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Chapter21-IntroPharm
Introduction to Pharmacology
Question | Answer |
---|---|
What can drug salts end with in drugs? | Mesylate, Tartrate, Citrate, Hydrochloride, Sodium, or Potassium |
What can drug names indicate? | Drug class or use |
The mechanism of action of a drug is classified by the different what within the body? | Biological or biochemical changes |
Drugs within the same class often have similiar: | Mechanisms of action, adverse effects, and contraindications |
What does DOC stand for? | Drug of Choice |
What is a drug or drug class that is superior in treating certain conditions? | Drug of Choice |
What is the most frequently prescribed drug called? | Drug of Choice |
What are first line drugs? | Drugs that have acceptable adverse effect profiles |
What drugs are less effective and have more adverse effects? | 2nd, 3rd, 4th line of drugs |
What is pharmacokinetics? | The study of movement and changes in the drug within the body |
What are the four parts of pharmacokinetics? | Absorption, distribution, metabolism, and elimination |
How the drug gets into the bloodstream is the definition to which of the four parts of pharmacokinetics? | Absorption |
What drugs are not absorbed? | IV drugs |
What are the drug absorption factors? | pH of the compartment, lipid solubility, and vascularity of the administration site |
When will a drug stay intact when it enters a body compartment? | When the acidity of the drug and body enviroment are similiar |
The drug ionizes when what happens? | When the acidity of the drug and the body enviroment are dissimiliar |
Drugs are only absorbed as what? | Intact molecules |
When are drugs better absorbed? | In "like" enviroments |
What happens when the body cavity pH is altered? | The drug uptake will also be altered |
What drugs pass easily through the cell membrane? | Lipid soluble drugs |
What are some highly lipid soluble drugs? | Most CNS drugs and anesthetics |
What happens once the drug enters the bloodstream? | The drug disseminates throughtout the body |
Once in the bloodstream, part of the drug remains where? | Free in the plasma |
Once in the bloodstream, the other part of the drug that isn't free in the plasma goes where? | May be stored either bound to plasma proteins or in fat |
Highly lipid soluble drugs stored in fatty tissue include? | Liver, spleen, CNS, and stored fat |
The drugs are also stored as protein-drug complexes bound to either what? | Tissue proteins or plasma proteins |
Drugs bound to proteins exist in equilibrium between what two drug types in the plasma? | Bound drugs and "free" drugs |
What type of drug has a therapeutic effect and can be eliminated from the body? | "Free" drug |
The volume of space the drug occupies in the body is the what? | Volume of Distribution(VD) |
What is large VD? | When the drug is distributed throughtout different body compartments |
What is small VD? | When the drug is concentrated mainly in one place |
What is the loading dose? | A large initial doesage to quickly reach therapeutic levels |
What is drug metabolism? | When drugs undergo changes in the body |
What metabolizes drugs? | Enzymes |
What enzyme is involved in the metabolism of most drugs in the liver? | Cytochrome P450 |
What is Cytochrome P450? | Cytochrome mixed function oxidase system |
In order to be filtered by the kidneys during clearance, drugs must not be what? | Lipid soluble or protein bound |
How are drugs secreted? | Liver, bile, then feces |
What is contraindicate? | When some drugs cannot be used with certain illnesses |
The amount of time it takes for 1/2 of the drug dosage to clear the body is the what? | Drug half-life |
What two things is the drug half-life influenced by? | Rate of elimination and how quickly a drug might be inactivated in the body by enzymes |
What alters drug half-lives? | Altering the clearance rate, pH, altering the elimination rate, and renal and liver dysfunction |
What are some examples that alter drug half-lives? | Acetylcholines and Enterohepatic recycling |
What can range from uncomfortable to life threatening? | Adverse effects |
Adverse effects advise to understand the mechanism of drug's action with what to determine the possible effects? | Physiology background |
What are the 3 absorption level drug drug interactions? | Binding interactions, change pH of the enviroment, and change in local blood flow |
What is the drug distribution interaction? | Protein binding interactions |
Many drugs bind to the same what? | Plasma proteins |
Most drugs bind to what protein? | Albumin |
During interactions at clearance, how does the body expel the drug? | Lungs, urine, and bile |
Some drugs "compete" for the same enzyme or what? | Limit the enzymes activity |
What is agonists? | A drug that mimics the actions of a substance in the body |
What type of substance does the agonist mimic? | Endogeneous substances |
What are two ways an agonists can work? | Stimulating a cellular or biochemical pathway or inhibiting the breakdown of endogeneous substances |
When one drug decreases or prevents the actions of another drug is called what? | Antagonistic effect |
The antagonistic effect prevents the function of what when binded to it? | Receptor |
When is a receptor stimulated? | At the moment of contact |
What are partial agonists? | Weak agonists that acts as agonists unless a stronger agonists is present then it acts as an antagonist |
When are partial agonists useful? | When there are erratic levels of strong agonists |
When two drugs have the same effect, the effect of one will be added to the effect of the other is called what? | Additive effects |
What is synergistic effect? | When two drugs have the same physiological effect, but different mechanisms and one potentials the effect of the other such that the combined effect is greater than the sums of both drugs |
What two substances have a dangerous synergistic effect? | CNS depressants and alcohol |
What is it called when one drug decreases or blocks the actions of another drug? | Antagonistic effect |