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Questions and Answers
What is the most effective route of administration for adrenaline during an anaphylactic shock?
What is the most effective route of administration for adrenaline during an anaphylactic shock?
Which type of hypersensitivity can be detected through intradermal drug sensitivity tests?
Which type of hypersensitivity can be detected through intradermal drug sensitivity tests?
Which drug is noted for causing minimal or no physical dependence despite its addiction potential?
Which drug is noted for causing minimal or no physical dependence despite its addiction potential?
What constitutes the essential feature of drug addiction?
What constitutes the essential feature of drug addiction?
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Which term describes physiological changes from repeated drug use, manifesting in withdrawal symptoms upon discontinuation?
Which term describes physiological changes from repeated drug use, manifesting in withdrawal symptoms upon discontinuation?
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Which scenario best illustrates drug abuse?
Which scenario best illustrates drug abuse?
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How do 'addiction' and 'habituation' fundamentally differ?
How do 'addiction' and 'habituation' fundamentally differ?
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Which drug is known to cause significant adverse effects upon sudden discontinuation following chronic use?
Which drug is known to cause significant adverse effects upon sudden discontinuation following chronic use?
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What is the relationship between drug toxicity and poisoning?
What is the relationship between drug toxicity and poisoning?
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Which substance's poisoning allows emetic use for removal?
Which substance's poisoning allows emetic use for removal?
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An immunologically mediated drug reaction with symptoms unrelated to its pharmacodynamics is termed what?
An immunologically mediated drug reaction with symptoms unrelated to its pharmacodynamics is termed what?
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Drugs that cause allergic reactions typically act as which of the following?
Drugs that cause allergic reactions typically act as which of the following?
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Which allergic drug reaction is caused by circulating antibodies?
Which allergic drug reaction is caused by circulating antibodies?
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Which treatment is identified as the only life-saving measure during anaphylactic shock?
Which treatment is identified as the only life-saving measure during anaphylactic shock?
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Type II, type III, and type IV hypersensitivity reactions can be suppressed by which of the following?
Type II, type III, and type IV hypersensitivity reactions can be suppressed by which of the following?
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What distinguishes idiosyncratic adverse drug reactions?
What distinguishes idiosyncratic adverse drug reactions?
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Which of the following acts as an intracellular second messenger in receptor mediated signal transduction?
Which of the following acts as an intracellular second messenger in receptor mediated signal transduction?
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What mechanism of receptor transduction has the fastest response times?
What mechanism of receptor transduction has the fastest response times?
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Which of the following receptors exhibits intrinsic enzymatic activity?
Which of the following receptors exhibits intrinsic enzymatic activity?
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What defines an 'orphan drug'?
What defines an 'orphan drug'?
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What can lead to down regulation of receptors?
What can lead to down regulation of receptors?
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Which route of drug administration is most susceptible to first-pass metabolism?
Which route of drug administration is most susceptible to first-pass metabolism?
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Which statement regarding the log dose-response curve is not true?
Which statement regarding the log dose-response curve is not true?
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When is a drug said to exhibit a therapeutic window phenomenon?
When is a drug said to exhibit a therapeutic window phenomenon?
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Transdermal drug delivery systems are beneficial except for which characteristic?
Transdermal drug delivery systems are beneficial except for which characteristic?
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Which of the following describes a characteristic of drug potency?
Which of the following describes a characteristic of drug potency?
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Which administration route is best suited for titrating drug doses with the patient’s response?
Which administration route is best suited for titrating drug doses with the patient’s response?
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Which drug is commonly administered via intra-nasal spray for systemic effects?
Which drug is commonly administered via intra-nasal spray for systemic effects?
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Which drug is least likely to exhibit a therapeutic window phenomenon?
Which drug is least likely to exhibit a therapeutic window phenomenon?
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How does intramuscular injection compare to subcutaneous injection?
How does intramuscular injection compare to subcutaneous injection?
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Which route carries the highest risk of harming vital functions?
Which route carries the highest risk of harming vital functions?
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What type of drugs does alkalinization of urine expedite the excretion of?
What type of drugs does alkalinization of urine expedite the excretion of?
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Which type of uptake is blocked by reserpine?
Which type of uptake is blocked by reserpine?
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What primarily terminates the action of noradrenaline released from adrenergic nerve endings?
What primarily terminates the action of noradrenaline released from adrenergic nerve endings?
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Which of the following is not a basis for subclassifying β adrenergic receptors into β1 and β2?
Which of the following is not a basis for subclassifying β adrenergic receptors into β1 and β2?
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The β3 adrenoceptor is characterized by which of the following features?
The β3 adrenoceptor is characterized by which of the following features?
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Where are α2 adrenoceptors located?
Where are α2 adrenoceptors located?
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Which substance acts exclusively by releasing noradrenaline from nerve endings?
Which substance acts exclusively by releasing noradrenaline from nerve endings?
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Which sympathomimetic amine has agonistic action on α1, α2, β1, and β3 adrenoceptors, but not on β2?
Which sympathomimetic amine has agonistic action on α1, α2, β1, and β3 adrenoceptors, but not on β2?
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What common effect is mediated by both α and β receptors?
What common effect is mediated by both α and β receptors?
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What characteristic distinguishes dobutamine from dopamine?
What characteristic distinguishes dobutamine from dopamine?
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Which drug is specifically known for its selective adrenergic β1 agonistic activity without dopaminergic effects?
Which drug is specifically known for its selective adrenergic β1 agonistic activity without dopaminergic effects?
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Which of the following effects is NOT produced by amphetamine at therapeutic doses?
Which of the following effects is NOT produced by amphetamine at therapeutic doses?
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Which pressor agent is known to act both directly and indirectly, causing vasoconstriction and cardiac stimulation?
Which pressor agent is known to act both directly and indirectly, causing vasoconstriction and cardiac stimulation?
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What effect does phenylephrine have when instilled in the eye?
What effect does phenylephrine have when instilled in the eye?
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Which of the following drugs is most suitable for treating hypotension during a surgical procedure?
Which of the following drugs is most suitable for treating hypotension during a surgical procedure?
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Ephedrine shares which feature with adrenaline?
Ephedrine shares which feature with adrenaline?
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Which type of adrenergic effects does ephedrine produce?
Which type of adrenergic effects does ephedrine produce?
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Study Notes
Drug Administration Routes and Metabolism
- Orphan drugs are medications used to treat or prevent rare diseases.
- Oral administration is most likely to undergo first-pass metabolism.
- Transdermal drug delivery systems (e.g., patches) provide a consistent plasma drug concentration and avoid the liver's first-pass metabolism, but they have higher peak plasma concentrations.
- Inhalational and nasal insufflation routes allow for dose titration based on patient response.
- Intra-nasal sprays are used for systemic effects for drugs like Desmopressin.
- Intramuscular injections produce a faster response than subcutaneous injections, although subcutaneous can be for depot preparations.
- Intra-arterial injection carries the highest risk of affecting vital functions.
Pharmacokinetics and Excretion
- Alkalinization of urine enhances the excretion of weakly basic drugs.
- Drugs administered intravenously are subjected to first-pass metabolism.
- Different receptor transduction mechanisms have varying response time-courses. The fastest is intrinsic ion channel operation.
- Intracellular second messengers, such as cyclic AMP and inositol trisphosphate, are crucial components of receptor-mediated signal transduction. G proteins are not intracellular second messengers
- The insulin receptor has enzymatic properties
Receptor Regulation and Drug Effects
- Continuous use of agonists can lead to receptor downregulation.
- Log dose-response curves are almost linear except at the extremes and are useful to compare different agonists.
- A drug with a narrow therapeutic window has significant therapeutic effect at and only at a narrow concentration range.
- Potency is the drug dose needed for a specific response.
Drug Toxicity and Poisoning
- Poisoning is a toxic effect that needs specific treatment and endangers life. Toxicity is often from drugs, while poisoning is from other harmful chemicals
- An emetic should not be used to induce vomiting for strychnine, caustic soda, or kerosene poisoning. It is contraindicated in cases of poisoning by these substances. Ferrous sulfate should only be treated using emetics in specific cases where contraindicated
- Idiosyncratic reactions are adverse drug reactions that are not predictable.
- Immunologically mediated adverse reactions unrelated to pharmacological action are hypersensitivity reactions.
- Drugs causing allergic reactions are haptens (not full antigens), and serum sickness is an allergic reaction caused by circulating antibodies.
- Intramuscular adrenaline is the life-saving measure in anaphylactic shock.
- Type I, II, and III hypersensitivity reactions can be suppressed by corticosteroids.
- Intradermal drug tests detect type I hypersensitivity.
- Drug addiction has both physical and psychological dependence components.
Autonomic Nervous System and Sympathomimetics
- Reserpine blocks axonal, granular, and extraneous uptake for noradrenaline.
- Noradrenaline's action terminates through axonal reuptake.
- β-adrenergic receptors are distinguished by agonist and antagonist selectivity, and different transduction pathways.
- β3 receptors primarily differ by avoiding standard propranolol doses.
- α2 receptors are located pre- and postjunctionally.
- Clonidine is a selective α2 receptor agonist.
- Ephedrine and tyramine are similar to noradrenaline release.
- Adrenaline has effects on both α and β receptors.
- Dobutamine has β1 agonistic activity, but no dopaminergic effects, used short-term in heart failure.
- Amphetamine increases attention span, wakefulness, and delays fatigue, but lowers the threshold level of seizures, and potentiates neuroleptics
- Phenylephrine constricts blood vessels as well as stimulates the heart and dilates pupils
- Noradrenaline is injected intramuscularly to increase blood pressure.
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Description
This quiz explores various drug administration routes and their impact on pharmacokinetics and metabolism. It covers methods such as oral, transdermal, inhalational, and intravenous administration, detailing how each route affects drug absorption and excretion. Test your knowledge on these essential topics in pharmacology.