questions Flashcards

1
Q

What is metformins mode of action?

A
  • Reduces glucose produced by the liver
  • increases sensitivity of muscles cells to insulin produced
  • delays transfer of glucose from intestinal tract to blood after meal
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2
Q

Metformin half life?

A

Three hours

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3
Q

Onset to drug action of metformin?

A

2.5 hrs

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4
Q

Name a plasma protein and drug which is highly plasma protein bound

Discuss their role in binding drugs and affecting their availability for pharmacodynamic action

A

Albumin

Warfarin

Drugs bound are pharmacologically inert, don’t reach site of action

Can mean oral dose is greater than needed due to bioavailability being reduced due to plasma protein bonding

Can be displaced by other drugs from their binding sites

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5
Q

What is bioavailability?

A

Percentage of administered drug that reaches systemic circulation after absorption

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6
Q

What is steady state?

A

When drug going into the body is equal to going out, achieved after 5 half lives

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7
Q

Which organ produces plasma proteins?

A

Liver

In liver disease there are changes to plasma proteins meaning less of the drug is protein bound and more of the drug can exert effect- lower dose needed

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8
Q

Example for pharmacokinetic drug interaction

A

Can occur when drug alters after adme eg magnesium reduces ansorbion of iron so should be separated by time (in bnf)

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9
Q

Example of pharmacodynamic interaction

A

Competition at receptor sites eg propanalol (antagonist) and salbutamol (agonist)

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10
Q

2 types of ADRs

A

Augmented- predicted by pharmacology

Bizarre- wholly unpredictable eg anaphylaxis

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11
Q

How to avoid/minimise ADRs

A
Prescribe familiar drugs
Only prescribe if indicated
Check for allergies
Ref meds reviews to check for polypharmacy
Give clear instruction to the pt
Check bloods
Advise others of potential side effects
Previous reactions to medications
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12
Q

What is an ADR

A

Unwanted or harmful reaction, always unwanted

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13
Q

What to consider when prescribing in the elderly

A
Decreased metabolism and excretion
Polypharmacy
Check for renal/liver impairment
Only prescribe if good indication
Review regularly
Check nutrition status
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14
Q

Factors to consider when prescribing in renal impairment

A

Only px if definite indication
Choose drug with minimal nephrotoxicity
Monitor pt carefully- rev bloods

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15
Q

Factors to consider when prescribing a drug

A
Route
Allergies
Co morbidities
Age
Other medications
Patient agreement
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16
Q

What factors influence metabolism?

A

Genetics
Age- 1st pass maybe reduced in older people

Liver and cardiac disease (reduced blood flow in cardiac, liver disease reduces metabolic potential

17
Q

What factors can influence ‘time to onset’

A

Route of administration
Rate at which it is absorbed
How it is distributed by the body

18
Q

What are pharmacokinetics?

A

The way the drugs move through the body

19
Q

Pharmacodynamics?

A

The effect the drug has on the body

20
Q

Physiological factors affecting absorption

A

Blood flow

Total surface area (intestine, large surface area)

Contact time at site

21
Q

Physio chemical factors affecting absorption

A

Solubility

Chemical stability

Lipid to water partition coefficient (cells made from phospho-lipid layer- drugs dissolve well in lipids eg anaesthetic, benzodiazepines

Degree of ionisation

22
Q

What affects distribution

A

Distribution of body fluids (plasma, interstitial, and intercellular fluid)

Uptake to organs (eg iodine- thyroid gland)

Extent of plasma protein binding

Passage through barriers (eg placenta)

23
Q

2 phases of metabolism

A

Phase 1- oxidation (chemical reaction that changes drug properties), reduction, hydrolysis

Phase 2- conjugation

24
Q

What factors affect metabolism?

A

Nutrition

Age- enzyme activity declines

Alcohol

Genetics

Disease process, such as heart failure

25
Q

Where does excretion mainly take place? And how?

A

Kidney

Via renal elimination- active glomeral filtration (ionised drugs are secreted into proximal tubule and pushed out into urine

Distal tubule- passive reabsorotion and excretion of drug by taking drug from high to low concentration by diffusion

26
Q

Object of medication review

A
Check pts understanding
Reduce polypharmacy
Check bloods
Check concordance
ADRs
Side effects
27
Q

Ligand

A

Chemical/drug that binds to a receptor (benzodiazepine)

28
Q

Ion channel

A

Provide receptors which drugs can react with (blockers and modulators)

29
Q

What is an enzyme?

A

Biological catalyst that increase rate of chemical reaction eg elanopril (acei)

30
Q

Eg of transport systems?

A

Serotonin released from neurone-taken back up by same neurone using serotonin re uptake system (recycling)

Fluoxetine blocks uptake transporter- resulting in increased serotonin (increase in mood)

31
Q

What is biotransformation?

A

Process of metabolising drugs

Mainly in the liver

32
Q

Eg of a pro drug

A

Aspirin

Drugs which are activated by metabolism