Pharmacology Flashcards
What is a medicine?
Any substance or combination of substances presented as having properties for treating
or preventing disease in human beings
What are the two regulatory restrictions for drugs?
Intended mode of action
How they are supplied
What are OTC - PO drugs?
Over the counter and sold / supplied under pharmacist supervison.
What are OTC GSL drugs?
Over the counter, general sales and grocery stores
What are Analgesics?
Codeine, paracetamol, aspirin, ibuprofen.
What are Laxatives?
Bisacodyl, Senna
What are PPIs?
Omeprazole
What are cough mixtures?
Diphenydramine
What are Anti-Histamines?
Cetririzine
What are Decongestants?
Pseudoephedrine
What’s the difference between an active and inactive ingredient?
Active delivers the mode of action and is responsible for side effects (ibuprofen to reduce inflammation)
Inactive alter the physical properties of the drug (filler, colouring, gluten)
What do we mean by ‘drug class’
Penicillin is an antibiotic
What do we mean by ‘Indication’
What the drug is intended for
What do we mean by contraindication?
When the drug must not be used
What do we mean by side effects?
Ibu can produce gastric ulcers
What do we mean by interactions?
A drug’s activity is affected by another substance causing a new effect.
What do drugs not do?
They do not target the underlying cause.
Describe Willow Bark and its connection to aspirin.
It contains salicin, which does not convert to salicylic acid until it reaches the bloodstream and body tissues.
It reduces fever, inflammation and pain without SEs
Aspirin was synthetically developed from salicylic acid and can cause gastric problems.
What do we call movement of drugs within the body?
Pharmacokinetics
What do we call how drugs interact with the body to exert their effect?
Pharmacodynamics
What is ADME?
Linked to pharmacokinetics
A: How is the drug ABSORBED
D: How is the drug distributed
M: How is the drug METABOLISED
E: How is the drug EXCRETED
What is the process where drugs taken orally are absorbed from the gIT and taken via the Portal Vein into the liver to be metabolised, reducing the effect of the drug by the time it enters the systemic circulation.
First pass metabolism