Chapter 1 Flashcards

(32 cards)

1
Q

______________ Occurs when the true effect of one drug are change with presence another drug or food or environmental chemical agent.

A

Drug Interaction

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2
Q
  • not all drug interaction are ________
  • It’s not just the drugs themselves that interact, it’s their ________ too.
  • Many interactions are ______ related.
  • Some interaction can be accommodated by using another member of the _________.
A
  • bad
  • metabolites
  • dose
  • same group
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3
Q

Mechanism of drug interaction:

A
  1. Pharmacokinetics Interaction
  2. Pharmacodynamic interaction:
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4
Q

_________ When the interaction can affect the process by which drug absorbed, distributed, metabolized, excreted (ADME)

A

Pharmacokinetics interaction

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5
Q

___________ When the effect of one drug changed by presence of another drug at its site of action.

A

Pharmacodynamic interaction

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6
Q
  1. Pharmacokinetics interaction:
    A) Drug absorption interaction:
    - example 1:
A
  1. Drug affected: penicillin.
  2. Interacting drug: Neomycin.
  3. Effect of interaction: Neomycin induce malabsorption stage.
  4. Type of interaction: pharmacokinetic antagonism at absorption stage.
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7
Q
  1. Pharmacokinetics interaction:
    A) Drug absorption interaction:
    - example 2:
A
  1. Drug affected: Tetracycline
  2. Interaction drug: Antacid containingCa2+ , Mg2+,milk, Fe2+
  3. Effect of interaction: Formation of poorly absorbed soluble chelate resulting in reduced antibiotic absorption.
  4. Type of interaction: pharmacokinetic antagonism at absorption stage.
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8
Q
  1. Pharmacokinetics interaction:
    A) Drug absorption interaction:
    - example 3:
A
  1. Drug affected: Quinolone antibiotic
  2. Interaction drug: Antacid containing Al3+ , Mg2+,milk, Fe2+
  3. Effect of interaction: Formation of poorly absorbed complex.
  4. Type of interaction: pharmacokinetic antagonism at absorption stage.
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9
Q
  1. Pharmacokinetics interaction:
    B) Drug displacement (protein- binding) interaction:
A
  • affect mainly the highly bound protein such as : sulfonamides, phenylbutazone.
  • Type of interaction: pharmacokinetic synergism at displacement stage.
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10
Q

Why Drug displacement (protein- binding) is a good interaction?

A

Some drugs bind albumin and become inactive. High protein-affinity drugs like phenylbutazone displace them, increasing their free form and distribution.

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11
Q

_________ converting drug molecules into more polar compounds ( less active and water soluble ) to decrease reabsorption in the kidney and increase drug elimination.

A

metabolism

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12
Q
  1. Pharmacokinetics interaction:
    C) Drug metabolism (biotransformation) interaction: ( Enzyme induction )
A
  1. Drug affect: corticosteroids, Theophylline
  2. Inducing agent: Barbiturate , Rifampin
  3. Effect of interaction: reduce effect
  4. Type of interaction: pharmacokinetic antagonism at metabolism stage
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13
Q

How inducing agent reduce affect of drug?

A

The inducing agent stimulates liver enzymes, so when the drug reaches the liver, its effect will be reduced.

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14
Q
  1. Pharmacokinetics interaction:
    C) Drug metabolism (biotransformation) interaction: ( Enzyme inhibition )
A
  1. Drug affect: Anticoagulant
  2. Inducing agent: phenybutazone
  3. Effect of interaction: increase effect
  4. Type of interaction: pharmacokinetic synergism at metabolism stage
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15
Q
  1. Pharmacokinetics interaction:
    C) Drug metabolism (biotransformation) interaction: ( Change in blood flow through the liver )
A
  1. Interaction drug: cimetidine.
  2. Effect of interaction: interaction drug decrease blood flow in the liver lead to decrease metabolism and first pass effect and increase bioavailability.
  3. Type of interaction: pharmacokinetic synergism at metabolic stage
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16
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
A
  • Change in urinary pH
  • Change in kidney blood flow
  • Change in active kidney tubule excretion
  • Biliary excretion and entero-hepatic shunt
17
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in urinary pH ( synergism acid )
A
  1. Affect drug: Acid
  2. Interacting agent: Acid (e.g: ammonium chloride)
  3. Effect of interaction: Decreases ionization → decreases excretion → increases effect
  4. Type on interaction: pharmacokinetic synergism at excretion stage
18
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in urinary pH ( antagonism acid )
A
  1. Affect drug: Acid
  2. Interacting agent: base (e.g: sodium bicarbonate)
  3. Effect of interaction: increase ionization → increase excretion → decreases effect
  4. Type on interaction: pharmacokinetic antagonism at excretion stage
19
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in urinary pH ( synergism base )
A
  1. Affect drug: bas
  2. Interacting agent: base (e.g: sodium bicarbonate )
  3. Effect of interaction: Decreases ionization → decreases excretion → increases effect
  4. Type on interaction: pharmacokinetic synergism at excretion stage
20
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in urinary pH ( antagonism base )
A
  1. Affect drug: base
  2. Interacting agent: acid (e.g: ammonium chloride)
  3. Effect of interaction: increase ionization → increase excretion → decreases effect
  4. Type on interaction: pharmacokinetic antagonism at excretion stage
21
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in kidney blood flow
A
  • NSAID (non steroidal anti inflammatory drug) - e.g: phenylbutazone:
    It decrease blood flow in Kidney and decrease excretion of another drug
22
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in active kidney tubule excretion
A
  • Some drug compete the site of excretion of other drug at the kidney tubule.
23
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Change in active kidney tubule excretion:
A
  1. Effect drug: penicillin
  2. Interaction drug: probenecid
  3. Interaction effect: reduces active excretion of penicillin, allowing it to be passively reabsorbed by the kidneys.
  4. Type of interaction: pharmacokinetics antagonism at excretion stage
24
Q
  1. Pharmacokinetics interaction:
    D) Interaction due to change in excretion:
    • Biliary excretion and entero-hepatic shunt
A
  1. normal circulation (entro intestine hepatic circulation):
    - Lipid soluble drug exerted in bile - metabolized by gut flora - return parent compound - reabsorb drug (this process elongate the drug action)
  2. Abnormal circulation (entero hepatic shunt):
    - antibiotic reduce the flora action - quick loss of drug.
25
2. Pharmacodynamic interaction:
1. Additive or synergistic interaction and combined toxicity. 2. Antagonistic or opposing interaction. 3. Interaction due to change in drug transport mechanism.
26
2. Pharmacodynamic interaction: A) Additive or synergistic interaction and combined toxicity:
1. Drug: Nephrotoxic drug + Nephrotoxic drug ( gentamicin - gram(-) + cephalothin - gram(+) ) 2. Result of interaction: increase nephrotoxitycity. 3. Pharmacodynamics synergism
27
2. Pharmacodynamic interaction: A) Additive or synergistic interaction and combined toxicity:
1. Drug: Neuromuscular blocker + Neuromuscular blocking effect (Gallamine + Aminoglycosides) 2. Result of interaction: Increase Neuromuscular blocking 3. Pharmacodynamics synergism at neuromuscular
28
2. Pharmacodynamic interaction: B) Antagonistic or opposing interaction
1. Drug effect: Anticoagulant - heparin 2. Drug interactions: vitamin K 3. Result of interaction: decrease anticoagulant effect 4. Type of interaction: pharmacodynamic antagonism
29
2. Pharmacodynamic interaction: B) Antagonistic or opposing interaction
1. Drug effect: hypnotic drug 2. Drug interactions: caffeine 3. Result of interaction: decrease hypnotic effect 4. Type of interaction: pharmacodynamic antagonism
30
2. Pharmacodynamic interaction: B) Antagonistic or opposing interaction
1. Drug effect: Bactericidal agent 2. Drug interactions: Bacteriostatic agent 3. Result of interaction: Decrease bactericidal effect 4. Type of interaction: pharmacodynamic antagonism
31
Examples - bacteriostatic
1. Tetracycline 2. Aminocyclitols 3. Macrolides 4. Sulfonamides 5. CHPC 6. Lincosamides
32
Examples - bactericidal:
1. beta - lactams 2. Aminoglycosides 3. Fluoroquinolones