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69 Cards in this Set

  • Front
  • Back

Pharmacology

study of drugs and their interactions with living systems

Drug

any chemical that can affect living processes

Clinical Pharmacology

study of drugs in humans

Therapeutics

use of drugs to diagnose, prevent, or treat disease or to prevent pregnancy


the medical use of drugs

Generic name

name associated w/ specific drug molecule


(acetaminophen)

Trade name

associated with manufacturer


(Tylenol)


can be multiple trade names

Pharmacokinetics

study of drug movement throughout the body


what the body does to the drug


(absorption, distribution, metabolism, excretion)

pharmacodynamics

study of biochemical and physiologic effects of drugs and the molecular mechanism by which those effects are produced


(what the drug does to the body)

indication

what a drug can be used for

Contraindication

pre-existing condition that precludes use of particular drug

precaution

pre-existing condition that significantly increases risk of an adverse reaction to particular drug

adverse drug reaction

any noxious, unintended, and undesired effect that occurs at normal drug doses

Toxicity

adverse reaction caused by excess of drug

drug interaction

drug's activity/effects are altered by another factor


drug-drug, drug-food, drug-supplement

adherence

extent to which a pt's behavior coincides w/ medical advice

tolerance

decreased responsiveness as a result of repeated drug administration

tachyphylaxis

tolerance that develops due to repeated doses over short time

pharmacogenetics

study of how genetic variations affect individual drug responses

FDA

safety and efficacy, drug approval process

Drug Enforcement Administration (DEA)

Enforcement of controlled substances Act


illegal drugs, legal use of controlled subst.

CII

Controlled/scheduled; list by state

Pure Food and Drug Act of 1906

adulteration and misbranding of foods/drugs

Food, Drug, and Cosmetic Act of 1938

sulfanilamide tragedy


testing for safety

Durham-Humphrey Amendment of 1951

prescription/nonprescription categories

Kefauver-Harris Amendment of 1962

effectiveness as well as safety


formalized drug approval process

Controlled Subts Act of 1970

categories for drugs that have a high potential for abuse and addiction


5 schedules

Schedule 1

high potential for abuse (heroin, LSD)


none in US

Schedule II

high potential for abuse, w/ accepted medical use


must have prescription - no refills

Schedule III

lower abuse potential (anabolic steroids, tylenol w/ codeine)


up to 5 refills in 6 months

Schedule IV

lower abuse potential


refill up to 5 times in 6 months


(Valium, Xanax)

Schedule V

lowest abuse potential


OTC in some states


SD does not have any schedule V

Poison Prevention Packaging Act of 70

child-resistant containers

Federal Anti-tempering act of 82

tamper evident packaging - foil covers

Dietary supplement health and education act of 94

classify vitamins, minerals, and herbal products as dietary supplements

Drug Approval Process

takes 10-15 years to get approved


-Preclinical testing (lab & animal)


-Phase I (healthy vol.; safety/pharmacokinetics)


-Phase II (safety and efficacy)


-Phase III (pt w/ condition; effectiveness & adverse effects)


-Phase IV (post market surveillance)

Side Effect

secondary effect produced at therapeutic doses- predictable

Allergic reaction

immune response

Idiosyncratic effect

uncommon drug response; not necessarily be assoc. w/ drug - opposite of what was expected


(Benadryl)

Iatrogenic disease

disease produced by drugs

physical dependence

withdrawal symptoms upon termination

Carcinogenic effect

cancer-causing

Teratogenic effect

drug-induced birth defect


difficult to identify


Cat. A - remote risk


Cat B - slightly more risk (studies not done in women)


Cat C - greater risk


Cat X - proven risk of fetal harm(risk outweighs benefit)

absorption

movement of drug from its site of administration into the blood

Distribution

drug movement from the blood to the interstitial space of tissues & from there into the cells

Metabolism

enzymatically mediated alteration of drug structure

Excretion

movement of drugs and their metabolites out of body

Bioavailability

ability of drug to reach the circulation intact from site of administration

enteric-coated preparations

dissolve in intestine

Sustained release

steadily release drug over long period

absorbency during pregnancy

increased absorption time

pediatric absorption

lower acidity (higher pH)

Geriatric absorption

rate of absorption is slower, gastric acidity reduced

Distribution factors

1. blood flow to tissues


2. ability of drug to exit vasculature


3. ability of drug to enter cells

Peds protein binding

limited due to low albumin; increase in free amt of drug (adult level by 1)

Metabolism

(biotransformation)


most occurs in liver


cytochrome P450

metabolic tolerance

accelerated drug metabolism - drug clears system faster

metabolism in pregnancy

increases

Steps in renal drug excretion

1. glomerular filtration


2. tubular reabsorption


3. active tubular secretion

Excretion in pregnancy

increase - double renal blood flow by 3rd trimester

Pediatric excretion

decreased - low renal blood flow

how to assess renal function

creatinine clearance

half-life

time required for amt of drug in body to decrease 50%

receptors

functional macromolecule in a cell to which a drug binds to produce its effects

Affinity

strength of attraction between drug and receptor (potency)

intrinsic activity

ability of drug to activate receptor after binding (efficacy)

Agonist

activate receptors; bind well & produce response

Antagonists

block actions; decrease body's response

partial agonists

mimic action like agonist w/ reduced intensity

physical or chemical interactions

do not involve receptors