Lesson 2 Flashcards

1
Q

aspirin can relieve pain

A

analgesic

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2
Q

reduce fever

A

antipyretic

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3
Q

name assigned to the drug differentiated from trade name by initial lowercase letter; never capitalized.

A

Common or general name

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4
Q

Individual drugs that represent groups of drugs.
May be the first drugs of this group to be developed (e.g., penicillin for antibiotics, morphine for opioid analgesics)

A

Prototype drugs

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5
Q

the name which the pharmaceutical company identifies it’s product; copyrighted and used exclusively by that company; can be distinguished from generic name by Capitalized first letter and often shown on labels and references with the symbol after the name (for registered trademark)

A

Trade name

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6
Q

The exact molecular formula of the drug; usually a long, very difficult name to pronounce and of little concern to the health care worker.

A

Chemical name

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7
Q

name of the drug as it appears in the official reference, the USP/NF; generally the same as the generic name

A

Official name

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8
Q

prescription drug; determined unsafe for OTC purchase because of possible side effects if taken indiscriminately; includes birth control pills, antibiotics, cardiac drugs, hormones etc..indicated in the Physician’s desk Reference by the symbol to the far right of the trade name

A

Legend drugs

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9
Q

drug controlled by prescription requirement because of the danger of addiction or abuse..indicated by schedule of numbers C-I to C-V.

A

Controlled substance

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10
Q

not approved for medical use and have high abuse potentials; LSD, heroin, peyote, ecstasy (3,4 methyenedioxy-methamphetamine)

A

Schedule I

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11
Q

used medically. High abuse potential (methadone, meperidine, cocaine, pentobarbital, Tylox)

A

Schedule II

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12
Q

less potential for abuse than I and II but may lead to psychological or physical dependence (Vicodin, Tylenol with codeine)

A

Schedule III

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13
Q

drugs have some potential for abuse (Valium, Dalmane, Klonopin)

A

Schedule IV

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14
Q

contain moderate amounts of controlled substances. An example is Lomotil (atropine and diphenoxylate)

A

Schedule V

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15
Q

studies in pregnant women failed to show risk to the fetus

A

Category A

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16
Q

animal studies have failed to show a risk to the fetus but there are no adequate studies in women

A

Category B

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17
Q

animal studies have shown an adverse effect on the fetus, no adequate human studies, benefits may outweigh risks

A

Category C

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18
Q

positive evidence of human fetal risk

A

Category D

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19
Q

animal or human studies have shown fetal abnormalities or toxicity

A

Category X

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20
Q

a list of medical conditions or diseases for which the drug is meant to be used. Ex. Diphenhydramine HCL (Benadryl) indicated fro allergic rhinitis, mild allergic skin reactions, motion sickness and mild cases of parkinsonism.

A

indications

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21
Q

A description of the cellular changes that occur as a result of the drug. Ex. Benadryl appears to compete with histamine for cell receptor sites on effector cells.

A

actions

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22
Q

A lists of conditions for which the drug should not be given. Ex. Benadryl should not be given on pregnant and lactating mothers

A

contraindication

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23
Q

a list of conditions or types of patients that warrant closer observation for the specified side effects when given the drug.
Ex. Benadryl have atropine like effect and must be used cautiously with patient with bronchial asthma or hypertension or with older adults

A

cautions

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24
Q

a list of possible unpleasant or dangerous secondary effects, other than desired effect. Ex Benadryl side effects includes dizziness, sedation, disturbed coordination, epigastric distress, anorexia and thickening of bronchial secretions

A

Side effects and adverse reactions

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25
3 side effects associated with antibiotics
- ototoxicity - nephrotoxicity - photosensitivity
26
A lists of drugs or foods that may alter the effect of the drug and usually should not be given during the same course of therapy. Ex. MAO inhibitors intensify effect of Benadryl causing serious BP  changes and death when taken with other drugs and some food.
interactions
27
SOURCES OF DRUGS
- PLANTS - MINERALS - ANIMALS - SYNTHETIC
28
reaches widespread area of the body
Systemic
29
is limited to area of the body where it administered
Local
30
describes the pharmacokinetic processes which follow a given dosage regimen.
LADME
31
the release of the drug from it's dosage form.
liberation
32
the movement of drug from the site of administration to the blood circulation.
absorption
33
the process by which drug diffuses or is transferred from intravascular space to extravascular space (body tissues).
distribution
34
the chemical conversion or transformation of drugs into compounds which are easier to eliminate.
metabolism
35
the elimination of unchanged drug or metabolite from the body via renal, biliary, or pulmonary processes
excretion
36
the first step in the process by which medication enters the body and liberates the active ingredient that has been administered. The pharmaceutical drug must separate from the vehicle or the excipient that it was mixed with during manufacture.
liberation
37
process that occurs from the time a drug enters the body to the time it enters the bloodstream to be circulated
absorption
38
Factors affecting absorption
dosage form, route of administration, blood flow to the site of administration, gastrointestinal function, presence of food or other drugs
39
Is the portion of a dose that reaches the systemic circulation and is available to act on body cells
bioavailability
40
refers to the measurement of the time it takes the body to break down and excrete one half of the drug. This is an important factor in the creation of drugs because it tells the manufacturer how long it takes the body to rid itself of the drug.
half life
41
Involves the transport of drug molecules within the body Protein binding is an important factor in drug distribution
distribution
42
After the drug is absorbed into the bloodstream, it is carried by the blood or tissue fluids to its sites of pharmacologic action, metabolism and excretion
distribution
43
is composed of capillaries with tight walls which limits movement of drug molecules into brain tissue
Blood-brain barrier
44
Drug distribution during pregnancy and lactation is unique as most drugs cross the?
placenta or in the case of lactation, pass into breast milk
45
Most drugs form a compound with plasma proteins,--------, which act as carriers
albumin
46
allows a part of a drug dose to be stored and released as needed
protein binding
47
Method by which drugs are inactivated or biotransformed by the body
metabolism
48
Most drugs are metabolized by the --------- enzymes in the liver Liver contains complex system of enzymes, three of which are key in the metabolism of medications/drugs
cytochrome p450
49
catalyze the chemical reactions which ultimately metabolize the medications
CYP enzymes
50
accelerates drug metabolism. Result is that larger doses of the drug may be need for therapeutic effects.
enzyme induction
51
may occur with concurrent administration of two or more drugs that compete for the same metabolizing enzymes (e.g., Dilantin, EES(erythromycin ethyl succinate), Tagamet)
enzyme inhibition
52
Oral meds are generally absorbed by the GI tract and carried to the liver. Drug may undergo extensive metabolism leaving little for systemic use. This is called the?
first pass effect
53
is a phenomenon of drug metabolism whereby the concentration of a drug, specifically when administered orally, is greatly reduced before it reaches the systemic circulation.
first pass effect
54
Lab measurement of the amount of a drug in the blood at a particular time
serum drug levels
55
must be present before a drug exerts its pharmacologic action on body cells
Minimum effective concentration (MEC)
56
time during which serum drug levels are at or above the MEC (may measure serum drug levels when the drugs have a low therapeutic index)
duration of action
57
Refers to the elimination of a drug from the body Most are excreted by the kidneys although some are excreted in the bile then the feces
excretion
58
 is a major mechanism for terminating drug action and eliminating drug molecules from the body
Hepatic drug metabolism or clearance
59
the response of the body to the drug. It refers to the relationship between drug concentration at the site of action and any resulting effects namely, the intensity and time course of the effect and adverse effects.
PHARMACODYNAMICS
60
Involves drug actions on target cells and the resulting alterations in cellular biochemical reactions
Pharmacodynamics--Receptors
61
Most drugs chemically bind with receptors at the cellular level
Pharmacodynamics--Receptors
62
Drug-receptor complex initiates physiochemical reactions that stimulate or inhibit cellular functions
Pharmacodynamics--Receptors
63
Receptors vary in type, location, number and functional capacity
Pharmacodynamics--Receptors
64
When drug molecules chemically bind with cell receptors, pharmacologic effects result from agonism or antagonism
Pharmacodynamics--Receptors
65
are drugs that produce effects similar to those produced by naturally occurring hormones, neurotransmitters and others. May accelerate or slow normal cellular processes depending on the type of receptor activated. Examples of Opioid -------: Morphine, Hydrocodone (pain relief /euphoria)
Agonists
66
drugs that inhibit cell function by occupying receptor sites. Not all drugs act on receptors. Examples include: antacids, osmotic diuretics, chelators example of Opioid receptors, examples of ------- are Naloxone (Narcan), Naltrexone and Nalmefene.
Antagonists
67
is a drug, chelating substance, or a chemical that counteracts (neutralizes) the effects of another drug or a poison.
antidote
68
the action of 2 drugs working together in which one helps the other simultaneously for an effect that neither could produce alone.  Drugs that work together are synergistic. Ex. Use of two opioids like morphine and oxycodone may be more effective than just one because both opioids have a slightly different action on opioid receptors
Synergism
69
giving small amounts can relieve pain safely ex. Promethazine (phenergan) and meperidine (demerol).  Large amounts could be addictive.
desirable synergism
70
sedatives and barbiturates given in combination can depress CNS to dangerous levels depending on the strength of each
undesirable synergism
71
the action of 2 drugs in which one prolongs or multiplies the effect of the other. EX, many macrolides (erythromycin, troleandomycin), which are antibiotics, potentiate the effects of ergot derivatives such as ergotamine which is a vasoconstrictor agent. The explanation of this potentiation responsible of serious adverse effects is that macrolides inhibit the inactivation of ergotamine which accumulates in the body at toxic levels
potentiation
72
to build up a high level of some forms of penicillin (antibiotic) in the blood, the drug probenecid (benemid) antigout  given simultaneously.  Benemid potentiates the effect of penicillin by slowing the excretion rate of the antibiotic
desirable potentiation
73
toxic effect may result if cimetidine (tagamet/gastric antisecretory) is given simultaneously with tofranil(antidepressant).  Tagamet potentiates the level of antidepressant concentration in the blood.
undesirable potentiation
74
Variables that affect drug actions
- Dosage - Route - Drug-diet interactions. Food may slow absorption or foods may actually interact with certain medications (tyramine and MAO inhibitors; tetracycline and milk products; ingestion when taking certain antihypertensive medications - Drug-drug interations-additive effects such as seen with sedatives and ethanol. Synergism as seen with acetaminophen and codeine. - Antidote—drug can be given to antagonize the toxic effects of another drug
75
Variables that affect drug actions
- Age - Pregnancy - Body weight - Gender-hormonal effects - Pathologic conditions - Placebo response
76
amount of drug given for a particular therapeutic or desired effect.
dosage
77
smallest amount of drug that produce therapeutic effect
minimum dose
78
largest amount of drugs that will produce desired effect without producing symptoms of toxicity
maximum dose
79
initial high dose (Max. dose) use to quickly elevate the level of drug in the blood followed by a series of low maintenance doses.
loading dose
80
dose required to keep the blood level at a steady state in order to maintain the desired effect
maintenance dose
81
amount that will produce harmful side effects or symptoms of poisoning
toxic dose
82
dose that causes death
lethal dose
83
customarily given (ave. adult dose based on body weight of 150lbs; adjusted according to variations from the norm
therapeutic dose
84
ROUTE 2 Category
1.GI routes Oral (PO) Nasogastric (NG) Rectal (R) 2.  Parenteral Sublingual( SL) or buccal Injection routes ·Intravenous (IV) ·Intramuscular (IM) ·Subcutaneous (subQ) ·Intradermal (ID) ·Intracardiac, intraspinal, intracapular Topical (T) ·Dermal (D) ·Mucosal Inhalation
85
Oral route
easiest
86
fastest administered by IV push or bolus (Concentrated drug solution)or diluted infused slowly by IVdrip. Best route for emergency treatment
IV route
87
are choice if NPO status or drug not suitable for GI absorption
PARENTERAL ROUTES
88
is fairly rapid because muscles are highly vascular, desirable to retard the speed of absorption, can be added to oily base drugs
IM route
89
causes development of physical defects to fetus in vitro
teratogenic
90
unique, unusual response to a drug. Ex. Tranquilizer causes agitation and excitement  rather than tranquility
idiosyncracy
91
Opposite effect from that expected
paradoxical
92
decreased response to a drug that develops after repeated doses.  To achieve desired effect dosage is increased or replaced.
tolerance
93
Acquired need for a drug that may produce psychological or physical symptoms of withdrawal when drug is discontinued. Psychological-craving, no physical symptoms of withdrawal other than anxiety Physical – cells actually have need of the drug like retching, nausea, pain tremors or sweating
dependence
94
immune response (allergy) to a drug in varying degrees -rash , hives after 3-4 days of drug therapy
hypersensitivity
95
severe, possibly fatal. Allergic (hypersensitivity) response -signs are itching, urticarial(hives), hyperemia (reddened warm skin) vascular collapse, shock, cyanosis, laryngeal edema, dyspnea.
anaphylactic reaction