Full download : http://alibabadownload.com/product/pharmacology-an-introduction-6th-edition-hitner-test-bank/ Pharmacology An Introduction 6th Edition Hitner Test Bank
This document provides an overview of key pharmacokinetic concepts including bioavailability, Cmax, distribution, half-life, Tmax, and area under the curve (AUC). Bioavailability describes the amount of drug that reaches systemic circulation. Cmax is the maximum drug concentration in blood plasma. Distribution describes drugs binding to plasma proteins. Half-life is the time for drug concentration to reduce by half. Tmax is the time to reach Cmax. AUC represents total drug absorption over time.
Pharmacodynamics is the study of how drugs act on the body and examines the biochemical and physiologic effects of drugs. It focuses on the drug's effects on cells and tissues. There are three main ways drugs can exert their effects: receptor interactions, enzyme interactions, and nonspecific interactions. The goal of drug therapy is to produce a therapeutic effect, while minimizing adverse effects. Drug response is monitored to evaluate therapeutic effects and detect undesirable side effects or toxicity.
This document contains 13 multiple choice or multiple answer questions about pharmacology concepts. The questions cover topics such as types of chemical bonds between drugs and receptors, drug transport mechanisms, factors influencing drug movement, weak acids and bases, and renal drug excretion.
This document discusses pharmacokinetics and pharmacodynamics. Pharmacokinetics refers to the relationship between drug dose and concentration in plasma over time, and includes concepts like absorption, distribution, metabolism and excretion. Pharmacodynamics refers to the relationship between drug concentration and effect, and includes concepts like potency, efficacy and therapeutic windows. Specific pharmacokinetic concepts discussed include volume of distribution, clearance, protein binding and compartmental models. Specific pharmacodynamic concepts discussed include receptor theory, agonists, antagonists, and evaluating drug effects through potency, efficacy and dose response curves.
This document appears to be a 10 page exam for pharmacology and dental materia medica consisting of 43 multiple choice questions. The questions cover topics such as general pharmacology, the autonomic nervous system, sedative-hypnotics, analgesics, local anesthetics, antimicrobial agents, and dental antiseptics. Each question is followed by 5 possible answers with the key/correct answer indicated at the end. The questions probe students' knowledge of medication mechanisms of action, side effects, treatment choices for various medical conditions, and more.
This document discusses adverse drug reactions (ADRs), including their definition, frequency, impact on public health, classification, management, and prevention. Some key points:
- ADRs are the 4th-6th leading cause of death among hospitalized patients in the US.
- They are classified based on factors like onset (acute, subacute, latent), type (augmented, bizarre, continuous), and severity (minor to lethal).
- Common causes of ADRs include dosage errors, allergies, drug interactions, and failure to follow dosing regimens. Patient risk factors include age, sex, genetics, and concurrent diseases or medications.
- Prevention strategies include proper dosing, screening
Toxicology
Principles of Toxicology
Dose-response relationship
Risk = Hazard X Exposure
Factors that influence toxicity
Drug Toxicology
Therapeutic index
Therapeutic window
Idiosyncrasy
Pharmcogenetics
Drug allergy
Test for prediction drug allergy
Toxicology is a branch of biology, chemistry, and medicine that concerned with the study of the adverse effects of chemicals on living organisms.
This document provides an overview of key pharmacokinetic concepts including bioavailability, Cmax, distribution, half-life, Tmax, and area under the curve (AUC). Bioavailability describes the amount of drug that reaches systemic circulation. Cmax is the maximum drug concentration in blood plasma. Distribution describes drugs binding to plasma proteins. Half-life is the time for drug concentration to reduce by half. Tmax is the time to reach Cmax. AUC represents total drug absorption over time.
Pharmacodynamics is the study of how drugs act on the body and examines the biochemical and physiologic effects of drugs. It focuses on the drug's effects on cells and tissues. There are three main ways drugs can exert their effects: receptor interactions, enzyme interactions, and nonspecific interactions. The goal of drug therapy is to produce a therapeutic effect, while minimizing adverse effects. Drug response is monitored to evaluate therapeutic effects and detect undesirable side effects or toxicity.
This document contains 13 multiple choice or multiple answer questions about pharmacology concepts. The questions cover topics such as types of chemical bonds between drugs and receptors, drug transport mechanisms, factors influencing drug movement, weak acids and bases, and renal drug excretion.
This document discusses pharmacokinetics and pharmacodynamics. Pharmacokinetics refers to the relationship between drug dose and concentration in plasma over time, and includes concepts like absorption, distribution, metabolism and excretion. Pharmacodynamics refers to the relationship between drug concentration and effect, and includes concepts like potency, efficacy and therapeutic windows. Specific pharmacokinetic concepts discussed include volume of distribution, clearance, protein binding and compartmental models. Specific pharmacodynamic concepts discussed include receptor theory, agonists, antagonists, and evaluating drug effects through potency, efficacy and dose response curves.
This document appears to be a 10 page exam for pharmacology and dental materia medica consisting of 43 multiple choice questions. The questions cover topics such as general pharmacology, the autonomic nervous system, sedative-hypnotics, analgesics, local anesthetics, antimicrobial agents, and dental antiseptics. Each question is followed by 5 possible answers with the key/correct answer indicated at the end. The questions probe students' knowledge of medication mechanisms of action, side effects, treatment choices for various medical conditions, and more.
This document discusses adverse drug reactions (ADRs), including their definition, frequency, impact on public health, classification, management, and prevention. Some key points:
- ADRs are the 4th-6th leading cause of death among hospitalized patients in the US.
- They are classified based on factors like onset (acute, subacute, latent), type (augmented, bizarre, continuous), and severity (minor to lethal).
- Common causes of ADRs include dosage errors, allergies, drug interactions, and failure to follow dosing regimens. Patient risk factors include age, sex, genetics, and concurrent diseases or medications.
- Prevention strategies include proper dosing, screening
Toxicology
Principles of Toxicology
Dose-response relationship
Risk = Hazard X Exposure
Factors that influence toxicity
Drug Toxicology
Therapeutic index
Therapeutic window
Idiosyncrasy
Pharmcogenetics
Drug allergy
Test for prediction drug allergy
Toxicology is a branch of biology, chemistry, and medicine that concerned with the study of the adverse effects of chemicals on living organisms.
This document discusses pharmacokinetics, specifically the absorption and distribution phases. It defines absorption as the transfer of a drug from its site of administration to the bloodstream. There are several factors that can affect drug absorption, including dissolution rate, particle size, lipid solubility, formulation, pH, gastrointestinal transit time, and disease states. Distribution is defined as the movement of drugs throughout the body via passive diffusion, active transport, or vesicles. Key determinants of distribution include blood flow, capillary permeability, drug structure, binding to plasma proteins, and barriers like the blood-brain barrier and placenta. The apparent volume of distribution is used to describe the hypothetical volume that a drug distributes into following intravenous administration.
This document outlines the contents of a pharmacology textbook. It is divided into 6 chapters covering general pharmacology principles, agents that control the peripheral and central nervous systems, organ-specific drugs, metabolic drugs, and chemotherapeutic drugs. The first chapter discusses pharmacokinetics, including absorption, distribution, metabolism and excretion of drugs in the body. It also addresses concepts such as bioavailability, routes of administration, and the first-pass effect.
This document discusses several case studies related to clinically important drug interactions. It begins by providing background on the prevalence of drug interactions and the importance of reviewing drug alerts and reports to prevent serious interactions. The document then discusses how group discussion of case studies can reinforce learning, promote critical thinking, and foster problem-solving skills. It presents six case studies related to drug interactions between aspirin and sulfonylureas, rifampin and oral contraceptives, methotrexate and folic acid, diuretics and hypokalemia, simvastatin and amlodipine, and finally choosing an appropriate antibiotic route for a child with pneumonia. For each case it provides questions and discusses the relevant drug interactions and management considerations
The document discusses various concepts in pharmacokinetics including absorption, distribution, metabolism, and excretion of drugs in the body over time. It explains key mechanisms of absorption such as passive diffusion and carrier-mediated transport. Distribution of drugs in tissues is described using the volume of distribution concept. Metabolism and excretion of drugs via different routes is also summarized. The relationship between pharmacokinetics and pharmacodynamics is explained using drug concentration-time curves. Clinical applications of pharmacokinetic principles including therapeutic drug monitoring and dosage adjustment are also highlighted.
This document contains an outline of 6 chapters covering general principles of pharmacology and various classes of drugs. Chapter 1 discusses pharmacokinetics, including absorption, distribution, metabolism and excretion of drugs. Chapter 2 covers agents that control the peripheral nervous system, including local anesthetics, cholinergic drugs, anticholinergic drugs, adrenergic drugs and antagonists. Subsequent chapters address agents controlling the central nervous system, organ-specific drugs, metabolic profile drugs, and chemotherapeutic drugs.
Pharmacoeconomics is a branch of health economics which compares the value of one drug or a drug therapy to another.
By understanding the principles, methods, and application of pharmacoeconomics, healthcare professionals will be prepared to make better decisions regarding the use of pharmaceutical products and services.
This document contains a collection of questions from various ANZCA exams on the topics of pharmacology and general anaesthetics. The questions cover topics such as pharmacokinetics, drug properties, mechanisms of action, volatile anaesthetic agents, and minimum alveolar concentration. The questions are multiple choice format and cover basic concepts as well as specific drug properties.
Pharmacodynamics is the study of how drugs act on the body and their mechanisms of action. Drugs can act through receptors, enzymes, ion channels, or physical properties. Receptors are molecules that drugs bind to, like G-protein coupled receptors, inducing cellular changes. Affinity is a drug's ability to bind receptors, while intrinsic activity is its ability to produce an effect after binding. Agonists fully activate receptors, antagonists block receptors' effects. Drug efficacy is the maximum effect, while potency is the amount needed to produce an effect. Drug actions can be modified by factors like age, genetics, psychological state, diseases, other drugs, and tolerance from repeated use.
This document discusses various methods for quantitatively estimating drugs, including biological, physico-chemical, radioimmunological, and microbiological methods. It also describes dose-response relationships and different metrics used to characterize drug potency and efficacy such as ED50, LD50, TD50, and therapeutic index. Key concepts covered include quantal vs graded dose-response curves, the significance of potency vs efficacy, and using dose-response data to understand drug interactions and sites of action.
This document discusses the rational use of antibiotics. It emphasizes that antibiotics should only be used when necessary for bacterial infections, as overuse can lead to antibiotic resistance and increased healthcare costs. When prescribing antibiotics, the doctor should consider whether an antibiotic is needed, which antibiotic is most appropriate for the aetiological agent and patient factors, what dose and regimen to use, and monitor the treatment's efficacy with an early review. Antibiotics should generally be used for the minimum effective duration and oral therapy is preferred over parental when possible.
This document defines drug interactions and describes the main types and mechanisms. Drug interactions occur when one drug alters the effects of another drug. There are several types including drug-drug, drug-food, and drug-disease interactions. Mechanisms include pharmaceutical, pharmacokinetic, and pharmacodynamic interactions which can impact absorption, distribution, metabolism, excretion, or the pharmacological effects of drugs. Factors like multiple drug use, diseases, age, and non-compliance can contribute to interactions. Careful consideration of a patient's drug history and risks can help reduce negative interactions.
This document summarizes key concepts in pharmacodynamics from a third semester pharmaceutical sciences group project. It defines pharmacodynamics as how drugs act on the body and influence the magnitude of response based on drug concentration. Most drugs exert their effects by interacting with receptors, and substances that can bind receptors and produce biological responses are called agonists. The relationship between drug concentration and response is shown using drug response curves, where efficacy is the maximum response and potency is the amount needed to produce the maximum effect, such as Candesartan being more potent than Ibesartan due to its lower dose range.
this slide share will provide information about drug discovery and development.in this, how the drug is discovered and what type of procedures and instructions followed during discovery and development of a new drug and also give limitations of drug discovery and development process.
The document provides an overview of basic concepts in pharmacology including definitions of key terms like pharmacy, pharmacology, pharmacokinetics, pharmacodynamics, clinical pharmacology, and toxicology. It also discusses essential drug concepts, drug nomenclature, sources of drugs, routes of drug administration including local and systemic routes, and factors governing the choice of administration route.
Drug induced hematological disorders @rxvichu!!!RxVichuZ
This is my 35th powerpoint..published here in Google Slideshare...
And I wish to thank everyone who have supported me in my 2 year long journey......
This ppt is regarding DRUG INDUCED HEMATOLOGICAL DISORDERS, covering the definitions, causative drugs, pathophysiological mechanisms, manifestations,and management of 5 blood disorders.
Do go through this ppt, and send me ur reviews!!
Regards,
Vishnu.R.Nair.
This document discusses general principles of drug therapy, including:
1) Dose-response relationships and how drug effects are related to the dose and concentration of the drug. Higher doses result in greater drug effects until a maximum effect is reached.
2) Time-response relationships, where the drug effect occurs only after a certain amount of time as the drug accumulates and binds to receptors in the body.
3) Different types of drug-receptor interactions including agonists that activate receptors, antagonists that block receptors, and concepts like potency, efficacy, competitive vs. noncompetitive antagonism.
4) Factors that can influence individual responses to drugs like tolerance from repeated use and differences in drug
The document discusses bioavailability, which is the rate and amount of an administered drug that reaches systemic circulation. Bioavailability can be affected by physiological, formulation, and drug properties. It is assessed by parameters like time to peak concentration, maximum concentration, area under the curve, onset and duration of action, which are illustrated using plasma concentration versus time curves. Absolute and relative bioavailability are defined and can be calculated from these parameters or from urinary drug excretion data.
The document discusses pharmacokinetics and pharmacodynamics. It describes the four main processes of pharmacokinetics - absorption, distribution, metabolism and elimination - and how they determine the effects of drugs in the body. It also discusses factors that influence absorption and distribution of drugs. The document then covers pharmacodynamics concepts such as dose-response relationships, therapeutic indices, and interactions between drugs. Mechanisms of drug interactions including pharmacokinetic and pharmacodynamic interactions are explained. Common types of drug interactions and ways to prevent adverse drug effects are also summarized.
This presentation includes basic concepts about pharmacodynamics. It discusses about:
Definition of Pharmacodynamics
Types of drug tragets
Stay tuned for more!
The document discusses pharmacokinetics and its four main processes - absorption, distribution, metabolism, and excretion. It defines pharmacokinetics as the study of how the body affects a drug. The key processes of absorption discussed are diffusion, transporters, and factors affecting absorption like solubility, dosage form properties, and physiological conditions. Distribution and excretion involve transfer of drugs between blood, tissues, and elimination routes like the kidneys, lungs, and bile.
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
This document discusses pharmacokinetics, specifically the absorption and distribution phases. It defines absorption as the transfer of a drug from its site of administration to the bloodstream. There are several factors that can affect drug absorption, including dissolution rate, particle size, lipid solubility, formulation, pH, gastrointestinal transit time, and disease states. Distribution is defined as the movement of drugs throughout the body via passive diffusion, active transport, or vesicles. Key determinants of distribution include blood flow, capillary permeability, drug structure, binding to plasma proteins, and barriers like the blood-brain barrier and placenta. The apparent volume of distribution is used to describe the hypothetical volume that a drug distributes into following intravenous administration.
This document outlines the contents of a pharmacology textbook. It is divided into 6 chapters covering general pharmacology principles, agents that control the peripheral and central nervous systems, organ-specific drugs, metabolic drugs, and chemotherapeutic drugs. The first chapter discusses pharmacokinetics, including absorption, distribution, metabolism and excretion of drugs in the body. It also addresses concepts such as bioavailability, routes of administration, and the first-pass effect.
This document discusses several case studies related to clinically important drug interactions. It begins by providing background on the prevalence of drug interactions and the importance of reviewing drug alerts and reports to prevent serious interactions. The document then discusses how group discussion of case studies can reinforce learning, promote critical thinking, and foster problem-solving skills. It presents six case studies related to drug interactions between aspirin and sulfonylureas, rifampin and oral contraceptives, methotrexate and folic acid, diuretics and hypokalemia, simvastatin and amlodipine, and finally choosing an appropriate antibiotic route for a child with pneumonia. For each case it provides questions and discusses the relevant drug interactions and management considerations
The document discusses various concepts in pharmacokinetics including absorption, distribution, metabolism, and excretion of drugs in the body over time. It explains key mechanisms of absorption such as passive diffusion and carrier-mediated transport. Distribution of drugs in tissues is described using the volume of distribution concept. Metabolism and excretion of drugs via different routes is also summarized. The relationship between pharmacokinetics and pharmacodynamics is explained using drug concentration-time curves. Clinical applications of pharmacokinetic principles including therapeutic drug monitoring and dosage adjustment are also highlighted.
This document contains an outline of 6 chapters covering general principles of pharmacology and various classes of drugs. Chapter 1 discusses pharmacokinetics, including absorption, distribution, metabolism and excretion of drugs. Chapter 2 covers agents that control the peripheral nervous system, including local anesthetics, cholinergic drugs, anticholinergic drugs, adrenergic drugs and antagonists. Subsequent chapters address agents controlling the central nervous system, organ-specific drugs, metabolic profile drugs, and chemotherapeutic drugs.
Pharmacoeconomics is a branch of health economics which compares the value of one drug or a drug therapy to another.
By understanding the principles, methods, and application of pharmacoeconomics, healthcare professionals will be prepared to make better decisions regarding the use of pharmaceutical products and services.
This document contains a collection of questions from various ANZCA exams on the topics of pharmacology and general anaesthetics. The questions cover topics such as pharmacokinetics, drug properties, mechanisms of action, volatile anaesthetic agents, and minimum alveolar concentration. The questions are multiple choice format and cover basic concepts as well as specific drug properties.
Pharmacodynamics is the study of how drugs act on the body and their mechanisms of action. Drugs can act through receptors, enzymes, ion channels, or physical properties. Receptors are molecules that drugs bind to, like G-protein coupled receptors, inducing cellular changes. Affinity is a drug's ability to bind receptors, while intrinsic activity is its ability to produce an effect after binding. Agonists fully activate receptors, antagonists block receptors' effects. Drug efficacy is the maximum effect, while potency is the amount needed to produce an effect. Drug actions can be modified by factors like age, genetics, psychological state, diseases, other drugs, and tolerance from repeated use.
This document discusses various methods for quantitatively estimating drugs, including biological, physico-chemical, radioimmunological, and microbiological methods. It also describes dose-response relationships and different metrics used to characterize drug potency and efficacy such as ED50, LD50, TD50, and therapeutic index. Key concepts covered include quantal vs graded dose-response curves, the significance of potency vs efficacy, and using dose-response data to understand drug interactions and sites of action.
This document discusses the rational use of antibiotics. It emphasizes that antibiotics should only be used when necessary for bacterial infections, as overuse can lead to antibiotic resistance and increased healthcare costs. When prescribing antibiotics, the doctor should consider whether an antibiotic is needed, which antibiotic is most appropriate for the aetiological agent and patient factors, what dose and regimen to use, and monitor the treatment's efficacy with an early review. Antibiotics should generally be used for the minimum effective duration and oral therapy is preferred over parental when possible.
This document defines drug interactions and describes the main types and mechanisms. Drug interactions occur when one drug alters the effects of another drug. There are several types including drug-drug, drug-food, and drug-disease interactions. Mechanisms include pharmaceutical, pharmacokinetic, and pharmacodynamic interactions which can impact absorption, distribution, metabolism, excretion, or the pharmacological effects of drugs. Factors like multiple drug use, diseases, age, and non-compliance can contribute to interactions. Careful consideration of a patient's drug history and risks can help reduce negative interactions.
This document summarizes key concepts in pharmacodynamics from a third semester pharmaceutical sciences group project. It defines pharmacodynamics as how drugs act on the body and influence the magnitude of response based on drug concentration. Most drugs exert their effects by interacting with receptors, and substances that can bind receptors and produce biological responses are called agonists. The relationship between drug concentration and response is shown using drug response curves, where efficacy is the maximum response and potency is the amount needed to produce the maximum effect, such as Candesartan being more potent than Ibesartan due to its lower dose range.
this slide share will provide information about drug discovery and development.in this, how the drug is discovered and what type of procedures and instructions followed during discovery and development of a new drug and also give limitations of drug discovery and development process.
The document provides an overview of basic concepts in pharmacology including definitions of key terms like pharmacy, pharmacology, pharmacokinetics, pharmacodynamics, clinical pharmacology, and toxicology. It also discusses essential drug concepts, drug nomenclature, sources of drugs, routes of drug administration including local and systemic routes, and factors governing the choice of administration route.
Drug induced hematological disorders @rxvichu!!!RxVichuZ
This is my 35th powerpoint..published here in Google Slideshare...
And I wish to thank everyone who have supported me in my 2 year long journey......
This ppt is regarding DRUG INDUCED HEMATOLOGICAL DISORDERS, covering the definitions, causative drugs, pathophysiological mechanisms, manifestations,and management of 5 blood disorders.
Do go through this ppt, and send me ur reviews!!
Regards,
Vishnu.R.Nair.
This document discusses general principles of drug therapy, including:
1) Dose-response relationships and how drug effects are related to the dose and concentration of the drug. Higher doses result in greater drug effects until a maximum effect is reached.
2) Time-response relationships, where the drug effect occurs only after a certain amount of time as the drug accumulates and binds to receptors in the body.
3) Different types of drug-receptor interactions including agonists that activate receptors, antagonists that block receptors, and concepts like potency, efficacy, competitive vs. noncompetitive antagonism.
4) Factors that can influence individual responses to drugs like tolerance from repeated use and differences in drug
The document discusses bioavailability, which is the rate and amount of an administered drug that reaches systemic circulation. Bioavailability can be affected by physiological, formulation, and drug properties. It is assessed by parameters like time to peak concentration, maximum concentration, area under the curve, onset and duration of action, which are illustrated using plasma concentration versus time curves. Absolute and relative bioavailability are defined and can be calculated from these parameters or from urinary drug excretion data.
The document discusses pharmacokinetics and pharmacodynamics. It describes the four main processes of pharmacokinetics - absorption, distribution, metabolism and elimination - and how they determine the effects of drugs in the body. It also discusses factors that influence absorption and distribution of drugs. The document then covers pharmacodynamics concepts such as dose-response relationships, therapeutic indices, and interactions between drugs. Mechanisms of drug interactions including pharmacokinetic and pharmacodynamic interactions are explained. Common types of drug interactions and ways to prevent adverse drug effects are also summarized.
This presentation includes basic concepts about pharmacodynamics. It discusses about:
Definition of Pharmacodynamics
Types of drug tragets
Stay tuned for more!
The document discusses pharmacokinetics and its four main processes - absorption, distribution, metabolism, and excretion. It defines pharmacokinetics as the study of how the body affects a drug. The key processes of absorption discussed are diffusion, transporters, and factors affecting absorption like solubility, dosage form properties, and physiological conditions. Distribution and excretion involve transfer of drugs between blood, tissues, and elimination routes like the kidneys, lungs, and bile.
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version
TEST BANK For Basic and Clinical Pharmacology, 15th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
Pharmacology An Introduction 7th Edition Hitner Test BankJuarezer
Full download : http://alibabadownload.com/product/pharmacology-an-introduction-7th-edition-hitner-test-bank/ Pharmacology An Introduction 7th Edition Hitner Test Bank
Test Bank - Karch Focus on Nursing Pharmacology 9th Edition by Rebecca Tucker...Donc Test
Test Bank - Karch Focus on Nursing Pharmacology
9th Edition by Rebecca Tucker
Chapters 1 - 59
Test Bank - Karch Focus on Nursing Pharmacology
9th Edition by Rebecca Tucker
Chapters 1 - 59
Pharmacology Principles and Applications 3rd Edition Fulcher Test Bankhymaq
This document contains a test bank with multiple choice and matching questions about pharmacology fundamentals from Fulcher's Pharmacology: Principles and Applications 3rd Edition textbook. The questions cover topics such as medication components, sources of drugs, factors affecting drug absorption, distribution, metabolism and excretion, major drug actions, and definitions of various pharmacology terms.
Clinical pharmacokinetics is the application of pharmacokinetic principles to the safe and effective therapeutic management of drugs in an individual patient. Primary goals of clinical pharmacokinetics include enhancing efficacy and decreasing toxicity of a patient's drug therapy.
The success of drug therapy is highly dependent on the choice of the drug, the drug product, and the design of the dosage regimen. The choice of the drug is generally made by the physician after careful patient diagnosis and physical assessment.
Test Bank For Karch's Focus on Nursing Pharmacology 9th Edition by Rebecca Tu...nursing premium
A Test bank is a ready-made electronic Q&A testing resource that is tailored to the contents of an individual textbook. Feedback is often provided on answers given by students, containing page references to the book.
Test Bank For Karch's Focus on Nursing Pharmacology 9th Edition by Rebecca Tu...nursing premium
A Test bank is a ready-made electronic Q&A testing resource that is tailored to the contents of an individual textbook. Feedback is often provided on answers given by students, containing page references to the book.
Test bank calculating drug dosages a patient safe approach to nursing and mat...robinsonayot
Test bank calculating drug dosages a patient safe approach to nursing and math 2nd edition by castillo werner mccullough (1).pdf
Test bank calculating drug dosages a patient safe approach to nursing and math 2nd edition by castillo werner mccullough (1).pdf
This document provides an introduction to pharmacology. It defines key terms like efficacy, potency, therapeutic index, and adverse drug reactions. It describes pharmacokinetic principles such as absorption, distribution, metabolism and elimination of drugs. It also discusses pharmacodynamics concepts like agonists, antagonists, and drug-receptor interactions. The document outlines various drug classifications and therapeutic categories. It discusses routes of drug administration including enteral and parental routes. It also covers topics like drug interactions, drug labeling, and patient records.
The document discusses bioequivalence, biosimilar drug products, and the biopharmaceutics classification system (BCS). It defines key terms like bioavailability, bioequivalence, innovator products, and generic products. It describes the different types of bioequivalence studies including in vivo, in vitro, pharmacodynamic, and comparative clinical trials. It outlines the elements of a bioequivalence study protocol and discusses study design, population, procedures, and data analysis. It also covers the study submission and drug review process.
This document provides an introduction to pharmacy and pharmacology. It defines pharmacy as the profession dealing with all aspects of drugs, including identification, preservation, extraction, manufacturing, packaging, and dispensing. The main types of pharmacy practice are described as community pharmacy, hospital pharmacy, clinical pharmacy, and nuclear pharmacy. Pharmacology is defined as the study of drug action and effects, while clinical pharmacology involves the relationship between drugs and humans. Key terms used in pharmacology like half-life, minimum effective concentration, bioavailability, and indications are also explained.
Practice Quiz for Napsrx1. How are drugs sorted into therapeutic.docxChantellPantoja184
Practice Quiz for Napsrx
1. How are drugs sorted into therapeutic group and classes?
A. First by the conditions that they are used to treat, and then by their mechanisms of action
B. First by their mechanisms of action, and then by their therapeutic effects
C. First by their side effects, and then by their therapeutic effects
D. First by their toxicity, and then by their effectiveness
2. What section of a drug’s package insert describes situations in which the drug should not be used because the risks outweigh the therapeutic benefits?
A. Adverse reactions
B. Contraindications
C. Overdosage
D. Warming/precautions
3. Which of the following is NOT one of the stages in the classic approach to band development strategy covered in your manual?
A. Band personality
B. Band positioning
C. Band quality
D. Band values
4. What is the name of the condition that occurs after a specific dose of a drug is given at such regular intervals that absorption and elimination (and therefore drug plasma concentration) have become fairly constant?
A. homeostasis
B. steady state
C. titration
D. tolerance
5. Which entity/entities invest/s the most money in pharmaceutical R&D?
A. Canadian pharmaceutical companies
B. The NIH
C. The U.S Government
D. U.S pharmaceutical companies
6. Over the last few decades, what has happened to legal limitations sales’ reps discussions about off label uses?
A. Limitations have decreased.
B. Limitations have increased significantly.
C. Limitations have increased slightly.
D. Limitations have remained about the same.
7. Why are novice sales representatives often placed in charge of negotiating MCO formularies?
A. to become more familiar with the healthcare industry
B. to be more familiar with their territories
C. P&T committees are more receptive to new experienced reps.
D. They are not. This job is usually reserved for more experienced reps.
8. Which of the following is an example of a central value?
A. I buy Advil to show that I’m modern consumer.
B. I like Advil because we were both born in the 80s.
C. I prefer Advil because I like the flavor.
D. I prefer Advil because it’s easier to swallow.
9. Which of the following specialties likely has the MOST emergency calls?
A. Cardiology
B. Psychiatry
C. Urology
D. All specialists have the same number of emergency calls
10. What affects the rate of active transport?
A. The availability of carriers, but not energy
B. The availability of energy, but not carriers
C. The availability of carriers and energy
D. Neither the availability of carriers nor the availability of energy
11. Over the last few decades, what has happened to the FDA approval time for new drugs?
A. It has been lengthened to ensure safer drug products.
B. It has been lengthened to limit DTC marketing.
C. It has been shortened to improve drug quality.
D. It has been shortened to reduce the cost of new drug development.
12. Which of the following would NOT help improve compliance?
A. Patients liking their providers.
Pharmacoepidemiology is the study of the use and effects of drugs in large populations. It applies epidemiological methods to issues in pharmacology. Descriptive studies examine disease and exposure rates, while analytic studies compare exposed and unexposed groups to test hypotheses. Pharmacoepidemiology aims to optimize drug use by quantifying known effects, discovering new effects, and informing safe and effective prescribing practices at a population level.
Bioavailability refers to the amount of drug that enters systemic circulation and is available at the site of action. It depends on the rate and extent of drug absorption from its dosage form. Many physiological and drug-specific factors can affect bioavailability such as pH, enzymes, blood flow, and food interactions. Careful evaluation and standardization of bioavailability is important for drug development and quality control to ensure accurate and safe dosing.
The document discusses bioavailability and bioequivalence studies. It defines bioavailability as the rate and extent of an active drug reaching systemic circulation and being available at its site of action. Bioequivalence refers to comparing the bioavailability of a drug from different formulations. The document outlines the objectives, types of study designs, important considerations like sampling, subjects, and analysis methods for bioavailability and bioequivalence studies.
Fundamental concept of modified drug releaseAbhinayJha3
Different Terminologies used in a modified release
1. Sustained release
2. Delayed release
3. Prolonged release
4. Extended-release
5. Controlled release
6. Site-specific targeting and receptor targeting
SELECTION OF DRUG CANDIDATE FOR ORAL SUSTAINED RELEASE SYSTEMS, BIOPHARMACEUTICAL CLASSIFICATION SYSTEM.
Fundamental concept of modified drug releaseAbhinayJha3
BIOPHARMACEUTICAL CLASSIFICATION SYSTEM
Different Terminologies used in a modified release
1. Sustained release
2. Delayed release
3. Prolonged release
4. Extended-release
5. Controlled release
6. Site-specific targeting and receptor targeting
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This presentation includes basic of PCOS their pathology and treatment and also Ayurveda correlation of PCOS and Ayurvedic line of treatment mentioned in classics.
Pharmacology An Introduction 6th Edition Hitner Test Bank
1. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-1
Multiple Choice Questions
1. Identify the term used for the process by which a drug enters the bloodstream from its site
of administration.
A. Drug absorption
B. Drug excretion
C. Drug distribution
D. Drug metabolism
2. Identify the most common drug available as a transdermal patch system.
A. Nitroglycerin
B. Clonidine
C. Estrogen
D. All of these are correct.
3. Identify the dosage form that contains dried and finely ground drugs or drug extract.
A. Powders
B. Tablets
C. Troches
D. Capsules
4. Match the dosage form commonly known as a "troche" to the medical condition it is used
to treat.
A. Asthma
B. Tonsillitis
C. Sore throat
D. Toothache
Pharmacology An Introduction 6th Edition Hitner Test Bank
Full Download: http://alibabadownload.com/product/pharmacology-an-introduction-6th-edition-hitner-test-bank/
This sample only, Download all chapters at: alibabadownload.com
2. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-2
5. Among the factors that affect drug distribution, the factor that plays the biggest role in how
much drug penetrates the brain is:
A. Lipid solubility
B. Plasma protein binding
C. Blood circulation
D. GI absorption rate
6. Match the proper preparation name to a solution that is described as containing water and
sugar and added drug.
A. Elixir
B. Tincture
C. Syrup
D. Fluid extract
7. Compare the processes of drug absorption, drug distribution, drug metabolism, and drug
excretion. These are all components of the study known as:
A. Half-life
B. Pharmacokinetics
C. Bioavailability
D. Enzyme induction
8. Match the correct alcohol concentration range to the dosage form that is referred to as an
alcoholic preparation and that includes the elixirs, spirits, tinctures, and fluid extracts.
A. 5 to 10 percent
B. 10 to 15 percent
C. 10 to 25 percent
D. 5 to 20 percent
3. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-3
9. The fact that adipose tissue receives a relatively poor blood supply can be interpreted as
indicating that adipose tissue:
A. Accumulates large amounts of drug
B. Does not accumulate large amounts of drug
C. Does not metabolize large amounts of drug
D. Metabolizes large amounts of drug
10. Use the term drug tolerance, drug dependence, or drug addiction to document the reason
why a patient's dose of an analgesic agent he uses for chronic pain has been increased two
times over the last 12 months.
A. The drug's effect decreases due to repeated administration of the product.
B. Reliance on the administration of the drug leads to a psychological and or physical
condition for the patient.
C. Compulsive dependence on a drug dominates all other activities in the patient's life.
D. None of these are correct.
11. Use a half-life of 8 hours to determine how much drug is left in the body at 4 p.m. after a
500-mg dose was taken at 8 am.
A. 250 mg
B. 125 mg
C. 375 mg
D. None of these are correct.
12. Use a half-life of 4 hours to determine how much drug is left in the body at 2 p.m. after a
200-mg dose was given by the intravenous route of administration at 6 a.m.
A. 25 mg
B. 12.5 mg
C. 50 mg
D. None of these are correct.
4. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-4
13. Implementing a patient education program should include educating patients to take their
drug products properly. Patients should be instructed to take enteric-coated products:
A. On an empty stomach
B. One hour before meals
C. Two hours after meals
D. All of these are correct.
14. Compare the routes of administration based on the parameters of patient safety and ease of
drug use in order to select the correct route of administration for a patient with a busy lifestyle
and a hectic schedule.
A. Parenteral administration
B. Oral administration
C. Topical administration
D. Inhalation administration
15. Use onset of action to determine which of the following routes of administration will lead
to the slowest therapeutic response.
A. Inhalation
B. Transdermal
C. Intramuscular
D. Sublingual
16. Use onset of action to determine which of the following routes of administration will lead
to the quickest therapeutic response.
A. Inhalation
B. Transdermal
C. Intramuscular
D. Sublingual
5. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-5
17. Using the factors of individual variation, select the statement that best describes the
placebo effect.
A. Excitement can lead to perceived symptom improvement.
B. Positive attitude can lead to perceived symptom improvement.
C. Less body fat can lead to perceived symptom improvement.
D. None of these are correct.
18. Differentiate between the routes of drug administration in order to select the route that is
restricted to use in the hospital setting due to immediate onset of action and high percentage
of drug bioavailability.
A. IM injection method
B. IV injection method
C. Topical application method
D. Suppository insertion method
19. Differentiate between the transport mechanisms to determine how cells allow drugs to
pass through the cell membrane.
A. Filtration
B. Passive transport
C. Active transport
D. All of these are correct.
20. Select the basic principle in passive transport by which most drug molecules diffuse
through the cell membrane.
A. Drug passes from an area of high concentration to an area of low concentration.
B. Drug passes from an area of low concentration to an area of high concentration.
C. Drug passes from an area of high concentration to an area of high concentration.
D. Drug passes from an area of low concentration to an area of low concentration.
6. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-6
21. Differentiate between tolerance, antagonism, and synergism in order to select the drug
interaction that occurs during antagonism.
A. The combined effect of two drugs, by the same mechanism of action, is equal to the sum of
their individual effects.
B. The combined effect of two drugs, by a different mechanism of action, is equal to the sum
of their individual effects.
C. The combined effect of two drugs is less than the sum of their individual effects.
D. The combined effect of two drugs is larger than the sum of their individual effects.
22. Differentiate between the FDA pregnancy categories to determine the proper category for
a drug for which studies on animals have not demonstrated fetal risk and no studies have been
performed in pregnant women.
A. Pregnancy Category A
B. Pregnancy Category B
C. Pregnancy Category D
D. None of these are correct.
23. When differentiating between enzyme induction and enzyme inhibition, enzyme induction
can be interpreted as resulting in a(an):
A. Increase in the rate of drug metabolism in the liver, leading to a decreased duration of
action
B. Decrease in the rate of drug metabolism in the liver, leading to a decreased duration of
action
C. Unchanged rate of drug metabolism in the liver, leading to an increased duration of action
D. None of these are correct.
24. When differentiating between free drug molecules and drug molecules that have bound to
plasma proteins, the main focus is:
A. Only unbound or free drug molecules can exert a pharmacological effect.
B. Only drug molecules that have bound to plasma can exert a pharmacological effect.
C. Free drug molecules exert the same level of pharmacological effect as drug molecules that
are bound to plasma.
D. None of these are correct
7. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-7
25. You have been asked to explain to a patient the possibility that he will experience drug
interactions while taking his newly prescribed medications. Select the appropriate statement
you will use when explaining "synergism" to the patient.
A. Drugs may increase each other's effect equal to the sum of their individual effects.
B. Drugs may increase each other's effect greater than the sum of their individual effects.
C. Drugs may cancel each other's effect or lead to a response that is less than the sum of their
individual effects.
D. None of these are correct.
26. Select the proper method by which you can conclude that there will be 100 percent
bioavailability in the circulatory system immediately after administration of the drug product.
A. Subcutaneous injection method
B. Inhalation method
C. Transdermal patch method
D. Intravenous injection method
27. Select the most appropriate reason why a patient with cirrhosis of the liver does not get
the therapeutic response expected from the medications that she is taking.
A. The patient's ability to absorb drug is impaired.
B. The patient's ability to distribute drug throughout the body is impaired.
C. The patient's ability to metabolize drug is impaired.
D. The patient's ability to excrete unused drug from the body is impaired.
28. A patient has an order in the chart that reads, "Take two tablets by mouth today; then take
one tablet by mouth daily for the next 4 days." Select the term that represents the part of the
order that reads, "Take two tablets by mouth today."
A. Maintenance dose
B. Therapeutic dose
C. Loading dose
D. None of these are correct.
8. Chapter 002 Pharmacokinetics and Factors of Individual Variation
2-8
29. Select the most likely reason why a patient who has been diagnosed with end-stage renal
disease must have routine blood work drawn to check his blood levels of a prescribed drug.
A. Due to the renal disease, the patient is unable to effectively eliminate the drug, causing
accumulation of the drug in the plasma.
B. Due to the renal disease, the patient is unable to effectively metabolize the drug, causing
low levels of the drug in the plasma.
C. Due to the renal disease, the patient is unable to effectively absorb the drug, causing low
levels of the drug in the plasma.
D. None of these are correct.
9. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-9
Multiple Choice Questions
1. (p. 20) Identify the term used for the process by which a drug enters the bloodstream from its
site of administration.
A. Drug absorption
B. Drug excretion
C. Drug distribution
D. Drug metabolism
Drug absorption refers to the entrance of a drug into the bloodstream.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Remembering
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Easy
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
2. (p. 19) Identify the most common drug available as a transdermal patch system.
A. Nitroglycerin
B. Clonidine
C. Estrogen
D. All of these are correct.
Transdermal products are administered through a bandage or patch. Nitroglycerin, estrogen,
and clonidine are drugs available in this form.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Remembering
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Easy
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
10. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-10
3. (p. 18) Identify the dosage form that contains dried and finely ground drugs or drug extract.
A. Powders
B. Tablets
C. Troches
D. Capsules
Powders are drugs or drug extracts that are dried and ground into fine particles.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Remembering
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Easy
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
4. (p. 18) Match the dosage form commonly known as a "troche" to the medical condition it is
used to treat.
A. Asthma
B. Tonsillitis
C. Sore throat
D. Toothache
Troches are flattened tablets that are allowed to dissolve in the mouth. They are commonly
used for colds and sore throats.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Understanding
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Easy
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
11. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-11
5. (p. 22) Among the factors that affect drug distribution, the factor that plays the biggest role in
how much drug penetrates the brain is:
A. Lipid solubility
B. Plasma protein binding
C. Blood circulation
D. GI absorption rate
Since the brain is composed of a large amount of lipid (nerve membranes and myelin), lipid-
soluble drugs pass readily into the brain. As a general rule, then, a drug must have a certain
degree of lipid solubility if it is to penetrate this barrier and gain access to the brain.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Understanding
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Easy
Learning Outcome: 2.3 Identify how half-life, blood drug level, and bioavailability relate to drug response.
6. (p. 18) Match the proper preparation name to a solution that is described as containing water
and sugar and added drug.
A. Elixir
B. Tincture
C. Syrup
D. Fluid extract
A syrup is a solution of water and sugar to which a drug is added.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Understanding
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Easy
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
12. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-12
7. (p. 18) Compare the processes of drug absorption, drug distribution, drug metabolism, and
drug excretion. These are all components of the study known as:
A. Half-life
B. Pharmacokinetics
C. Bioavailability
D. Enzyme induction
Pharmacokinetics is a study of the factors that determine drug absorption, drug distribution,
drug metabolism, and drug excretion.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies.
Bloom's: Understanding
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Easy
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
8. (p. 18) Match the correct alcohol concentration range to the dosage form that is referred to as
an alcoholic preparation and that includes the elixirs, spirits, tinctures, and fluid extracts.
A. 5 to 10 percent
B. 10 to 15 percent
C. 10 to 25 percent
D. 5 to 20 percent
Elixirs, spirits, tinctures, and fluid extracts are drugs dissolved in various concentrations of
alcohol, usually in the range of 5 to 20 percent.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Understanding
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Easy
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
13. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-13
9. (p. 22) The fact that adipose tissue receives a relatively poor blood supply can be interpreted
as indicating that adipose tissue:
A. Accumulates large amounts of drug
B. Does not accumulate large amounts of drug
C. Does not metabolize large amounts of drug
D. Metabolizes large amounts of drug
Some tissues, such as adipose tissue, receive a relatively poor blood supply and, as a result, do
not accumulate large amounts of drug.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies.
Bloom's: Understanding
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Easy
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
10. (p. 28–29) Use the term drug tolerance, drug dependence, or drug addiction to document the
reason why a patient's dose of an analgesic agent he uses for chronic pain has been increased
two times over the last 12 months.
A. The drug's effect decreases due to repeated administration of the product.
B. Reliance on the administration of the drug leads to a psychological and or physical
condition for the patient.
C. Compulsive dependence on a drug dominates all other activities in the patient's life.
D. None of these are correct.
Drug tolerance is defined as a decreased drug effect that occurs after repeated administration.
In order to attain the previous drug effect, the dosage must be increased.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.7 Explain the basic terminology of chronic drug administration and drug dependence.
14. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-14
11. (p. 23) Use a half-life of 8 hours to determine how much drug is left in the body at 4 p.m.
after a 500-mg dose was taken at 8 am.
A. 250 mg
B. 125 mg
C. 375 mg
D. None of these are correct.
The half-life of a drug is the time required for the blood or plasma concentration of the drug
to fall to half of its original level.
ABHES Competency: 6. Pharmacology a. Demonstrate accurate occupational math and metric conversions for proper medication
administration. b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification, usual dosage, usual
side effects, and contraindications.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.3 Identify how half-life, blood drug level, and bioavailability relate to drug response.
12. (p. 23) Use a half-life of 4 hours to determine how much drug is left in the body at 2 p.m.
after a 200-mg dose was given by the intravenous route of administration at 6 a.m.
A. 25 mg
B. 12.5 mg
C. 50 mg
D. None of these are correct.
The half-life of a drug is the time required for the blood or plasma concentration of the drug
to fall to half of its original level.
ABHES Competency: 6. Pharmacology a. Demonstrate accurate occupational math and metric conversions for proper medication
administration. b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification, usual dosage, usual
side effects, and contraindications.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.3 Identify how half-life, blood drug level, and bioavailability relate to drug response.
15. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-15
13. (p. 19) Implementing a patient education program should include educating patients to take
their drug products properly. Patients should be instructed to take enteric-coated products:
A. On an empty stomach
B. One hour before meals
C. Two hours after meals
D. All of these are correct.
Enteric-coated products should be taken on an empty stomach with water, either 1 hour before
or 2 hours after meals.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. 9. Medical Office Clinical Procedures d. Recognize and understand various
treatment protocols.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
14. (p. 19) Compare the routes of administration based on the parameters of patient safety and
ease of drug use in order to select the correct route of administration for a patient with a busy
lifestyle and a hectic schedule.
A. Parenteral administration
B. Oral administration
C. Topical administration
D. Inhalation administration
The oral administration route is the safest and the most convenient method.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. 9. Medical Office Clinical Procedures d. Recognize and understand various
treatment protocols.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
16. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-16
15. (p. 20) Use onset of action to determine which of the following routes of administration will
lead to the slowest therapeutic response.
A. Inhalation
B. Transdermal
C. Intramuscular
D. Sublingual
The transdermal route of administration has an onset of action of approximately 30 to 60
minutes.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. 9. Medical Office Clinical Procedures d. Recognize and understand various
treatment protocols.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
16. (p. 20) Use onset of action to determine which of the following routes of administration will
lead to the quickest therapeutic response.
A. Inhalation
B. Transdermal
C. Intramuscular
D. Sublingual
The inhalation route of administration has an onset of action within one minute of
administration.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. 9. Medical Office Clinical Procedures d. Recognize and understand various
treatment protocols.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
17. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-17
17. (p. 25) Using the factors of individual variation, select the statement that best describes the
placebo effect.
A. Excitement can lead to perceived symptom improvement.
B. Positive attitude can lead to perceived symptom improvement.
C. Less body fat can lead to perceived symptom improvement.
D. None of these are correct.
It has been observed that if patients have a positive attitude and think that the drug or
treatment will help, chances are the patients claim an improvement whether there actually is
one or not.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. 9. Medical Office Clinical Procedures d. Recognize and understand various
treatment protocols.
Bloom's: Applying
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Medium
Learning Outcome: 2.4 List several factors of individual variation that can alter drug response.
18. (p. 19) Differentiate between the routes of drug administration in order to select the route
that is restricted to use in the hospital setting due to immediate onset of action and high
percentage of drug bioavailability.
A. IM injection method
B. IV injection method
C. Topical application method
D. Suppository insertion method
Intravenous (IV) injection is usually restricted to use in the hospital. IV injection offers the
fastest means of drug absorption because the drug is delivered directly into the circulation;
therefore, the onset of drug action is almost immediate.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. 9. Medical Office Clinical Procedures d. Recognize and understand various
treatment protocols.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Hard
Learning Outcome: 2.1 List different forms of drug products and the routes by which they are administered.
18. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-18
19. (p. 20) Differentiate between the transport mechanisms to determine how cells allow drugs
to pass through the cell membrane.
A. Filtration
B. Passive transport
C. Active transport
D. All of these are correct.
Cells have special transport mechanisms that allow various substances (including drugs) to
pass through the cell membrane. These mechanisms include filtration, passive transport, and
active transport.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Hard
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
20. (p. 20–21) Select the basic principle in passive transport by which most drug molecules
diffuse through the cell membrane.
A. Drug passes from an area of high concentration to an area of low concentration.
B. Drug passes from an area of low concentration to an area of high concentration.
C. Drug passes from an area of high concentration to an area of high concentration.
D. Drug passes from an area of low concentration to an area of low concentration.
Most drugs pass through membranes by passive transport. An important principle in passive
transport is that the concentration of drug on each side of the membrane differs. In passive
transport, drug molecules diffuse from an area of high concentration to an area of low
concentration (law of diffusion).
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Hard
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
19. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-19
21. (p. 29) Differentiate between tolerance, antagonism, and synergism in order to select the
drug interaction that occurs during antagonism.
A. The combined effect of two drugs, by the same mechanism of action, is equal to the sum of
their individual effects.
B. The combined effect of two drugs, by a different mechanism of action, is equal to the sum
of their individual effects.
C. The combined effect of two drugs is less than the sum of their individual effects.
D. The combined effect of two drugs is larger than the sum of their individual effects.
Antagonism occurs when the combined effect of two drugs is less than the sum of their
individual effects.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Hard
Learning Outcome: 2.6 Define the different types of drug interaction.
22. (p. 26) Differentiate between the FDA pregnancy categories to determine the proper
category for a drug for which studies on animals have not demonstrated fetal risk and no
studies have been performed in pregnant women.
A. Pregnancy Category A
B. Pregnancy Category B
C. Pregnancy Category D
D. None of these are correct.
Pregnancy Category B: Drug studies have not been performed in pregnant women and animal
studies have not demonstrated fetal risk.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Hard
Learning Outcome: 2.5 Understand the drug factors that relate to pediatric drug administration.
20. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-20
23. (p. 22) When differentiating between enzyme induction and enzyme inhibition, enzyme
induction can be interpreted as resulting in a(an):
A. Increase in the rate of drug metabolism in the liver, leading to a decreased duration of
action
B. Decrease in the rate of drug metabolism in the liver, leading to a decreased duration of
action
C. Unchanged rate of drug metabolism in the liver, leading to an increased duration of action
D. None of these are correct.
By stimulating the microsomal metabolizing system, the drugs actually increase the amount of
enzymes (cytochrome P450's) in the system; this process is referred to as enzyme induction.
With an increase in the amount of enzymes, there is a faster rate of drug metabolism.
Consequently, the duration of drug action is decreased for all drugs metabolized.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Hard
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
24. (p. 22) When differentiating between free drug molecules and drug molecules that have
bound to plasma proteins, the main focus is:
A. Only unbound or free drug molecules can exert a pharmacological effect.
B. Only drug molecules that have bound to plasma can exert a pharmacological effect.
C. Free drug molecules exert the same level of pharmacological effect as drug molecules that
are bound to plasma.
D. None of these are correct
Only unbound or free drug molecules can exert a pharmacological effect.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Hard
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
21. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-21
25. (p. 29) You have been asked to explain to a patient the possibility that he will experience
drug interactions while taking his newly prescribed medications. Select the appropriate
statement you will use when explaining "synergism" to the patient.
A. Drugs may increase each other's effect equal to the sum of their individual effects.
B. Drugs may increase each other's effect greater than the sum of their individual effects.
C. Drugs may cancel each other's effect or lead to a response that is less than the sum of their
individual effects.
D. None of these are correct.
Synergism occurs when the combined effect of two drugs is greater than the sum of their
individual effects.
ABHES Competency: 6. Pharmacology b. Properly utilizePDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Hard
Learning Outcome: 2.6 Define the different types of drug interaction.
26. (p. 24) Select the proper method by which you can conclude that there will be 100 percent
bioavailability in the circulatory system immediately after administration of the drug product.
A. Subcutaneous injection method
B. Inhalation method
C. Transdermal patch method
D. Intravenous injection method
Bioavailability is the percentage of the dose of a drug that is actually absorbed into the
bloodstream. Differences in drug formulation, route of administration, and factors that affect
GI absorption can influence bioavailability.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Hard
Learning Outcome: 2.3 Identify how half-life, blood drug level, and bioavailability relate to drug response.
22. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-22
27. (p. 22) Select the most appropriate reason why a patient with cirrhosis of the liver does not
get the therapeutic response expected from the medications that she is taking.
A. The patient's ability to absorb drug is impaired.
B. The patient's ability to distribute drug throughout the body is impaired.
C. The patient's ability to metabolize drug is impaired.
D. The patient's ability to excrete unused drug from the body is impaired.
Drug metabolism, also referred to as biotransformation, is the chemical alteration of drugs and
foreign compounds in the body. The liver is the main organ involved in drug metabolism.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications.
ABHES Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Hard
Learning Outcome: 2.2 Understand the pharmacokinetic factors that determine the absorption, distribution, metabolism, and excretion of
drugs.
28. (p. 24) A patient has an order in the chart that reads, "Take two tablets by mouth today; then
take one tablet by mouth daily for the next 4 days." Select the term that represents the part of
the order that reads, "Take two tablets by mouth today."
A. Maintenance dose
B. Therapeutic dose
C. Loading dose
D. None of these are correct.
A loading dose is usually an initial higher dose of drug, often administered IV, to rapidly
attain the therapeutic drug level and drug effects. Loading doses are usually followed by
maintenance doses that are smaller and calculated to maintain the drug level within the
therapeutic range.
ABHES Competency: 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to identify a drug's classification,
usual dosage, usual side effects, and contraindications. c. Identify and define common abbreviations that are accepted in prescription
writing.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 11. Identify the classifications of medications, including desired effect, side effects, and
adverse reactions.
Difficulty: Hard
Learning Outcome: 2.3 Identify how half-life, blood drug level, and bioavailability relate to drug response.
23. Chapter 002 Pharmacokinetics and Factors of Individual Variation Key
2-23
29. (p. 26) Select the most likely reason why a patient who has been diagnosed with end-stage
renal disease must have routine blood work drawn to check his blood levels of a prescribed
drug.
A. Due to the renal disease, the patient is unable to effectively eliminate the drug, causing
accumulation of the drug in the plasma.
B. Due to the renal disease, the patient is unable to effectively metabolize the drug, causing
low levels of the drug in the plasma.
C. Due to the renal disease, the patient is unable to effectively absorb the drug, causing low
levels of the drug in the plasma.
D. None of these are correct.
Patients with hepatic or renal disease suffer a greater incidence of adverse drug effects
because they are unable to eliminate the drug and its metabolites effectively. Consequently,
plasma drug levels are much higher in these patients due to accumulation of the drug in the
plasma.
ABHES Competency: 2. Anatomy and Physiology b. Identify and apply the knowledge of all body systems; their structure and functions; and
their common diseases, symptoms, and etiologies. 6. Pharmacology b. Properly utilize PDR, drug handbook, and other drug references to
identify a drug's classification, usual dosage, usual side effects, and contraindications.
Bloom's: Analyzing
CAAHEP Competency: I. Anatomy & Physiology 12. Describe the relationship between anatomy and physiology of all body systems and
medications used for treatment in each.
Difficulty: Hard
Learning Outcome: 2.3 Identify how half-life, blood drug level, and bioavailability relate to drug response.
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