1. Pharmacology Flashcards
Definition of a pre-drug Definition of a drug Function of a drug Types of dental drugs (4) Action of ion channels
Inactive form of a drug activated in first-pass metabolism Substance that acts on living tissues, via receptors, enzymes or ion channels, to produce a measurable change in tissue function Simulate/interrupt normal communication and act on non-host organisms to aid body defences LA, anxiolytics, antimicrobials, analgesics Ion channels (LA, anti-diabetic drugs) disrupt cell ion balance
Types of autonomic drugs (4)
Autonomic nerve control of HR
B-agonist, B-antagonist, cholinergic agonist, cholinergic antagonist
SyNS increases HR via B-receptors; PSyNS decreases HR via cholinergic receptors
Drug receptor interactions (2) and response (1)
Affinity, occupancy and efficacy
Methods of drug administration (2)
Examples of drug administration
Advantages (1) and disadvantages (4) of oral administration
When is oral route not preferred (3)
Advantages (2) and disadvantages (3) of parenteral route
Definition of first-pass metabolism
Enteral and parenteral
Oral, IV, IM, SC, TD, inhalation
Socially acceptable; slow onset, variable absorption, affected by first-pass metabolism, drug formulation
Emesis, absorption irregularities, destruction by digestive enzymes/gastric acid
No first-pass metabolism, predictable plasma levels, higher cost, more severe allergic reactions, access difficulties
Enterally administered drugs pass through liver once before entering circulation - activation or inactivation
Definition of bioavailability
What is bioavailability modified by
Proportion of ingested drug available for clinical effect
Dosage form, poor absorption, first=pass metabolism
Phases of drug metabolism (2) Phase 1 description Phase 1 reactions (3) Phase 2 description Phase 2 reactions (2) Methods of drug excretion (5)
Phase 1 and phase 2 Drug inactivation Reduction, oxidation, hydrolysis Preparing drug for removal Conjugation - methylation, sulphanation Renal (urine), liver, lung, sweat, saliva
Definition of volume of distribution
Types of drug distribution (2)
What is drug distribution affected by (2)
Body compartments the drug is diluted in (usually uneven)
Single (evenly distributed around body), two compartments (equilibrium with different body tissues)
Lipid binding and binding to plasma proteins
Drug clearance components (2)
Features of first-order kinetics (3)
Features of zero-order kinetics (3)
Plasma half-life and kinetics
Elimination/absorption is passive. T0.5 is constant. Removal is proportional to concentration
Elimination is active and can be saturated. Maximum rate of elimination is constant regardless of concentration. Predictable
Definition of drug accumulation
Features of drug scheduling (2)
What is drug efficiency effected by
What controls access of endogenous substances and xenobiotics (2)
Measure of how plasma concentration builds due to repeated doses
Too much - toxic plasma levels. Too little - no clinical effect
Degree bound - less bound (free drug), less predictable
Blood-brain barrier and blood-CSF barrier
Features of aspirin (what it is, what it does)
How is aspirin eliminated from the body
Side effects of aspirin (4)
Blood thinner/antiplatelet drug - reduces MI/bowel cancer risk
By first-order kinetics
Gastric irritation, inhibits platelets (increased bleeding), bronchospasm, allergic reaction
Action of NSAIDs (2)
Side effects of ibuprofen vs aspirin
Features of diclofenac
Features of COX II inhibitors (side effects, action)
Reduce inflammatory mediators, inhibit prostaglandin synthesis
Ibuprofen less than aspirin
Diclofenac more potent (lower doses)
Less gastric irritation. Better long-term (arthritis) but cause cardiac death
Action of corticosteroids (4) What do corticosteroids not do Side effects (7)
Reduce inflammation by inhibiting WBC migration, bradykinin formation and capillary permeability. Reduce eicosanoid synthesis
Do not treat cause/underlying problem
HTN, weight gain, fat distribution change (buffalo hump, moonface), adrenal suppression, risk of osteoporosis, diabetes, gastric ulcers
Dental medical emergency drugs (8)
Adrenaline injection, glucagon injection, oral glucose, oxygen cylinder, midazolam, salbutamol inhaler, aspirin dispersible tablet, GTN spray
What are pharmacodynamic interactions
What are pharmacokinetic interactions
Between drugs with similar/antagonistic effects/side effects
When one drug alters the absorption, distribution, metabolism or excretion of another