Lec 9- Interactions Flashcards

1
Q

How do we define an interaction

A
  • A change in one drugs effect when administered with another drug, food or other substance
  • FOOD = Milk
  • HERBALS= St Johns Wort
  • DRUGS= Any
  • LIFESTYLE= Alcohol, smoking
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2
Q

Will it be important

A
  • Mostly No / Yes
  • Depends on a number of factors
  • High risk drugs: Narrow TI
  • High risk Patients: pregnant, geriatric, liver/renal disease
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3
Q

Polypharmacy: use of medicine in the preceding week

A
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4
Q

Interactions- clinical presentation

A
  • BENEFICIAL
    • POTENTIATE: Combination anti-biotics (Additive/Synergistic)
    • ANTAGONISM: ‘Antidote’ for overdose (Antagonistic =Lessened effects)
  • Undesirable
    • TOXICITY: Diuretics and NSAIDs worsening renal impairment (Additive/Synergistic)
    • LOSS OF EFFECT: Carbamazepine reducing warfarin’s blood thinning effect (Antagonistic =Lessened effects)
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5
Q

Interactions- Clinical presentation

Warfarin example

A
  • An 87-year-old woman is brought to the A&E by ambulance.
  • Her INR is 6 (Therapeutic range 2-3) and this is her CT scan
  • Her daughter tells you she is usually on warfarin and has recently been taking some other tablets for a UTI
  • This patient was prescribed erythromycin for her UTI
  • It turns out that erythromycin is able to inhibit the metabolism of warfarin and thereby leading to a cranial haemorrhage
  • Something as simple as erythromycin is potentially lethal as an interaction for those taking warfarin
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6
Q

Interactions- ADME processes

A
  • An interactions can occur at different points in the PK of a drugs, depending on the route of administration
  • ABSORPTION: Often at the level of the stomach Or small-intestine
  • DISTRIBUTION: At a tissue level
  • METABOLISM: At the liver
  • ELIMINATION: At the kidneys
  • For example and orally dosed agent may have more of a clinical problem with an interaction compared to one which dosed through an IV bolus
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7
Q

Interactions- Impact on absorption

A
  • For orally dosed therapeutics, interactions at the level of the stomach and small-intestine are important and impact on the process of drug absorption
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8
Q

Interactions- Impact on distribution

A
  • For drugs to be able to distribute out of the circulation and into target tissues, diffusion across cellular membranes is important
  • Interactions often occur at the level of plasma protein
  • Albumin has two main drug binding sites, the bindings depends on the affinity of a drug towards the proteins
  • Co-administer a drug with higher binding affinity than the victim drug leads to displacement from binding site
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9
Q

What is the impact of this on the PK of a drug and does it impact on drugs with a low or high Fu

A
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10
Q

Interactions- Impact on metabolism

A
  • For orally dosed therapeutics, interactions at the level of the small intestine and liver can be clinically significant as they often impact upon drug metabolism
  • The main target is often CYP450 enzymes
  • The perpetrator drug will cause one of these
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11
Q

Interactions- impact on metabolism

A
  • The drug agent causing the change in metabolism (perpetrator) itself has to undergo ADME processes
  • Less enzyme (function)=> Inhibitor => Time to see effect depends on the half-life of the drug and time it takes to reach a steady state
  • More enzyme (amount) => Inducer => Can take a few weeks to see maximum effects and a few weeks to recover
  • Manifests as changes in clearance or half-life and plasma concentrations
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12
Q

Interactions- Impact on metabolism

A
  • Inhibitor-
    • Macrolide AB (–mycins)
    • Ca2+ blockers (verapamil / Diltiazem)
    • HIV anti-virals
    • Azoles (Keto/itra)
  • Inducer
    • Anti-epileptics (Carbamazepine, Phenytoin)
    • St Johns Wort
    • Rifampicin
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13
Q

Interactions- impact on metabolism (examples)

What will happen?

A
  • Increased elimination
  • Reduced Half-life
  • Reduction in immune-suppresion
  • Organ rejection
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14
Q

Interactions- impact on metabolism

A
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15
Q

Interactions- impact on metabolism (examples)

A
  • Inducers (rifampicin)- Note that the effect is NOT instantaneous
  • Inducers require some time to manifest an effect on the metabolism of drugs
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16
Q

Interactions- impact on metabolism (examples)

A
  • INDUCER (CYP2C9)
    • Antiepileptics (carbamazepine, phenytoin)
    • Rifampicin
    • St Johns Wort
  • INHIBITOR
    • Amiodarone
    • Fluoxetine
    • FLuconazole
  • Narrow TI drug
  • Control of PK important
  • Increased or decrease in clotting
  • Alters elimination
  • Alters half-life
17
Q

Interactions- impact on metabolism (examples)

Clonzapine

A
  • Food / Lifestlye interaction
  • Smokers have a Cmax that is 20% lower than non-smokers
  • Tobacco INDUCES the expression of CYP1A2 (hence 20% reduction)
  • Patients admitted or unable to smoke should get a dose reduction
18
Q

Interactions- impact on metabolism

A
  • Food / Lifestyle interaction
  • Grapefruit juice contains chemicals which strongly inhibit the function of CYP3A4
  • This can have an effect on a wide range of drugs
19
Q

Interactions- impact on renal elimination

A
  • The kidney play a major role in the elimination of drugs
  • Patients with renal failure are more prone to presenting with more significant ADR as a result of an interaction
  • NSAIDS- alter renal blood flow change GFR; Affects methotrexate (toxic) reduced elimination
  • Thiazides diuretic- Alter fluid secretion/reabsorption; Affects lithium (depression) reduced elimination
  • Bicarbonates- Alters urine pH; Encourages elimination of aspirin in OD cases
20
Q

Summary

A
  • Describe the term interactions in the context of alterations in the ADMA of a victim drug
  • Illustrate examples of interactions at the level of ADME
  • Describe the consequence on the PK of the victim drug