Questions and Answers
What does the term pharmacokinetics refer to?
Which of the following is NOT part of the pharmacokinetic process?
What does pharmacodynamics primarily focus on?
Which route of drug administration is mentioned as the most common?
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What is one of the main treatment modalities mentioned for the problems of excess output in infants?
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Which of the following best describes the undesirable effects of medication?
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What is the impact of metabolism within the pharmacokinetic process?
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What does the 'E' in ADME stand for?
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Which of the following factors is NOT related to drug absorption?
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Why are drugs generally absorbed more effectively in the small intestine than in the stomach?
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How does food intake generally affect drug absorption?
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What is bioavailability mainly defined as?
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Which of the following drugs may be better absorbed when taken with fatty food?
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What is the effect of a fatty meal on gastric emptying?
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Which statement accurately describes drug absorption via intravenous administration?
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What role does lipid-water solubility play in drug absorption?
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Where is most drug absorption likely to occur when a drug is administered orally?
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What characteristic of weakly acidic drugs aids in their absorption in the stomach?
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Which factor does NOT affect oral drug absorption?
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What happens to peptide drugs such as insulin when taken orally?
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Why does the small intestine allow for increased drug absorption compared to the stomach?
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What is a likely outcome for weakly basic drugs when absorbed?
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Which of the following statements about gastrointestinal absorption is true?
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What is a significant barrier for drug absorption in the stomach?
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What happens to the plasma drug concentration when a larger average volume concentration (AVC) is administered to Patient A?
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Which statement is true regarding T max following intravenous bolus administration?
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What aspect of drug administration is absent when drugs are given via intravenous bolus?
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How is drug administration via intravenous bolus often compared to other methods?
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What occurs immediately after administering a drug intravenously?
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What is one effect of having a smaller Area under the curve (Arc)?
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Faster elimination of a drug typically correlates with which outcome?
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Following intravenous administration, what does the graph generally depict in terms of plasma drug concentration over time?
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What type of drug is less likely to be administered orally due to its difficulty in crossing membranes?
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Which of the following factors does NOT affect oral drug absorption?
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When might a weak acid drug be most effectively absorbed in the body?
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What happens to a weak base drug when placed in the stomach?
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The pKa of a drug is crucial because it determines the ratio of which types of forms?
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Under which condition does a weak acid primarily exist in its un-ionized form?
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Which characteristic aids in the absorption of drugs across the phospholipid bilayer?
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What is the result of a drug's ionization status on its oral absorption?
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Study Notes
Pharmacology Overview
- Pharmacokinetics studies how drugs move through the body, involving absorption, distribution, metabolism, and excretion (ADME).
- Pharmacodynamics refers to the effects produced by drugs, differentiating it from pharmacokinetics.
Drug Administration
- The most common drug administration route is oral, although topical routes are also utilized.
- Routes and methods significantly influence drug absorption and bioavailability.
Drug Absorption Factors
- Drug-related Factors: Includes drug formulation, molecular size, lipid solubility, and ionization status.
- Individual-related Factors: Encompasses absorptive surface area, pH of the gastrointestinal tract, and food intake.
Absorption Mechanisms
- Oral drugs must withstand low pH and gastrointestinal secretions to be absorbed effectively.
- Absorption is primarily through the small intestine due to a larger surface area facilitated by villi, compared to the stomach.
Influence of pH on Drug Absorption
- Weakly acidic drugs are better absorbed in acidic conditions (stomach), while weakly basic drugs absorb better in more alkaline conditions (small intestine).
- Ionization status is influenced by the pH relative to the drug's pKa; un-ionized drugs are more easily absorbed.
Bioavailability Insights
- Bioavailability measures the fraction of the drug that reaches systemic circulation unchanged.
- Intravenous (IV) administration has nearly 100% bioavailability, unlike other routes where absorption is incomplete.
Food Interactions
- Food can slow gastric emptying and alter absorption rates; some drugs are better absorbed on an empty stomach while others may benefit from food, particularly fatty foods.
Drug Excretion and Elimination
- After IV administration, drugs do not experience an absorption phase, as the entire dose enters circulation directly.
- Factors such as surface area and gastrointestinal blood flow affect the extent of drug absorption and subsequent therapeutic effects.
Key Points on Drug Forms
- Acidic drugs remain un-ionized in the stomach, facilitating absorption, while basic drugs tend to be ionized.
- The ionization level influences lipid solubility and the ability of the drug to cross cell membranes.
Pharmacokinetic Parameters
- Plasma concentration over time shows that rapid absorption leads to a shorter time to reach maximum concentration (T max) compared to slower absorption profiles.
- The pharmacokinetic profile guides dosage and administration strategies for effective treatment.
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Description
Explore the challenges faced in pharmacology, focusing on drug issues related to excess output in infants and reduced input in adults. Understand how IV fluids containing glucose can be crucial in treatment. This quiz covers key pharmacokinetic principles and their applications.