Lecture Pharmacology Flashcards
define: pharmacoprophylaxis
use of drugs to prevent disease, or slow the course of a disease
define Pharmacodiagnostics
pre-treatment testing to determine patient response to a drug therapy
define pharmacokinetics
how the body deals with a drug in terms of the way it is administered, absorbed, distributed, and eliminated
define pharmacodynamics
what a drug does to the body, including the mechanism by which it exerts its effect
define toxicology
the study of the harmful effects of drugs (incl. medication, toxins & poisons)
what are 3 classifications of drug naming?
chemical, brand/trade, generic
describe the dose response curve
Threshold dose - dose at which the response begins to occur
Potency - dose required to produce a given response
Maximal efficacy or Peak response – maximum amplitude of response (coincides with ceiling effect)
Ceiling effect – plateau effect in the curve, indicating that no further response occurs beyond the given dose
describe administration types (pharmacokinetics) - advantages and disadvantages
Enteral administration means that drug enters the body via the alimentary canal.
Parenteral administration means that the drug enters the body through non-alimentary routes.
First-pass inactivation means that the drug entering the enteral route will be metabolized by the liver before reaching its target site. Thus dosage must be adjusted to ensure adequate amount of drug reach the tissue after being partially metabolized by the liver.
describe bioavailability
The bioavailability of a drug is the extent to which the drug reaches the systemic circulation, and is expressed as a percentage of the drug administered that reaches the bloodstream. For example, for a 100mg dose, if 50mg eventually reaches the bloodstream, that drug is said to be 50% bioavailable.
what does bioavailability depend on and what are the 4 ways it can occur?
explain drug distribution
explain drug storage
describe pharmacokinetic elimitation
describe pharmacokinetic elimination rate
describe individual drug responses
describe drug receptors
NSAIDs - what it does, properties, and adverse effects
- inhibits COX (1 and 2) enxymes, except for COX-2 selective NSAIDs which inhibits only COX2
four general properties:
Anti-inflammatory - reduce inflammation
Analgesic - reduce mild to moderate pain
Antipyretic - reduce elevated body °T (fever)
Anticoagulant - reduce blood clotting (platelet aggregation) **COX-2 selective NSAID doesn’t do this
primary adverse effects of this family of NSAIDs are:
Gastrointestinal damage
High dose: liver damage
Renal problems in patients with impaired renal function
Reye syndrome in children
NSAIDs guidelines for musculoskeletal injuries
- interferes with normal inflammatory response and therefore should avoid use within first 48 hours post-injury (avoid use over 5 days)
- not more effective than simple analgesic (tylenol)
- NOT recomended for DOMS (use simple analgesic instead)