BRS Pharmacology (Board Review Series) (6th Edition) - download pdf or read online

By Gary C. Rosenfeld, David S. Loose

ISBN-10: 1451175353

ISBN-13: 9781451175356

BRS Pharmacology is designed for clinical scholars, dental scholars, and different scholars getting ready to go into the well-being care professions. It is meant essentially to aid scholars arrange for licensing examinations, comparable to the USMLE, yet can be utilized for direction evaluation or as a supplementary textual content. This e-book offers succint descriptions of ways medicines act at the significant physique platforms, offering readers with very important info with no overloading them with extraneous info. Written with a physique structures technique, the ebook starts with a bankruptcy dedicated to the final rules of drug mechanisms, and keeps with chapters that aspect how medications act at the significant physique platforms. different chapters talk about a number of well known medications, like autocoids, ergots, anti inflammatory medications, and immunosuppresive brokers. Readers also will know about medicines used to deal with anemia, problems of hemostatis, infectious ailments, and melanoma. also, the textual content covers pharmacological ideas linked to toxicology.

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Additional info for BRS Pharmacology (Board Review Series) (6th Edition)

Sample text

MUSCARINIC-RECEPTOR ANTAGONISTS A. 5) 1. Muscarinic-receptor antagonists are competitive antagonists of ACh at all muscarinic cholinoceptors. 2. , propantheline [Pro-Banthine], ipratropium [Atrovent]). 3. Tertiary amines are often used for their effects on the CNS. Quaternary amines, which have minimal CNS actions, are often used for their effects on peripheral systems. B. Pharmacologic effects 1. 3) a. Muscarinic-receptor antagonists produce cycloplegia by blocking parasympathetic tone, leading to paralysis of the ciliary muscle and loss of accommodation.

A) Alters the mechanism of action of an agonist (B) Alters the potency of an agonist (C) Shifts the dose–response curve of an agonist to the right (D) Decreases the maximum response to an What is the half-life (in hours) of drug X? (A) 1 (B) 2 (C) 4 (D) 5 (E) 9 23. Which of the following factors will determine the number of drug–receptor complexes formed? (A) (B) (C) (D) (E) Efficacy of the drug Receptor affinity for the drug TI of the drug Half-life of the drug Rate of renal secretion agonist (E) Binds to the same site on the receptor as the agonist 25.

Administration of an IV loading dose to a patient of drug X yields an initial plasma concentration of 100 mcg/L. The table below illustrates the plasma concentration of X as a function of time after the initial loading dose. Chapter 1 General Principles of Drug Action 23 Time (hours) 0 1 5 9 Plasma conc. 5 24. Which of the following is an action of a noncompetitive antagonist? (A) Alters the mechanism of action of an agonist (B) Alters the potency of an agonist (C) Shifts the dose–response curve of an agonist to the right (D) Decreases the maximum response to an What is the half-life (in hours) of drug X?

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BRS Pharmacology (Board Review Series) (6th Edition) by Gary C. Rosenfeld, David S. Loose


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