Lec 9- Interactions Flashcards
How do we define an interaction
- 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
Will it be important
- Mostly No / Yes
- Depends on a number of factors
- High risk drugs: Narrow TI
- High risk Patients: pregnant, geriatric, liver/renal disease
Polypharmacy: use of medicine in the preceding week

Interactions- clinical presentation
- 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)
Interactions- Clinical presentation
Warfarin example
- 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

Interactions- ADME processes
- 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
Interactions- Impact on absorption
- For orally dosed therapeutics, interactions at the level of the stomach and small-intestine are important and impact on the process of drug absorption

Interactions- Impact on distribution
- 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

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

Interactions- impact on metabolism
- 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

Interactions- Impact on metabolism
-
Inhibitor-
- Macrolide AB (–mycins)
- Ca2+ blockers (verapamil / Diltiazem)
- HIV anti-virals
- Azoles (Keto/itra)
-
Inducer
- Anti-epileptics (Carbamazepine, Phenytoin)
- St Johns Wort
- Rifampicin

Interactions- impact on metabolism (examples)
What will happen?
- Increased elimination
- Reduced Half-life
- Reduction in immune-suppresion
- Organ rejection

Interactions- impact on metabolism

Interactions- impact on metabolism (examples)
- Inducers (rifampicin)- Note that the effect is NOT instantaneous
- Inducers require some time to manifest an effect on the metabolism of drugs

Interactions- impact on metabolism (examples)
- 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
Interactions- impact on metabolism (examples)
Clonzapine
- 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

Interactions- impact on metabolism
- 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

Interactions- impact on renal elimination
- 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
Summary
- 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