click below
click below
Normal Size Small Size show me how
Pharmacology first
Exam 1
| Question | Answer |
|---|---|
| drug | any chemical that can affect the living process - all chemicals fall into this category |
| pharmacology | study of drugs and their actions with living systems |
| clinical pharmacology | study of drugs in humans, both patients and in healthy volunteers |
| therapeutics | use of drugs to diagnose, prevent or treat disease, or prevent pregnancy. or use of medical drugs |
| 3 most important characteristics that any drug can have | effectiveness, safety, selectivity |
| effectiveness | elicits response for which is given - most important property a drug can have |
| safety | safe drug that cannot produce harmful effects - even if administered in very high doses for a very long time. no such thing as a safe drug |
| selectivity | elicits only the response for which it is given - no such thing as selective drug, all drugs produce side effects |
| reversible action | drug actions to subside within an appropriate time |
| predictability | would be very help if we knew how a given patient will respond. predictions cannot be guaranteed, must tailor therapy to the individual |
| ease of administration | simple to administer, convenient route |
| freedom from drug interaction | when taking two or more drugs, those drugs can interact |
| low cost | easy to afford |
| chemical stability | ideal drug would have a long shelf-life |
| simple generic name | drug name that is easy to pronounce and recall |
| therapeutic objective | provide maximum benefit with minimum harm |
| factors that determine the intensity of drug responses | administration, pharmacokinetics, pharmacodynamics |
| administration | dosage size and the route and timing are important determinants of drug responses |
| pharmacokinetics | drug absorption, drug distribution, drug metabolism, and drug excretion |
| pharmacodynamics | impact of drugs on the body |
| generic drug or nonproprietary name | assigned by US adopted names council, or nonproprietary or US adoptive name, less complex than chem names but more complex than trade names |
| trade or proprietary name | names which a drug is marketed, with intention that they will be easy for nurses, md, etc to recall and pronounce, must be approved by fda |
| functional or class drug name | classified in two ways: pharmacologic family ( beta-adrenergic blockers) and therapeutic family (drugs for angina pectoris, drugs for hiv infection) |
| Legal drug description | |
| controlled substances act of 1970 | set rules for the manufacture and distribution of drugs considered to have the potential for abuse and defines the 5 categories of substances - schedule, I, II, III, IV, V |
| schedule I | no accepted medical use in US and are deemed to have high potential for abuse. heroin, mescaline, lsd |
| schedule II | drugs must be typed or filled-out by prescriber. opiods - codeine, psychostimulants - amphetamine, barbiturates - amobarbital |
| schedule III | precription may be oral or written. opioids - hydrocodone, stimulants - aprobarbital, anabolic steroids - testosterone |
| schedule IV | has a low potential for abuse relative to the drugs or other substances in schedule III, has a currently accepted medical use, Abuse of the drug or other substance may lead to limited physical dependence or psychological dependence |
| schedule V | has a low potential for abuse relative to the drugs or other substances in schedule IV, The drug or other substance has a currently accepted medical use in treatment. |
| study of drugs in humans | clinical pharmacology |
| study of drugs and their interactions with living systems is the definition of | pharmacology |
| therapeutics or pharmacotherapeutics | is defined as the use of drugs to diagnose, prevent, or treat disease to prevent pregnancy |
| any chemical that can affect living processes is a | drug |
| three most important characteristics that any drug can have are | effectiveness, safety, selectivity |
| pharmakon | drug or poison |
| antibacterial effects of tetracycline are reduced by | dairy, antacids, or iron |
| objective of drug therapy is to provide | max benefit with min harm |
| four major pharmacokinetic processes are | absorption, distribution, metabolism, excretion |
| pharmacodynamics may be thought of as | study of what drugs do to the body and how they do it |
| six rights of drug administration | drug, patient, dose, route, time, and documantation |
| most likely member of the healthcare team to observe and evaluate drug responses | the nurse |
| 3 basic goals of pre-administration assessment of medications are | baseline data, ID high risk patients, assess patients capacity for self care |
| important predisposing factors in ID of high-risk patients are | pathophysiology, genetic, drug allergies, pregnancy, old age, and extreme youth |
| Certain drugs have more than one indication, and the dosage may differ depending on the indication for which the drug is used. Aspirin is given in low doses to ____________ and in high doses to __________? | relieve pain, suppress inflamation |
| Measures to reduce adverse effects of medication administration include _______________, ___________________, and? | ID high risk pts, pt education, and causes of adverse effects |
| Patients taking insulin therapy should be taught that early signs of hypoglycemia include __________ and? | sweating, increased HR |
| A _____can be defined as a preexisting condition that significantly increases the risk of an adverse reaction to a particular drug, but not to a degree that is life threatening? | contraindication |
| Among geriatric patients, the most common cause of failed self-medication is? | drug was not needed in dosage prescribed |
| A harmless side effect of rifampin is? | loss of appetite, HA |
| The first legislation to regulate drug safety passed in 1938 was the? | food, drug, and cosmetic act |
| In 1962, Congress passed the___in response to the thalidomide tragedy that occurred in Europe in the early 1960s. | harris-kefauver amendments |
| The first American law to regulate drugs was the? | federal pure food and drug act of 1906 |
| In the early 1960s, thalidomide was widely used by pregnant women, and thousands of infants were born with____, a rare birth defect characterized by the gross malformation or complete absence of arms or legs. | phocomelia |
| Under conditions of the Controlled Substance Act, Schedule I drugs have | no accepted medical use in the us and deemed to have high potential for abuse - heroin, mesculine, LSD |
| In the United States, the estimated cost of developing a new drug can exceed _ and require____to _____ years for completion. | 800 million, 6 to 12 years |
| are the most reliable way to objectively assess drug therapies? | RCT's or randomized controlled trials |
| Phase I drug trials are usually conducted in ___________, whereas Phase II and Phase III trials are tested in? | healthy volunteers, patients |
| The ___constitutes a description of a drug using the nomenclature of chemistry. The ____is assigned by the U.S. Adopted Names Council, and the_____, __, or __ are names under which a drug is marketed | Chemical name, generic, tradename, proprietary or brandname |
| Drugs that can be purchased without a prescription are referred to as? | OTC |
| is the study of drug movement through the body? | pharmacokinetics |
| In order for a drug to directly penetrate membranes, it must be? | lipid soluable |
| Factors that affect drug absorption include? | rate of dissolution, surface area, bloodflow, lipid solubility, ph partitioning |
| consist of drugs that have been covered with a material designed to dissolve in the intestine but not the stomach? | enteric coating |
| most drug metabolism takes place in the?` | liver |
| Nonrenal routes of drug excretion include? | bile, lungs, sweat, saliva, breast milk, feces |
| Three procedures that can be used to reduce fluctuations in drug levels are? | continuous infusion, depot preparation, reduce size and dose and dosing interval |
| The therapeutic range of a drug lies between the____and____? | MEC or minimum effective concentration, toxic concentration |
| the____account for the majority of drug excretion? | kidneys |
| oral administration is | easy, convenient, inexpensive |
| is defined as the study of the biochemical and physiologic effects of drugs and the molecular mechanisms by which those effects are produced? | pharmacodynamics |
| largest effect a drug can produce is called the | maximal efficacy |
| refers to the amount of drug we must give to elicit an effect | potency |
| is any functional macromolecule in a cell to which a drug binds to produce its effects? | receptor |
| The function of the transcription factors is to? | regulate protein synthesis |
| The modified theory ascribes two qualities to drugs: affinity and intrinsic activity. Affinity refers to the____, and intrinsic activity refers to? | strength, ability to activate a receptor upon binding |
| Drugs that mimic the body’s own regulatory molecules are called __, and drugs that block the actions of endogenous regulators are called? | agonists, antagonist |
| When the receptors of a cell are continually exposed to an agonist, the cell usually becomes less responsive; the cell is said to be ___or __or to have undergone___? | desensitized, refractory, down regulation |
| The four primary families of receptors are? | cell membrane-embedded enzymes, ligand-gated ion channels, g protein-coupled receptor systems, transcription |
| The therapeutic index, determined using laboratory animals, is defined as? | measure of drugs safety |
| Patients receiving both halothane and succinylcholine may develop? | malignant hyperthermia |
| When two drugs interact, there are three possible outcomes? | 1. one drug intensifies effects of other. 2. reduces effects of other 3. combo produce new response not seen with either drug alone |
| When a patient is taking two medications and one drug may intensify the effects of the other, the interaction is termed? | potentiative |
| Interactions that result in reduced drug effects are often termed? | inhibitory |
| Direct interactions are most commonly found when drugs are combined? | in IV solutions |
| Interactions are especially important for drugs that have a___therapeutic index. | low or small |
| Some foods cause decreased absorption of drugs. Absorption of digoxin is significantly reduced by? | wheat bran, rolled oats, sunflower seeds |
| The most dramatic example of drug-food interactions that sometimes increase toxicity is the interaction between? | monoamine oxidase inhibitors and tyramine rich foods |
| Grapefruit juice raises drug levels mainly by inhibiting? | metabolism |
| When grapefruit juice is consumed on a regular basis, inhibition can persist up to how long after the last glass? | 3 days |
| Any noxious, unintended, and undesired effect that occurs at normal drug doses is defined by the World Health Organization as? | adverse drug reaction, or ADR |
| Among the more mild adverse drug reactions are? | drowsiness, nausea, itching, and rash |
| Severe adverse drug reactions include? | depression, neutropenia, hepatocellular injury, anaphylaxis, hemorrhage, or death |
| a side effect is defined as? | nearly unavoidable secondary drug effect produced by therapeutic doses |
| is an adverse drug reaction caused by excessive dosing? | toxicity |
| Most serious reactions are caused by just one drug family? | penicillins |
| Other drugs are noted for causing allergic reactions include the __and the ___of compounds? | NSAIDS, Sulfonamide group |
| An uncommon drug response resulting from a genetic predisposition is called? | idiosyncratic |
| which term is used to denote a disease produced by drugs? | iatrogenic disease |
| A state in which the body has adapted to prolonged drug exposure in such a way that an abstinence syndrome will result if drug use is discontinued is known as? | physical dependence |
| Drug-induced birth defects are referred to as? | teratogenic |
| The patient’s last line of defense against medication errors made by others is the? | Nurse |
| Dosage adjustments based on which method provide a more precise means of controlling drug responses than do adjustments based on weight alone? | surface area |
| Drug sensitivity varies with age. In_____heightened drug sensitivity is the result of? | very young, organ immaturity |
| In the___heightened sensitivity results largely from? | elderly, organ degeneration |
| Why do we not know much about gender-related differences in drug therapy? | drug research only done on men |
| Perhaps the most important example of an altered drug effect occurring in response to electrolyte imbalance involves digoxin and? | potassium levels, when depressed - induced dysrhythmias |
| Decreased responsiveness to a drug, as a result of repeated drug administration, is called? | tolerance |
| The type of tolerance associated with long-term administration of drugs such as morphine and heroin is? | pharmacodynamic |
| A form of tolerance that can be defined as a reduction in drug responsiveness brought on by repeated dosing over a short time is called? | tachyphylaxis |
| is defined as that component of a drug response that is caused by psychologic factors and not by the biochemical or physiologic properties of the drug? | placebo effect |
| refers to the ability of a drug to reach the systemic circulation from its site of administration? | bioavailablity |
| Is the study of how genes affect individual drug responses? | pharmacogenomics |
| By the third trimester, renal blood flow in the pregnant woman has? | doubled, causing a large increase in glomerular filtration rate |
| False, all drugs can closs | |
| The effect of a teratogen is highly dependent on? | when the drug is given |
| Symptoms of withdrawal syndrome in the infant include? | shrill crying, vomiting, extreme irritability |
| Of the genetically based anomalies,which is the most common? | down syndrome |
| Gross malformations are produced by exposure to teratogens during the? | embryonic period |
| Teratogen exposure during which period usually disrupts the function rather than gross anatomy? | fetal period |
| to produce a monster | teratogen |
| which teratogen is an estrogenic substance that causes vaginal cancer in female offspring 18 or so years after birth? | diethylstolbestol |
| which category are the most dangerous drugs and known to cause human fetal harm? | category X |
| One criterion to prove that a drug is a teratogen is the drug must cause a? | characteristic set of malformations |
| Which drugs are able to enter breast milk readily? | lipid soluble |
| Drug sensitivity in the very young results largely from? | organ system immaturity |
| Drug sensitivity in the elderly results largely from? | organ system degeneration |
| The pediatric age group includes all patients younger than? | age 16 |
| Premature infants? | less than 36 weeks |
| Full-term infants | 36 to 40 weeks |
| Neonates | 1st 4 postnatal weeks |
| infants | weeks 5-52 postnatal |
| children | 1-12 years |
| adolescents | 12-16 years |
| Pediatric drug therapy is difficult because of? | insufficient drug information |
| Gastric acidity does not reach adult values until which years? | 2 years old |
| How do drugs affect the blood-brain barrier of the infant? | its not developed at birth, easy access to CNS |
| Complete maturation of the liver is accomplished by age? | 1 year |
| Adult levels of renal function are achieved by age? | 1 year |
| In the pediatric population, adverse drug reactions to fluoroquinolones may cause? | tendon rupture |
| pediatric population, adverse drug reactions to nalidixic acid may cause? | cartilage erosion |
| Although pharmacokinetically similar to adults, children do differ in one important way: They metabolize drugs? | faster than adults |
| The method of conversion of adult dosages of drugs to pediatric dosages of drugs used most commonly is based on? | surface area |
| The principles underlying complication to drug therapy in the elderly include? | poor adherence, multi drug therapy, multi severe illnesses, altered pharmacokinetics |
| Altered absorption of drugs in the elderly may result in? | delayed drug response |
| The four major factors that can alter drug distribution in the elderly include? | increase % body fat, decrease % in lean body mass, decrease in total body water, decrease concentration of serum albumin |
| Because of reduced _____levels, protein binding of drugs decreases, causing level of? | albumin, free drug to rise |
| The most important cause of adverse drug reactions in the elderly is? | accumulation secondary to reduce renal excretions |
| In the elderly, the proper index of renal function is? | creatinine clearance |
| Adverse drug reactions are how many times more common in the elderly than in younger adults. | 7 times more common |
| Factors underlying the increase in adverse reactions in the geriatric population include? | decreased renal function, polypharmacy, increase severity of illness, multi pathologies, drugs that have a low therapeutic index, altered pharmacokinetics, inadequate supervision of long term therapy, poor patient adherence |
| Identifies drugs with a high likelihood of causing adverse effects in the elderly? | beers list |
| which percent or more of elderly patients fail to take their medications as prescribed. | as many as 40% |