state management on the prevention of drugs, analysis and assessment of the state of the state management on the prevention of drugs in Vietnam, fellows establish and implement the scientific foundation to propose practical solutions to improve system ef ciency of state management on the prevention of drugs in Vietnam during the integration period.

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  • Chapter 14 - Venous access and medication administration. In this chapter you will learn about the following: Convert selected units of measurement into the household, apothecary, and metric systems; identify the steps in the calculation of drug dosages; calculate the correct volume of drug to be administered in a given situation;...

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  • Food, Drug Administration (FDA) là cơ quan thuộc Bộ Y Tế Hoa Kỳ, tập hợp nhiều nhà khoa học kỹ thuật của Hoa Kỳ để đề ra và giám sát thực hiện các biện pháp đảm bảo an toàn tiêu dùng đối với thực phẩm, dược phẩm và dụng cụ y tế và mỹ phẩm sản xuất tại Hoa Kỳ và nhập khẩu từ các nước ngoài vào lãnh thổ Hoa Kỳ.

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  • Ô nhiễm không khí Thức ăn truyền thống 100 N thải tiết 61 Amonia thoát ra Tích luỹ nitơ 39 Thức ăn tháp protein + axit amin TĂ bổ sung và vấn đề ATTP Hormone và chất kích thích dùng trong chăn nuôi - BST (Bovine Somatotropin) do thuỳ trước tuyến yên của bò tiết ra. US Food and Drug Administration (FDA) cho phép sử dụng từ 1994, Hội đồng Marketing Sữa của Anh cũng cho phép sử dụng Sữa tăng 16-41%, bò cái tơ tăng trọng cao hơn 10% - rBGH (recombinant Bovine Growth Hormone. FDA cho phép sử dụng,...

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  • For decades we have been learning about the interplay between tumors and the immune system. Our knowledge seemed somewhat incomplete and indirect, like listening to the ocean waves through a shell. Only recently, cancer immunotherapy has started to become a reality, with Provenge (Dendreon Corporation, WA), an autologous antigen-presenting cell preparation, earning the approval of United States Food and Drug Administration (FDA) for the treatment of advanced prostate cancer in 2010.

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  • Background Definitions Causation: degrees of certainty Pharmacovigilance and pharmacoepidemiology Classification Causes Allergy in response to drugs Effects of prolonged administration: chronic organ toxicity Adverse effects on reproduction Background Cur'd yesterday of my disease I died last night of my physician.1 Nature is neutral, i.e. it has no 'intentions' towards humans, though it is often unfavourable to them.

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