Competency 1 Flashcards
Pharmacodynamics
Pharmacodynamics is the study of the way drugs affect the body.
Dose response
Dose response is the relationship between the minimal versus the maximal amount of drug dose needed to produce the desired drug response.
- Some patients respond to a lower drug dose
- others need a high drug dose to get desired response.
Maximal efficacy
- max drug effect
- Ex. morphine and tramadol hydrochloride (Ultram) are prescribed to relieve pain.
- The maximum efficacy of morphine is greater than tramadol hydrochloride, regardless of how much tramadol hydrochloride is given.
- The pain relief with the use of tramadol hydrochloride is not as great as it is with morphine.
Onset of action
Onset of action is the time it takes to reach the minimum effective concentration (MEC) after a drug is administered.
Peak action
Peak action occurs when the drug reaches its highest blood or plasma concentration.
Duration of action
Duration of action is the length of time the drug has a pharmacologic effect.
Minimum effective concentration
the threshold level of a drug in plasma below which the efficiency of the drug as a treatment drops off sharply.
Drug interaction
A drug interaction is defined as an altered or modified action or effect of a drug as a result of interaction with one or multiple drugs.
Adverse drug reaction
An adverse drug reaction is an undesirable drug effect that ranges from mild untoward effects to severe toxic effects, including hypersensitivity reaction and anaphylaxis
Drug incompatibility
Drug incompatibility is a chemical or physical reaction that occurs among two or more drugs in vitro. In other words, the reaction occurs between two or more drugs within a syringe, IV bag, or other artificial environment outside of the body.
Drug-induced photosensitivity
A drug-induced photosensitivity reaction is a skin reaction caused by exposure to sunlight.
- caused by the interaction of a drug and exposure to ultraviolet A (UVA) light, which can cause cellular damage.
- two types:photoallergy and phototoxicity.
Enzyme inducers
- drugs that promote induction of enzymes, by binding to it or activating
- produce cascade effect of drug function
- ex. Barbiturates like phenobarbital
Enzyme inhibitors
Ex . Anitulcer drug cimetidine ( Tagamet) , decreases metabolism of certain drugs like theophylline, causing increase plasma concentration of theophylline
Receptor theory
Drugs act through receptors by binding to the receptor to produce (initiate) a response or to block (prevent) a response. The activity of many drugs is determined by the ability of the drug to bind to a specific receptor. The better the drug fits at the receptor site, the more biologically active the drug is. It is similar to the fit of the right key in a lock.
Agonist
Drugs that produce a response
Antagonist
drugs that block a response
Nonspecific drug effects
Drugs that affect various sites are nonspecific drugs and have properties of nonspecificity.
-effects may be either desirable or harmful. Drugs that evoke a variety of responses throughout the body have a nonspecific response.
Nonselective drug effects
Drugs that affect various receptors are nonselective drugs or have properties of nonselectivity.
-Drugs that produce a response but do not act on a receptor may act by stimulating or inhibiting enzyme activity or hormone production
Therapeutic index
- therapeutic index (TI) estimates the margin of safety of a drug through the use of a ratio that measures the effective (therapeutic) dose (ED) in 50% of people (ED50) and the lethal dose (LD) in 50% of people (LD50)
- The closer the ratio is to 1, the greater the danger of toxicity.
Therapeutic drug range
The therapeutic range (therapeutic window) of a drug concentration in plasma is the level of drug between the minimum effective concentration in the plasma for obtaining desired drug action and the minimum toxic concentration (the toxic effect).
- includes both protein-bound and unbound portions of the drug
- If the therapeutic range is narrow, such as for digoxin (0.5 to 1 ng/mL), the plasma drug level should be monitored periodically to avoid drug toxicity.
Protein bound drugs
As drugs are distributed in the plasma, many are bound to varying degrees (percentages) with protein (primarily albumin). Drugs that are greater than 89% bound to protein are known as highly protein-bound drugs
Half-life
The half-life (1/2) of a drug is the time it takes for one half of the drug concentration to be eliminated.
peak drug level
the highest plasma concentration of a drug at a specific time
trough level
the lowest plasma concentration of a drug. The trough level measures the rate at which a drug is eliminated; levels are drawn immediately before the next dose of a drug is given.
side effects
physiologic effects not related to desired drug effects
drug toxicity
refers to how poisonous or harmful a substance can be. In the context of pharmacology, drug toxicity occurs when a person has accumulated too much of a drug in his bloodstream, leading to adverse effects within the body.Mar 7, 2016