Pharmacology Overview Quiz
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Questions and Answers

It involves the analysis, assessment, and evaluation of circulating concentrations of drugs in serum, plasma, or whole blood.

  • Therapeutic Drug Monitoring
  • Drug Testing
  • Drug Metabolism
  • Toxicology Testing (correct)

It is the biochemical pathway responsible for the greatest portion of drug metabolism.

  • CYP 450 (correct)
  • MFO System
  • CYP 2D6
  • MFA System

It describes the relationship between drug concentration at the target site and the response of the tissues.

  • Pharmacokinetics
  • Pharmacogenomics
  • Pharmacodynamics (correct)
  • Pharmacology

The study of genes that effect the performance of a drug in an individual.

<p>Pharmacogenomics (C)</p> Signup and view all the answers

This describes the relationship between drug dose and drug blood level.

<p>Pharmacokinetics (D)</p> Signup and view all the answers

It is the fraction of the drug dose that reaches the blood.

<p>Therapeutic Fraction (C)</p> Signup and view all the answers

This is often the type of reaction involved in drug absorption.

<p>Passive Diffusion (B)</p> Signup and view all the answers

Which of the following are examples of drug metabolism?

<p>Conversion of active drugs to inactive drugs (A), Conversion of a toxic component of a drug to a non-toxic form (B), Conversion of hydrophobic drug to a hydrophilic drug (C), Conversion of a prodrug to the active form of the drug (D)</p> Signup and view all the answers

Which of the following cardioactive drugs is not a rapid sodium channel blocker?

<p>Xylocaine (A)</p> Signup and view all the answers

Which of the following statements is/are incorrect?

<p>Example of a class II cardioactive drug is Xylocaine (B), Class I cardioactive drugs are rapid potassium channel blockers. (C), All of the above (D)</p> Signup and view all the answers

Flashcards

Therapeutic Drug Monitoring (TDM)

The analysis, assessment, and evaluation of drug concentrations in blood, serum, or plasma.

CYP 450 System

The primary biochemical pathway responsible for drug metabolism, involving a family of enzymes known as cytochrome P450.

Pharmacogenomics

The study of how an individual's genes influence their response to a drug.

Pharmacokinetics

The relationship between drug dose and drug blood level, describing how the body processes a drug.

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Bioavailability

The fraction of a drug dose that reaches the bloodstream, indicating absorption efficiency.

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Drug Metabolism

The process by which drugs are broken down and eliminated from the body, often involving enzymes like CYP 450.

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Reduction

A type of drug metabolism reaction where a molecule gains electrons, often involving enzymes.

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Pharmacodynamics

The relationship between drug concentration at the target site and the resulting effect on tissues.

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Class I Cardioactive Drugs

A class of cardioactive drugs that act as rapid sodium channel blockers, affecting heart rhythm.

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Class IV Cardioactive Drugs

A class of cardioactive drugs that block calcium channels, affecting heart rate and contraction.

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Lidocaine

A cardioactive drug that is a rapid sodium channel blocker, used to treat arrhythmias.

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Disopyramide

A cardioactive drug that blocks potassium channels in cardiac muscles, used to treat ventricular arrhythmias.

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Propranolol

A beta-blocker used for various cardiovascular conditions, known for its effects on heart rate and blood pressure.

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Vancomycin

An antibiotic effective against various bacterial infections, particularly gram-positive bacteria.

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Lithium

A psychoactive drug used for treating bipolar disorders, known for its mood-stabilizing effects.

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Phenobarbital

A drug commonly used for controlling and preventing seizures, known for its antiepileptic properties.

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Tacrolimus

An immunosuppressive drug used for preventing organ rejection after transplantation, known for its role in modulating the immune system.

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Acetaminophen (Tylenol)

A common analgesic and anti-inflammatory drug, known for its potential to cause liver damage with overdose.

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Neuroleptic Drugs

A category of psychoactive drugs used for managing symptoms of schizophrenia and other mental illnesses.

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Timing of Specimen Collection

The timing of specimen collection in Therapeutic Drug Monitoring (TDM), crucial for determining accurate drug levels.

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Verapamil

A cardioactive drug that is a calcium channel blocker, used for conditions like hypertension and angina.

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Dilantin (Phenytoin)

An antiepileptic drug used to treat various types of epilepsy.

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Fluoxetine (Prozac)

A psychoactive drug used to treat depression, known for its role in regulating serotonin levels.

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FK-506 (Tacrolimus)

An immunosuppressive drug used for preventing organ rejection after transplantation.

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Drug Absorption

The process by which drugs are absorbed into the bloodstream, often involving passive diffusion.

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Oxidation

A type of drug metabolism reaction where a molecule loses electrons, often involving enzymes.

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Prodrug

A drug molecule that is inactive when administered but is converted into an active form by the body.

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Drug Excretion

The process by which drugs are eliminated from the body, often involving the kidneys and liver.

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Half-life

The time it takes for the concentration of a drug in the body to decrease by half.

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Therapeutic Range

The range of drug concentrations that produce the desired therapeutic effect without causing toxicity.

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Study Notes

Instructions for the Exam

  • Read the questions carefully and choose the best answer.
  • If there are any alterations in the given options of the exam, choose the answer corresponding to that alteration
  • Use black ballpoint pen only.

Pharmacology concepts

  • Studying pharmacology involves analysis, assessment, and evaluation of circulating concentrations of drugs in serum, plasma, or whole blood.

  • It encompasses the study of medications and their interactions with the body.

Pharmacokinetics

  • The study of how medications move throughout the body.

  • This includes absorption, distribution, metabolism, and excretion of medications.

  • It describes chemical pathway responsible for the greatest portion of drug metabolism.

  • It is the study of the relationship between drug concentration at the target site and the response of the tissues.

Pharmacodynamics

  • The study of how medications produce their effects on the body.

  • The study of the effects that affect the performance of a drug in the individual

  • It describes the relation between drug dose and blood level.

  • Describes the relationship between drug dose and drug blood levels.

  • This defines the fraction of the drug dose that reaches the blood.

Drug Absorption

  • A process by which medications move from the site of administration into the bloodstream.
  • This often involves passive diffusion.

Drug Metabolism

  • A process of drug chemical modifications to either activate or inactivate the drug, often through oxidation, reduction, or hydrolysis

  • Includes conversions of active drugs to inactive drugs,

  • Also includes the conversion of prodrugs into an active form,

  • Includes the conversion of a hydrophobic drug to a hydrophilic drug,

  • Includes the conversion of a drug to a nontoxic form,

  • Includes all the processes mentioned above, except number 4.

Therapeutic Range

  • A range of drug doses that produces therapeutic effects without significant side effects.

Important Concepts

  • Pharmacokinetics is the study of what the body does to the drug.
  • Pharmacodynamics is the study of what the drug does to the body.

Additional Concepts (Multiple choice questions)

  • Amiodarone is a class III cardiac drug. It's used as a substitute for quinidine and is quickly absorbed orally.
  • Vancomycin is a glycopeptide antibiotic, effective against various bacteria (Staphylococcus, Streptococcus, and Bacillus anthracis).
  • Prozac is a psychoactive drug used to treat bipolar and other related disorders.
  • An immunosuppressive drug, taken orally, is used to prevent host-versus-graft rejection, Sirolimus.
  • A common analgesic and antipyretic drug, Aspirin, can lead to hepatotoxicity in overdose cases.
  • Drugs used to treat acute schizophrenia include antipsychotics.
  • Identifying single most important factors in determining the timing of peak and trough concentrations in a patient.

Additional Concepts (Multiple choice questions- continued)

  • Important factor in determining the timing of peak and trough concentrations is the timing of specimen collection
  • Quinidine and Lidocaine are not rapidly acting medications.
  • The incorrect statement about classes of cardiac medications involves the statement that class IV cardiac drugs are calcium channel blockers. Class II cardiac medications are calcium channel blockers and Xylocaine is an example of a class II drug.

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Description

Test your knowledge on the fundamental concepts of pharmacology, including pharmacokinetics and pharmacodynamics. This quiz covers how drugs interact with the body, their movements, and their effects. Prepare to deepen your understanding of medication mechanisms.

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