Podcast
Questions and Answers
It involves the analysis, assessment, and evaluation of circulating concentrations of drugs in serum, plasma, or whole blood.
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.
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.
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.
The study of genes that effect the performance of a drug in an individual.
This describes the relationship between drug dose and drug blood level.
This describes the relationship between drug dose and drug blood level.
It is the fraction of the drug dose that reaches the blood.
It is the fraction of the drug dose that reaches the blood.
This is often the type of reaction involved in drug absorption.
This is often the type of reaction involved in drug absorption.
Which of the following are examples of drug metabolism?
Which of the following are examples of drug metabolism?
Which of the following cardioactive drugs is not a rapid sodium channel blocker?
Which of the following cardioactive drugs is not a rapid sodium channel blocker?
Which of the following statements is/are incorrect?
Which of the following statements is/are incorrect?
Flashcards
Therapeutic Drug Monitoring (TDM)
Therapeutic Drug Monitoring (TDM)
The analysis, assessment, and evaluation of drug concentrations in blood, serum, or plasma.
CYP 450 System
CYP 450 System
The primary biochemical pathway responsible for drug metabolism, involving a family of enzymes known as cytochrome P450.
Pharmacogenomics
Pharmacogenomics
The study of how an individual's genes influence their response to a drug.
Pharmacokinetics
Pharmacokinetics
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Bioavailability
Bioavailability
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Drug Metabolism
Drug Metabolism
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Reduction
Reduction
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Pharmacodynamics
Pharmacodynamics
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Class I Cardioactive Drugs
Class I Cardioactive Drugs
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Class IV Cardioactive Drugs
Class IV Cardioactive Drugs
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Lidocaine
Lidocaine
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Disopyramide
Disopyramide
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Propranolol
Propranolol
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Vancomycin
Vancomycin
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Lithium
Lithium
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Phenobarbital
Phenobarbital
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Tacrolimus
Tacrolimus
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Acetaminophen (Tylenol)
Acetaminophen (Tylenol)
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Neuroleptic Drugs
Neuroleptic Drugs
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Timing of Specimen Collection
Timing of Specimen Collection
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Verapamil
Verapamil
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Dilantin (Phenytoin)
Dilantin (Phenytoin)
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Fluoxetine (Prozac)
Fluoxetine (Prozac)
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FK-506 (Tacrolimus)
FK-506 (Tacrolimus)
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Drug Absorption
Drug Absorption
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Oxidation
Oxidation
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Prodrug
Prodrug
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Drug Excretion
Drug Excretion
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Half-life
Half-life
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Therapeutic Range
Therapeutic Range
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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
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Studying pharmacology involves analysis, assessment, and evaluation of circulating concentrations of drugs in serum, plasma, or whole blood.
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It encompasses the study of medications and their interactions with the body.
Pharmacokinetics
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The study of how medications move throughout the body.
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This includes absorption, distribution, metabolism, and excretion of medications.
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It describes chemical pathway responsible for the greatest portion of drug metabolism.
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It is the study of the relationship between drug concentration at the target site and the response of the tissues.
Pharmacodynamics
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The study of how medications produce their effects on the body.
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The study of the effects that affect the performance of a drug in the individual
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It describes the relation between drug dose and blood level.
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Describes the relationship between drug dose and drug blood levels.
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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
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A process of drug chemical modifications to either activate or inactivate the drug, often through oxidation, reduction, or hydrolysis
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Includes conversions of active drugs to inactive drugs,
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Also includes the conversion of prodrugs into an active form,
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Includes the conversion of a hydrophobic drug to a hydrophilic drug,
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Includes the conversion of a drug to a nontoxic form,
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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.