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For most of the psychoactive pharmaceuticals as well as various other drugs that are misused, the site of action


A) is neurons in the central nervous system.
B) is on the contralateral side of the body from where it was administered.
C) involves the kidneys during the biotransformation process.
D) depends on how the substance was administered.

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If 99 percent of test subjects have the desired response to the same medication identified in the last question at a dosage level of 20 mg, this would be called:


A) the LD99.
B) the ED99.
C) the minimal effective dose.
D) the therapeutic half-life of that compound at the 99th percentile.

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Drugs that are abused comprise a special class of chemicals that are different from drugs that are used pharmaceutically.

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The term "skin popping" used by some drug addicts refers to the route of drug administration.


A) subcutaneous
B) intravenous
C) transdermal
D) enteral

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The dosage level that would kill 5 % of those people who took an overdose of medication "X" (medication from last question) is 400 mg.This would mean that


A) this compound has a large therapeutic window.
B) this compound has a narrow therapeutic window.
C) the compound is highly toxic.
D) the elimination of medication "X" from their body at this dosage level will be difficult for most people.

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A

Which of the following is true regarding drugs of abuse?


A) The speed at which the compound begins to take effect varies as a result of the drug-specific site of action.
B) The heart and cardiovascular system are of minimal importance to the process of biotransformation.
C) The site of action is the central nervous system.
D) Rectal administration is quite common, although it is relatively inefficient.

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Define the terms effective dose and lethal dose.Explain how these might be used to calculate the therapeutic index of a drug.

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The effective dose (ED) is the amount of a drug or treatment that produces the desired effect in a certain percentage of the population. It is often expressed as the dose required to achieve a specific therapeutic effect in 50% of the population (ED50). The lethal dose (LD) is the amount of a drug or treatment that causes death in a certain percentage of the population. It is often expressed as the dose that is lethal to 50% of the population (LD50). The therapeutic index of a drug is a measure of its safety and efficacy. It is calculated by dividing the lethal dose by the effective dose (TI = LD50/ED50). A higher therapeutic index indicates that the drug is safer, as it means that the effective dose is much lower than the lethal dose. This means that there is a wider margin of safety between the dose that produces the desired effect and the dose that could be lethal. By using the effective dose and lethal dose to calculate the therapeutic index of a drug, healthcare professionals can determine the safety and efficacy of the drug. This information is crucial for determining the appropriate dosage and monitoring for potential adverse effects in patients. It also helps in comparing the safety profiles of different drugs and making informed decisions about their use in clinical practice.

The biotransformation process for pharmaceuticals was once called


A) drug metabolism.
B) vascularization.
C) absorption.
D) distribution.

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A

Which process is affected by factors such as the individual's sex, state of hydration, genetic heritage, general health, and muscle/adipose tissue ratio?


A) Peak effect
B) Drug interaction
C) Diffusion
D) Distribution

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Which of the following is most accurate in regards to bioavailability?


A) It is concerned with the biotransformation process after a compound is administered into the human body.
B) It forces the body to absorb a compound more rapidly.
C) It is only 1/100,000th of an inch from drug molecules and the circulatory system.
D) It reflects the concentration of unchanged chemical at the site of action.

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Describe the term distribution half-life, including its two subforms.

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The term distribution half-life refers t...

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An advantage of administering a drug parenterally is


A) the drug is not delayed by the stomach emptying process.
B) it avoids the danger of the drug being mixed with food in the GI tract.
C) the drug is not exposed to gastric juices.
D) all of these answers.

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A drug that has a narrow therapeutic window would


A) be easy to overdose.
B) be difficult to overdose.
C) never reach its peak effect.
D) reach its peak effect slowly.

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Jared is experiencing an overdose of heroin.He is rushed to the hospital and given another drug that blocks his opioid receptor sites, thus preventing the effects of the overdose from stopping his respiration.Jared was most likely given


A) Naltraxone.
B) Disulfiram
C) Narcan.
D) Buspirone.

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Which of the following statements is true concerning the bioavailability of chemical compounds related to drug misuse and abuse?


A) There is little known about drug distribution patterns in overdose situations.
B) The main site of biotransformation is the pancreas.
C) The effects of any compound are the same in animals as in humans.
D) The method of administration for a compound does not matter in pharmacokinetics.

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Describe the actions and effects of agonists and antagonists on a receptor sites.

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Agonists are molecules that bind to a re...

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Describe the processes of neurotransmitter reuptake and destruction, noting where these processes take place.

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Neurotransmitter reuptake and destructio...

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Describe the process of biotransformation.

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Biotransformation is the process by whic...

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According to your text, drugs of abuse and pharmaceuticals both


A) destroy emerging potentials within the body.
B) cause a disruption in protein absorption for most persons.
C) destroy most of the essential enzymes found in the brain.
D) modify a potential that already exists in the body or brain.

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If 95 % of test subjects have the desired response to medication "X" at a dosage level of 15 mg, this would be called the


A) LD95.
B) ED95.
C) minimal effective dose.
D) therapeutic half-life of that compound at the 95th %ile.

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