Drug Interactions Flashcards

1
Q

Drug interaction

A

One drug/vehicle alters effect of another; not an adverse reaction (unexpected), not toxic effect (overdose), not side effect (expected)

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2
Q

What are the major types of drug interactions?

A

Pharmacological, Pharmacodynamic, Pharmacokinetic

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3
Q

Pharmacologic interaction

A
  • Physical/chemical interaction between drugs, drug solutions, dosing equipment
  • Ex: Doxy and temp. (becomes less active w/ improper storage) - detrimental
    • Enrofloxacin + LRS (LRS chelates abx and makes inactive) - detrimental
  • Often caused by MIXING - cloudy, precipitation, catheter flushing
  • Consequences: difficult to predict, precipitates can be toxic/irritants, drugs can be inactivated or NOT biologically available - treatment failure
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4
Q

Pharmacodynamic interactions

A
  • Additive, synergistic, or antagonistic interaction of the effect of combining two drugs and effect on patient
  • Ex: synergistic activity of two antibiotics - helpful
  • Either act on same receptors or those that regulate common process - direct vs. physiological interaction or elicit effects that are not receptor-mediated but have final common pathways - systemic interaction
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5
Q

Pharmacokinetic interactions

A
  • Interactions b/t drugs which impact the absorption, distribution, metabolism or excretion of the drug
  • most common and most difficult to keep track of
  • Ex: herbal supplements in combination with prescription drugs (not FDA regulated, can have toxic SE, can affect metabolism of other drugs) - can be detrimental
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6
Q

What are some detrimental drug interactions?

A

Toxicity and Treatment failure

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7
Q

What are helpful drug interactions?

A

Using known interaction to increase the efficacy of some treatments or decrease the incidence of adverse drug effects

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8
Q

How to prevent pharmacologic interactions

A
  • Don’t mix drugs prior to injection
  • sequential rather than simultaneous drug addition to IV
  • Flush catheter!!!
  • Use immediately after preparation
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9
Q

Additive pharmacodynamic interaction

A
  • Sedation - e.g barbiturates and benzodiazepines
  • Analgesia - combo of opioids and NSAIDs (Physiological interactions)
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10
Q

Synergistic Pharmacodynamic Interactions

A

Greater than expected increase in drug activity from drug combo; e.g. Penicillins + aminoglycosides

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11
Q

Antagonistic interactions

A

Pharmacodynamic effects are the basis of the use of reversal agents which often have same drug target or biological pathway Ex: metdetomidine (analgesic) and atipamezole (reversal)

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12
Q

Complex physiological interactions

A
  • Diuretics (furosemide)
    • Interact w/ many drugs due to effects on renal function
  • Ex: Digitalis
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13
Q

Absorption Pharmacokinetic Interactions

A

Can affect uptake of drug by the body

  • Oral absorption - drug binding:
    • pH effect on uptake
    • Gut drug transporters - either bringing in or out of gut lumen/portal circulation
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14
Q

Oral Drug Physical Interactions

A
  • Cations interaction with drugs is common mechanism- decrease uptake/bioavailability
  • Ex: oral antacids, gastric protectants (sucralfate), cation rich feed/oral supplements, Milk diets in nursing animals are high in Ca, Can be used for drug overdose tx
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15
Q

Pharmacokinetic interaction alterations in Gastric pH

A
  • Can impact dissolution/uptake
  • For non-transport (passive) mediated uptake
    • Antacids (incr pH) decr absorption of weak acids
    • Infections (decr pH) incr absorption of weak acids Ex: antifungals - absorption pH sensitive
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16
Q

Distribution Interactions

A

Phenylbutazone (NSAID) + Warfarin (anti-coagulant) -increases free warfarin drug levels - incr bleeding risk

17
Q

Metabolism interactions

A

Metabolic inactivation - Drugs can compete with each for metabolism P450 enzymes

  • involved in conversion/bioactivation of P450
    • Inducers - phenobarb, rifampin, decr duration/potency of other drugs
    • Inhibitors - cimetidine, chloramphenicol, ketoconazole; incr duration/potency of others
    • Metabolites - diazepam, ketamine, morphine
18
Q

Metabolism interactions with CYP Inhibition

A
  • Chlormaphenicol/Ketoconazole - reduces metabolism of phenobarb
    • Increases serum levels of many drugs metabolized by P450
    • Used to increase anticonvulsant responses of PB
19
Q

Other Metabolism Interactions

A

Behavior modifying drugs - Selegiline inhibits MAO - co-administered with other drugs that increase circulating serotonin levels can lead to serotonin syndrome

20
Q

Elimination Interactions

A
  • Renal- competition for same renal tubular system, alter urinary pH (ion trapping), alter renal blood flow
  • Biliary - enterohepatic recirculation, antibiotics alter microbial flora Respiratory