Xem 1-20 trên 30 kết quả Drug dosage
  • (BQ) Part 1 book "Pharmacology for dentistry" presents the following contents: General pharmacology, drug dosage forms, drugs acting on autonomic nervous system, drugs acting on autonomic nervous system, renal pharmacology, drugs acting on central nervous system.

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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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  • Pharmacology has undergone major intellectual changes in the recent years and has become increasingly important to all medical, dental and other health professionals. The graduate students of dentistry may have to handle medical emergency during various dental procedures on the dental chair. Besides this, dentists have to look into various drug associated interactions. The broad goal of teaching pharmacology to undergraduate students is to inculcate rational and scientific basis of therapeutics keeping in view the dental curriculum and profession.

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  • (BQ) The second section contains topics relevant to the critically ill patients, including factors that may affect drug prescribing and management of medical emergencies. There is also a key data section showing weight conversions, BMI and corresponding dosage calculations, and an invaluable chart indicating drug compatibility for IV administration.

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  • (BQ) The best and easiest way to learn essential information about the top 300 drugs. Every card includes: Generic and common name, class, dosage forms, approved dose and indications, off-label use, contraindications, adverse reactions, drug interactions,...

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  • It has been over eight years since the first edition of the Handbook of Pharmaceutical Granulation Technology was published. The enthusiastic reception afforded by the scientific community was heartwarming. The basic science of granulation has not changed much over the last few years; however, a better understanding of the theory of granulation and the proliferation of different dosage forms has.

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  • This Handbook of Manufacturing Techniques focuses on a new aspect of the drug development challenge: producing and administering the physical drug products that we hope are going to provide valuable new pharmacotherapeutic tools in medicine. These 34 chapters cover the full range of approaches to developing and producing new formulations and new approaches to drug delivery. Also addressed are approaches to the issues of producing and packaging these drug products (that is, formulations).

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  • This work is subject to copyright. All rights are reserved, whether the whole or part of the material is concerned, specifically those of, translation, reprinting, re-use of illustrations, broadcasting, reproduction by photocopying machines or similar means, and storage in data banks. Product liability. The publisher can give no guarantee for all the information contained in this book. This also refers to that on drug dosage and application thereof. In each individual case the respective user

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  • Adjusting Drug Dosages While elimination half-life determines the time required to achieve steadystate plasma concentrations (Css), the magnitude of that steady state is determined by clearance (Cl) and dose alone.

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  • The subspecialty of population pharmacokinetics was introduced into clinical pharmacology / pharmacy in the late 1970s as a method for analyzing observational data collected during patient drug therapy in order to estimate patient-based pharmacokinetic parameters. It later became the basis for dosage individualization and rational pharmacotherapy. The population pharmacokinetics method (i.e., the population approach) was later extended to the characterization of the relationship between pharmacokinetics and pharmacodynamics, and into the discipline of pharmacometrics.

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  • Renal Disease Renal excretion of parent drug and metabolites is generally accomplished by glomerular filtration and by specific drug transporters, only now being identified. If a drug or its metabolites are primarily excreted through the kidneys and increased drug levels are associated with adverse effects, drug dosages must be reduced in patients with renal dysfunction to avoid toxicity. The antiarrhythmics dofetilide and sotalol undergo predominant renal excretion and carry a risk of QT prolongation and arrhythmias if doses are not reduced in renal disease.

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  • Seven distinct antigenic botulinum toxins (BNT-A, -B, -C, -D, -E, -F, and -G) produced by different strains of Clostridium botulinum have been described. The human nervous system is susceptible to five toxin serotypes (BNT-A, -B, -E, -F, -G) and unaffected by 2 (BNT-C, -D). Although all toxins have different molecular targets, their action leads to the blockade of the cholinergic nerves. However, only the A and B toxins are available as drugs.

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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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  • Chapter 51 prepares you to understand the fundamentals of drug administration, including the following: Routes of medication administration, dosage calculations, techniques involved with various types of parenteral injections, seven rights of drug administration, patient education.

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  • Chapter 51 - Drug administration. Chapter 51 prepares you to understand the fundamentals of drug administration, including the following: Routes of medication administration, dosage calculations, techniques involved with various types of parenteral injections, seven rights of drug administration, patient education.

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  • Chapter 20 provides knowledge of drug administration. After studying this chapter you will be able to: Identify your responsibilities regarding drug administration, execute dosage calculations accurately, check the patient before administering any drug, identify the rights of drug administration, describe the various techniques of drug administration,...

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  • Chapter 10, Pediatric and geriatric considerations. This chapter includes drug orders based upon body weight. It introduces body surface area (BSA) calculations. Discussions of special concerns for pediatric and geriatric patients are also presented.

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  • (BQ) Part 1 book "Fundamental pharmacology for pharmacy technicians" presentation of content: Introduction to pharmacology, drug legislation, and regulation; drug sources and dosage forms, biopharmaceutics, drug therapy for the autonomic nervous system, anesthetic drugs, anticoagulant drugs, drug therapy for allergies and respiratory disorders,... and other content.

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  • The selection of the most commonly prescribe meications was base on a number of reports evaluating meication use base on the number of prescriptions fille in the Unite States an the cost of those prescriptions. Most estimates rely on data from IMS Health, using data from their National Prescription Au it

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  • What is the definition of a formulation? Why is it needed? What is the importance of a formulation? These are some important questions that need to be addressed during the development of a potential drug product. The strict definition of the word is to specify a formula or to express a formula in systematic terms or concepts. The formula, in the current case, is a pharmaceutical dosage form. A formulation is needed to deliver the drug or the active pharmaceutical ingredient (API) to its targeted site. In order to overcome some of the physiochemical limitations of an API,...

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