Pharmacology — Drug Classifications

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Pharmacokinetics

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All Terms (35)

Pharmacokinetics

The study of how drugs move through the body including absorption, distribution, metabolism, and excretion.

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Pharmacodynamics

The study of the biochemical and physiological effects of drugs and their mechanisms of action.

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First-pass metabolism

The process by which the concentration of a drug is significantly reduced before it reaches the systemic circulation.

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Bioavailability

The proportion of a drug that enters the circulation when introduced into the body and is able to have an active effect.

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Half-life of a drug

The time required for the concentration of a drug to reduce to half its initial value.

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Agonist

A substance that activates a receptor to produce a biological response.

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Antagonist

A substance that interferes with or inhibits the physiological action of another.

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Therapeutic index

The ratio between the toxic dose and the therapeutic dose of a drug.

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What is the mechanism of action of statins?

Statins inhibit HMG-CoA reductase, the enzyme involved in the synthesis of cholesterol, thereby lowering blood cholesterol levels.

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Prodrug

A drug that is administered in an inactive form and is metabolized in the body to produce an active compound.

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Enzyme induction

The increase in enzyme activity that results in greater metabolism of drugs.

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Enzyme inhibition

The decrease in enzyme activity that results in reduced metabolism of drugs.

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What is the role of cytochrome P450 enzymes?

Cytochrome P450 enzymes are involved in the metabolism of many drugs, affecting their activation or deactivation.

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Volume of distribution

The theoretical volume that a drug would have to occupy to provide the same concentration as in the blood plasma.

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Loading dose

An initial higher dose of a drug given to rapidly achieve a therapeutic concentration in the body.

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Maintenance dose

The dose of a drug that maintains or keeps the drug in the therapeutic range.

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Pharmacogenomics

The study of how genes affect a person's response to drugs.

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What is the significance of the blood-brain barrier in pharmacology?

The blood-brain barrier restricts the passage of substances from the bloodstream into the brain, affecting drug delivery and effectiveness.

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Potency

The amount of drug needed to produce a given effect.

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Efficacy

The maximum effect that can be achieved with a drug, regardless of dose.

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What are beta blockers used for?

Beta blockers are used to manage cardiac arrhythmias, protect the heart after a heart attack, and treat hypertension.

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Tachyphylaxis

A rapid decrease in response to a drug after initial or repeated use.

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Therapeutic window

The range of drug doses which can treat disease effectively while staying within the safety range.

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What is the mechanism of action of ACE inhibitors?

ACE inhibitors block the conversion of angiotensin I to angiotensin II, leading to vasodilation and reduced blood pressure.

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Additive effect

The effect of two chemicals is equal to the sum of the effect of the two chemicals taken separately.

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Synergistic effect

The effect of two drugs taken together is greater than the sum of their separate effects.

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What are the primary routes of drug excretion?

Drugs are primarily excreted via the kidneys (urine), liver (bile), lungs (exhalation), and skin (sweat).

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Enterohepatic circulation

The recycling of drugs and other substances by the circulation of bile through the intestine and liver.

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What is the role of P-glycoprotein in drug resistance?

P-glycoprotein is a transporter protein that pumps drugs out of cells, often leading to decreased drug efficacy and drug resistance.

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What is an example of a drug with a narrow therapeutic index?

Warfarin, a common anticoagulant, has a narrow therapeutic index and requires careful monitoring.

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Placebo effect

A beneficial effect produced by a placebo drug or treatment, which cannot be attributed to the properties of the placebo itself.

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What is the action of diuretics?

Diuretics increase the excretion of water and salts from the body, often used to treat hypertension and edema.

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Bioequivalence

When two drugs have the same bioavailability and same effect at the site of physiological activity.

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First-order kinetics

A constant fraction of the drug is eliminated per unit time, leading to a logarithmic decrease in drug concentration.

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Zero-order kinetics

A constant amount of drug is eliminated per unit time, leading to a linear decrease in drug concentration.

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