1. Nutritional Pharmacology Flashcards
(128 cards)
What types of drugs are:
Codeine
Paracetamol
Aspirin
Ibuprofen
Examples of analgesics
What types of drugs are:
Bisacodyl
Senna
Examples of laxatives
What type of drug is omeprazole?
Example of a PPI
What type of drugs are:
Cetirizine
Chlorphenamine
Examples of anti-histamines
What is the active ingredient of a drug?
Delivers the mode of action
Responsible for side effects
What is the inactive ingredient of a drug?
Alters the physical properties of the drug - colours, fillers, preservatives, lactose, gluten
What kind of reactions can inactive ingredients trigger?
Allergic reactions
Food intolerances
What is aspirin used for?
Reduces pain, fever, inflammation
What are the potential side effects of using aspirin?
GI bleeding
Peptic ulceration
Hypersensitivity
Which compound in aspirin triggers the side effects?
Salicylic acid
What is the natural alternative to aspirin?
Willow bark
Why is willow bark a better alternative to aspirin?
Contains salicin which doesn’t convert to salicylic acid
Same benefits without the side effects
What is meant by pharmacokinetics?
The timed movement of drugs into, through and out of the body
What is meant by pharmacodynamics?
How drugs interact with the body to exert their effect (mode of action)
What are the 4 key processes of pharmacokinetics?
Absorption
Distribution
Metabolism
Elimination
Why is absorption important in pharmacokinetics?
A drug must be absorbed into the bloodstream so it can exert its mode of action
Why is distribution important in pharmacokinetics?
Once in the bloodstream, the drug can now be distributed to its target site (normally a receptor) to exert its action
Why is metabolism important in pharmacokinetics?
Once the drug and receptor have interacted, the drug returns to the bloodstream and progresses to the liver to be metabolised and then eliminated from the body
Why is excretion important in pharmacokinetics?
Once metabolised, excretion normally takes place via urine or bile
What is first pass hepatic metabolism?
The process by which drugs taken orally are absorbed from the GIT and taken via the portal vein into the liver to be metabolised
What happens when a drug is extensively metabolised?
The amount of drug entering the bloodstream is greatly reduced
Effect exertion is reduced
How should drugs that are extensively metabolised by administered?
By a different route
e.g. nitro glycerine (GTN) spray for angina
Which two factors determine whether or not a drug reaches its target site of action?
Bioavailability
Route of administration
What is the bioavailability of a drug?
The proportion of the drug that can reach the bloodstream and is, therefore, available for distribution to its intended site of action