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
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
3
Q
Polypharmacy: use of medicine in the preceding week
A
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)
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
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
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
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
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
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
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
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
13
Q
Interactions- impact on metabolism (examples)
What will happen?
A
- Increased elimination
- Reduced Half-life
- Reduction in immune-suppresion
- Organ rejection
14
Q
Interactions- impact on metabolism
A
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