Pharmacology: Drug Action and Classification

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Questions and Answers

A patient with liver cirrhosis may experience impaired drug metabolism. This primarily affects which pharmacokinetic process?

  • Distribution
  • Metabolism (correct)
  • Excretion
  • Absorption

Which classification method groups drugs based on their clinical application?

  • Pharmacological classification
  • Chemical classification
  • Toxicological classification
  • Therapeutic classification (correct)

A drug that binds to a receptor and prevents the action of an endogenous substance is known as what?

  • Agonist
  • Partial agonist
  • Enzyme
  • Antagonist (correct)

If a drug has a high affinity for plasma proteins, what effect would this have on drug distribution?

<p>Decreased distribution to tissues (B)</p> Signup and view all the answers

Which of the following routes of administration typically results in the highest bioavailability?

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

A drug interaction that alters the absorption, distribution, metabolism, or excretion of another drug is classified as what type of interaction?

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

Which of the following best describes the term 'efficacy' in pharmacodynamics?

<p>The maximum effect a drug can produce (A)</p> Signup and view all the answers

In toxicology, what term describes the ability of a drug to cause birth defects?

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

Cytochrome P450 enzymes play a critical role in which pharmacokinetic process?

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

Why is patient adherence important in pharmacotherapy?

<p>To maximize therapeutic benefits and minimize risks (D)</p> Signup and view all the answers

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Flashcards

Pharmacology

The study of drugs and their effects on living organisms, covering pharmacokinetics, pharmacodynamics, toxicology, and therapeutics.

Chemical Classification

Grouping drugs by similar chemical structures.

Pharmacological Classification

Grouping drugs based on how they work in the body.

Pharmacokinetics

The movement of drugs within the body, including absorption, distribution, metabolism, and excretion (ADME).

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Absorption

The process by which a drug enters the bloodstream from its administration site.

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Bioavailability

The fraction of an administered dose of drug that reaches the systemic circulation.

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Distribution

The process by which a drug is transported throughout the body to its target tissues.

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Metabolism

The process by which the body chemically modifies a drug, often in the liver.

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Excretion

The process by which the drug is removed from the body, primarily via the kidneys.

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Pharmacodynamics

Describes the effects of a drug on the body and its mechanism of action.

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Study Notes

  • Pharmacology is the study of drugs and their effects on living organisms.
  • Encompasses pharmacokinetics (how drugs are absorbed, distributed, metabolized, and excreted) and pharmacodynamics (effects on the body).
  • Also covers toxicology (adverse effects of drugs) and therapeutic use in treating diseases.

Drug Classification

  • Drugs are classified based on chemical structure, mechanism of action, or therapeutic use.
  • Chemical classification groups drugs with similar chemical structures.
  • Pharmacological classification groups drugs based on their mechanism of action.
  • Therapeutic classification groups drugs based on their clinical use.

Pharmacokinetics

  • Pharmacokinetics describes the movement of drugs within the body.
  • Involves four main processes: absorption, distribution, metabolism, and excretion (ADME).
  • Absorption is the process by which a drug enters the bloodstream from its site of administration.
  • Factors affecting absorption include the route of administration, the drug's formulation, and physiological factors like gastric emptying and intestinal motility.
  • Distribution is the process by which a drug is transported throughout the body to its target tissues.
  • Factors affecting distribution include blood flow, tissue permeability, and binding to plasma proteins.
  • Metabolism (or biotransformation) is the process by which the body chemically modifies a drug.
  • Often occurs in the liver and can result in the drug becoming more water-soluble, which facilitates excretion.
  • Enzymes, such as those in the cytochrome P450 (CYP) family, play a vital role in drug metabolism.
  • Excretion is the process by which the drug is removed from the body.
  • The kidneys are the primary organs involved in excretion, but drugs can also be excreted in the bile, feces, sweat, and breath.
  • Understanding pharmacokinetics is crucial for determining appropriate drug dosages and dosing intervals.
  • Bioavailability refers to the fraction of an administered dose of drug that reaches the systemic circulation.

Pharmacodynamics

  • Pharmacodynamics describes the effects of a drug on the body and its mechanism of action.
  • Drugs typically exert their effects by interacting with specific receptors, enzymes, or ion channels.
  • Receptors are proteins on cell surfaces or within cells that bind to drugs and initiate a biological response.
  • Agonists are drugs that bind to receptors and activate them, producing a response.
  • Antagonists are drugs that bind to receptors but do not activate them; instead, they block the binding of agonists and prevent a response.
  • Enzyme inhibitors bind to enzymes and decrease their activity.
  • Ion channel blockers bind to ion channels and block the flow of ions across cell membranes.
  • Dose-response relationships describe the relationship between the dose of a drug and the magnitude of its effect.
  • The potency of a drug refers to the amount of drug needed to produce a given effect.
  • The efficacy of a drug refers to the maximum effect a drug can produce.

Toxicology

  • Toxicology is the study of the adverse effects of drugs and other chemicals on living organisms.
  • Adverse drug reactions (ADRs) are unintended and undesirable effects of drugs.
  • ADRs can range from mild to severe and can include allergic reactions, organ damage, and death.
  • Factors that can increase the risk of ADRs include high doses, multiple drug use, and certain pre-existing medical conditions.
  • Drug interactions occur when one drug affects the activity of another drug.
  • Interactions can be pharmacokinetic (affecting ADME) or pharmacodynamic (affecting the drug's mechanism of action).
  • Overdose occurs when a drug is taken in excessive amounts, leading to toxic effects.
  • Treatment for overdose may involve supportive care, administration of antidotes, and measures to enhance drug elimination.
  • Some drugs can cause birth defects if taken during pregnancy (teratogenicity).
  • Carcinogenicity refers to the ability of a drug to cause cancer.
  • Mutagenicity refers to the ability of a drug to cause gene mutations.

Therapeutic Uses

  • Drugs are used to treat a wide range of diseases and conditions.
  • Antibiotics are used to treat bacterial infections.
  • Antiviral drugs are used to treat viral infections.
  • Antifungal drugs are used to treat fungal infections.
  • Analgesics are used to relieve pain.
  • Anti-inflammatory drugs are used to reduce inflammation.
  • Antidepressants are used to treat depression.
  • Antipsychotics are used to treat psychosis.
  • Antihypertensive drugs are used to treat high blood pressure.
  • Chemotherapy drugs are used to treat cancer.
  • Immunosuppressants are used to suppress the immune system.
  • Hormone therapies are used to treat hormone deficiencies or imbalances.
  • The selection of a drug for therapeutic use depends on various factors, including the diagnosis, the severity of the condition, and the patient's individual characteristics.
  • Considerations include the drug's efficacy, safety, cost, and potential for drug interactions.
  • The goal of pharmacotherapy is to maximize the therapeutic benefits of a drug while minimizing its risks.
  • Patient adherence (taking medications as prescribed) is essential for successful pharmacotherapy.

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